材料科学
甲脒
钙钛矿(结构)
能量转换效率
异质结
钝化
锡
光电子学
结晶度
锌黄锡矿
开路电压
手套箱
纳米技术
图层(电子)
化学工程
捷克先令
电压
太阳能电池
化学
电气工程
复合材料
有机化学
冶金
工程类
作者
Tianyue Wang,Hok‐Leung Loi,Jiupeng Cao,Zhaotong Qin,Zhiqiang Guan,Yang Xu,Haiyang Cheng,Guijun Li,Chun‐Sing Lee,Xinhui Lu,Feng Yan
标识
DOI:10.1002/advs.202200242
摘要
Abstract 2D–3D mixed tin halide perovskites are outstanding candidate materials for lead‐free perovskite solar cells (PSCs) due to their improved stability and decreased trap density in comparison with their pure 3D counterparts. However, the mixture of multiple phases may lead to poor charge transfer across the films and limit the device efficiency. Here, a stacked quasi‐2D (down)–3D (top) double‐layered structure in perovskite films prepared via vacuum treatment is demonstrated, which can result in a planar bilayer heterojunction. In addition, it is found that the introduction of guanidinium thiocyanate (GuaSCN) additive can improve the crystallinity and carrier mobility in the 2D perovskite layer and passivate defects in the whole film, leading to a long carrier lifetime (>140 ns) in photoluminescence measurements. As a result, the PSCs show a high open circuit voltage (V OC ) up to 1.01 V with a voltage loss of only 0.39 V, which represents the record values ever reported for tin‐based PSCs. The champion device exhibits a power conversion efficiency (PCE) of 13.79% with decent stability, retaining 90% of the initial PCE for 1200 h storage in N 2 ‐filled glovebox.
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