材料科学
钙钛矿(结构)
能量转换效率
光电子学
图层(电子)
带隙
卤化物
结晶
纳米技术
化学工程
无机化学
工程类
化学
作者
Benfang Niu,Haoran Liu,Yanchun Huang,Emely Gu,Minxing Yan,Ziqiu Shen,Kangrong Yan,Buyi Yan,Jizhong Yao,Yanjun Fang,Hongzheng Chen,Chang‐Zhi Li
标识
DOI:10.1002/adma.202212258
摘要
Abstract Challenges remain hindering the performance and stability of inverted perovskite solar cells (PSCs), particularly for the nonstable interface between lead halide perovskite and charge extraction metal oxide layer. Herein, a simple yet scalable interfacial strategy to facilitate the assemble of high‐performance inverted PSCs and scale‐up modules is reported. The hybrid interfacial layer containing self‐assembly triphenylamine and conjugated poly(arylamine) simultaneously improves the chemical stability, charge extraction, and energy level alignment of hole‐selective interface, meanwhile promoting perovskite crystallization. Consequently, the correspondent inverted PSCs and modules achieve remarkable power conversion efficiencies (PCEs) of 24.5% and 20.7% (aperture area of 19.4 cm 2 ), respectively. The PSCs maintain over 80% of its initial efficiency under one‐sun equivalent illumination of 1200 h. This strategy is also effective to perovskite with various bandgaps, demonstrating the highest PCE of 19.6% for the 1.76‐eV bandgap PSCs. Overall, this work provides a simple yet scalable interfacial strategy for obtaining state‐of‐the‐art inverted PSCs and modules.
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