材料科学
钙钛矿(结构)
调制(音乐)
化学工程
纳米技术
光电子学
哲学
工程类
美学
作者
Yu Wang,Feng Wang,Jiaxing Song,Jingchuan Ye,Jieying Cao,Xinxing Yin,Zhen Su,Yingzhi Jin,Lin Hu,Han Zuilhof,Zaifang Li,Wensheng Yan,Feng Gao
标识
DOI:10.1002/adfm.202402632
摘要
Abstract As the core component of sandwich‐like perovskite solar cells (PSCs), the quality of perovskite layer is a challenge for further progress in PSCs due to the unfavorable defects and uncontrollable crystallization. Here, a surface post‐treatment strategy employing ethyl thioglycolate (ET) as ligand molecule is developed for property manipulation of perovskite films. ET can lower surface energy of perovskite facets and induces secondary growth of grains, giving films with higher crystallinity and lower defect density. Meanwhile, both carbonyl and sulfhydryl in ET can bind to the Pb 2+ , thus forming bidentate anchoring on the surface for defect passivation. Besides, the perovskite/ET/C 60 interface presents improved charge transfer owing to the well‐aligned energy levels. Consequently, the power‐conversion‐efficiency (PCE) is boosted to 22.42% and 23.56% (certified 23.29%) for the FA 0.85 Cs 0.15 Pb(I 0.95 Br 0.05 ) 3 and FA 0.9 MA 0.05 Cs 0.05 Pb(I 0.95 Br 0.05 ) 3 PSCs, respectively, and the FA 0.85 Cs 0.15 Pb(I 0.95 Br 0.05 ) 3 ‐based PSC with a larger area (1.03 cm 2 ) delivers a PCE of 20.01%. Importantly, ET demonstrates effective management of I 2 and PbI 2 , thereby preventing accelerated degradation and lead leakage of devices. Thanks to the multiple effects of ET, the resulting devices exhibit significantly enhanced ambient stability over a course of 800 h, and a thermal stability of over 1500 h while maintaining 80.4% of its original efficiency.
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