钝化
开路电压
材料科学
钙钛矿(结构)
介观物理学
能量转换效率
光电子学
电压
纳米技术
电气工程
化学
凝聚态物理
结晶学
物理
图层(电子)
工程类
作者
Dang Xu,Dongjie Wang,Jiale Liu,Jianhang Qi,Kai Chen,Wending Zhu,Tao Ying,Zheling Zhang,Anyi Mei,Jian Zhang
出处
期刊:Small
[Wiley]
日期:2024-04-26
卷期号:20 (31)
被引量:3
标识
DOI:10.1002/smll.202311755
摘要
Abstract Numerous defects exist at the buried interface between the perovskite and adjacent electron transport layers in perovskite solar cells, resulting in severe non‐radiative recombination and excessive open‐circuit voltage ( V OC ) loss. Herein, a dual defect passivation strategy utilizing guanidine sulfate (GUA 2 SO 4 ) as an interface modifier is first reported. On the one hand, the SO 4 2− preferentially interacts with Pb‐related defects, generating water‐insoluble lead oxysalts complexes. Additionally, GUA + diffuses into the perovskite and induces the formation of low‐dimensional perovskite. These reactions effectively suppress trap states at the buried interface and perovskite boundaries in printable mesoscopic perovskite solar cells (p‐MPSCs), thus increasing the carrier lifetime. Meanwhile, GUA 2 SO 4 optimizes the interface energy band alignment, thus accelerating the charge extraction and transfer at the buried interface. This synergistic effect of trap passivation and interface energy band alignment modulation is strongly demonstrated by an increase in average V OC of 70 mV and the power conversion efficiency improvement from 17.51% to 18.70%. This work provides a novel approach to efficiently improve the performance of p‐MPSCs through dual‐targeted defect passivation at the buried interface.
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