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Regulation of Interfacial Charge Transfer and Recombination for Efficient Planar Perovskite Solar Cells
Author(s) -
Shi Xiaoqiang,
Chen Ruochen,
Jiang Tingting,
Ma Shuang,
Liu Xuepeng,
Ding Yong,
Cai Molang,
Wu Jihuai,
Dai Songyuan
Publication year - 2020
Publication title -
solar rrl
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.544
H-Index - 37
ISSN - 2367-198X
DOI - 10.1002/solr.201900198
Subject(s) - perovskite (structure) , materials science , recombination , planar , hysteresis , optoelectronics , electron , electron transfer , thin film , ion , deposition (geology) , atomic layer deposition , nanotechnology , chemical physics , chemistry , condensed matter physics , crystallography , photochemistry , paleontology , biochemistry , physics , computer graphics (images) , organic chemistry , quantum mechanics , sediment , biology , computer science , gene
Control of dynamics at the electron transport layer–perovskite interface, such as charge transfer and recombination, is essential in achieving high‐efficiency planar perovskite solar cells (PSCs). Herein, it was observed that the trade‐off between unfavorable electron transport of a thick SnO 2 film and serious electron recombination at thin SnO 2 film/perovskite interfaces is essential for the performance of SnO 2 ‐based planar PSCs. The optimized efficiency of devices beyond 20% is obtained by using a two‐step deposition of SnO 2 . Moreover, trap‐assisted carrier recombination is significantly suppressed by using the diethylenetriaminepentaacetic acid passivator via the formation of coordination with undercoordinated Sn and Pb 2+ ions. As a result, the champion device demonstrates a promising efficiency of 21.28% with negligible hysteresis and much improved environmental stability, i.e., retaining 98% of the initial efficiency under ambient atmosphere over 1000 h.