Effect of surface termination on electronic and optical properties of lead-free tin-based eco-friendly perovskite solar cell: A first principal study
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Abstract
The lead (Pb) based halide perovskites have been reported to be promising materials for photovoltaic applications, however, presence of toxic lead in them concerns the environmental and health issues. In this work, we have, therefore, studied the lead-free and non-toxic tin-based halide perovskite, CsSnI 3 , which is an eco-friendly material with high power conversion efficiency thus being a potential candidate for photovoltaic applications. We have investigated the influence of CsI and SnI 2 - terminated (001) surfaces on structural, electronic and optical properties of lead-free tin-based halide perovskite CsSnI 3 from the first principal calculations, based on density functional theory (DFT). The calculations of electronic and optical parameters are performed under the parameterization of PBE_Sol for exchange correlation functions conjugated with modified- Beche-Johnshon (mBJ) exchange potential. The optimised lattice constant, the energy band structure and the density of states (DoS) have been calculated for the bulk and different terminated surface structures. The optical properties of CsSnI 3 are computed in terms of the real and imaginary part of absorption coefficient, dielectric function, refractive index, conductivity, reflectivity, extinction coefficient and electron energy loss. The photovoltaic characteristics for CsI- termination are found to be better than the bulk and SnI 2 - terminated surfaces. This study reveals that optical and electronic properties can be tuned by selecting proper surface termination in halide perovskite CsSnI 3 . The CsSnI 3 surfaces exhibit semiconductor behaviour with a direct energy band gap and a high value of absorption power in the ultraviolet and visible region rendering these inorganic halide perovskite materials important for eco-friendly and efficient optoelectronic devices.
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- last seen: 2026-05-19T01:45:01.086888+00:00