Periodic Acid Modification of Chemical‐Bath Deposited SnO2 Electron Transport Layers for Perovskite Solar Cells and Mini Modules

Author:

Wu Ziyi1ORCID,Su Jiazheng1,Chai Nianyao2,Cheng Siyang3456,Wang Xuanyu1,Zhang Ziling1,Liu Xuanling1,Zhong Han1ORCID,Yang Jianfei1,Wang Zhiping3456,Liu Jianbo7,Li Xin8,Lin Hong1ORCID

Affiliation:

1. State Key Laboratory of New Ceramics and Fine Processing School of Materials Science and Engineering Tsinghua University Beijing 100084 P. R. China

2. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 P. R. China

3. Key Lab of Artificial Micro‐ and Nano‐Structures of Ministry of Education of China School of Physics and Technology Wuhan University Wuhan 430072 P. R. China

4. Hubei Luojia Laboratory Wuhan 430072 P. R. China

5. Wuhan Institute of Quantum Technology Wuhan 430206 P. R. China

6. School of Microelectronics Wuhan University Wuhan 430072 P. R. China

7. Key Laboratory of Advanced Materials of Ministry of Education of China School of Materials Science and Engineering Tsinghua University Beijing 100084 P. R. China

8. School of Electronic Science and Engineering Xiamen University Xiamen 361005 P. R. China

Abstract

AbstractChemical bath deposition (CBD) has been demonstrated as a remarkable technology to fabricate high‐quality SnO2 electron transport layer (ETL) for large‐area perovskite solar cells (PSCs). However, surface defects always exist on the SnO2 film coated by the CBD process, impairing the devices’ performance. Here, a facile periodic acid post‐treatment (PAPT) method is developed to modify the SnO2 layer. Periodic acid can react with hydroxyl groups on the surface of SnO2 films and oxidize Tin(II) oxide to Tin(IV) oxide. With the help of periodic acid, a better energy level alignment between the SnO2 and perovskite layers is achieved. In addition, the PAPT method inhibits interfacial nonradiative recombination and facilitates charge transportation. Such a multifunctional strategy enables to fabricate PSC with a champion power conversion efficiency (PCE) of 22.25%, which remains 93.32% of its initial efficiency after 3000 h without any encapsulation. Furthermore, 3 × 3 cm2 perovskite mini‐modules are presented, achieving a champion efficiency of 18.10%. All these results suggest that the PAPT method is promising for promoting the commercial application of large‐area PSCs.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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