Enhanced efficiency and stability of carbon-based CsPbI2Br perovskite solar cells by introducing metal organic framework-derived Fe3O4@NC interfacial layer

被引:8
|
作者
Yang, Xiaoyu [1 ]
Qi, Ying [1 ]
Wei, Peng [1 ]
Hu, Qixu [1 ]
Cheng, Jian [2 ]
Xie, Yahong [1 ]
机构
[1] Xinjiang Univ, Sch Chem Engn & Technol, State Key Lab Chem & Utilizat Carbon Based Energy, Urumqi 830017, Peoples R China
[2] Hanyang Univ, Dept Mat & Chem Engn, Seoul 04763, South Korea
基金
中国国家自然科学基金;
关键词
C-PSCs; CsPbI2Br; UVO; Fe-MOF; Interfacial layer; ELECTRON-TRANSPORT LAYER; ELECTROCATALYSTS; COMPOSITE; SNO2;
D O I
10.1016/j.jpowsour.2023.232927
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Carbon-based CsPbI2Br perovskite solar cells (C-PSCs) have the advantages of low cost and stable performance, but the poor contact and energy mismatch between the perovskite layer and the carbon electrode lead to low power conversion efficiency (PCE). In this work, uniform spindle-shaped Fe3O4@NC composites have prepared by calcining Fe-based metal organic framework (Fe-MOF) NH2-MIL-88B(Fe), which has synthesized by sol-vothermal reaction using 2-aminoterephthalic acid as nitrogen and carbon sources. Using Fe3O4@NC composite and UV-Ozone treated Fe3O4@NC composite (Fe3O4@NC UVO) as the interfacial layer between the perovskite layer and the carbon electrode, the devices with a structure of FTO/SnO2/CsPbI2Br/interfacial layer/Carbon exhibit a maximum PCE of 12.25%, which is about 19.28% higher than that of the pristine device. The improved optoelectronic performance is mainly attributed to more matched energy level, denser interface contact, better carrier separation performance and better conductivity. After 19 days of storage at room temperature and ambient humidity, Fe3O4@NC UVO device has retained 87% of the initial PCE. This work provides a simple and effective strategy to improve the PCE and stability of carbon-based CsPbI2Br PSCs with Fe-MOFs-derived carbon materials.
引用
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页数:11
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