Efficient Inorganic Vapor-Assisted Defects Passivation for Perovskite Solar Module

被引:27
|
作者
Zhang, Kun [1 ,2 ,3 ]
Wang, Yang [1 ,2 ]
Tao, Mingquan [1 ,2 ,3 ]
Guo, Lutong [1 ,2 ,3 ]
Yang, Yongrui [1 ,2 ,3 ]
Shao, Jiangyang [2 ,4 ]
Zhang, Yanyan [2 ,5 ]
Wang, Fuyi [2 ,3 ,5 ]
Song, Yanlin [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Inst Chem, Key Lab Green Printing, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Inst Chem, CAS Res Educ Ctr Excellence Mol Sci, Beijing 100190, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Chinese Acad Sci, Inst Chem, Key Lab Photochem, Beijing 100190, Peoples R China
[5] Chinese Acad Sci, Inst Chem, Key Lab Analyt Chem Living Biosyst, Beijing 100190, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
inorganic passivation layer; modules; perovskite; photovoltaics; vapor-assisted passivation; FILMS; CELLS;
D O I
10.1002/adma.202211593
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Surface trap as intrinsic defects-mediated non-radiative charge recombination is a major obstacle to achieving the reliable fabrication of high-efficiency and large-area perovskite photovoltaics. Here a CS2 vapor-assisted passivation strategy is proposed for perovskite solar module, aiming to passivate the iodine vacancy and uncoordinated Pb2+ caused by ion migration. Significantly, this method can avoid the disadvantages of inhomogeneity film caused by spin-coating-assisted passivation and reconstruction of perovskite surface from solvent. The CS2 vapor passivated perovskite device presents a higher defect formation energy (0.54 eV) of iodine vacancy than the pristine (0.37 eV), while uncoordinated Pb2+ is bonded with CS2. The shallow level defect passivation of iodine vacancy and uncoordinated Pb2+ has obviously enhanced the device efficiencies (25.20% for 0.08 cm(2) and 20.66% for 40.6 cm(2)) and the stability, exhibiting an average T-80-lifetime of 1040 h working at the maximum power point, and maintaining over 90% of initial efficiency after 2000 h at RH = 30% and 30 degrees C.
引用
收藏
页数:9
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