材料科学
晶界
钙钛矿(结构)
钝化
微晶
成核
载流子寿命
化学工程
纳米技术
能量转换效率
光电子学
硅
化学
复合材料
冶金
有机化学
微观结构
工程类
图层(电子)
作者
Tianyuan Luo,Gang Ye,Xiayan Chen,Haixin Chang,Tian Ye,Chunyan Zhao,Wenfeng Zhang,Haixin Chang
出处
期刊:ACS applied energy materials
[American Chemical Society]
日期:2021-10-20
卷期号:4 (11): 12290-12297
被引量:6
标识
DOI:10.1021/acsaem.1c02113
摘要
The degeneration of organic–inorganic hybrid perovskite solar cells (PSCs) under ambient air is a serious challenge that prevents the commercialization of PSCs. The introduction of hydrophobic long-chain organic cations into the perovskite film is a promising way to improve the long-term stability of devices. However, this approach always comes with the sacrifice of the power conversion efficiency (PCE). In this work, we introduce a novel one-step double ion passivation route together using phenylethylamine ion (PEA+) and SCN– to passivate the grain boundary and surface of the perovskite polycrystalline film by crystal engineering to fabricate all air-processed, stable PSCs. Compared with three-dimensional (3D) MAPbI3 perovskite films, the PEA+ and SCN– codoped MAPbI3 perovskite films from the single crystal engineering have a larger grain size and better stability with a longer carrier lifetime and lower electron trap state density. The champion PCE of 18.04% with negligible hysteresis was achieved for the 0.05 M PEA+ and SCN– codoped PSCs, which exhibit 25% higher efficiency than the MAPbI3 solar cell fabricated using the traditional precursor solution mixing method. The devices without encapsulation still maintain 82% of their original PCE when stored over 750 h under ambient air conditions with a relative humidity of 50%.
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