非阻塞I/O
钙钛矿(结构)
材料科学
卤化物
能量转换效率
带隙
光电子学
兴奋剂
光伏
甲脒
光伏系统
无机化学
化学
结晶学
电气工程
催化作用
工程类
生物化学
作者
Liming Liu,Yajie Ma,Yousheng Wang,Qiaoyan Ma,Zixuan Wang,Zigan Yang,Meixiu Wan,Tahmineh Mahmoudi,Yoon‐Bong Hahn,Yaohua Mai
出处
期刊:Nano-micro Letters
[Springer Science+Business Media]
日期:2023-04-30
卷期号:15 (1)
被引量:30
标识
DOI:10.1007/s40820-023-01088-4
摘要
Abstract NiO x -based inverted perovskite solar cells (PSCs) have presented great potential toward low-cost, highly efficient and stable next-generation photovoltaics. However, the presence of energy-level mismatch and contact-interface defects between hole-selective contacts (HSCs) and perovskite-active layer (PAL) still limits device efficiency improvement. Here, we report a graded configuration based on both interface-cascaded structures and p-type molecule-doped composites with two-/three-dimensional formamidinium-based triple-halide perovskites. We find that the interface defects-induced non-radiative recombination presented at HSCs/PAL interfaces is remarkably suppressed because of efficient hole extraction and transport. Moreover, a strong chemical interaction, halogen bonding and coordination bonding are found in the molecule-doped perovskite composites, which significantly suppress the formation of halide vacancy and parasitic metallic lead. As a result, NiO x -based inverted PSCs present a power-conversion-efficiency over 23% with a high fill factor of 0.84 and open-circuit voltage of 1.162 V, which are comparable to the best reported around 1.56-electron volt bandgap perovskites. Furthermore, devices with encapsulation present high operational stability over 1,200 h during T 90 lifetime measurement (the time as a function of PCE decreases to 90% of its initial value) under 1-sun illumination in ambient-air conditions.
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