Melanin-like nanofibers with highly ordered structures achieve unprecedented specific electromagnetic interference shielding efficiency

Melanin-like nanofibers with highly ordered structures achieve unprecedented specific electromagnetic interference shielding efficiency | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Article Melanin-like nanofibers with highly ordered structures achieve unprecedented specific electromagnetic interference shielding efficiency Yiwen Li, Peng Chen, Shibo He, Tianyou Wang, Chencan Wang, Junru Tao This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-6020493/v1 This work is licensed under a CC BY 4.0 License Status: Published Journal Publication published 03 Aug, 2025 Read the published version in Nature Communications → Version 1 posted You are reading this latest preprint version Abstract Lightweight, high-performance electromagnetic shielding materials are crucial for protection and detection, relying heavily on the precise design of electromagnetic response structures. Conventional shielding materials often involve complex fabrication of conjugated composites or graphitization of organic materials, facing challenges in balancing their performance and processability. As such, seeking intrinsically conjugated materials with superior processability is crucial. Natural melanin and melanin-like polymers have garnered considerable attention as emerging promising energy-dissipating substances with a wide range from ionizing radiation to infrared light. In this work, we have engineered those bioinspired polymers with highly ordered microstructures as a new class of promising high-performance and lightweight electromagnetic shielding materials for the first time. The key process is to use 5, 6-dihydroxyindole ring tetramer framework to construct highly ordered melanin-like nanofibers by tuning the intramolecular π-π stacking, which could facilitate the well regulation of long-range electron conduction and electromagnetic matching features. The resulting melanin-like nanofibers could be easily transformed into carbon aerogels with outstanding microwave absorption performance, i.e. a maximum reflection loss of -68.87dB and effective absorption bandwidth of 5.25GHz during 2-18GHz. In the X-band, the aerogel reached the considerable absolute EMI shielding effectiveness value of 47909.9 dB cm 2 /g, the highest for organic carbon materials reported to date. This work represented the first successful extension of the electromagnetic response of melanin-like polymers into the microwave spectrum, paving the way for practical applications of bioinspired polymers in EMI shielding and stealth technologies. Scientific community and society/Business and industry/Engineering/Electrical and electronic engineering Biological sciences/Biotechnology/Nanobiotechnology/Nanostructures melanin polydopamine microwave absorption electromagnetic interference shielding nanofiber Figures Figure 1 Figure 2 Figure 3 Figure 4 Figure 5 1. Introduction With the increasingly stringent requirements of aerospace and military equipment for combat speed and concealment in complex environments, electromagnetic shielding materials are undergoing iterative upgrades, aiming for higher performance and lighter weight. 1 , 2 Conventional metal materials and their composites usually suffer from unsatisfactory density, leading to the increasing attentions on highly conjugated inorganic materials such as carbon nanotubes and graphene, graphene, etc., which could be compounded with polymers or directly processed into material forms via customized methods. However, due to their poor compatibility, there is an inevitable dilemma that conjugate structures make it difficult to construct effective adaptive networks. 3 , 4 An Alternative strategy is to graphitize natural or organic materials to obtain a high degree of conjugated structures, However, the inherent defects would be present in the graphitized products, which is difficult to regulate accurately. The resulting electromagnetic shielding materials often exhibited limited performance. 5 Therefore, the key to breaking through the lightweight and high-performance electromagnetic shielding materials is to develop a new class of intrinsic conjugated organic materials with well-regulated structures and functions. 2 Melanin has been regarded as a class of emerging promising energy-dissipating biomacromolecules in nature, which could efficiently absorb and transform a broad spectrum of energy due to its unique and chaotic assembled structures. 6 – 9 Melanin and melanin-like polymers offer abundant chemical versatility and significant potential for structural regulation, making them easily combinable with various materials. Considerable research has been focused on the structural and interaction regulation of melanin-like polymers, which have shown remarkable responses to a wide range of electromagnetic waves, from ionizing radiation to near-infrared (NIR) light, offering radiation protection, visible light absorption, and photothermal conversion. 10 – 15 However, reports on melanin-like materials exhibiting effective absorption in the microwave band are quite lacking, since their disordered structures cannot support long-range electron transfer paths to respond to long-wavelength energy. 8 Thus, if we could construct melanin-like materials with highly ordered microstructure through appropriate supramolecular engineering strategies, it is expected to extend the energy dissipation range of melanin-inspired polymers and break the performance limitations in lightweight, high-performance materials for electromagnetic shielding. Theoretically, the formation process of melanin and melanin-like polymers involves both chemical processes(oxidation, isomerization, rearrangement into 5,6-dihydroxyindole(DHI) tetramers, and coupling reactions between intermediates) and physical assembly through intermolecular interactions, including π-π stacking and hydrogen bonding. Traditional methods typically result in disordered melanin-like materials due to complicated macromolecular structures and cross-linked hydrogen bond networks formed by phenolic hydroxyl groups, which severely inhibit the establishment of long-range ordered structures. Therefore, we speculated that highly ordered melanin structures can be achieved by enhancing the π-π interactions between DHI tetramers and minimizing random chemical reactions and hydrogen bond crosslinking within the macromolecular networks. The resulting highly ordered melanin-like polymers might enable long-range electron conduction and improve electromagnetic response capabilities. One possible way to realize this goal is to increase the proportion of cyclized indole and reduce the disordered crosslinking caused by hydrogen bonding. To accomplish this, we strived to use indole analogs as active species to induce the polymerization process, resulting in improved π-π stacking of the DHI tetramers. This approach could achieve the successful formation of highly ordered melanin-like nanofibers for the first time, to the best of our knowledge. These nanofibers were then processed into ultra-light, high-performance carbon aerogels through typical freeze-drying and pyrolysis treatments. Remarkably, the resulting melanin-inspired aerogels exhibited exceptional electromagnetic interference (EMI) shielding and microwave absorption(MA) properties, with a maximum reflection loss (RL) of -68.87 dB and an effective absorption bandwidth (EAB) of 5.25 GHz in the 2–18 GHz range. In the X-band, with a density of 3.11 mg/cm³ and a thickness of 2 mm, the aerogel achieved an impressive absolute EMI shielding effectiveness (SSE/t), defined as the shielding effectiveness (SE) value divided by the surface density, reaching 47,909.9 dB·cm²/g—currently the highest reported value for organic carbon materials. Additionally, radar cross-section (RCS) simulations were performed, confirming the potential application of these aerogels as intelligent electromagnetic shielding materials for stealth technology. This work demonstrates the successful construction of melanin-like polymers with highly ordered microstructures through the rational regulation of interaction forces, offering a novel way for optimizing the properties of a broad range of bioinspired materials. 2. Result and Discussion 2.1. Fabrication and Characterization of melanin-like nanofibers Conventional melanin-like polymers, such as polydopamine (PDA), typically form isotropic nanoparticles due to their disordered structures. In this work, we introduced indole units with different hydroxyl groups into the conventional melanin polymerization process, aiming to reduce the influence of hydrogen bonding. A one-pot copolymerization of different indole analogs and dopamine monomer in a mixture solution of water and alcohol at room temperature in the presence of ammonium hydroxide was facilely performed, as the typical experimental condition for PDA nanoparticles preparation (Fig. 1 A). We discovered that the PDAs formed with indole or 5,6-dihydroxy indole maintained traditional black nanoparticles, while those synthesized with 5-hydroxyindole exhibited distinct yellow nanofibers prepared under similar conditions (Fig. 1 B-C and Figure S1 ). Ultraviolet-visible spectra further confirmed the presence of characteristic absorption between 300–450 nm (Figure S2), while there is almost no absorption in the rest of the visible region, suggesting that the optical properties of PDA nanofibers are quite different from conventional PDA nanoparticles. Furthermore, we confirmed the existence of the highly ordered structures by transmission electron microscopy (TEM), which revealed a layered structure with an interlayer spacing of approximately 3.4 Å, consistent with classical π-π stacking (Fig. 1 D). We then carefully investigated their chemical structures in detail. Firstly, we used X-ray photoelectron spectroscopy (XPS) to determine the element proportions, which revealed that the molar ratio of hydroxyl indole was 17.8%, consistent with the results from elemental analysis (EA) (Fig. 1 E and Figure S6). Next, we performed the disassembly experiments in various solvents (Figure S7). It was found that the nanofibers were completely disassembled in methanol and acetonitrile, indicating that their assembly was driven by supramolecular forces. The dissolution likely occurred due to the disruption of hydrogen bonds, caused by solvent interactions and competition. Electrospray ionization mass spectrometry (ESI-MS) analysis of the disassembled PDA nanofibers in methanol solution revealed prominent peaks that closely matched the coupled molecules of DHI and 5-hydroxyindole (M1), the dimer of DHI (M2), and the ring tetramer of DHI (M3) (Figure S7). Additionally, the ring tetramer of DHI was successfully isolated using Ultraperformance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS) (Fig. 1 H). Based on the elemental analysis, we calculated the M1 to M3 ratio as 11:10, consistent with the N and O element ratios. To better understand the self-assembly process, we used GROMACS 16 , 17 simulations to model the interactions between these two molecular species at the same ratio, under identical solvent and temperature conditions (Fig. 1 G). Over a simulation time of 1000 ns, the molecules exhibited a general tendency to form fibrous assemblies. Key structural analysis revealed that the tetramer (M3) favored axial packing, likely contributing to the formation of nanofibers (structure 1). Additionally, the interplay of hydrogen bonding, cation-π interactions, and hydrophilic-hydrophobic forces, combined with the planar deflection angles of M1 and M3, led to a deflected, side-by-side arrangement of the fibers. M1 co-stacked via hydrogen bonding and π-π interactions, producing a variety of typical arrangements and corresponding interlayer spacings (structures 2–4). 18 Based on these results, we proposed that the formation of PDA nanofibers follows a specific pathway: in a base-catalyzed environment, dopamine undergoes oxidation, cyclization, and rearrangement to generate 5,6-dihydroxyindole (DHI). During this process, quinone free radicals are formed, which initiate both self-polymerization and copolymerization with indole. Since 5-hydroxyindole has only a single hydroxyl group, it cannot support multidirectional hydrogen bond cross-linking. This limitation facilitates the formation of M3 with outward-facing hydrogen bonds. 