卤化物
钙钛矿(结构)
光伏
碘化物
材料科学
化学工程
能量转换效率
惰性
相(物质)
光电子学
纳米技术
水分
工作(物理)
薄膜
半导体
溶解过程
科技与社会
光伏系统
作者
Asayil Alsulami,Ahmed Ali Said,İlhan Yavuz,Luis Lanzetta,Christopher E. Petoukhoff,Sofiia Kosar,Shynggys Zhumagali,Luis Huerta Hernandez,Xu Han,Yongcao Zhang,Anirudh Sharma,Stefaan De Wolf,Derya Baran
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-10-30
卷期号:10 (11): 5825-5833
被引量:2
标识
DOI:10.1021/acsenergylett.5c02922
摘要
All-inorganic tin–lead halide perovskites (CsPbxSn1–xI3) are promising absorber materials for next-generation photovoltaics due to their near-ideal bandgaps (∼1.3–1.4 eV) and favorable optoelectronic characteristics. Their practical application, however, is limited by intrinsic instabilities, including Sn2+ oxidation, halide migration, and phase transitions. Here, we introduce an additive engineering approach using dimethylammonium iodide (DMAI) to address these challenges. DMAI simultaneously passivates deep-level defects, inhibits Sn2+ oxidation, reduces iodide migration, and improves moisture resistance, thereby enhancing environmental stability. CsPbxSn1–xI3 films treated with DMAI maintain stable perovskite phases in air and exhibit improved optoelectronic properties. Devices fabricated with these films achieve power conversion efficiencies up to 14.2%, compared to 8.9% for untreated controls, and retain more than 94% of their initial performance after 3000 h of inert storage. This work highlights additive-driven stabilization as a pathway toward durable, high-efficiency all-inorganic perovskite solar cells.
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