钝化
卤化物
钙钛矿(结构)
非阻塞I/O
材料科学
异质结
磁滞
化学
化学工程
无机化学
图层(电子)
结晶学
光电子学
纳米技术
有机化学
催化作用
凝聚态物理
物理
工程类
作者
Hui Ju,Yajie Ma,Ye Cao,Zixuan Wang,Liming Liu,Meixiu Wan,Tahmineh Mahmoudi,Yoon‐Bong Hahn,Yousheng Wang,Yaohua Mai
出处
期刊:Solar RRL
[Wiley]
日期:2022-02-08
卷期号:6 (6)
被引量:17
标识
DOI:10.1002/solr.202101082
摘要
The passivation of perovskite bulk and heterointerface defects is one of the most significant ways to enhance the efficiency and operational stability of perovskite solar cells (PSCs). So far, ammonium‐based alkylamine halides have been considered as effective passivation materials to reduce defects of the perovskite absorber layer. Herein, roles of long‐chain alkylamine ligands (LALs) in triple‐halide perovskites are systematically studied for achieving efficient NiO x ‐based inverted PSCs. Two kinds of LALs oleylammonium (OAm) and phenethylammonium (PEA), as perovskite bulk and interface passivation agents, respectively, are introduced. It is found that both OAm and PEA ligands cannot only assist their crystal growth with vertical orientation, but also suppress triple‐halide perovskite bulk and interface defects. As precursor additives, OAm ligands can be used as organic spacers to assist the generation of the 2D@3D perovskite bulk crystals. 2D@3D/2D perovskite heterostructures are further formed when the 2D@3D perovskite bulk film is post‐treated by PEA ligands. As a result, such strategies enable hysteresis‐free and highly efficient NiO x ‐based triple‐halide inverted PSCs.
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