18 , 19 Additionally, M3 exhibits a strong π-π conjugation tendency, with the delocalized π-electron cloud over the indole ring promoting directional axial packing. This axial packing provides a potential mechanism for π-electron transport within the material. 19 As the degree of crosslinking varies due to hydrogen bonding between the tetramer and other conjugated structures, nanofibers with different length-to-diameter ratios are formed. This hypothesis was further supported by X-ray diffraction (XRD) analysis (Fig. 1 H), which revealed a highly ordered stacking structure that differs significantly from the amorphous peaks typically observed in conventional PDA nanoparticles. The peaks between 20° and 25° correspond to the π-π stacking region, while the smaller angle peaks likely result from multistage diffraction or other assembled structures. 19 , 20 These findings closely align with the structural predictions obtained from GROMACS simulations. An integral analysis of the XRD data indicated that the amorphous envelope peak region accounts for only 2.1%, further confirming the high degree of ordered microstructures within the PDA nanofibers. Raman spectroscopy (Fig. 1 I) provided additional evidence for the ordered structure. The PDA nanofibers were found to exhibit a sharp and narrow G-peak at 1580 cm⁻¹, in stark contrast to the broader, multiple peaks characteristic of conventional PDA nanoparticles. This sharp G-peak suggested that the molecules within the nanofibers primarily undergo in-plane stretching vibrations, with boundary vibrations suppressed due to their fixed, lattice-like arrangement. This result strongly correlated with the vibration characteristics of the DHI ring tetramer. The narrow peak width further indicates a high degree of uniformity among the molecular units participating in in-plane vibrations within the PDA nanofibers. 21 Upon magnifying the Raman spectrum, a very small signal in the D-peak region was detected. Although this peak was visually masked, its area accounts for only 1.61% of the G-peak area. This result was consistent with the XRD findings, reaffirming the highly ordered structures within the PDA nanofibers. 2.2. Fabrication and characterization of PDA carbon aerogels The as-synthesized PDA nanofiber aerogels were carbonized in a tubular furnace under a flowing nitrogen atmosphere at various temperatures (600°C, 700°C, 800°C, and 900°C) for 2 hours, with a heating rate of 5°C/min(Fig. 2 A). The resulting carbon aerogel samples were designated as NFAG-i (i = NFAG-600, NFAG-700, NFAG-800, NFAG-900), respectively. SEM imaging in Fig. 2 B- 2 D confirmed that the carbonized aerogels still retained their long fibrous morphologies, indicating structural stability during carbonization. XPS survey scans shown in Fig. 2 C revealed the removal of N and O elements, leading to the formation of oxygen vacancies and electron-hole pairs within the NFAG samples. These defects act as polarization centers, significantly enhancing the dielectric properties of the material (Fig. 2 E). Additionally, the proportion of sp² carbon in the NFAG samples increased with rising pyrolysis temperatures, which is favorable for electron transport. This trend was further validated by Raman spectroscopy (Fig. 2 F), where the D band (centered at ~ 1350 cm⁻¹) and G band (centered at ~ 1590 cm⁻¹) intensities were analyzed. The D/G ratio (I D /I G ), indicative of the relative proportions of disordered and graphitic carbon, showed a gradual increase in the graphite phase with rising temperatures, reaching an I D /I G value of 82.21% for NFAG-900.FTIR spectra (Fig. 2 G) further corroborated these findings, showing a significant reduction or complete disappearance of organic C = O and C–N peaks, consistent with the XPS results. Notably, π-π stacking in NFAG not only facilitated π-conjugated electron transportation but also contributed to the formation of micropores during heat treatment, since its higher bond length made it more susceptible to such structural changes compared to typical covalent bonds. N₂ adsorption-desorption characterization was used to evaluate the specific surface area (SSA) and pore size distribution of the NFAG samples. The high air-phase volume fraction provided a potential impedance-matching advantage for NFAG in dielectric applications. All samples (Fig. 2 H) exhibited typical type IV isotherms with H1 hysteresis loops, indicative of capillary condensation of N₂. Remarkably, NFAG-900 demonstrated an excellent surface area of 885.65 m²/g, ཞfour times higher than that of carbonized PDA nanoparticles reported previously. 22 The predominant micropores (< 2 nm) play a crucial role in facilitating ion transport, improving electrical applications, and enabling the construction of abundant gas-solid heterostructures. 2.3. Electromagnetic absorption of NFAGs Figures 3 A and 3 B illustrated the primary loss mechanisms in NFAGs. The extensive specific surface area and micropores contributed significantly to the interfacial loss in NFAGs, while the multistage core-skin structure of the fibers generated additional heterogeneous interfacial systems. Debye relaxation polarization in NFAGs could be attributed to numerous defects and residual groups, including oxygen vacancies and electron-hole pairs induced by heat treatment, which facilitated electron accumulation, transfer, and dipole formation. Furthermore, the excellent electrical conductivity of the PDA nanofibers, owing to their ordered structure, played a significant role in ohmic loss. This effect was further amplified by the large aspect ratio and three-dimensional interconnected conductive network formed during heat treatment and sinteringNext, the electromagnetic absorption capacity of NFAGs (NFAG-600, NFAG-700, NFAG-800, NFAG-900) was evaluated, respectively. Generally, an RL value below − 10 dB is considered the threshold for effective absorption, indicating that more than 90% of incident microwaves are absorbed 1 . The corresponding microwave frequency range is referred to as the effective absorption bandwidth (EAB), a critical parameter for assessing the broadband performance of microwave-absorbing (MA) materials. The RL values of NFAGs were calculated using Equations 4 and 5 , with the results presented in Fig. 3 C-D and Figure S14. The data revealed that the shielding ability of NFAGs improved with increasing pyrolysis temperature. Among the samples, NFAG-900 demonstrated remarkable performance, achieving a minimum reflection loss (RL min ) of − 68.87 dB at 10.62 GHz and an EAB of 5.25 GHz at a thickness of 2.5 mm. These results surpassed most of the recently reported microwave-absorbing materials (Fig. 3 E). To further clarify the absorbing mechanism, we discussed the electromagnetic parameters of all samples. The real part (ɛ′) and imaginary part (ɛ′′) of complex permittivity represent the ability to store and dissipate electrical energy, respectively. As shown in Figure S15, the electromagnetic parameters of NFAG-900 were characterized. Firstly, it was observed that the ɛ′ values of all samples tend to decrease with increasing frequency. This behavior could be attributed to polarization hysteresis at higher frequencies and typical frequency dispersion. Additionally, both ε' and ε" increased with rising pyrolysis temperatures, attributed to the higher graphite phase ratio, enhanced sintering degree, and the formation of electron-hole pairs, interfaces, and micropores. These factors collectively contributed to a denser electron transport network, enhancing the material's dielectric loss. 1 , 2 Impedance matching (Z = |Z in /Z 0 |) is employed to assess the alignment between the material and free space, with optimal matching achieved when the Z in /Z 0 ratio approaches 1. As shown in Fig. 3 F, NFAG-900 displayed excellent impedance matching over a wide frequency range, where the position of the maximum absorption corresponded to the optimal impedance-matching position. This facilitated the penetration of significant electromagnetic waves into the material. Furthermore, when comparing the attenuation constant, NFAG-900 exhibited high values, confirming its effective ability to dissipate electromagnetic waves (Figure S16). Moreover, Fig. 3 G illustrates the EAB range of NFAG-900 at various thicknesses, showing that complete coverage of the 2–18 GHz frequency range was achieved with a thickness below 5 mm. This highlighted the exceptional broadband absorption capability and efficiency of NFAG-900 as a lightweight, high-performance MA material. According to Debye's theory, the presence of Cole–Cole semicircles in the ε′−ε′′ plots suggested Debye relaxation processes. As shown in Fig. 3 G, the curve displayed two distinct sections with varying characteristics. In the low-frequency region, the Cole-Cole plot exhibited an approximately linear relationship, primarily attributed to dielectric loss due to interface polarization, while in the high-frequency region, the classical Cole–Cole semicircle revealed significant Debye relaxation polarization. 1 , 4 This phenomenon is understandable, as interface polarization occurs at heterogeneous interfaces and requires charge accumulation or complete dipole migration, which necessitates a longer response time. In contrast, Debye relaxation polarization involves directional dipole polarization of lower intensity. Upon removal of the external field relaxation, the dipole loses its orientation under thermal motion, leading to a significantly shorter response time compared to interface polarization. 2.4. Electromagnetic shielding performances of NFAGs Figure 4 A illustrated the mechanism for the exceptionally high EMI shielding performance of NFAGs, based on transmission line theory. First, impedance matching occurred at the interface of the NFAGs. A small portion of the electromagnetic wave was reflected, while a large amount penetrated into the material. Once inside, the electromagnetic waves were trapped within the NFAG structure, where they were attenuated by losses in conduction and polarization between the cross-linked carbon nanofiber networks. This process converted electromagnetic energy into heat. Additionally, the dense skin structure of the nanofibers allowed repeated reflections of the remaining electromagnetic waves, ensuring that the energy was completely absorbed, contributing to excellent shielding efficiency. 36 Notably, the core-shell structure of the self-assembled nanofibers further created rich heterogeneous interfaces, which were conducive to interface polarization and loss, further enhancing the material’s shielding capability. 37 , 38 To further expand its application scenario of NFAGs, we investigated their shielding performance in the common X-band. As shown in Fig. 4 C, NFAGs exhibited excellent electrical conductivity, which could be attributed to the remarkable electron transport capacity of the highly ordered microstructures. Interestingly, the conductivity of NFAG-900 reached 103.47 S/m, several orders of magnitude higher than the graphitized PDA nanoparticles, which typically exhibit conductivities in the range of 10 − 4 -10 − 6 S·m − 1 . 39 Correspondingly, the shielding efficiency of NFAGs increased with the heat treatment temperature. Electromagnetic shielding generally involves three primary mechanisms: reflection (R), absorption (A), and transmission (T). 2 We further calculated the contribution of each shielding through theoretical calculation. The shielding performance of NFAGs is primarily dominated by absorption, in contrast to traditional conjugated materials, which often suffer from poor impedance matching. The higher degree of graphitization and the increased number of polarization centers, resulting from higher heat treatment temperatures, were crucial factors contributing to the enhanced absorption. In addition, NFAGs, due to their simple preparation method, offer the flexibility to adjust the final material density by varying the concentration of the lyophilized solution, as practically needed. Specifically, a 2 mm thick NFAG-900 sample, with a density of 21.38 mg/cm³, achieved an electromagnetic shielding efficiency (SE) of 65 dB. To evaluate the comprehensive EMI shielding properties, we calculated the specific EMI shielding effectiveness (SSE/t), which accounts for the material's absolute shielding effectiveness (SE) considering its thickness (t) and density (ρ), as given by the following equation: $$\:\frac{SSE}{\text{t}}=\text{S}{E}_{T}/\left({\rho\:}\text{t}\right)$$ 2 Excitingly, the specific shielding effectiveness (SSE/t) of NFAGs at a density of 3.11 mg/cm³ and a thickness of 2 mm reached an impressive 47,909.9 dB·cm²/g, the highest reported value for organic carbon materials (Fig. 4 B). Analysis of the parameters revealed that the reflection (R) increased with density, which can be attributed to the formation of a higher-density fiber network and a denser outer cortex. SEM and TEM images revealed the multiscale skin-core structure of the NFAGs. Notably, NFAG-900 exhibited a dense shell formed by the curling and sintering of the outermost fibers during heat treatment, which led to fiber entanglement at the interface and a tightly packed shell structure. Furthermore, high-resolution observations of the graphitized nanofibers showed enhanced π-π stacking near the surface, likely due to the extended period available for surface refinement during the later stages of the reaction, after the chemical process had terminated. The skin-core structure introduced additional heterogeneous interfaces, which enhanced the ability of NFAGs to dissipate electromagnetic waves. This phenomenon was consistent with previous reports on the role of heterogeneous interfaces in improving wave dissipation. 