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Suppressed Defects and Improved Stability of All‐Inorganic CsSnI <sub>3</sub> Films by Solid Additive‐Assisted Chemical Vapor Deposition Process

Hongyu LiMaterials Genome Institute Shanghai University Shanghai 200444 P. R. ChinaChao YeMaterials Genome Institute Shanghai University Shanghai 200444 P. R. ChinaYichen JinSchool of Science Shanghai University Shanghai 200444 P. R. ChinaLifang WuMaterials Genome Institute Shanghai University Shanghai 200444 P. R. ChinaYouguang MaQian‐Wei‐Chang College Shanghai University Shanghai 200444 P. R. ChinaHongliang DongCenter for High Pressure Science and Technology Advanced Research Shanghai 201203 P. R. ChinaLuis K. OnoOkinawa Institute of Science and Technology Graduate University (OIST) 1919‐1 Tancha, Onna‐son, Kunigami‐gun Okinawa 904‐0495 JapanYabing QiGlobal Institute of Future Technology Shanghai Jiao Tong University Shanghai 200240 P. R. ChinaS. B. DonaevFaculty of Electronics and Automation Tashkent State Technical University University Str. 2 Tashkent 100095 UzbekistanLin JiangSchool of Microelectronics Shanghai University Shanghai 201800 P. R. ChinaZhifang WuMaterials Genome Institute Shanghai University Shanghai 200444 P. R. ChinaChang XueMaterials Genome Institute Shanghai University Shanghai 200444 P. R. ChinaShenghao WangMaterials Genome Institute Shanghai University Shanghai 200444 P. R. China
Smalljournal2025en
ABI

Аннотация

Abstract All‐inorganic Sn‐based halide perovskite CsSnI 3 is a promising candidate for perovskite solar cells (PSCs) owing to its narrower bandgap (≈1.3 eV) and lower toxicity as compared with traditional organic–inorganic hybrid Pb‐based counterparts. However, CsSnI 3 rapidly degrades in ambient air and simultaneously generates intrinsic defect states, thus seriously impairing the optoelectronic property of the film, as well as the corresponding device performance. Herein, a solid additive‐assisted chemical vapor deposition (SACVD) method is reported to prepare CsSnI 3 films with high quality. Combining with theoretical calculations, Fourier transform infrared spectroscopy, temperature‐dependent photoluminescence, and scanning Kelvin probe techniques prove that the lone electron pairs in the solid additive form coordination interactions with Sn 2+ , resulting in the suppression of Sn 2+ oxidizing to Sn 4+ and thus reducing defect density. This work not only provides a new strategy to prepare eco‐friendly and stability‐improved tin halide perovskite thin films for PSCs, but also reveals the underlying physical properties of CsSnI 3 film upon solid state modification (i.e., without any organic solvent).

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