材料科学
钙钛矿(结构)
带隙
能量转换效率
光电子学
光致发光
开路电压
钝化
串联
纳米技术
电压
化学
结晶学
复合材料
电气工程
工程类
图层(电子)
作者
Rui He,Zongjin Yi,Yi Luo,Jincheng Luo,Qi Wei,Huagui Lai,Hao Huang,Bingsuo Zou,Guangyao Cui,Wenwu Wang,Chuanxiao Xiao,Shengqiang Ren,Cong Chen,Changlei Wang,Guichuan Xing,Fan Fu,Dewei Zhao
标识
DOI:10.1002/advs.202203210
摘要
Surface post-treatment using ammonium halides effectively reduces large open-circuit voltage (VOC ) losses in bromine-rich wide-bandgap (WBG) perovskite solar cells (PSCs). However, the underlying mechanism still remains unclear and the device efficiency lags largely behind. Here, a facile strategy of precisely tailoring the phase purity of 2D perovskites on top of 3D WBG perovskite and realizing high device efficiency is reported. The transient absorption spectra, cross-sectional confocal photoluminescence mapping, and cross-sectional Kelvin probe force microscopy are combined to demonstrate optimal defect passivation effect and surface electric-field of pure n = 1 2D perovskites formed atop 3D WBG perovskites via low-temperature annealing. As a result, the inverted champion device with 1.77-eV perovskite absorber achieves a high VOC of 1.284 V and a power conversion efficiency (PCE) of 17.72%, delivering the smallest VOC deficit of 0.486 V among WBG PSCs with a bandgap higher than 1.75 eV. This enables one to achieve a four-terminal all-perovskite tandem solar cell with a PCE exceeding 25% by combining with a 1.25-eV low-bandgap PSC.
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