材料科学
钙钛矿(结构)
钙钛矿太阳能电池
钝化
离子液体
卤化物
太阳能电池
离子键合
磁滞
图层(电子)
降级(电信)
化学工程
光伏系统
光电子学
能量转换效率
纳米技术
离子
无机化学
电子工程
电气工程
催化作用
生物化学
量子力学
有机化学
化学
工程类
物理
作者
Xuejie Zhu,Shaoan Yang,Yuexian Cao,Lianjie Duan,Minyong Du,Jiangshan Feng,Yuxiao Jiao,Jiang Xiao,Youming Sun,Hui Wang,Shengnan Zuo,Yucheng Liu,Shengzhong Liu
标识
DOI:10.1002/aenm.202103491
摘要
Abstract Metal‐halide perovskite has emerged as an effective photovoltaic material for its high power conversion efficiency (PCE), low cost and straightforward fabrication techniques. Unfortunately, its long‐term operational durability, mainly affected by halide ion migration and undercoordinated Pb 2+ is still the bottleneck for its large‐scale commercialization. In this work, an ionic liquid (IL) is designed to effectively cap the grain surface for improved stability and reduced trap density. More specifically, the Br − in the IL passivates the undercoordinated Pb 2+ by chemically bonding to it, resulting in a thin layer of ionic‐liquid‐perovskite formed on the surface, leading to improved photovoltaic performance and better stability. Specifically, the solar cell exhibits an open‐circuit voltage of 1.192 V and PCE of 24.33% under one‐sun illumination with negligible hysteresis, and a large area (10.75 cm 2 ) integrated module achieves PCE of 20.33%. Moreover, the bare device maintains over 90% of its initial efficiency after 700 h of aging at 65 °C. It also shows outstanding stability with only about 10% degradation after being exposed to the ambient environment for 1000 h. The superior efficiency and stability demonstrate that the present IL passivating strategy is a promising approach for high‐performance large area perovskite solar cell applications.
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