Surface engineering based on ionic liquids for efficient and stable CsPbI3 perovskite solar cells

被引:8
|
作者
Rui, Dong [1 ]
Fu, Jianfei [2 ]
Chen, Qiaoyun [1 ]
Cao, Ji [1 ]
Wu, Wenting [1 ]
Chen, Lei [3 ]
Zhang, Jing [3 ]
Zhang, Zelong [1 ]
Zhou, Yi [1 ]
Song, Bo [1 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Lab Adv Optoelect Mat, Suzhou Key Lab Novel Semicond Mat & Devices, Suzhou 215123, Peoples R China
[2] NingboTech Univ, Sch Mat Sci & Engn MSE, Ningbo 315100, Peoples R China
[3] Changzhou Univ, Natl Expt Demonstrat Ctr Mat Sci & Engn, Sch Mat Sci & Engn, Jiangsu Prov Cultivat base State Key Lab Photovolt, Changzhou 213164, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
STABILITY; LAYERS; LEAD;
D O I
10.1039/d3ta06841b
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 perovskite CsPbI3 is widely recognized as a promising material for photovoltaic applications in single-junction or tandem solar cells. However, the spontaneous phase transition of CsPbI3 remains a crucial obstacle to commercialization. In this study, we propose a surface engineering approach using a tetra-n-butylammonium hexafluorophosphate (TBAPF(6)) ionic liquid to prevent the perovskite-to-non-perovskite phase transition induced by moisture. The experimental results demonstrate that by chemically bonding excess lead iodide (PbI2) with a tetrabutylammonium cation (TBA(+)), a low-dimensional stable and hydrophobic material called [TBA]PbI3 was achieved, which effectively enhances the stability of the CsPbI3 perovskite structure. Furthermore, we found that the hexafluorophosphate anion (PF6-) can effectively passivate surface iodine vacancies and interact with uncoordinated Pb2+. Consequently, the CsPbI3-based perovskite solar cells (C-PSCs) employing the TBAPF6 treatment achieved an impressive power conversion efficiency (PCE) of 17.47%. Moreover, the unencapsulated devices retained more than 70% of their initial PCE after being stored in ambient air for 168 hours.
引用
收藏
页码:7847 / 7855
页数:9
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