卤化物
锡
钙钛矿(结构)
路易斯酸
基础(拓扑)
无机化学
化学
材料科学
催化作用
冶金
结晶学
有机化学
数学分析
数学
作者
Shurong Wang,Cheng Wu,Tai‐Sing Wu,Huanhuan Yao,Yong Hua,Feng Hao
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-02-26
卷期号:9 (3): 1168-1175
被引量:8
标识
DOI:10.1021/acsenergylett.4c00094
摘要
Lead-free tin halide perovskite solar cells (TPSCs) have driven much research attention for their environmental friendliness. However, the low efficiency and large open-circuit voltage (Voc) deficit limit their further development. Here, we introduced a π-conjugated Lewis base, 1H-pyrrolo[2,3-b]pyridin-6-ylaamine (1H6An), a N donor for the unique electron-donating role of pyridine and pyrrole N with unpaired lone pair electrons to interact with the tin halide perovskites and thus retard the oxidation of Sn2+ during the aging process of precursors. Meanwhile, the interaction stabilized the perovskite lattice and decreased the microstrain of deposited films. The carrier kinetics further revealed a notably enhanced carrier extraction and transport as well as decreased nonradiative recombination with 1H6An. Consequently, this approach delivered an efficiency of 13.28% with a remarkable Voc enhancement from 853 to 907 mV. Meanwhile, the 1H6An device exhibited an extended lifespan of over 2500 h with around 90% retention of its initial value in a N2 atmosphere.
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