钝化
卤化物
钙钛矿(结构)
能量转换效率
离子液体
化学工程
材料科学
图层(电子)
无机化学
离子键合
熔点
化学
纳米技术
离子
催化作用
光电子学
有机化学
工程类
作者
Xinmeng Zhuang,Xinfu Chen,Lin Xu,Shuainan Liu,Yanjie Wu,Zhichong Shi,Qingqing Zhou,Bo Li,Haixia Yan,Peter Reiß,Hongwei Song
标识
DOI:10.1016/j.jcis.2022.04.117
摘要
Long-term stability remains a great challenge for metal halide perovskite solar cells (PSCs). The utilization of ionic liquids (ILs) is a promising strategy to solve the stability problem. However, few studies have focused on controlling the halide anions of ILs, in which different organic cations can modulate the melting point of ILs and film crystal growth. Here, ILs with a 1-ethyl-3-methylimidazolium (EMIM+) cation and different halide anions (X = Cl, Br, and I) are employed in inverted PSCs. The results show that EMIMX can form a 1D passivation layer by the in situ growth technique and influence the surface morphology of the perovskite film. These EMIMX-treated layers simultaneously suppress the surface defects and nonradiative energy losses and improve the hydrophobic properties. As a result, a power conversion efficiency (PCE) of 20.0% is obtained for the EMIMBr-modified PSCs compared to 18.06% for the control device. Moreover, the unencapsulated devices maintain more than 90% of their initial PCE over 3000 h under ambient air, which is among the best long-term stabilities reported for NiOx-based inverted PSCs. It also retains 74.2% and 49.5% of the initial PCE value after aging under harsher conditions, such as an 85 ± 5% relative humidity (RH) environment and at 85 °C for 48 h, respectively.
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