钙钛矿(结构)
光电流
光活性层
磁滞
材料科学
异质结
卤化物
光电子学
图层(电子)
光伏系统
钙钛矿太阳能电池
太阳能电池
纳米技术
化学
聚合物太阳能电池
无机化学
凝聚态物理
结晶学
物理
电气工程
工程类
作者
Konrad Wojciechowski,Tomas Leijtens,С. В. Сипрова,Christoph Schlueter,Maximilian T. Hörantner,Jacob Tse‐Wei Wang,Chang‐Zhi Li,Alex K.‐Y. Jen,Tien‐Lin Lee,Henry J. Snaith
标识
DOI:10.1021/acs.jpclett.5b00902
摘要
Organic-inorganic halide perovskite solar cells have rapidly evolved over the last 3 years. There are still a number of issues and open questions related to the perovskite material, such as the phenomenon of anomalous hysteresis in current-voltage characteristics and long-term stability of the devices. In this work, we focus on the electron selective contact in the perovskite solar cells and physical processes occurring at that heterojunction. We developed efficient devices by replacing the commonly employed TiO2 compact layer with fullerene C60 in a regular n-i-p architecture. Detailed spectroscopic characterization allows us to present further insight into the nature of photocurrent hysteresis and charge extraction limitations arising at the n-type contact in a standard device. Furthermore, we show preliminary stability data of perovskite solar cells under working conditions, suggesting that an n-type organic charge collection layer can increase the long-term performance.
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