36 , 40 Through the pre-regulation of melanin-based organic structures, we have successfully developed ultra-lightweight and highly efficient electromagnetic shielding and microwave-absorbing materials. Note that nature offers numerous examples where alterations in the aggregation state and interaction forces of organic materials lead to varied energy responses. For instance, non-covalently arranged porphyrin derivatives serve as the primary chromophores in the light-harvesting systems of plants and algae, enabling them to capture light of different wavelengths by modulating their aggregation state. Inspired by this, our work highlights the potential of pre-regulating the structure of organic materials or synthetic molecules to achieve enhanced energy-responsive architectures while preserving strong processability. At the same time, this work also showed that π-π stacking might be a new adaptive characteristic structure of electromagnetic energy dissipation, and it had better impedance-matching and microstructure than the traditional conjugate structure, which was expected to greatly expand the material candidate pool in the field of energy dissipation applications. 2.5. Radar Cross-Section (RCS) Simulation To verify the practical application potential, FEKO software was employed to simulate the Radar Cross Section (RCS) of the composite aerogel at different temperatures, using the classic stealth fighter F-35 as the model (Fig. 5 A, B). 57 , 58 NFAG-900 was applied as a 2.5 mm thick coating on the F-35’s surface, and its performance was compared with that of an ideal coating of the same thickness. The simulation was conducted using monostatic RCS and plane wave propagation, with incident angles of 10°, 0°, and − 10° to cover different flight attitudes, and a frequency of 10.46 GHz (the optimal absorption frequency). 57 – 59 The results showed that NFAG-900 exhibited excellent radar stealth capabilities, with ΔRCS values consistently below − 20 dB. Specifically, the average ΔRCS was − 35.88 dB at 0°, -36.56 dB at 10°, and − 35.45 dB at -10°. At an incident angle of 10°, the F-35 demonstrated the best RCS value of -50.47 dB at 153°, indicating that NFAG-900 provides outstanding radar stealth performance across a range of angles. These findings suggested that NFAGs have promising potential as intelligent microwave-absorbing materials, adaptable for real-time use in diverse applications, particularly in the defense and aerospace sectors. 3. Conclusions In summary, distinct from traditional strategies that focus on the engineering of conjugated precursors or the pyrolysis of natural materials, we have proposed the structural pre-regulation strategy to construct melanin-like polymers with highly ordered microstructures to achieve optimal electromagnetic matching for the first time. Indole analogs were employed to regulate the interaction forces during the melanin polymerization process, successfully constructing ordered PDA nanofibers with stacked DHI ring tetramers. Through typical freeze-drying and heat treatment, we have successfully fabricated ultra-light, conductive, and multi-scale core-skin structured NFAGs, which are well-suited for electromagnetic absorption and shielding applications. This multi-scale core-skin ordered structure significantly enhanced the electromagnetic wave propagation path and created abundant heterojunctions, thereby improving dielectric loss. As a result, NFAGs showed excellent EM absorption performance, with a maximum RL of -68.87dB and EAB of 5.25 GHz. In the X-band, with a density of 3.11mg/cm 3 and a thickness of 2 mm, Its SSE/t value reaches 47909.9 dB cm 2 /g, which is the highest reported value for organic carbon materials to date. This strategy is expected to extend to the design and application of a broader range of bio-inspired polymers in energy response dissipation, thereby driving material innovation in the electromagnetic and stealth fields. 4. Experimental Section Materials : Dopamine hydrochloride (98%), 5-hydroxyindole (98%) and ammonia aqueous solution (25–28 wt%)were all purchased from Titan Scientific Co. Ltd (Shanghai, China). Ethanol (SafeDry), methyl alcohol (SafeDry), ethyl acetate (SafeDry), acetonitrile (SafeDry), NaOH (99%), HCl (37%), THF (SafeDry), DMSO (SafeDry), and DMF (SafeDry) were acquired from Kelong Chemical Reagent Co., Ltd. (Chengdu, China). All chemical reagents were freshly used without any further purification in the research. Synthesis of PDA nanofibers: A total of 450 mg dopamine (DA) and 50 mg 5-hydroxyindole were dispersed in a mixed aqueous alcohol solution (90 mL H₂O and 40 mL ethanol) using ultrasonic treatment. Ammonia aqueous solution (NH₄OH, 3 mL, 28–30%) was then added to the above solution. The color of the mixture immediately changed to light brown, gradually transitioning to dark green. After 24 hours of reaction, the yellow PDA nanofibers were obtained by centrifugation and washed three times with deionized water. Fabrication of PDA carbon aerogels: The PDA aerogel was prepared by freeze-drying the dispersion, which was evenly dispersed in water at a specific concentration. The as-synthesized PDA nanofiber aerogel was carbonized at a specific temperature(600℃, 700℃, 800℃, 900℃) for 2 hours at a heating rate of 5 ℃ min − 1 in a flow nitrogen atmosphere to prepare PDA nanofiber carbon aerogel sample (NFAG-600, NFAG-700, NFAG-800, NFAG-900). Characterization : The surface morphologies of the series of materials mentioned were acquired on a Scanning electron microscope (SEM) of FEI Quanta 250. The transmission electron microscope (TEM) images and the EELS mapping analysis were acquired on Talos F200i (Thermo Scientific, Czech). The ESI-MS spectrum of the disassembly solution of PDA nanofibers was applied on Applied Biosystems API 2000 with positive anion mode electrospray ionization with the 10 µL min − 1 flow rate. The UPLC-MS was performed by Agilent 1290 UPLC and Agilent QTOF 6550 with positive anion mode electrospray ionization with 0.3 min − 1 flow rate; (Chromatographic column: waters BEH C 18 2.1*100mm 1.7µm; 20% mobile phase A: 0.1% Aqueous formic acid; 80% mobile phase B: Methanol). Raman spectra were obtained with a Raman spectrometer (HORIBA HR Evolution) using an Ar ion laser (532 nm) as the emission source to characterize the degree of graphitization. UV-vis spectroscopy was performed by PerkinElmer Lambda 650 UV–vis spectrophotometer. Fourier transform infrared spectra (FTIR, Thermo Fisher Nicolet iS50), X-ray photoelectron spectra (XPS, Thermo Fisher Thermo Scientific K-Alpha+) and X-ray diffraction (XRD, Rigaku Ultima IV) were employed to analyze the chemical structure of samples. The pore characteristics and specific surface areas of the samples were evaluated using Micromeritics ASAP 2020 at liquid Ar temperature. EIS measurements were conducted on a CHI760E electrochemical workstation. Electromagnetic parameter characterization : Corresponding electrical conductivity (σ) was examined by an RTS-9 four-point probe tester at the temperature of 25°C according to the modified ASTM F 390 − 98. Electromagnetic parameters were obtained by Agilent E5071C vector network analyzer in the frequency range of 2–12 GHz based on a coaxial method. The measured samples were prepared by adding the absorbents (10–30 wt%) into molten paraffin uniformly mixing them, followed by modeling into a coaxial ring with an outer diameter of 7.0 mm and inner diameter of 3.0 mm. In order to further analyze the shielding capability in the X band (8.2–12.4 GHz), the Electromagnetic parameters were obtained on the basis of a waveguide method. The EMI performance is calculated according to the scattering parameters, including SE total (SET), SE reflection (SER) and SE absorption (SEA), the coefficients of absorption (A), transmission (T) and reflection (R). Molecular Simulation : The molecular ratio was calculated as DA tetramer (structure 1): Bimolecular conjugate (structure 1) = 11:1 according to the proportion of elements obtained by EA, which was used to simulate molecular stacking in GROMACS. For random insertion of molecules, the GROMACS insert-molecules tool was used. The amber14sb force field parameters were used for both molecules, and the system was solvated using the TIP3P model. The system containing a total of 1800 water molecules,800 molecules of ethanol, which is consistent with the reaction environment, 11 molecules of structure 1 and 1 molecule of structure 2 was used for the simulation. The steepest descent method was used to minimize the energy of the system and NPT ensemble was performed with 100ps. The production of the simulation was run for 100 ns using a 2 fs time step. The V-rescale method was used for temperature coupling and the Parrinello-Rahman method was used for pressure coupling. The Particle Mesh Ewald (PME) method was used for long-range electrostatic interactions. 14 Å cut-off was employed for van der waals force (VdW) and short-range coulombic interaction. MD calculations were performed with the GROMACS molecular dynamic simulation package. Pymol was used for all molecular visualizations. The Antechamber program was used to generate complex force field parameters, and the team (Amber 18.0 Module) was used to generate the molecular topology. The HF/6-31G* method and basis set were used to calculate the electrostatic potential (ESP) and then the result was employed to calculate the restricted ESP(RESP)2 charge. Simulation details and methodology of electromagnetic paramete : The RL values were calculated based on the transmission line theory $$\:{Z}_{in}=\sqrt{{\mu\:}_{r}/{{\epsilon\:}}_{r}}\text{tan}\text{h}\left|-j\left(2{\pi\:}fc\right)\right|\sqrt{{\mu\:}_{r}{{\epsilon\:}}_{r}}$$ 4 $$\:RL\left(dB\right)=-20log\left|{Z}_{in}-\frac{1}{{Z}_{in}}+1\right|$$ 5 where εr and 𝜇r are the complex permittivity (εr = ε′ − jε′′) and permeability (𝜇r = 𝜇′ − j𝜇′′), respectively, f is the frequency of microwave, c is the velocity of light, d is the thickness, and Zin is the normalized input impedance of the sample. Additionally, The EMI SE of shielding materials can be defined as the logarithmic ratio of the incident power (PI) to transmitted power (PT) of an EM wave, and can be expressed in the following equation: $$\:{SE}_{T}=10\text{log}\left(\frac{{P}_{I}}{{P}_{T}}\right)={SE}_{R}+{SE}_{A}+{SE}_{M}$$ 6 As the SE T > 15 dB, the SE M is generally neglected, and the SET is determined by the sum of SE R and SE A : $$\:{SE}_{T}={SE}_{R}+{SE}_{A}$$ 7 $$\:{SE}_{R}=-10\text{l}\text{o}\text{g}(1-R)$$ 8 $$\:{SE}_{A}=-10\text{l}\text{o}\text{g}(T/\left|1-R\right|)$$ 9 \(\:R={\left|{S}_{11}\right|}^{2}\) , \(\:T={\left|{S}_{12}\right|}^{2}\) , \(\:A=1-R-T\) (10) Where A, R, and T are the reflection coefficient, absorption coefficient, and transmission coefficient, respectively. To evaluate the comprehensive EMI shielding property, the specific EMI SE (SSE/t) representing the absolute SE of a material considering the contribution of thickness (t) and density (ρ) was calculated from the following equation: $$\:\frac{SSE}{\text{t}}=\text{S}{E}_{T}/\left({\rho\:}\text{t}\right)$$ 11 RCS Simulations: The RCS value simulations were performed by FEKO 2017 software, using F35 as models. The scanning simulations were performed using the adaptive scanning technology AFS (Function Method of MoM Green-SGF). The simulated model was made up of an upper absorbing layer (NFAG-900, 2.5 mm) and a bottom perfect electric conductor layer (PEC, 2.5mm). The measured permittivity and permeability of NFAG-900 were used as EM parameters for input materials. The scattering directions were set as ≈ 0 ~ 360° for θ, and 0°, -10° and 10° for aircraft attitude inclination ϕ. The monitor frequency is set as 10.46 GHz, which shows the highest ΔRL values for NFAG-900. Declarations Supporting Information Supporting Information is available from the Wiley Online Library or from the author. Acknowledgments This work was supported by National Natural Science Foundation of China (552225311), Sichuan Science and Technology Program (2025NSFTD0011), and the Fundamental Research Funds for Central Universities. References M. Qin, L. Zhang and H. Wu, Adv Sci (Weinh) , 2022, 9 , e2105553. H. L. Lv, Z. H. Yang, H. G. Pan and R. B. Wu, Progress in Materials Science , 2022, 127 , 52-64. M. Green and X. B. Chen, Journal of Materiomics , 2019, 5 , 503-541. Z. C. Wu, H. W. Cheng, C. Jin, B. T. Yang, C. Y. Xu, K. Pei, H. B. Zhang, Z. Q. Yang and R. C. Che, Advanced Materials , 2022, 34 , 202107538. Y. Shi, M. J. Wu, S. B. Ge, J. Z. Li, A. S. Alshammari, J. Luo, M. A. Amin, H. Qiu, J. X. Jiang, Y. M. Asiri, R. Z. Huang, H. Hou, Z. M. El-Bahy, Z. H. Guo, C. Jia, K. M. Xu and X. M. Chen, Nano-Micro Letters , 2025, 17 . J. F. Hu, L. Yang, P. Yang, S. H. Jiang, X. H. 