钝化
钙钛矿(结构)
能量转换效率
单独一对
材料科学
图层(电子)
路易斯酸
化学工程
化学
光电子学
纳米技术
结晶学
催化作用
有机化学
分子
工程类
作者
Mingming Zhao,Wei‐Min Gu,Ke‐Jian Jiang,Xinning Jiao,Kun Gong,Fengzhu Li,Xueqin Zhou,Yanlin Song
标识
DOI:10.1002/anie.202418176
摘要
The regulation of interfaces remains a critical and challenging aspect in the pursuit of highly efficient and stable perovskite solar cells (PSCs). Here, 2,2′‐bipyridyl‐4,4′‐dicarboxylic acid (HBPDC) is incorporated as an interfacial layer between SnO2 and perovskite layers in PSCs. The two carboxylic acid moieties on HBPDC bind to SnO2 through esterification, while its nitrogen atoms, possessing lone electron pairs, interact with uncoordinated lead (Pb2+) atoms through Lewis acid‐base interactions. This dual functionality enables simultaneous passivation of surface defects on both the SnO2 and buried perovskite layers. In addition, the electron‐deficient nature of HBPDC enhances interfacial energy band alignment and facilitates electron transfer from the perovskite to SnO2. Furthermore, the incorporation of HBPDC strengthens the interfacial adhesion, improving mechanical reliability. As a result, the PSCs exhibited an impressive power conversion efficiency (PCE) of 25.41% under standard AM 1.5G conditions, along with remarkable environmental stability.
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