串联
制作
成核
光伏
能量转换效率
钙钛矿(结构)
结晶
材料科学
限制
相容性(地球化学)
纳米技术
化学工程
分子工程
热稳定性
光伏系统
卤化物
位阻效应
八面体
化学
能量转换
合理设计
钙钛矿太阳能电池
太阳能
催化作用
表面能
作者
Huifang Han,Jie Xu,Xueqi Zhang,Qianzheng Shi,Zhixue Li,Yao Fu,Kun Lang,Zhenxu Sun,Yahan Wu,Xu Pan,Yi Ding,Mohammad Khaja Nazeeruddin,Jianxi Yao
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2026-04-08
卷期号:11 (5): 3833-3842
被引量:1
标识
DOI:10.1021/acsenergylett.6c00044
摘要
High Resolution Image Download MS PowerPoint Slide All-inorganic CsPbI 3 perovskite holds promise for photovoltaics owing to its optoelectronic properties and thermal stability. However, its high nucleation barrier and thermodynamic instability hinder low-temperature crystallization, limiting compatibility with flexible and tandem devices. Herein, a synergistic additive strategy combining lead acetate (PbAc 2 ) and ammonium benzenesulfonate (ABS) enables the fabrication of γ-CsPbI 3 below 100 °C. Acetate anions lower the nucleation energy barrier, while tailored ABS analogs stabilize the γ-phase via chelation and steric hindrance, suppressing octahedral tilting. This work establishes a mechanistic framework linking additive chemistry to the low-temperature crystallization of CsPbI 3 perovskite, providing guidance for the rational design of all-inorganic perovskite formulations toward flexible and tandem photovoltaics. This approach achieves a record power conversion efficiency (PCE) of 16.33% for CsPbI 3 solar cells processed at temperatures below 100 °C, and retains 91% of the initial PCE after 600 h in dry air. Furthermore, flexible devices reach 13.53% PCE, demonstrating direct compatibility with flexible substrates.
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