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Also discoverable on Platform About Our Team In Review Editorial Policies Advisory Board Help Center Resources Author Services Accessibility API Access RSS feed Manage Cookie Preferences © Research Square 2026 | ISSN 2693-5015 (online) Privacy Policy Terms of Service Do Not Sell My Personal Information {"props":{"pageProps":{"initialData":{"identity":"rs-6020493","acceptedTermsAndConditions":true,"allowDirectSubmit":false,"archivedVersions":[],"articleType":"Article","associatedPublications":[],"authors":[{"id":418675963,"identity":"a1d48740-f3ee-45a5-9a4d-1dac4de0fafc","order_by":0,"name":"Yiwen Li","email":"data:image/png;base64,iVBORw0KGgoAAAANSUhEUgAAAZAAAAAyAQMAAABI0h/eAAAABlBMVEX///8AAABVwtN+AAAACXBIWXMAAA7EAAAOxAGVKw4bAAAAqUlEQVRIiWNgGAWjYFAC5oYDHyAsA2K1MDYcnEGyFmYekrQY3EhsPGzzxy6xgb15mwRDzR2itDQczm1LTmzgOVYmwXDsGRFaboO0NBxIbJDIMZNgbDhMpBaLP0At8m9I0cLABrKFh0gtkvcfNhzsbUs2buNJK7ZIOEaEFr4zhw9/+PHHTraf/fDGGx9qiNCicADKYAMRCYQ1MDDINxCjahSMglEwCkY2AABSKj81ny7ocgAAAABJRU5ErkJggg==","orcid":"","institution":"Sichuan University","correspondingAuthor":true,"prefix":"","firstName":"Yiwen","middleName":"","lastName":"Li","suffix":""},{"id":418675964,"identity":"4d9e5115-0206-4ed8-9424-6d0de36b23b0","order_by":1,"name":"Peng Chen","email":"","orcid":"","institution":"Sichuan University","correspondingAuthor":false,"prefix":"","firstName":"Peng","middleName":"","lastName":"Chen","suffix":""},{"id":418675965,"identity":"36a63fb4-9099-42ee-91a6-993eb1942b03","order_by":2,"name":"Shibo He","email":"","orcid":"","institution":"Sichuan University","correspondingAuthor":false,"prefix":"","firstName":"Shibo","middleName":"","lastName":"He","suffix":""},{"id":418675966,"identity":"ae598889-b024-43f3-810d-b6d85e8c5fbd","order_by":3,"name":"Tianyou Wang","email":"","orcid":"","institution":"Sichuan University","correspondingAuthor":false,"prefix":"","firstName":"Tianyou","middleName":"","lastName":"Wang","suffix":""},{"id":418675967,"identity":"94953bdf-bbae-443e-9f6b-31b2d9f8b97b","order_by":4,"name":"Chencan Wang","email":"","orcid":"","institution":"Sichuan University","correspondingAuthor":false,"prefix":"","firstName":"Chencan","middleName":"","lastName":"Wang","suffix":""},{"id":418675968,"identity":"4bb82c5b-f805-40a3-af75-d9f649ad3501","order_by":5,"name":"Junru Tao","email":"","orcid":"","institution":"Sichuan University","correspondingAuthor":false,"prefix":"","firstName":"Junru","middleName":"","lastName":"Tao","suffix":""}],"badges":[],"createdAt":"2025-02-13 07:20:22","currentVersionCode":1,"declarations":"","doi":"10.21203/rs.3.rs-6020493/v1","doiUrl":"https://doi.org/10.21203/rs.3.rs-6020493/v1","draftVersion":[],"editorialEvents":[{"content":"https://doi.org/10.1038/s41467-025-62367-9","type":"published","date":"2025-08-03T04:00:00+00:00"}],"editorialNote":"","failedWorkflow":false,"files":[{"id":78109527,"identity":"f4852907-0095-4ad9-a7c9-ceeab256d1e4","added_by":"auto","created_at":"2025-03-10 04:47:46","extension":"png","order_by":1,"title":"Figure 1","display":"","copyAsset":false,"role":"figure","size":1030378,"visible":true,"origin":"","legend":"\u003cp\u003e\u003cstrong\u003eFabrication and Characterization of melanin-like nanofibers. \u003c/strong\u003e(A) Preparation and application diagram of traditional PDA nanoparticles and PDA nanofibers. (B) Optical photograph of PDA nanofibers aerogel (C) SEM image of PDA nanofibers. (D) HRTEM image of PDA nanofibers. The red line shows the π-π stacking spacing. (E) XPS survey spectra and element proportion of PDA nanofibers. (F) UPLC-MS spectra of PDA nanofibers. (G) Graphical result of molecular stacking at time t (t=0, 20, 50, 100 ns) in GROMACS and specific characteristic structures and corresponding interlayer spacing. (H)XRD patterns of PDA nanofibers. (I) Raman spectra of PDA nanofibers.\u003c/p\u003e","description":"","filename":"image1.png","url":"https://assets-eu.researchsquare.com/files/rs-6020493/v1/2b8e727a3e94a999058ac4a0.png"},{"id":78109528,"identity":"f554109e-2c93-4eee-aa31-a74c07ca19d3","added_by":"auto","created_at":"2025-03-10 04:47:46","extension":"png","order_by":2,"title":"Figure 2","display":"","copyAsset":false,"role":"figure","size":859360,"visible":true,"origin":"","legend":"\u003cp\u003e\u003cstrong\u003eFabrication and characterization of PDA carbon aerogels\u003c/strong\u003e. (A) Schematic illustration of the NFAGs. (B)-(D) SEM image of NFAGs. (E) XPS survey, (F) Raman spectra, and (G) FTIR spectra of NFAGs. (H) Nitrogen adsorption-desorption isotherms and pore width distributions of NFAGs.\u003c/p\u003e","description":"","filename":"image2.png","url":"https://assets-eu.researchsquare.com/files/rs-6020493/v1/df4ba387cb8e116abad2553f.png"},{"id":78109532,"identity":"0a2bd669-9b57-47f5-9796-106f95f029ae","added_by":"auto","created_at":"2025-03-10 04:47:46","extension":"png","order_by":3,"title":"Figure 3","display":"","copyAsset":false,"role":"figure","size":811994,"visible":true,"origin":"","legend":"\u003cp\u003e\u003cstrong\u003eMicrowave absorption behaviors of NFAGs\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003e(A) Schematic illustration of the microwave absorption process. (B)Microwave absorption mechanism of NAFGs. (C) RL value of NFAG-900. (D) Three-dimensional representations and two-dimensional projection images of RL value of NFAG-900. (E) Comparison of RL and EAB of typical reported carbon aerogels. \u003csup\u003e23-35\u003c/sup\u003e \u0026nbsp;(F) Impedance-matching of NFAG-900 at different thicknesses. (G) EAB of NFAG-900 with different thicknesses. (H) Cole-Cole plot of NFAG-900.\u003c/p\u003e","description":"","filename":"image3.png","url":"https://assets-eu.researchsquare.com/files/rs-6020493/v1/33a7657beddfd3a5c966f131.png"},{"id":78110579,"identity":"3d3d99da-94ef-4668-b2ce-da1db9a9adad","added_by":"auto","created_at":"2025-03-10 05:03:46","extension":"png","order_by":4,"title":"Figure 4","display":"","copyAsset":false,"role":"figure","size":736926,"visible":true,"origin":"","legend":"\u003cp\u003e\u003cstrong\u003eElectromagnetic shielding performance of NFAGs in X band.\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003e(A) Schematic illustration of the EMI mechanism of the skin-core structure. (B) Comparison of SSE/t of typical reported carbon aerogels as a function of density. \u003csup\u003e36, 41-56\u003c/sup\u003e (C)–(E) C) Conductivity, D) EMI shielding efficiency, E) EMI shielding parameter of NFAGs at different heat treatment temperatures. (F)–(H) F) Conductivity, G) EMI shielding efficiency, H) EMI shielding parameter of NFAGs in different concentrations. (I) SEM and TEM images of multi-scale skin core structure.\u003c/p\u003e","description":"","filename":"image4.png","url":"https://assets-eu.researchsquare.com/files/rs-6020493/v1/1a7e2349535086d5759f942f.png"},{"id":78110430,"identity":"c15b5aff-d168-4a01-a387-2de19bfe0c06","added_by":"auto","created_at":"2025-03-10 04:55:46","extension":"png","order_by":5,"title":"Figure 5","display":"","copyAsset":false,"role":"figure","size":789182,"visible":true,"origin":"","legend":"\u003cp\u003e\u003cstrong\u003eRadar Cross-Section (RCS) Simulation of MA performance.\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003e(A) the model of the F-35B Stealth fighter. (B) Schematic diagram of Target detection of aircraft by radar in RCS. (C)-(E) Radar cross-section of the F-35B when the aircraft pitch Angle is 0°, 10°, -10°.\u003c/p\u003e","description":"","filename":"image5.png","url":"https://assets-eu.researchsquare.com/files/rs-6020493/v1/f7d4b289b0a761e95f9bb1f0.png"},{"id":88180795,"identity":"b60be065-d447-4149-acfe-3b6efaf43c40","added_by":"auto","created_at":"2025-08-03 07:06:40","extension":"pdf","order_by":0,"title":"","display":"","copyAsset":false,"role":"manuscript-pdf","size":5078820,"visible":true,"origin":"","legend":"","description":"","filename":"manuscript.pdf","url":"https://assets-eu.researchsquare.com/files/rs-6020493/v1/19880819-ba4e-4f69-8f3f-d05d30839644.pdf"},{"id":78109529,"identity":"90c2f8ac-4280-427e-b0a3-dfbc8521f0d9","added_by":"auto","created_at":"2025-03-10 04:47:46","extension":"pdf","order_by":1,"title":"","display":"","copyAsset":false,"role":"supplement","size":1322325,"visible":true,"origin":"","legend":"Supporting Information","description":"","filename":"SupportingInformation.pdf","url":"https://assets-eu.researchsquare.com/files/rs-6020493/v1/7ada1af803004697f8413845.pdf"},{"id":78110428,"identity":"af8e0808-4b3f-4084-8763-dc5781b8e6e2","added_by":"auto","created_at":"2025-03-10 04:55:46","extension":"docx","order_by":2,"title":"","display":"","copyAsset":false,"role":"supplement","size":733373,"visible":true,"origin":"","legend":"","description":"","filename":"ToC.docx","url":"https://assets-eu.researchsquare.com/files/rs-6020493/v1/4ebf1656977ee9b146c82e2e.docx"}],"financialInterests":"There is \u003cb\u003eNO\u003c/b\u003e Competing Interest.","formattedTitle":"Melanin-like nanofibers with highly ordered structures achieve unprecedented specific electromagnetic interference shielding efficiency","fulltext":[{"header":"1. Introduction","content":"\u003cp\u003eWith the increasingly stringent requirements of aerospace and military equipment for combat speed and concealment in complex environments, electromagnetic shielding materials are undergoing iterative upgrades, aiming for higher performance and lighter weight.\u003csup\u003e\u003cspan citationid=\"CR1\" class=\"CitationRef\"\u003e1\u003c/span\u003e, \u003cspan citationid=\"CR2\" class=\"CitationRef\"\u003e2\u003c/span\u003e\u003c/sup\u003e Conventional metal materials and their composites usually suffer from unsatisfactory density, leading to the increasing attentions on highly conjugated inorganic materials such as carbon nanotubes and graphene, graphene, etc., which could be compounded with polymers or directly processed into material forms \u003cem\u003evia\u003c/em\u003e customized methods. However, due to their poor compatibility, there is an inevitable dilemma that conjugate structures make it difficult to construct effective adaptive networks. \u003csup\u003e\u003cspan citationid=\"CR3\" class=\"CitationRef\"\u003e3\u003c/span\u003e, \u003cspan citationid=\"CR4\" class=\"CitationRef\"\u003e4\u003c/span\u003e\u003c/sup\u003e An Alternative strategy is to graphitize natural or organic materials to obtain a high degree of conjugated structures, However, the inherent defects would be present in the graphitized products, which is difficult to regulate accurately. The resulting electromagnetic shielding materials often exhibited limited performance.\u003csup\u003e\u003cspan citationid=\"CR5\" class=\"CitationRef\"\u003e5\u003c/span\u003e\u003c/sup\u003e Therefore, the key to breaking through the lightweight and high-performance electromagnetic shielding materials is to develop a new class of intrinsic conjugated organic materials with well-regulated structures and functions.\u003csup\u003e\u003cspan citationid=\"CR2\" class=\"CitationRef\"\u003e2\u003c/span\u003e\u003c/sup\u003e\u003c/p\u003e \u003cp\u003eMelanin has been regarded as a class of emerging promising energy-dissipating biomacromolecules in nature, which could efficiently absorb and transform a broad spectrum of energy due to its unique and chaotic assembled structures.