Synergistic effects of bithiophene ammonium salt for high-performance perovskite solar cells

被引:23
|
作者
Xu, Chang [1 ]
Zuo, Lijian [1 ,2 ]
Hang, Pengjie [3 ]
Guo, Xiangwei [2 ,6 ]
Pan, Youwen [1 ]
Zhou, Guanqing [4 ]
Chen, Tianyi [1 ]
Niu, Benfang [1 ]
Xu, Xingqi [7 ]
Hong, Zijian [6 ]
Wang, Dawei [7 ]
Zhu, Haiming [2 ,5 ]
Yu, Xuegong [3 ]
Yang, Deren [3 ]
Chen, Hongzheng [1 ]
机构
[1] Zhejiang Univ, State Key Lab Silicon Mat, MOE Key Lab Macromol Synth & Functionalizat, Dept Polymer Sci & Engn, Hangzhou 310027, Peoples R China
[2] Zhejiang Univ Hangzhou Global Sci & Technol Innov, Hangzhou 310014, Peoples R China
[3] Zhejiang Univ, State Key Lab Silicon Mat, Sch Mat Sci & Engn, Hangzhou 310027, Peoples R China
[4] Shanghai Jiao Tong Univ, Frontiers Sci Ctr Transformat Mol, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
[5] Zhejiang Univ, Dept Chem, Hangzhou 310027, Peoples R China
[6] Zhejiang Univ, Sch Mat Sci & Engn, Lab Dielect Mat, Hangzhou 310027, Peoples R China
[7] Zhejiang Univ, Interdisciplinary Ctr Quantum Informat & Zhejiang, Dept Phys, Hangzhou 310027, Peoples R China
基金
中国国家自然科学基金;
关键词
INORGANIC HYBRID PEROVSKITE; ELECTRON; INTERLAYERS; LENGTHS;
D O I
10.1039/d2ta01349e
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
Simultaneously improving the charge transfer and suppressing the charge recombination at the interface is essentially important for high-performance perovskite solar cells (PVSCs). To achieve this goat in this work, we modify the anode interface of PVSCs with a ligand, bithiophenethylammonium iodide (2TEAI), which comprises both long-conjugation bithiophene and ammonium groups. With 2TEAI, high-performance FAPbI(3) (FA: HC(NH2)(2)) based PVSCs with significantly increased efficiency from 21.7% to 23.6% have been demonstrated for small area devices, as well as 21.3% for large-area (2.25 cm(2)) devices. Comprehensive analysis of the carrier dynamics and first-principles simulations unveils that the 2TEAI modification can (1) enhance the interfacial charge transfer due to energy level alignment between the highest occupied molecular orbital and the perovskite valence band, and (2) mitigate the charge recombination by passivating the trap states owing to its strong chemical interaction perovskite layer and reduction of Pb-0. Our work demonstrates a reliable strategy to optimize the interface and paves the way toward high-performance PVSCs for commercialization.
引用
收藏
页码:9971 / 9980
页数:10
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