Post-Treatment-Free Dual-Interface Passivation via Facile 1D/3D Perovskite Heterojunction Construction

被引:5
作者
Wei, Ning [1 ]
Miao, Yanfeng [1 ]
Wang, Xingtao [1 ]
Qin, Zhixiao [1 ]
Liu, Xiaomin [1 ]
Chen, Haoran [1 ]
Wang, Haifei [1 ]
Liang, Yugang [1 ]
Wang, Shaowei [1 ]
Zhao, Yixin [1 ,2 ,3 ]
Chen, Yuetian [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Frontiers Sci Ctr Transformat Mol, Sch Environm Sci & Engn, Shanghai 200240, Peoples R China
[2] Shanghai Noncarbon Energy Convers & Utilizat Inst, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
来源
JACS AU | 2023年 / 3卷 / 12期
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
1D/3D heterojunction; perovskitesolar cell; metal oxide substrate functionalization; interface engineering; spontaneous ion diffusion; SOLAR-CELLS; PHASE; EFFICIENT; EVOLUTION; STATES;
D O I
10.1021/jacsau.3c00469
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
For achieving high-efficiency perovskite solar cells, it is almost always necessary to substantially passivate defects and protect the perovskite structure at its interfaces with charge transport layers. Such a modification generally involves the post-treatment of the deposited perovskite film by spin coating, which cannot meet the technical demands of scaling up the production of perovskite photovoltaics. In this work, we demonstrate one-step construction of buried and capped double 1D/3D heterojunctions without the need for any post-treatment, which is achieved through facile tetraethylammonium trifluoroacetate (TEATFA) prefunctionalization on the SnO2 substrate. The functional TEATFA salt is first deposited onto the SnO2 substrate and reacts on this buried interface. Once the FAPbI(3) perovskite precursor solution is dripped, a portion of the TEA(+) cations spontaneously diffuse to the top surface over film crystallization. The TEATFA-based water-resistant 1D/3D TEAPbI(3)/FAPbI(3) heterojunctions at both the buried and capped interfaces lead to much better photovoltaic performance and higher operational stability. Since this approach saves the need for any postsynthesis passivation, its feasibility for the fabrication of large-area perovskite photovoltaics is also showcased. Compared to similar to 15% for a pristine 5 cm x 5 cm FAPbI(3) mini-module without postsynthesis passivation, over 20% efficiency is achieved following the proposed route, demonstrating its great potential for larger-scale fabrication with fewer processing steps.
引用
收藏
页码:3324 / 3332
页数:9
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