\u003csup\u003e\u003cspan additionalcitationids=\"CR7 CR8\" citationid=\"CR6\" class=\"CitationRef\"\u003e6\u003c/span\u003e\u0026ndash;\u003cspan citationid=\"CR9\" class=\"CitationRef\"\u003e9\u003c/span\u003e\u003c/sup\u003e Melanin and melanin-like polymers offer abundant chemical versatility and significant potential for structural regulation, making them easily combinable with various materials. Considerable research has been focused on the structural and interaction regulation of melanin-like polymers, which have shown remarkable responses to a wide range of electromagnetic waves, from ionizing radiation to near-infrared (NIR) light, offering radiation protection, visible light absorption, and photothermal conversion.\u003csup\u003e\u003cspan additionalcitationids=\"CR11 CR12 CR13 CR14\" citationid=\"CR10\" class=\"CitationRef\"\u003e10\u003c/span\u003e\u0026ndash;\u003cspan citationid=\"CR15\" class=\"CitationRef\"\u003e15\u003c/span\u003e\u003c/sup\u003e However, reports on melanin-like materials exhibiting effective absorption in the microwave band are quite lacking, since their disordered structures cannot support long-range electron transfer paths to respond to long-wavelength energy.\u003csup\u003e\u003cspan citationid=\"CR8\" class=\"CitationRef\"\u003e8\u003c/span\u003e\u003c/sup\u003e Thus, if we could construct melanin-like materials with highly ordered microstructure through appropriate supramolecular engineering strategies, it is expected to extend the energy dissipation range of melanin-inspired polymers and break the performance limitations in lightweight, high-performance materials for electromagnetic shielding.\u003c/p\u003e \u003cp\u003eTheoretically, the formation process of melanin and melanin-like polymers involves both chemical processes(oxidation, isomerization, rearrangement into 5,6-dihydroxyindole(DHI) tetramers, and coupling reactions between intermediates) and physical assembly through intermolecular interactions, including π-π stacking and hydrogen bonding. Traditional methods typically result in disordered melanin-like materials due to complicated macromolecular structures and cross-linked hydrogen bond networks formed by phenolic hydroxyl groups, which severely inhibit the establishment of long-range ordered structures. Therefore, we speculated that highly ordered melanin structures can be achieved by enhancing the π-π interactions between DHI tetramers and minimizing random chemical reactions and hydrogen bond crosslinking within the macromolecular networks. The resulting highly ordered melanin-like polymers might enable long-range electron conduction and improve electromagnetic response capabilities.\u003c/p\u003e \u003cp\u003eOne possible way to realize this goal is to increase the proportion of cyclized indole and reduce the disordered crosslinking caused by hydrogen bonding. To accomplish this, we strived to use indole analogs as active species to induce the polymerization process, resulting in improved π-π stacking of the DHI tetramers. This approach could achieve the successful formation of highly ordered melanin-like nanofibers for the first time, to the best of our knowledge. These nanofibers were then processed into ultra-light, high-performance carbon aerogels through typical freeze-drying and pyrolysis treatments. Remarkably, the resulting melanin-inspired aerogels exhibited exceptional electromagnetic interference (EMI) shielding and microwave absorption(MA) properties, with a maximum reflection loss (RL) of -68.87 dB and an effective absorption bandwidth (EAB) of 5.25 GHz in the 2\u0026ndash;18 GHz range. In the X-band, with a density of 3.11 mg/cm\u0026sup3; and a thickness of 2 mm, the aerogel achieved an impressive absolute EMI shielding effectiveness (SSE/t), defined as the shielding effectiveness (SE) value divided by the surface density, reaching 47,909.9 dB\u0026middot;cm\u0026sup2;/g\u0026mdash;currently the highest reported value for organic carbon materials. Additionally, radar cross-section (RCS) simulations were performed, confirming the potential application of these aerogels as intelligent electromagnetic shielding materials for stealth technology. This work demonstrates the successful construction of melanin-like polymers with highly ordered microstructures through the rational regulation of interaction forces, offering a novel way for optimizing the properties of a broad range of bioinspired materials.\u003c/p\u003e"},{"header":"2. Result and Discussion","content":"\u003cdiv id=\"Sec3\" class=\"Section2\"\u003e\n \u003ch2\u003e2.1. Fabrication and Characterization of melanin-like nanofibers\u003c/h2\u003e\n \u003cp\u003eConventional melanin-like polymers, such as polydopamine (PDA), typically form isotropic nanoparticles due to their disordered structures. In this work, we introduced indole units with different hydroxyl groups into the conventional melanin polymerization process, aiming to reduce the influence of hydrogen bonding. A one-pot copolymerization of different indole analogs and dopamine monomer in a mixture solution of water and alcohol at room temperature in the presence of ammonium hydroxide was facilely performed, as the typical experimental condition for PDA nanoparticles preparation (Fig. \u003cspan class=\"InternalRef\"\u003e1\u003c/span\u003eA). We discovered that the PDAs formed with indole or 5,6-dihydroxy indole maintained traditional black nanoparticles, while those synthesized with 5-hydroxyindole exhibited distinct yellow nanofibers prepared under similar conditions (Fig. \u003cspan class=\"InternalRef\"\u003e1\u003c/span\u003eB-C and Figure \u003cspan class=\"InternalRef\"\u003eS1\u003c/span\u003e). Ultraviolet-visible spectra further confirmed the presence of characteristic absorption between 300\u0026ndash;450 nm (Figure S2), while there is almost no absorption in the rest of the visible region, suggesting that the optical properties of PDA nanofibers are quite different from conventional PDA nanoparticles. Furthermore, we confirmed the existence of the highly ordered structures by transmission electron microscopy (TEM), which revealed a layered structure with an interlayer spacing of approximately 3.4 \u0026Aring;, consistent with classical \u0026pi;-\u0026pi; stacking (Fig. \u003cspan class=\"InternalRef\"\u003e1\u003c/span\u003eD).\u003c/p\u003e\n \u003cp\u003eWe then carefully investigated their chemical structures in detail. Firstly, we used X-ray photoelectron spectroscopy (XPS) to determine the element proportions, which revealed that the molar ratio of hydroxyl indole was 17.8%, consistent with the results from elemental analysis (EA) (Fig. \u003cspan class=\"InternalRef\"\u003e1\u003c/span\u003eE and Figure S6). Next, we performed the disassembly experiments in various solvents (Figure S7). It was found that the nanofibers were completely disassembled in methanol and acetonitrile, indicating that their assembly was driven by supramolecular forces. The dissolution likely occurred due to the disruption of hydrogen bonds, caused by solvent interactions and competition. Electrospray ionization mass spectrometry (ESI-MS) analysis of the disassembled PDA nanofibers in methanol solution revealed prominent peaks that closely matched the coupled molecules of DHI and 5-hydroxyindole (M1), the dimer of DHI (M2), and the ring tetramer of DHI (M3) (Figure S7). Additionally, the ring tetramer of DHI was successfully isolated using Ultraperformance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS) (Fig. \u003cspan class=\"InternalRef\"\u003e1\u003c/span\u003eH). Based on the elemental analysis, we calculated the M1 to M3 ratio as 11:10, consistent with the N and O element ratios. To better understand the self-assembly process, we used GROMACS\u003csup\u003e\u003cspan class=\"CitationRef\"\u003e16\u003c/span\u003e, \u003cspan class=\"CitationRef\"\u003e17\u003c/span\u003e\u003c/sup\u003e simulations to model the interactions between these two molecular species at the same ratio, under identical solvent and temperature conditions (Fig. \u003cspan class=\"InternalRef\"\u003e1\u003c/span\u003eG). Over a simulation time of 1000 ns, the molecules exhibited a general tendency to form fibrous assemblies. Key structural analysis revealed that the tetramer (M3) favored axial packing, likely contributing to the formation of nanofibers (structure 1). Additionally, the interplay of hydrogen bonding, cation-\u0026pi; interactions, and hydrophilic-hydrophobic forces, combined with the planar deflection angles of M1 and M3, led to a deflected, side-by-side arrangement of the fibers. M1 co-stacked \u003cem\u003evia\u003c/em\u003e hydrogen bonding and \u0026pi;-\u0026pi; interactions, producing a variety of typical arrangements and corresponding interlayer spacings (structures 2\u0026ndash;4).\u003csup\u003e\u003cspan class=\"CitationRef\"\u003e18\u003c/span\u003e\u003c/sup\u003e Based on these results, we proposed that the formation of PDA nanofibers follows a specific pathway: in a base-catalyzed environment, dopamine undergoes oxidation, cyclization, and rearrangement to generate 5,6-dihydroxyindole (DHI). During this process, quinone free radicals are formed, which initiate both self-polymerization and copolymerization with indole. Since 5-hydroxyindole has only a single hydroxyl group, it cannot support multidirectional hydrogen bond cross-linking. This limitation facilitates the formation of M3 with outward-facing hydrogen bonds.\u003csup\u003e\u003cspan class=\"CitationRef\"\u003e18\u003c/span\u003e, \u003cspan class=\"CitationRef\"\u003e19\u003c/span\u003e\u003c/sup\u003e Additionally, M3 exhibits a strong \u0026pi;-\u0026pi; conjugation tendency, with the delocalized \u0026pi;-electron cloud over the indole ring promoting directional axial packing. This axial packing provides a potential mechanism for \u0026pi;-electron transport within the material. \u003csup\u003e\u003cspan class=\"CitationRef\"\u003e19\u003c/span\u003e\u003c/sup\u003e As the degree of crosslinking varies due to hydrogen bonding between the tetramer and other conjugated structures, nanofibers with different length-to-diameter ratios are formed.\u003c/p\u003e\n \u003cp\u003eThis hypothesis was further supported by X-ray diffraction (XRD) analysis (Fig. \u003cspan class=\"InternalRef\"\u003e1\u003c/span\u003eH), which revealed a highly ordered stacking structure that differs significantly from the amorphous peaks typically observed in conventional PDA nanoparticles. The peaks between 20\u0026deg; and 25\u0026deg; correspond to the \u0026pi;-\u0026pi; stacking region, while the smaller angle peaks likely result from multistage diffraction or other assembled structures.\u003csup\u003e\u003cspan class=\"CitationRef\"\u003e19\u003c/span\u003e, \u003cspan class=\"CitationRef\"\u003e20\u003c/span\u003e\u003c/sup\u003e These findings closely align with the structural predictions obtained from GROMACS simulations. An integral analysis of the XRD data indicated that the amorphous envelope peak region accounts for only 2.1%, further confirming the high degree of ordered microstructures within the PDA nanofibers. Raman spectroscopy (Fig. \u003cspan class=\"InternalRef\"\u003e1\u003c/span\u003eI) provided additional evidence for the ordered structure. The PDA nanofibers were found to exhibit a sharp and narrow G-peak at 1580 cm⁻\u0026sup1;, in stark contrast to the broader, multiple peaks characteristic of conventional PDA nanoparticles. This sharp G-peak suggested that the molecules within the nanofibers primarily undergo in-plane stretching vibrations, with boundary vibrations suppressed due to their fixed, lattice-like arrangement. This result strongly correlated with the vibration characteristics of the DHI ring tetramer. The narrow peak width further indicates a high degree of uniformity among the molecular units participating in in-plane vibrations within the PDA nanofibers.\u003csup\u003e\u003cspan class=\"CitationRef\"\u003e21\u003c/span\u003e\u003c/sup\u003e Upon magnifying the Raman spectrum, a very small signal in the D-peak region was detected. Although this peak was visually masked, its area accounts for only 1.61% of the G-peak area. This result was consistent with the XRD findings, reaffirming the highly ordered structures within the PDA nanofibers.