材料科学
钙钛矿(结构)
替代(逻辑)
窗口(计算)
过程(计算)
化学工程
工程物理
计算机科学
万维网
操作系统
工程类
程序设计语言
作者
Bo Zhao,Zhaohui Du,Yingjie Xie,Huan Lei,Jinxian Yang,Hui Zhang,Yonghua Chen
标识
DOI:10.1002/adfm.202508262
摘要
Abstract Dimethyl sulfoxide (DMSO) is frequently employed to boost the crystal quality of solution‐processed perovskites, while it is prone to remain trapped within the films and leads to defective interface within the resultant perovskite solar cells (PSCs). Herein, a small molecule of hydroxyethyl methacrylate (HEMA) is introduced to substitute the DMSO. The hydroxyl (─OH) and carbonyl (─C═O) groups in HEMA are simultaneously associated with formamidinium (FA + ) and Pb 2+ via hydrogen bonds and coordination bonds, respectively, which facilitates the formation of strongly bonded FAI‐HEMA‐PbI 2 complexes in the precursor solution to regulate perovskite crystallization with improved crystallinity and preferred orientation. Moreover, the solidification of residual HEMA via in situ polymerization can stabilize crystal structure with suppressed defects and released lattice strain. Consequently, PSCs based on HEMA‐treated perovskite films achieve a decent power conversion efficiency (PCE) of 25.31% with superior stability, retaining 90% of their initial PCE after 1000 h storage. Importantly, the incorporated hydrophilic HEMA can largely promote the moisture resistance of the precursor solution by preventing water molecules from direct contact with perovskite components. More than 90% of the initial efficiency is maintained by using old precursor solutions aged in ambient air for 20 days, indicating an extended process window for device fabrication.
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