材料科学
钙钛矿(结构)
异质结
兴奋剂
电子
费米能级
能量转换效率
光电子学
氧化物
氧化锡
离子键合
化学工程
离子
工程类
冶金
物理
量子力学
作者
Jianxing Xia,Junsheng Luo,Hua Yang,Fengjiao Zhao,Zhongquan Wan,Haseeb Ashraf Malik,Yu Shi,Keli Han,Xiaojun Yao,Chunyang Jia
标识
DOI:10.1002/adfm.202001418
摘要
Abstract In perovskite solar cells (PSCs), the interfaces of the halide perovskite/electron transport layer (ETL) and ETL/metal oxide electrode (MOE) always attract and trap free carriers via the surface electrostatic force, altering quasi‐Fermi level (EFq) splitting of contact interfaces, and significantly limit the charge extraction efficiency and intrinsic stability of devices. Herein, a graded “bridge” is first reported to link the MOE and perovskite interfaces by self vertical phase separation doping (PSD), diminishing the side effect of notorious ionic defects via both reinforced interface Ebi and the vacancies filling. Experimental and theoretical results prove that the inhomogeneous distribution of CsF in the bulk or surface of PC61BM would not only form metal–oxygen (M–O) dipole on MOE, reinforcing the interface Ebi, but also create a graded energy bridge to alleviate the disadvantage of band offset raised by the enhanced interface Ebi, which significantly avoid the carrier accumulation and recombination at defective interfaces. Employing PSD, the power conversion efficiency of the devices approaches 21% with a high open‐circuit voltage (1.148 V) and delivers a high stability of 89% after aging 60 days in atmosphere without encapsulation, which is the highest efficiency of organic electron transport layers for n–i–p PSCs.
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