\u003c/p\u003e\n\u003c/div\u003e\n\u003cdiv id=\"Sec4\" class=\"Section2\"\u003e\n \u003ch2\u003e2.2. Fabrication and characterization of PDA carbon aerogels\u003c/h2\u003e\n \u003cp\u003eThe as-synthesized PDA nanofiber aerogels were carbonized in a tubular furnace under a flowing nitrogen atmosphere at various temperatures (600\u0026deg;C, 700\u0026deg;C, 800\u0026deg;C, and 900\u0026deg;C) for 2 hours, with a heating rate of 5\u0026deg;C/min(Fig. \u003cspan class=\"InternalRef\"\u003e2\u003c/span\u003eA). The resulting carbon aerogel samples were designated as NFAG-i (i\u0026thinsp;=\u0026thinsp;NFAG-600, NFAG-700, NFAG-800, NFAG-900), respectively. SEM imaging in Fig. \u003cspan class=\"InternalRef\"\u003e2\u003c/span\u003eB-\u003cspan class=\"InternalRef\"\u003e2\u003c/span\u003eD confirmed that the carbonized aerogels still retained their long fibrous morphologies, indicating structural stability during carbonization. XPS survey scans shown in Fig. \u003cspan class=\"InternalRef\"\u003e2\u003c/span\u003eC revealed the removal of N and O elements, leading to the formation of oxygen vacancies and electron-hole pairs within the NFAG samples. These defects act as polarization centers, significantly enhancing the dielectric properties of the material (Fig. \u003cspan class=\"InternalRef\"\u003e2\u003c/span\u003eE). Additionally, the proportion of sp\u0026sup2; carbon in the NFAG samples increased with rising pyrolysis temperatures, which is favorable for electron transport. This trend was further validated by Raman spectroscopy (Fig. \u003cspan class=\"InternalRef\"\u003e2\u003c/span\u003eF), where the D band (centered at ~\u0026thinsp;1350 cm⁻\u0026sup1;) and G band (centered at ~\u0026thinsp;1590 cm⁻\u0026sup1;) intensities were analyzed. The D/G ratio (I\u003csub\u003eD\u003c/sub\u003e/I\u003csub\u003eG\u003c/sub\u003e), indicative of the relative proportions of disordered and graphitic carbon, showed a gradual increase in the graphite phase with rising temperatures, reaching an I\u003csub\u003eD\u003c/sub\u003e/I\u003csub\u003eG\u003c/sub\u003e value of 82.21% for NFAG-900.FTIR spectra (Fig. \u003cspan class=\"InternalRef\"\u003e2\u003c/span\u003eG) further corroborated these findings, showing a significant reduction or complete disappearance of organic C\u0026thinsp;=\u0026thinsp;O and C\u0026ndash;N peaks, consistent with the XPS results. Notably, \u0026pi;-\u0026pi; stacking in NFAG not only facilitated \u0026pi;-conjugated electron transportation but also contributed to the formation of micropores during heat treatment, since its higher bond length made it more susceptible to such structural changes compared to typical covalent bonds. N₂ adsorption-desorption characterization was used to evaluate the specific surface area (SSA) and pore size distribution of the NFAG samples. The high air-phase volume fraction provided a potential impedance-matching advantage for NFAG in dielectric applications. All samples (Fig. \u003cspan class=\"InternalRef\"\u003e2\u003c/span\u003eH) exhibited typical type IV isotherms with H1 hysteresis loops, indicative of capillary condensation of N₂. Remarkably, NFAG-900 demonstrated an excellent surface area of 885.65 m\u0026sup2;/g, ཞfour times higher than that of carbonized PDA nanoparticles reported previously.\u003csup\u003e\u003cspan class=\"CitationRef\"\u003e22\u003c/span\u003e\u003c/sup\u003e The predominant micropores (\u0026lt;\u0026thinsp;2 nm) play a crucial role in facilitating ion transport, improving electrical applications, and enabling the construction of abundant gas-solid heterostructures.\u003c/p\u003e\n\u003c/div\u003e\n\u003cdiv id=\"Sec5\" class=\"Section2\"\u003e\n \u003ch2\u003e2.3. Electromagnetic absorption of NFAGs\u003c/h2\u003e\n \u003cp\u003eFigures \u003cspan class=\"InternalRef\"\u003e3\u003c/span\u003eA and \u003cspan class=\"InternalRef\"\u003e3\u003c/span\u003eB illustrated the primary loss mechanisms in NFAGs. The extensive specific surface area and micropores contributed significantly to the interfacial loss in NFAGs, while the multistage core-skin structure of the fibers generated additional heterogeneous interfacial systems. Debye relaxation polarization in NFAGs could be attributed to numerous defects and residual groups, including oxygen vacancies and electron-hole pairs induced by heat treatment, which facilitated electron accumulation, transfer, and dipole formation. Furthermore, the excellent electrical conductivity of the PDA nanofibers, owing to their ordered structure, played a significant role in ohmic loss. This effect was further amplified by the large aspect ratio and three-dimensional interconnected conductive network formed during heat treatment and sinteringNext, the electromagnetic absorption capacity of NFAGs (NFAG-600, NFAG-700, NFAG-800, NFAG-900) was evaluated, respectively. Generally, an RL value below \u0026minus;\u0026thinsp;10 dB is considered the threshold for effective absorption, indicating that more than 90% of incident microwaves are absorbed \u003csup\u003e\u003cspan class=\"CitationRef\"\u003e1\u003c/span\u003e\u003c/sup\u003e. The corresponding microwave frequency range is referred to as the effective absorption bandwidth (EAB), a critical parameter for assessing the broadband performance of microwave-absorbing (MA) materials. The RL values of NFAGs were calculated using Equations \u003cspan class=\"InternalRef\"\u003e4\u003c/span\u003e and \u003cspan class=\"InternalRef\"\u003e5\u003c/span\u003e, with the results presented in Fig. \u003cspan class=\"InternalRef\"\u003e3\u003c/span\u003eC-D and Figure S14. The data revealed that the shielding ability of NFAGs improved with increasing pyrolysis temperature. Among the samples, NFAG-900 demonstrated remarkable performance, achieving a minimum reflection loss (RL\u003csub\u003emin\u003c/sub\u003e) of \u0026minus;\u0026thinsp;68.87 dB at 10.62 GHz and an EAB of 5.25 GHz at a thickness of 2.5 mm. These results surpassed most of the recently reported microwave-absorbing materials (Fig. \u003cspan class=\"InternalRef\"\u003e3\u003c/span\u003eE). To further clarify the absorbing mechanism, we discussed the electromagnetic parameters of all samples. The real part (ɛ\u0026prime;) and imaginary part (ɛ\u0026prime;\u0026prime;) of complex permittivity represent the ability to store and dissipate electrical energy, respectively. As shown in Figure S15, the electromagnetic parameters of NFAG-900 were characterized. Firstly, it was observed that the ɛ\u0026prime; values of all samples tend to decrease with increasing frequency. This behavior could be attributed to polarization hysteresis at higher frequencies and typical frequency dispersion. Additionally, both \u0026epsilon;\u0026apos; and \u0026epsilon;\u0026quot; increased with rising pyrolysis temperatures, attributed to the higher graphite phase ratio, enhanced sintering degree, and the formation of electron-hole pairs, interfaces, and micropores. These factors collectively contributed to a denser electron transport network, enhancing the material\u0026apos;s dielectric loss.\u003csup\u003e\u003cspan class=\"CitationRef\"\u003e1\u003c/span\u003e, \u003cspan class=\"CitationRef\"\u003e2\u003c/span\u003e\u003c/sup\u003e Impedance matching (Z = |Z\u003csub\u003ein\u003c/sub\u003e/Z\u003csub\u003e0\u003c/sub\u003e|) is employed to assess the alignment between the material and free space, with optimal matching achieved when the Z\u003csub\u003ein\u003c/sub\u003e/Z\u003csub\u003e0\u003c/sub\u003e ratio approaches 1. As shown in Fig. \u003cspan class=\"InternalRef\"\u003e3\u003c/span\u003eF, NFAG-900 displayed excellent impedance matching over a wide frequency range, where the position of the maximum absorption corresponded to the optimal impedance-matching position. This facilitated the penetration of significant electromagnetic waves into the material. Furthermore, when comparing the attenuation constant, NFAG-900 exhibited high values, confirming its effective ability to dissipate electromagnetic waves (Figure S16). Moreover, Fig. \u003cspan class=\"InternalRef\"\u003e3\u003c/span\u003eG illustrates the EAB range of NFAG-900 at various thicknesses, showing that complete coverage of the 2\u0026ndash;18 GHz frequency range was achieved with a thickness below 5 mm. This highlighted the exceptional broadband absorption capability and efficiency of NFAG-900 as a lightweight, high-performance MA material. According to Debye\u0026apos;s theory, the presence of Cole\u0026ndash;Cole semicircles in the \u0026epsilon;\u0026prime;\u0026minus;\u0026epsilon;\u0026prime;\u0026prime; plots suggested Debye relaxation processes. As shown in Fig. \u003cspan class=\"InternalRef\"\u003e3\u003c/span\u003eG, the curve displayed two distinct sections with varying characteristics. In the low-frequency region, the Cole-Cole plot exhibited an approximately linear relationship, primarily attributed to dielectric loss due to interface polarization, while in the high-frequency region, the classical Cole\u0026ndash;Cole semicircle revealed significant Debye relaxation polarization. \u003csup\u003e\u003cspan class=\"CitationRef\"\u003e1\u003c/span\u003e, \u003cspan class=\"CitationRef\"\u003e4\u003c/span\u003e\u003c/sup\u003e This phenomenon is understandable, as interface polarization occurs at heterogeneous interfaces and requires charge accumulation or complete dipole migration, which necessitates a longer response time. In contrast, Debye relaxation polarization involves directional dipole polarization of lower intensity. Upon removal of the external field relaxation, the dipole loses its orientation under thermal motion, leading to a significantly shorter response time compared to interface polarization.\u003c/p\u003e\n\u003c/div\u003e\n\u003cdiv id=\"Sec6\" class=\"Section2\"\u003e\n \u003ch2\u003e2.4. Electromagnetic shielding performances of NFAGs\u003c/h2\u003e\n \u003cp\u003eFigure \u003cspan class=\"InternalRef\"\u003e4\u003c/span\u003eA illustrated the mechanism for the exceptionally high EMI shielding performance of NFAGs, based on transmission line theory. First, impedance matching occurred at the interface of the NFAGs. A small portion of the electromagnetic wave was reflected, while a large amount penetrated into the material. Once inside, the electromagnetic waves were trapped within the NFAG structure, where they were attenuated by losses in conduction and polarization between the cross-linked carbon nanofiber networks. This process converted electromagnetic energy into heat. Additionally, the dense skin structure of the nanofibers allowed repeated reflections of the remaining electromagnetic waves, ensuring that the energy was completely absorbed, contributing to excellent shielding efficiency. \u003csup\u003e\u003cspan class=\"CitationRef\"\u003e36\u003c/span\u003e\u003c/sup\u003e Notably, the core-shell structure of the self-assembled nanofibers further created rich heterogeneous interfaces, which were conducive to interface polarization and loss, further enhancing the material\u0026rsquo;s shielding capability.\u003csup\u003e\u003cspan class=\"CitationRef\"\u003e37\u003c/span\u003e, \u003cspan class=\"CitationRef\"\u003e38\u003c/span\u003e\u003c/sup\u003e To further expand its application scenario of NFAGs, we investigated their shielding performance in the common X-band. As shown in Fig. \u003cspan class=\"InternalRef\"\u003e4\u003c/span\u003eC, NFAGs exhibited excellent electrical conductivity, which could be attributed to the remarkable electron transport capacity of the highly ordered microstructures. Interestingly, the conductivity of NFAG-900 reached 103.47 S/m, several orders of magnitude higher than the graphitized PDA nanoparticles, which typically exhibit conductivities in the range of 10\u003csup\u003e\u0026minus;\u0026thinsp;4\u003c/sup\u003e-10\u003csup\u003e\u0026minus;\u0026thinsp;6\u003c/sup\u003e S\u0026middot;m\u003csup\u003e\u0026minus;\u0026thinsp;1\u003c/sup\u003e.\u003csup\u003e39\u003c/sup\u003e Correspondingly, the shielding efficiency of NFAGs increased with the heat treatment temperature. Electromagnetic shielding generally involves three primary mechanisms: reflection (R), absorption (A), and transmission (T).