钝化
钙钛矿(结构)
能量转换效率
晶界
硅氧烷
热稳定性
材料科学
路易斯酸
化学工程
光伏系统
纳米技术
化学
图层(电子)
有机化学
催化作用
光电子学
复合材料
聚合物
微观结构
电气工程
工程类
作者
Lin Xie,Jiangzhao Chen,Parth Vashishtha,Xing Zhao,Gwang Su Shin,Subodh G. Mhaisalkar,Nam‐Gyu Park
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2019-08-07
卷期号:4 (9): 2192-2200
被引量:207
标识
DOI:10.1021/acsenergylett.9b01356
摘要
Here we report an efficient and reproducible multifunctional additive engineering strategy via methoxysilane cross-linking agents functionalized by the different terminal group, moderate electron-donating −SH, weak electron-donating −CH3, or strong electron-withdrawing −CN, into a PbI2 precursor solution. The power conversion efficiency (PCE) is increased from 18.4 to 20.8% after introduction of (3-mercaptopropyl)trimethoxysilane (MPTS) containing a −SH group as a consequence of improved voltage and current density, while 3-cyanopropyltriethoxysilane (CPTS) containing a −CN group deteriorates the overall photovoltaic performance. Moreover, −SH in MPTS is found to passivate defects effectively through a Lewis acid–base interaction with PbI2, resulting in a larger grain size and a longer carrier lifetime. Owing to the formation of a cross-linking siloxane network as a protective layer on the grain boundary, the thermal and moisture stability of the device are improved remarkably. The present work provides a guideline for multifunctional additive engineering for the purpose of simultaneous achievement of a high PCE and long-term stability.
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