钙钛矿(结构)
材料科学
能量转换效率
化学工程
八面体
相(物质)
Crystal(编程语言)
薄膜
纳米技术
光电子学
结晶学
晶体结构
有机化学
化学
程序设计语言
工程类
计算机科学
作者
Xiangyu Sun,Dongni Li,Lu Zhao,Yao Zhang,Qin Hu,Thomas P. Russell,Fangze Liu,Jing Wei,Hongbo Li
标识
DOI:10.1002/adma.202301115
摘要
Abstract Fabricating perovskite films with a dominant crystal orientation is an effective path to realizing quasi‐single‐crystal perovskite film, which can eliminate the fluctuation of the electrical properties in films arising from grain‐to‐grain variations, and improve the performance of perovskite solar cells (PSCs). Perovskite (FAPbI 3 ) films based on one‐step antisolvent methods usually suffer from chaotic orientations due to the inevitable intermediate phase conversion from intermediates of PbI 2 •DMSO, FA 2 Pb 3 I 8 •4DMSO, and δ ‐FAPbI 3 to α ‐FAPbI 3 . Here, a high‐quality perovskite film with (111) preferred orientation ((111)‐ α ‐FAPbI 3 ) using a short‐chain isomeric alcohol antisolvent, isopropanol (IPA) or isobutanol (IBA), is reported. The interaction between IPA and PbI 2 leads to a corner‐sharing structure instead of an edge‐sharing PbI 2 octahedron, sidestepping the formation of these intermediates. With the volatilization of IPA, FA + can replace IPA in situ to form α ‐FAPbI 3 along the (111) direction. Compared to randomly orientated perovskites, the dominantly (111) orientated perovskite ((111)‐perovskite) exhibits improved carrier mobility, uniform surface potential, suppressed film defects and enhanced photostability. PSCs based on the (111)‐perovskite films show 22% power conversion efficiency and excellent stability, which remains unchanged after 600 h continuous working at maximum power point, and 95% after 2000 h of storage in atmosphere environment.
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