\u003csup\u003e\u003cspan class=\"CitationRef\"\u003e2\u003c/span\u003e\u003c/sup\u003e We further calculated the contribution of each shielding through theoretical calculation. The shielding performance of NFAGs is primarily dominated by absorption, in contrast to traditional conjugated materials, which often suffer from poor impedance matching. The higher degree of graphitization and the increased number of polarization centers, resulting from higher heat treatment temperatures, were crucial factors contributing to the enhanced absorption. In addition, NFAGs, due to their simple preparation method, offer the flexibility to adjust the final material density by varying the concentration of the lyophilized solution, as practically needed. Specifically, a 2 mm thick NFAG-900 sample, with a density of 21.38 mg/cm\u0026sup3;, achieved an electromagnetic shielding efficiency (SE) of 65 dB. To evaluate the comprehensive EMI shielding properties, we calculated the specific EMI shielding effectiveness (SSE/t), which accounts for the material\u0026apos;s absolute shielding effectiveness (SE) considering its thickness (t) and density (\u0026rho;), as given by the following equation:\u003c/p\u003e\n \u003cdiv id=\"Equ1\" class=\"Equation\"\u003e\n \u003cdiv class=\"mathdisplay\" id=\"FileID_Equ1\" name=\"EquationSource\"\u003e$$\\:\\frac{SSE}{\\text{t}}=\\text{S}{E}_{T}/\\left({\\rho\\:}\\text{t}\\right)$$\u003c/div\u003e\n \u003cdiv class=\"EquationNumber\"\u003e2\u003c/div\u003e\n \u003c/div\u003e\n \u003cp\u003eExcitingly, the specific shielding effectiveness (SSE/t) of NFAGs at a density of 3.11 mg/cm\u0026sup3; and a thickness of 2 mm reached an impressive 47,909.9 dB\u0026middot;cm\u0026sup2;/g, the highest reported value for organic carbon materials (Fig. \u003cspan class=\"InternalRef\"\u003e4\u003c/span\u003eB). Analysis of the parameters revealed that the reflection (R) increased with density, which can be attributed to the formation of a higher-density fiber network and a denser outer cortex. SEM and TEM images revealed the multiscale skin-core structure of the NFAGs. Notably, NFAG-900 exhibited a dense shell formed by the curling and sintering of the outermost fibers during heat treatment, which led to fiber entanglement at the interface and a tightly packed shell structure. Furthermore, high-resolution observations of the graphitized nanofibers showed enhanced \u0026pi;-\u0026pi; stacking near the surface, likely due to the extended period available for surface refinement during the later stages of the reaction, after the chemical process had terminated. The skin-core structure introduced additional heterogeneous interfaces, which enhanced the ability of NFAGs to dissipate electromagnetic waves. This phenomenon was consistent with previous reports on the role of heterogeneous interfaces in improving wave dissipation.\u003csup\u003e\u003cspan class=\"CitationRef\"\u003e36\u003c/span\u003e, \u003cspan class=\"CitationRef\"\u003e40\u003c/span\u003e\u003c/sup\u003e\u003c/p\u003e\n \u003cp\u003eThrough the pre-regulation of melanin-based organic structures, we have successfully developed ultra-lightweight and highly efficient electromagnetic shielding and microwave-absorbing materials. Note that nature offers numerous examples where alterations in the aggregation state and interaction forces of organic materials lead to varied energy responses. For instance, non-covalently arranged porphyrin derivatives serve as the primary chromophores in the light-harvesting systems of plants and algae, enabling them to capture light of different wavelengths by modulating their aggregation state. Inspired by this, our work highlights the potential of pre-regulating the structure of organic materials or synthetic molecules to achieve enhanced energy-responsive architectures while preserving strong processability. At the same time, this work also showed that \u0026pi;-\u0026pi; stacking might be a new adaptive characteristic structure of electromagnetic energy dissipation, and it had better impedance-matching and microstructure than the traditional conjugate structure, which was expected to greatly expand the material candidate pool in the field of energy dissipation applications.\u003c/p\u003e\n\u003c/div\u003e\n\u003cdiv id=\"Sec7\" class=\"Section2\"\u003e\n \u003ch2\u003e2.5. Radar Cross-Section (RCS) Simulation\u003c/h2\u003e\n \u003cp\u003eTo verify the practical application potential, FEKO software was employed to simulate the Radar Cross Section (RCS) of the composite aerogel at different temperatures, using the classic stealth fighter F-35 as the model (Fig. \u003cspan class=\"InternalRef\"\u003e5\u003c/span\u003eA, B). \u003csup\u003e\u003cspan class=\"CitationRef\"\u003e57\u003c/span\u003e, \u003cspan class=\"CitationRef\"\u003e58\u003c/span\u003e\u003c/sup\u003e NFAG-900 was applied as a 2.5 mm thick coating on the F-35\u0026rsquo;s surface, and its performance was compared with that of an ideal coating of the same thickness. The simulation was conducted using monostatic RCS and plane wave propagation, with incident angles of 10\u0026deg;, 0\u0026deg;, and \u0026minus;\u0026thinsp;10\u0026deg; to cover different flight attitudes, and a frequency of 10.46 GHz (the optimal absorption frequency).\u003csup\u003e\u003cspan class=\"CitationRef\"\u003e57\u003c/span\u003e\u0026ndash;\u003cspan class=\"CitationRef\"\u003e59\u003c/span\u003e\u003c/sup\u003e The results showed that NFAG-900 exhibited excellent radar stealth capabilities, with \u0026Delta;RCS values consistently below \u0026minus;\u0026thinsp;20 dB. Specifically, the average \u0026Delta;RCS was \u0026minus;\u0026thinsp;35.88 dB at 0\u0026deg;, -36.56 dB at 10\u0026deg;, and \u0026minus;\u0026thinsp;35.45 dB at -10\u0026deg;. At an incident angle of 10\u0026deg;, the F-35 demonstrated the best RCS value of -50.47 dB at 153\u0026deg;, indicating that NFAG-900 provides outstanding radar stealth performance across a range of angles. These findings suggested that NFAGs have promising potential as intelligent microwave-absorbing materials, adaptable for real-time use in diverse applications, particularly in the defense and aerospace sectors.\u003c/p\u003e\n\u003c/div\u003e"},{"header":"3. Conclusions","content":"\u003cp\u003eIn summary, distinct from traditional strategies that focus on the engineering of conjugated precursors or the pyrolysis of natural materials, we have proposed the structural pre-regulation strategy to construct melanin-like polymers with highly ordered microstructures to achieve optimal electromagnetic matching for the first time. Indole analogs were employed to regulate the interaction forces during the melanin polymerization process, successfully constructing ordered PDA nanofibers with stacked DHI ring tetramers. Through typical freeze-drying and heat treatment, we have successfully fabricated ultra-light, conductive, and multi-scale core-skin structured NFAGs, which are well-suited for electromagnetic absorption and shielding applications. This multi-scale core-skin ordered structure significantly enhanced the electromagnetic wave propagation path and created abundant heterojunctions, thereby improving dielectric loss. As a result, NFAGs showed excellent EM absorption performance, with a maximum RL of -68.87dB and EAB of 5.25 GHz. In the X-band, with a density of 3.11mg/cm\u003csup\u003e3\u003c/sup\u003e and a thickness of 2 mm, Its SSE/t value reaches 47909.9 dB cm\u003csup\u003e2\u003c/sup\u003e/g, which is the highest reported value for organic carbon materials to date. This strategy is expected to extend to the design and application of a broader range of bio-inspired polymers in energy response dissipation, thereby driving material innovation in the electromagnetic and stealth fields.\u003c/p\u003e"},{"header":"4. Experimental Section","content":"\u003cp\u003e\u003cstrong\u003eMaterials :\u0026nbsp;\u003c/strong\u003eDopamine hydrochloride (98%), 5-hydroxyindole (98%) and ammonia aqueous solution (25\u0026ndash;28 wt%)were all purchased from Titan Scientific Co. Ltd (Shanghai, China). Ethanol (SafeDry), methyl alcohol (SafeDry), ethyl acetate (SafeDry), acetonitrile (SafeDry), NaOH (99%), HCl (37%), THF (SafeDry), DMSO (SafeDry), and DMF (SafeDry) were acquired from Kelong Chemical Reagent Co., Ltd. (Chengdu, China). All chemical reagents were freshly used without any further purification in the research.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eSynthesis of PDA nanofibers:\u0026nbsp;\u003c/strong\u003eA total of 450 mg dopamine (DA) and 50 mg 5-hydroxyindole were dispersed in a mixed aqueous alcohol solution (90 mL H₂O and 40 mL ethanol) using ultrasonic treatment. Ammonia aqueous solution (NH₄OH, 3 mL, 28\u0026ndash;30%) was then added to the above solution. The color of the mixture immediately changed to light brown, gradually transitioning to dark green. After 24 hours of reaction, the yellow PDA nanofibers were obtained by centrifugation and washed three times with deionized water.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eFabrication of PDA carbon aerogels:\u0026nbsp;\u003c/strong\u003eThe PDA aerogel was prepared by freeze-drying the dispersion, which was evenly dispersed in water at a specific concentration. The as-synthesized PDA nanofiber aerogel was carbonized at a specific temperature(600℃, 700℃, 800℃, 900℃) for 2 hours at a heating rate of 5 ℃ min\u003csup\u003e\u0026minus;\u0026thinsp;1\u003c/sup\u003e in a flow nitrogen atmosphere to prepare PDA nanofiber carbon aerogel sample (NFAG-600, NFAG-700, NFAG-800, NFAG-900).\u003c/p\u003e\n\u003cp\u003e\u003cem\u003e\u003cstrong\u003eCharacterization\u003c/strong\u003e\u003c/em\u003e: The surface morphologies of the series of materials mentioned were acquired on a Scanning electron microscope (SEM) of FEI Quanta 250. The transmission electron microscope (TEM) images and the EELS mapping analysis were acquired on Talos F200i (Thermo Scientific, Czech). The ESI-MS spectrum of the disassembly solution of PDA nanofibers was applied on Applied Biosystems API 2000 with positive anion mode electrospray ionization with the 10 \u0026micro;L min\u003csup\u003e\u0026minus;\u0026thinsp;1\u003c/sup\u003e flow rate. The UPLC-MS was performed by Agilent 1290 UPLC and Agilent QTOF 6550 with positive anion mode electrospray ionization with 0.3 min\u003csup\u003e\u0026minus;\u0026thinsp;1\u003c/sup\u003e flow rate; (Chromatographic column: waters BEH C\u003csup\u003e18\u003c/sup\u003e 2.1*100mm 1.7\u0026micro;m; 20% mobile phase A: 0.1% Aqueous formic acid; 80% mobile phase B: Methanol). Raman spectra were obtained with a Raman spectrometer (HORIBA HR Evolution) using an Ar ion laser (532 nm) as the emission source to characterize the degree of graphitization. UV-vis spectroscopy was performed by PerkinElmer Lambda 650 UV\u0026ndash;vis spectrophotometer. Fourier transform infrared spectra (FTIR, Thermo Fisher Nicolet iS50), X-ray photoelectron spectra (XPS, Thermo Fisher Thermo Scientific K-Alpha+) and X-ray diffraction (XRD, Rigaku Ultima IV) were employed to analyze the chemical structure of samples. The pore characteristics and specific surface areas of the samples were evaluated using Micromeritics ASAP 2020 at liquid Ar temperature. EIS measurements were conducted on a CHI760E electrochemical workstation.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eElectromagnetic parameter characterization :\u0026nbsp;\u003c/strong\u003eCorresponding electrical conductivity (\u0026sigma;) was examined by an RTS-9 four-point probe tester at the temperature of 25\u0026deg;C according to the modified ASTM F 390\u0026thinsp;\u0026minus;\u0026thinsp;98. Electromagnetic parameters were obtained by Agilent E5071C vector network analyzer in the frequency range of 2\u0026ndash;12 GHz based on a coaxial method. The measured samples were prepared by adding the absorbents (10\u0026ndash;30 wt%) into molten paraffin uniformly mixing them, followed by modeling into a coaxial ring with an outer diameter of 7.0 mm and inner diameter of 3.0 mm. In order to further analyze the shielding capability in the X band (8.2\u0026ndash;12.4 GHz), the Electromagnetic parameters were obtained on the basis of a waveguide method. The EMI performance is calculated according to the scattering parameters, including SE total (SET), SE reflection (SER) and SE absorption (SEA), the coefficients of absorption (A), transmission (T) and reflection (R).