结晶度
聚乙烯吡咯烷酮
材料科学
钙钛矿(结构)
碘化物
溶解
化学工程
氢键
能量转换效率
再结晶(地质)
晶界
水分
纳米技术
钙钛矿太阳能电池
化学
复合材料
无机化学
高分子化学
有机化学
微观结构
光电子学
工程类
古生物学
分子
生物
作者
Yunjuan Niu,Dingchao He,Zhengguo Zhang,Jun Zhu,Tulloch Gavin,Polycarpos Falaras,Linhua Hu
标识
DOI:10.1016/j.jechem.2021.10.029
摘要
• The hydrogen-bonding-initiated self-healing repairs the decayed perovskite solar cell back to the original state, continue to work, and alleviate long-term cell instability. Air moisture is the key issue for perovskites which invades the films and accelerates the damage of devices. Here, polyvinylpyrrolidone (PVP) is introduced to the methylammonium lead iodide (MAPbI 3 ) perovskite precursor to control crystal growth and endow the devices with self-healing ability in a moisture environment. The strong C Ο⋯Η Ν hydrogen bonding interactions between PVP and MAPbI 3 was confirmed by nuclear magnetic resonance measurements. By introducing hydrogen bonding in the MAPbI 3 -based PSCs, we form a compact perovskite film of excellent electronic quality with a power conversion efficiency (PCE) of up to 20.32%. Furthermore, the Ο⋯Η Ν hydrogen bonding interactions at the grain boundaries suppress the decomposition of methylammonium cations and improve the recyclable dissolution–recrystallization of perovskite. As a result, the MAPbI 3 -PVP based cells exhibited striking moisture stability and self-healing behavior, with negligible decay in efficiency after 500 h of operation in high humidity (65% ± 5% relative humidity) and rapid recovering ability after their removal from the humid environment.
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