Unraveling the Reasons Behind SnO2/Perovskite Defects and Their Cure Through Multifunctional Ti3C2TX

被引:4
|
作者
Khan, Danish [1 ]
Muhammad, Imran [2 ]
Qu, Geping [2 ]
Gao, Changqin [2 ]
Xu, Jiamin [3 ]
Tang, Zeguo [1 ]
Wang, Yang-Gang [2 ]
Xu, Zong-Xiang [2 ]
机构
[1] Shenzhen Technol Univ, Coll New Mat & New Energies, Shenzhen 518118, Guangdong, Peoples R China
[2] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Guangdong, Peoples R China
[3] Hong Kong Univ Sci & Technol, Div Integrat Syst & Design, Hong Kong 999077, Peoples R China
基金
中国国家自然科学基金;
关键词
buried interface; MXenes; PbI2; residue; SnO2/perovskite interface; PEROVSKITE SOLAR-CELLS; FILL FACTOR; TIN OXIDE; INTERFACES; EFFICIENT; PASSIVATION; LEAD; SNO2;
D O I
10.1002/adfm.202316169
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The rationale for low performances in perovskite solar cells with buried interface still needs to be clarified, owing to the complicated physiochemistry of metal oxides/perovskite interface, and literature offers a meager knowledge about the reactions at this interface. While exploring the SnO2/perovskite interfacial interactions, the reasons behind deteriorating perovskite at the interface are comprehensively investigated, and it is revealed that the PbI2 residue and metallic Pb-0 are the byproducts of this decomposed perovskite. Introducing an optimized amount of Ti3C2TX at the SnO2/perovskite interface detaches the SnO2 hydroxyls, which are found to be responsible for interfacial ion migrations. In addition, Ti3C2TX passivates the interface defects via its functional groups and establishes ballistic pathways for electrons with high chances of non-radiative recombination. Thus, 25.19% (certified as 24.41%) of efficiency with superior long-term operational stability is achieved.
引用
收藏
页数:12
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