A Soldering Flux Tackles Complex Defects Chemistry in Sn‐Pb Perovskite Solar Cells

Author:

Zhou Wentao1ORCID,Chen Yihua12ORCID,Li Nengxu1,Huang Zijian1,Zhang Yu1,Zhang Zhongyang2,Guo Zhenyu1,Yin Ruiyang1,Ma Yue1,Pei Fengtao2,Xie Haipeng3,Zai Huachao14,Wang Lina2,Qiu Zhiwen1,Chen Qi2,Zhou Huanping15ORCID

Affiliation:

1. Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials Key Laboratory of Polymer Chemistry and Physics of Ministry of Education School of Materials Science and Engineering Peking University Beijing 100871 P. R. China

2. Experimental Center of Advanced Materials School of Materials Science and Engineering Beijing Institute of Technology Beijing 100081 P. R. China

3. Institute of Super‐Microstructure and Ultrafast Process in Advance Materials School of Physics Central South University Changsha Hunan 410083 P. R. China

4. School of Materials Science and Technology China University of Geosciences (Beijing) Beijing 100083 P. R. China

5. Institute of Carbon Neutrality Peking University Beijing 100871 P. R. China

Abstract

AbstractDeveloping tin‐lead (Sn‐Pb) narrow‐bandgap perovskites is crucial for the deployment of all‐perovskite tandem solar cells, which can help to exceed the limits of single‐junction photovoltaics. However, the Sn‐Pb perovskite suffers from a large number of bulk traps and interfacial nonradiative recombination centers, with unsatisfactory open‐circuit voltage and the consequent device efficiency. Herein, for the first time, it is shown that abietic acid (AA), a commonly used flux for metal soldering, effectively tackles complex defects chemistry in Sn‐Pb perovskites. The conjugated double bond within AA molecule plays a key role for self‐elimination of Sn4+‐Pb0 defects pair, via a redox process. In addition, C═O group is able to coordinate with Sn2+, leading to the improved antioxidative stability of Sn‐Pb perovskites. Consequently, a ten‐times longer carrier lifetime is observed, and the defects‐associated dual‐peak emission feature at low temperature is significantly inhibited. The resultant device achieves a power conversion efficiency improvement from 22.28% (Ref) to 23.42% with respectable stability under operational and illumination situations.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

China Postdoctoral Science Foundation

Publisher

Wiley

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