掺杂剂
钙钛矿(结构)
兴奋剂
材料科学
氧化还原
离子
降级(电信)
吸收(声学)
光电子学
电导率
光化学
化学工程
纳米技术
化学
计算机科学
复合材料
有机化学
物理化学
电信
工程类
冶金
作者
Seul-Gi Kim,George C. Fish,Etienne Socie,Aaron T. Terpstra,Dong-Am Park,Kai Zhu,Michaël Grätzel,Jacques‐E. Moser,Nam‐Gyu Park
出处
期刊:Joule
[Elsevier]
日期:2024-04-15
卷期号:8 (6): 1707-1722
被引量:2
标识
DOI:10.1016/j.joule.2024.03.012
摘要
A widely used component of high-efficiency perovskite solar cells (PSCs) is the molecular hole-transport material (HTM) spiro-OMeTAD. This organic solid needs to be p-doped to acquire sufficient hole conductivity. However, the conventional doping method using LiTFSI in the air is slow, sensitive to the environment, and may lead to the deterioration of the PSCs by unintended oxidation or dopant migration. It is thus highly desirable to develop fast doping approaches that avoid exposing the PSC to ambient air and easy-to-move dopant ions. We report here that light absorption by spiro-OMeTAD itself triggers redox photochemistry that has so far been ignored. Strikingly, we found that Y(III) or La(III)-tBP complexes catalyze the symmetry-breaking charge separation of photo-excited spiro-OMeTAD, resulting in the efficient p-doping of the HTM. Using this photo-redox process, we realize PSCs with superior stability over cells using conventional doping that show no degradation under continuous illumination over 1,000 h.
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