CsF improved buried interface for efficient and stable inverted all-inorganic CsPbI2.85Br0.15 perovskite solar cells

被引:0
|
作者
Song, Zhicheng [1 ,2 ,3 ]
Chai, Wenming [1 ]
Zhu, Weidong [1 ]
Chen, Dazheng [1 ]
Zhang, Jincheng [1 ]
Zhang, Chunfu [1 ]
Hao, Yue [1 ]
机构
[1] Xidian Univ, Sch Microelect, State Key Lab Wide Bandgap Semicond Devices & Inte, Shaanxi Joint Key Lab Graphene, Xian 710071, Peoples R China
[2] Qinghai Huanghe Hydropower Dev Co Ltd, Xian Solar Power Branch, Xian 710000, Peoples R China
[3] Qinghai Huanghe Hydropower Dev Co Ltd, Xining 810007, Peoples R China
基金
中国国家自然科学基金;
关键词
All-inorganic; Interface reconstruction; Inverted structure; Defects passivation; FTO;
D O I
10.1016/j.mtener.2024.101763
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
All-inorganic CsPbIxBr3-x is frequently used as the top cells in tandem devices due to its tunable bandgap, making it highly promising for future development. However, CsPbIxBr3-x films typically contain numerous defects at the interfaces and grain boundaries, significantly hindering carrier transport and thus reducing the device performance. Interface modification is commonly employed to passivate defects and enhance carrier transport at the interfaces. In this work, CsF was used to modify the buried interface between the perovskite film and self- assembled monolayers (SAMs). The interaction between fluoride ions (F-) and uncoordinated Pb2+ contributed to reduce defect density, enhance crystallization quality, and suppress non-radiative carrier recombination at buried interface. Consequently, the efficiency of inverted CsPbI 2.85 Br 0.25 PSCs with CsF improved from 16.15 % to 18.24 %, compared to the control device. Moreover, the unencapsulated CsF-modified device retained 89 % of its initial efficiency after storing for 600 h in ambient air with room-temperature and relative humidity (RH) of 20 %. This demonstrates that CsF modification significantly enhances both the performance and stability of CsPbI 2.85 Br 0.15 perovskite solar cells.
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页数:8
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