Efficient and Stable Perovskite Solar Cells by Fluorinated Ionic Liquid–Induced Component Interaction

钙钛矿(结构) 离子液体 钝化 热稳定性 光致发光 卤化物 材料科学 化学工程 傅里叶变换红外光谱 化学 无机化学 纳米技术 有机化学 光电子学 工程类 催化作用 图层(电子)
作者
Yue Wang,Lingfeng Chao,Tingting Niu,Deli Li,Qi Wei,Hui Wu,Jian Qiu,Hui Lu,Chenxin Ran,Qi Zhong,Lin Song,Guichuan Xing,Yingdong Xia,Yonghua Chen,Peter Müller‐Buschbaum,Wei Huang
出处
期刊:Solar RRL [Wiley]
卷期号:5 (1) 被引量:29
标识
DOI:10.1002/solr.202000582
摘要

The instability of organic cations in lead halide perovskite materials is a major obstacle for the commercial breakthrough of perovskite photovoltaics due to desorption of organic cations during the thermal annealing and device operation. Herein, a novel strategy is reported to improve the performance and stability of organic halide perovskite solar cells containing organic cations by adding a small amount of the ionic liquid methylammonium difluoroacetate (MA + DFA − ). Nuclear magnetic resonance and Fourier‐transform infrared spectroscopy measurements show that MA + DFA − can anchor the organic cations via hydrogen bonding and enhance the Pb–O interaction in perovskite precursors, leading to the retardation of the perovskite crystallization and improved stability of the perovskite precursor solution. Dynamic light scattering and scanning electron microscopy verify the defect‐passivation effect of MA + DFA − on the perovskite precursors and films. The passivated perovskite film shows superior photo carrier dynamics as investigated by time‐resolved photoluminescence and transient absorption spectra. Moreover, the hydrogen bonding of the perovskite with MA + DFA − imparts excellent ambient and thermal stability to the film as revealed by X‐ray diffraction measurements. As a result, devices with a high efficiency of 21.46% and excellent stability over 180 days in nitrogen atmosphere at room temperature are achieved with the ionic liquid.
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