钝化
材料科学
钙钛矿(结构)
重组
载流子寿命
光电子学
分子
氟
化学工程
纳米技术
图层(电子)
硅
冶金
化学
有机化学
工程类
基因
生物化学
作者
Hang Su,Jing Zhang,Yingjie Hu,Xinyi Du,Ying Yang,Jiaxue You,Lili Gao,Shengzhong Liu
标识
DOI:10.1002/aenm.202101454
摘要
Abstract Defects in perovskite layers usually cause nonradiative recombination, impairing device performance and stability. Here, fluoroethylamine (FC 2 H 4 NH 3 , FEA) is integrated into the perovskite film to passivate defects. By engineering of different amounts of fluorine in the molecule, it is found that when 2‐fluoroethylamine (1FEA), in which one F bonds to the first carbon atom at the end of the molecule's structure, is used, the F atoms appear to be distributed throughout the bulk to the very surface. When 2,2‐difluoroethylamine (2FEA) and 2, 2, 2‐trifluoroethylamine (3FEA) are used, F is prone to distribution in the bulk of the perovskite film, while there appears to be no detectable F content on the surface. With the FEA passivation, the nonradiative recombination is suppressed, the carrier‐lifetime is improved to 840.01 ns, and the film‐air interface offers greater hydrophobicity, especially in the case of 1FEA, where because it is distributed throughout the film thickness, it passivates more defects and delivers the highest efficiency, as much as 23.40%. The device with 3FEA shows the best environmental stability; specifically, the bare cell without any encapsulation maintains 87% of its initial efficiency after exposure to the ambient environment for 1200 h.
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