\u003c/p\u003e\n\u003cp\u003e\u003cem\u003e\u003cstrong\u003eMolecular Simulation\u003c/strong\u003e\u003c/em\u003e: The molecular ratio was calculated as DA tetramer (structure 1): Bimolecular conjugate (structure 1)\u0026thinsp;=\u0026thinsp;11:1 according to the proportion of elements obtained by EA, which was used to simulate molecular stacking in GROMACS. For random insertion of molecules, the GROMACS insert-molecules tool was used. The amber14sb force field parameters were used for both molecules, and the system was solvated using the TIP3P model. The system containing a total of 1800 water molecules,800 molecules of ethanol, which is consistent with the reaction environment, 11 molecules of structure 1 and 1 molecule of structure 2 was used for the simulation. The steepest descent method was used to minimize the energy of the system and NPT ensemble was performed with 100ps. The production of the simulation was run for 100 ns using a 2 fs time step. The V-rescale method was used for temperature coupling and the Parrinello-Rahman method was used for pressure coupling. The Particle Mesh Ewald (PME) method was used for long-range electrostatic interactions. 14 \u0026Aring; cut-off was employed for van der waals force (VdW) and short-range coulombic interaction. MD calculations were performed with the GROMACS molecular dynamic simulation package. Pymol was used for all molecular visualizations. The Antechamber program was used to generate complex force field parameters, and the team (Amber 18.0 Module) was used to generate the molecular topology. The HF/6-31G* method and basis set were used to calculate the electrostatic potential (ESP) and then the result was employed to calculate the restricted ESP(RESP)2 charge.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eSimulation details and methodology of electromagnetic paramete :\u003c/strong\u003eThe RL values were calculated based on the transmission line theory\u003c/p\u003e\n\u003cdiv id=\"Equ2\" class=\"Equation\"\u003e\n \u003cdiv class=\"mathdisplay\" id=\"FileID_Equ2\" name=\"EquationSource\"\u003e$$\\:{Z}_{in}=\\sqrt{{\\mu\\:}_{r}/{{\\epsilon\\:}}_{r}}\\text{tan}\\text{h}\\left|-j\\left(2{\\pi\\:}fc\\right)\\right|\\sqrt{{\\mu\\:}_{r}{{\\epsilon\\:}}_{r}}$$\u003c/div\u003e\n \u003cdiv class=\"EquationNumber\"\u003e4\u003c/div\u003e\n\u003c/div\u003e\n\u003cdiv id=\"Equ3\" class=\"Equation\"\u003e\n \u003cdiv class=\"mathdisplay\" id=\"FileID_Equ3\" name=\"EquationSource\"\u003e$$\\:RL\\left(dB\\right)=-20log\\left|{Z}_{in}-\\frac{1}{{Z}_{in}}+1\\right|$$\u003c/div\u003e\n \u003cdiv class=\"EquationNumber\"\u003e5\u003c/div\u003e\n\u003c/div\u003e\n\u003cp\u003ewhere \u0026epsilon;r and 𝜇r are the complex permittivity (\u0026epsilon;r\u0026thinsp;=\u0026thinsp;\u0026epsilon;\u0026prime; \u0026minus; j\u0026epsilon;\u0026prime;\u0026prime;) and permeability (𝜇r = 𝜇\u0026prime; \u0026minus; j𝜇\u0026prime;\u0026prime;), respectively, f is the frequency of microwave, c is the velocity of light, d is the thickness, and Zin is the normalized input impedance of the sample.\u003c/p\u003e\n\u003cp\u003eAdditionally, The EMI SE of shielding materials can be defined as the logarithmic ratio of the incident power (PI) to transmitted power (PT) of an EM wave, and can be expressed in the following equation:\u003c/p\u003e\n\u003cdiv id=\"Equ4\" class=\"Equation\"\u003e\n \u003cdiv class=\"mathdisplay\" id=\"FileID_Equ4\" name=\"EquationSource\"\u003e$$\\:{SE}_{T}=10\\text{log}\\left(\\frac{{P}_{I}}{{P}_{T}}\\right)={SE}_{R}+{SE}_{A}+{SE}_{M}$$\u003c/div\u003e\n \u003cdiv class=\"EquationNumber\"\u003e6\u003c/div\u003e\n\u003c/div\u003e\n\u003cp\u003eAs the SE\u003csub\u003eT\u003c/sub\u003e \u0026gt; 15 dB, the SE\u003csub\u003eM\u003c/sub\u003e is generally neglected, and the SET is determined by the sum of SE\u003csub\u003eR\u003c/sub\u003e and SE\u003csub\u003eA\u003c/sub\u003e:\u003c/p\u003e\n\u003cdiv id=\"Equ5\" class=\"Equation\"\u003e\n \u003cdiv class=\"mathdisplay\" id=\"FileID_Equ5\" name=\"EquationSource\"\u003e$$\\:{SE}_{T}={SE}_{R}+{SE}_{A}$$\u003c/div\u003e\n \u003cdiv class=\"EquationNumber\"\u003e7\u003c/div\u003e\n\u003c/div\u003e\n\u003cdiv id=\"Equ6\" class=\"Equation\"\u003e\n \u003cdiv class=\"mathdisplay\" id=\"FileID_Equ6\" name=\"EquationSource\"\u003e$$\\:{SE}_{R}=-10\\text{l}\\text{o}\\text{g}(1-R)$$\u003c/div\u003e\n \u003cdiv class=\"EquationNumber\"\u003e8\u003c/div\u003e\n\u003c/div\u003e\n\u003cdiv id=\"Equ7\" class=\"Equation\"\u003e\n \u003cdiv class=\"mathdisplay\" id=\"FileID_Equ7\" name=\"EquationSource\"\u003e$$\\:{SE}_{A}=-10\\text{l}\\text{o}\\text{g}(T/\\left|1-R\\right|)$$\u003c/div\u003e\n \u003cdiv class=\"EquationNumber\"\u003e9\u003c/div\u003e\n\u003c/div\u003e\n\u003cp\u003e\u003cspan class=\"InlineEquation\"\u003e\u0026nbsp;\u003cspan class=\"mathinline\"\u003e\\(\\:R={\\left|{S}_{11}\\right|}^{2}\\)\u003c/span\u003e\u0026nbsp;\u003c/span\u003e, \u003cspan class=\"InlineEquation\"\u003e\u003cspan class=\"mathinline\"\u003e\\(\\:T={\\left|{S}_{12}\\right|}^{2}\\)\u003c/span\u003e\u003c/span\u003e, \u003cspan class=\"InlineEquation\"\u003e\u003cspan class=\"mathinline\"\u003e\\(\\:A=1-R-T\\)\u003c/span\u003e\u003c/span\u003e (10)\u003c/p\u003e\n\u003cp\u003eWhere A, R, and T are the reflection coefficient, absorption coefficient, and transmission coefficient, respectively.\u003c/p\u003e\n\u003cp\u003eTo evaluate the comprehensive EMI shielding property, the specific EMI SE (SSE/t) representing the absolute SE of a material considering the contribution of thickness (t) and density (\u0026rho;) was calculated from the following equation:\u003c/p\u003e\n\u003cdiv id=\"Equ8\" class=\"Equation\"\u003e\n \u003cdiv class=\"mathdisplay\" id=\"FileID_Equ8\" name=\"EquationSource\"\u003e$$\\:\\frac{SSE}{\\text{t}}=\\text{S}{E}_{T}/\\left({\\rho\\:}\\text{t}\\right)$$\u003c/div\u003e\n \u003cdiv class=\"EquationNumber\"\u003e11\u003c/div\u003e\n\u003c/div\u003e\n\u003cp\u003e\u003cstrong\u003eRCS Simulations:\u0026nbsp;\u003c/strong\u003eThe RCS value simulations were performed by FEKO 2017 software, using F35 as models. The scanning simulations were performed using the adaptive scanning technology AFS (Function Method of MoM Green-SGF). The simulated model was made up of an upper absorbing layer (NFAG-900, 2.5 mm) and a bottom perfect electric conductor layer (PEC, 2.5mm). The measured permittivity and permeability of NFAG-900 were used as EM parameters for input materials. The scattering directions were set as \u0026asymp;\u0026thinsp;0\u0026thinsp;~\u0026thinsp;360\u0026deg; for \u0026theta;, and 0\u0026deg;, -10\u0026deg; and 10\u0026deg; for aircraft attitude inclination ϕ. The monitor frequency is set as 10.46 GHz, which shows the highest \u0026Delta;RL values for NFAG-900.\u003c/p\u003e"},{"header":"Declarations","content":"\u003cp\u003e\u003cstrong\u003eSupporting Information\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eSupporting Information is available from the Wiley Online Library or from the author.\u0026nbsp;\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eAcknowledgments\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThis work was supported by National Natural Science Foundation of China (552225311), Sichuan Science and Technology Program (2025NSFTD0011), and the Fundamental Research Funds for Central Universities.\u003c/p\u003e"},{"header":"References","content":"\u003col\u003e\n\u003cli\u003eM. Qin, L. Zhang and H. Wu, \u003cem\u003eAdv Sci (Weinh)\u003c/em\u003e, 2022, \u003cstrong\u003e9\u003c/strong\u003e, e2105553.\u003c/li\u003e\n\u003cli\u003eH. L. Lv, Z. H. Yang, H. G. Pan and R. B. 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Seetharamdoo, \u003cem\u003eJournal of Applied Physics\u003c/em\u003e, 2019, \u003cstrong\u003e126\u003c/strong\u003e.\u003c/li\u003e\n\u003c/ol\u003e"}],"fulltextSource":"","fullText":"","funders":[],"hasAdminPriorityOnWorkflow":false,"hasManuscriptDocX":true,"hasOptedInToPreprint":true,"hasPassedJournalQc":"","hasAnyPriority":true,"hideJournal":false,"highlight":"","institution":"","isAcceptedByJournal":true,"isAuthorSuppliedPdf":false,"isDeskRejected":"","isHiddenFromSearch":false,"isInQc":false,"isInWorkflow":false,"isPdf":false,"isPdfUpToDate":true,"isWithdrawnOrRetracted":false,"journal":{"display":true,"email":"[email protected]","identity":"nature-portfolio","isNatureJournal":true,"hasQc":false,"allowDirectSubmit":false,"externalIdentity":"","sideBox":"","snPcode":"","submissionUrl":"","title":"Nature Portfolio","twitterHandle":"","acdcEnabled":false,"dfaEnabled":false,"editorialSystem":"ejp","reportingPortfolio":"","inReviewEnabled":true,"inReviewRevisionsEnabled":false},"keywords":"melanin, polydopamine, microwave absorption, electromagnetic interference shielding, nanofiber","lastPublishedDoi":"10.21203/rs.3.rs-6020493/v1","lastPublishedDoiUrl":"https://doi.org/10.21203/rs.3.rs-6020493/v1","license":{"name":"CC BY 4.0","url":"https://creativecommons.org/licenses/by/4.0/"},"manuscriptAbstract":"\u003cp\u003eLightweight, high-performance electromagnetic shielding materials are crucial for protection and detection, relying heavily on the precise design of electromagnetic response structures. Conventional shielding materials often involve complex fabrication of conjugated composites or graphitization of organic materials, facing challenges in balancing their performance and processability. As such, seeking intrinsically conjugated materials with superior processability is crucial. Natural melanin and melanin-like polymers have garnered considerable attention as emerging promising energy-dissipating substances with a wide range from ionizing radiation to infrared light. In this work, we have engineered those bioinspired polymers with highly ordered microstructures as a new class of promising high-performance and lightweight electromagnetic shielding materials for the first time. The key process is to use 5, 6-dihydroxyindole ring tetramer framework to construct highly ordered melanin-like nanofibers by tuning the intramolecular π-π stacking, which could facilitate the well regulation of long-range electron conduction and electromagnetic matching features. The resulting melanin-like nanofibers could be easily transformed into carbon aerogels with outstanding microwave absorption performance, i.e. a maximum reflection loss of -68.87dB and effective absorption bandwidth of 5.25GHz during 2-18GHz. In the X-band, the aerogel reached the considerable absolute EMI shielding effectiveness value of 47909.9 dB cm\u003csup\u003e2\u003c/sup\u003e/g, the highest for organic carbon materials reported to date. This work represented the first successful extension of the electromagnetic response of melanin-like polymers into the microwave spectrum, paving the way for practical applications of bioinspired polymers in EMI shielding and stealth technologies.\u003c/p\u003e","manuscriptTitle":"Melanin-like nanofibers with highly ordered structures achieve unprecedented specific electromagnetic interference shielding efficiency","msid":"","msnumber":"","nonDraftVersions":[{"code":1,"date":"2025-03-10 04:47:41","doi":"10.21203/rs.3.rs-6020493/v1","editorialEvents":[],"status":"published","journal":{"display":true,"email":"[email protected]","identity":"nature-communications","isNatureJournal":true,"hasQc":false,"allowDirectSubmit":false,"externalIdentity":"NCOMMS","sideBox":"Learn more about [Nature Communications](http://www.nature.com/ncomms/)","snPcode":"","submissionUrl":"https://mts-ncomms.nature.com/","title":"Nature Communications","twitterHandle":"","acdcEnabled":true,"dfaEnabled":true,"editorialSystem":"ejp","reportingPortfolio":"Nature Communications","inReviewEnabled":true,"inReviewRevisionsEnabled":false}}],"origin":"","ownerIdentity":"7bcca31d-352d-4991-a6a4-213315c282b6","owner":[],"postedDate":"March 10th, 2025","published":true,"recentEditorialEvents":[],"rejectedJournal":[],"revision":"","amendment":"","status":"published-in-journal","subjectAreas":[{"id":44641651,"name":"Scientific community and society/Business and industry/Engineering/Electrical and electronic engineering"},{"id":44641652,"name":"Biological sciences/Biotechnology/Nanobiotechnology/Nanostructures"}],"tags":[],"updatedAt":"2025-08-03T07:06:32+00:00","versionOfRecord":{"articleIdentity":"rs-6020493","link":"https://doi.org/10.1038/s41467-025-62367-9","journal":{"identity":"nature-communications","isVorOnly":false,"title":"Nature Communications"},"publishedOn":"2025-08-03 04:00:00","publishedOnDateReadable":"August 3rd, 2025"},"versionCreatedAt":"2025-03-10 04:47:41","video":"","vorDoi":"10.1038/s41467-025-62367-9","vorDoiUrl":"https://doi.org/10.1038/s41467-025-62367-9","workflowStages":[]},"version":"v1","identity":"rs-6020493","journalConfig":"researchsquare"},"__N_SSP":true},"page":"/article/[identity]/[[...version]]","query":{"redirect":"/article/rs-6020493","identity":"rs-6020493","version":["v1"]},"buildId":"8U1c8b4HqxoKbykW_rLl7","isFallback":false,"isExperimentalCompile":false,"dynamicIds":[84888],"gssp":true,"scriptLoader":[]}