化学
钙钛矿(结构)
脱质子化
胺气处理
非阻塞I/O
降级(电信)
能量转换效率
无机化学
功能群
稳定器(航空)
催化作用
组合化学
有机化学
材料科学
离子
聚合物
电信
光电子学
计算机科学
工程类
机械工程
作者
Mengjia Li,Jing Li,Qixin Zhuang,Dongmei He,Baibai Liu,Cong Chen,Boxue Zhang,Thierry Pauporté,Zhigang Zang,Jiangzhao Chen
标识
DOI:10.1002/ange.202206914
摘要
Abstract Perovskite solar cells suffer from poor reproducibility due to the degradation of perovskite precursor solution. Herein, we report an effective precursor stabilization strategy via incorporating 3‐hydrazinobenzoic acid (3‐HBA) containing carboxyl (−COOH) and hydrazine (−NHNH 2 ) functional groups as stabilizer. The oxidation of I − , deprotonation of organic cations and amine‐cation reaction are the main causes of the degradation of mixed organic cation perovskite precursor solution. The −NHNH 2 can reduce I 2 defects back to I − and thus suppress the oxidation of I − , while the H + generated by −COOH can inhibit the deprotonation of organic cations and subsequent amine‐cation reaction. The above degradation reactions are simultaneously inhibited by the synergy of functional groups. The inverted device achieves an efficiency of 23.5 % (certified efficiency of 23.3 %) with an excellent operational stability, retaining 94 % of the initial efficiency after maximum power point tracking for 601 hours.
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