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

Developing 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 recomb...

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Veröffentlicht in:Advanced materials (Weinheim) 2024-08, Vol.36 (35), p.e2405807-n/a
Hauptverfasser: Zhou, Wentao, Chen, Yihua, Li, Nengxu, Huang, Zijian, Zhang, Yu, Zhang, Zhongyang, Guo, Zhenyu, Yin, Ruiyang, Ma, Yue, Pei, Fengtao, Xie, Haipeng, Zai, Huachao, Wang, Lina, Qiu, Zhiwen, Chen, Qi, Zhou, Huanping
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Sprache:eng
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Zusammenfassung:Developing 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. Abietic acid (AA), a soldering flux, is introduced into Sn‐Pb perovskite solar cells to tackle complex defects chemistry. The C═C bond within AA continuously eliminates Sn4+ and Pb0 defects, while the presence of C═O bond enhances the antioxidation stability of Sn2+. This innovative and effective approach leads to 23.42% power conversion efficiency of Sn‐Pb perovskite solar cell.
ISSN:0935-9648
1521-4095
1521-4095
DOI:10.1002/adma.202405807