钙钛矿(结构)
重组
图层(电子)
氧化物
电子
无定形固体
材料科学
量子隧道
光电子学
金属
电荷(物理)
自由电子模型
纳米技术
化学
结晶学
物理
量子力学
基因
生物化学
冶金
作者
Wu‐Qiang Wu,Jin‐Feng Liao,Jun‐Xing Zhong,Yangfan Xu,Lianzhou Wang,Jinsong Huang
标识
DOI:10.1002/anie.202005680
摘要
Abstract 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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