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Suppressing Interfacial Charge Recombination in Electron‐Transport‐Layer‐Free Perovskite Solar Cells to Give an Efficiency Exceeding 21 %
Author(s) -
Wu WuQiang,
Liao JinFeng,
Zhong JunXing,
Xu YangFan,
Wang Lianzhou,
Huang Jinsong
Publication year - 2020
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.202005680
Subject(s) - perovskite (structure) , materials science , recombination , oxide , layer (electronics) , amorphous solid , optoelectronics , electron , quantum tunnelling , charge (physics) , metal , nanotechnology , chemistry , crystallography , physics , biochemistry , quantum mechanics , metallurgy , gene
The performances of electron‐transport‐layer (ETL)‐free perovskite solar cells (PSCs) are still inferior to ETL‐containing devices. This is mainly due to severe interfacial charge recombination occurring at the transparent conducting oxide (TCO)/perovskite interface, where the photo‐injected electrons in the TCO can travel back to recombine with holes in the perovskite layer. Herein, we demonstrate for the first time that a non‐annealed, insulating, amorphous metal oxyhydroxide, atomic‐scale thin interlayer (ca. 3 nm) between the TCO and perovskite facilitates electron tunneling and suppresses the interfacial charge recombination. This largely reduced the interfacial charge recombination loss and achieved a record efficiency of 21.1 % for n‐i‐p structured ETL‐free PSCs, outperforming their ETL‐containing metal oxide counterparts (18.7 %), as well as narrowing the efficiency gap with high‐efficiency PSCs employing highly crystalline TiO 2 ETLs.
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