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- W4385726962 abstract "Tin-based perovskites are one of the most promising candidates for the development of lead-free perovskite solar cells (PSCs) and have attracted lots of attention. Despite the extensive research efforts, the performance of tin-based PSCs (Sn-PSCs) still lags far behind the lead containing counterparts due to the poor stability and self-p-doping. Here, we perform first-principles density functional theory calculations combined with non-adiabatic molecular dynamics simulations to unveil the origins of the instability of tin iodine perovskite when exposed to O2. It is found that O2 is more thermally favorable to be adsorbed on iodine-vacancy (VI) defect sites in the defective surface rather than the pristine surface, and the generation of peroxide species on the VI sites dramatically accelerates the structural decomposition. The presence of VI defects on the surface of CsSnI3 decreases the band gap by inducing a local shallow state around conduction band minimum, significantly accelerating the electron–hole recombination. The adsorption of O2 on VI site slightly increases the band gap compared to that of the pristine one and decreases the influence of VI on the surface’s optoelectronic properties and the electron–hole recombination rate but significantly accelerates structural decomposition by weakening the defect tolerance ability of the [SnI6]4– octahedra as well as the carriers’ relaxation. The increased structural instability in combined VI and O2 points to the surface VI defect passivation as the main optimization scheme for efficient and stable Sn-PSCs." @default.
- W4385726962 created "2023-08-11" @default.
- W4385726962 creator A5001497356 @default.
- W4385726962 creator A5015411929 @default.
- W4385726962 creator A5033319328 @default.
- W4385726962 date "2023-08-10" @default.
- W4385726962 modified "2023-10-16" @default.
- W4385726962 title "Origins of the Accelerated Decomposition in Inorganic Tin Perovskites Contaminated by Oxygen: <i>Ab Initio</i> and Quantum Dynamics Study" @default.
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- W4385726962 doi "https://doi.org/10.1021/acs.jpcc.3c04066" @default.
- W4385726962 hasPublicationYear "2023" @default.
- W4385726962 type Work @default.