铷
钙钛矿(结构)
材料科学
相(物质)
工程物理
光电子学
纳米技术
化学
冶金
结晶学
物理
钾
有机化学
作者
Bo Xu,Rong Yang,Yu Chen,Jinfei Zhou,Wen Liang Tan,Pinghui Yang,Fengwei Wang,X X Wang,Wenbo Liu,Xuan Gao,Jingwei Li,Daliang Zhang,Christopher R. McNeill,Renzhi Li,Wei Huang,Jianpu Wang
标识
DOI:10.1021/acsenergylett.4c02883
摘要
Quasi-two-dimensional (2D) perovskites are notable for their diverse formulations and environmental stability. However, solution-processed quasi-2D perovskites often exhibit inherent multiple-quantum-well structures with broad phase distributions, limiting their efficiency in photovoltaic applications. Here, we demonstrate that incorporating rubidium ions effectively narrows the phase distribution in quasi-2D perovskite by accelerating the formation of the n = 1 2D perovskite phase during the initial crystallization stage. This leads to a decrease in the remaining free organic spacer cations, which in turn limits the transition to medium-n phases (n = 3, 4) and promotes the formation of high-quality 3D-like or large-n perovskites, ultimately enhancing charge transport of quasi-2D perovskite. Consequently, we achieve quasi-2D perovskite solar cells with a champion power conversion efficiency of 21.9%. Furthermore, the thermal stability of the unencapsulated devices containing rubidium is significantly improved, with the T80 lifetime under continuous 60 °C stress increasing from 1150 to over 3000 h.
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