钙钛矿(结构)
铵
能量转换效率
材料科学
格式化
甲酸铵
光致发光
化学工程
光电子学
钙钛矿太阳能电池
电压
纳米技术
工作(物理)
载流子
氯化铵
离子
光伏系统
作者
Farhan Yousuf (21794035),Chen-Fu Lin (10952917),Ming-Hsien Li (1766215),Peter Chen (261319)
出处
期刊:
[Figshare (United Kingdom)]
日期:2025-07-27
标识
DOI:10.1021/acsaem.5c01652.s001
摘要
The instability of wide-bandgap perovskite solar cells (PSCs) impedes their practical applications. Here, ammonium formate is incorporated into perovskite precursors to optimize composition, enhancing film quality, optoelectronic properties, and stability. Time-resolved photoluminescence reveals prolonged carrier lifetimes (reduced nonradiative recombination), while morphological analysis demonstrates enlarged grain sizes, enabling efficient charge transport and defect mitigation. Optimized devices achieve a power conversion efficiency of 20.37% (vs 17.47% for the control device) under AM 1.5G 1-sun illumination, with improved open-circuit voltage (1.14 V (with ammonium formate) vs 1.11 V (without ammonium formate)) and fill factor (81.10% (with ammonium formate) vs 74.14% (without ammonium formate)). Unencapsulated devices retain >80% of their initial efficiency after 300 h under light/dark cycling and 230 h under continuous 1-sun illumination (55 ± 5% humidity), outperforming control cells (<50% retention). Ammonium formate suppresses PbI2 formation and surface recombination, enhancing the operational durability. This work provides a facile compositional engineering strategy to advance long-term stability in wide-bandgap PSCs.
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