钝化
结晶度
材料科学
成核
钙钛矿(结构)
光伏
化学工程
结晶
能量转换效率
晶界
碳纤维
纳米技术
图层(电子)
光电子学
光伏系统
化学
微观结构
冶金
复合材料
有机化学
复合数
工程类
生态学
生物
作者
Zijun Niu,Weifeng Liu,Kexiang Wang,Weiwei Sun,Xiaonan Huo,Yanqin Miao,Tingting You,Penggang Yin
出处
期刊:ACS applied energy materials
[American Chemical Society]
日期:2024-04-17
卷期号:7 (9): 3635-3644
被引量:1
标识
DOI:10.1021/acsaem.3c03135
摘要
Inorganic CsPbI2Br carbon-based perovskite solar cells (C-PSCs) are considered as an alternative promising contender in the field of photovoltaics, attributed to their remarkable thermal stability and cost-effectiveness. However, the defects located at the electron transporting layer (ETL)/perovskite interface (i.e., buried interface) and unsatisfactory crystallinity of CsPbI2Br films hinder the progress in enhancing the power conversion efficiency (PCE). Herein, we put forward facile acetate-assisted buried interface engineering to passivate TiO2/perovskite interface defects along with regulate the crystallization process of CsPbI2Br. Multifunctional small molecule interface modifier zinc acetate (Zn(Ac)2) is introduced into the surface of TiO2 ETL, which can passivate the oxygen vacancy defects of TiO2 and optimize the energy level alignment at the TiO2/CsPbI2Br interface. Meanwhile, part of Ac– may be dissolved in the CsPbI2Br precursor to retard its nucleation process, leading to enhanced crystallinity with a larger grain size of the CsPbI2Br film. As a result, reduced interface defects and bulk defects as well as enhanced electron extraction are achieved, which substantially enhance the PCE of CsPbI2Br C-PSCs from 12.54% to 14.20%, among the highest values of this type of device. Besides, thermal and long-term storage stabilities of the optimized devices are improved.
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