材料科学
钝化
钙钛矿(结构)
聚合物
晶界
卤化物
化学工程
偶极子
光伏系统
光电子学
纳米技术
无机化学
复合材料
有机化学
生态学
图层(电子)
生物
微观结构
化学
工程类
作者
Yuhui Ma,Yuanhang Cheng,Xiuwen Xu,Menglin Li,Chujun Zhang,Sin Hang Cheung,Zixin Zeng,Dong Shen,Yue‐Min Xie,Ka Lok Chiu,Fen Lin,Shu Kong So,Chun‐Sing Lee,Sai‐Wing Tsang
标识
DOI:10.1002/adfm.202006802
摘要
Abstract Passivation of organometal halide perovskites with polar molecules has been recently demonstrated to improve the photovoltaic device efficiency and stability. However, the mechanism is still elusive. Here, it is found that both polymers with large and small dipole moment of 3.7 D and 0.6 D have negligible defect passivation effect on the MAPbI 3 perovskite films as evidenced by photothermal deflection spectroscopy. The photovoltaic devices with and without the polymer additives also have comparable power conversion efficiencies around 19%. However, devices with the additives have noticeable improvement in stability under continuous light irradiation. It is found that although the initial mobile ion concentrations are comparable in both devices with and without the additives, the additives can strongly suppress the ion migration during the device operation. This contributes to the significantly enhanced electrical‐field stress tolerance of the perovskite solar cells (PVSCs). The PVSCs with polymer additives can operate up to −2 V reverse voltage bias which is much larger than the breakdown voltage of −0.5 V that has been commonly observed. This study provides insight into the role of additives in perovskites and the corresponding device degradation mechanism.
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