Decoupling light- and oxygen-induced degradation mechanisms of Sn–Pb perovskites in all perovskite tandem solar cells

Efficiencies of all-perovskite tandem solar cells are dominantly constrained by the challenges pertaining to defects and stability within tin–lead (Sn–Pb) perovskite sub-cells. On top of the well-studied oxygen oxidation, defects related to iodide and the consequent generation of I 2 upon light illu...

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Published inEnergy & environmental science
Main Authors Bai, Yang, Tian, Ruijia, Sun, Kexuan, Liu, Chang, Lang, Xiting, Yang, Ming, Meng, Yuanyuan, Xiao, Chuanxiao, Wang, Yaohua, Lu, Xiaoyi, Wang, Jingnan, Pan, Haibin, Song, Zhenhua, Zhou, Shujing, Ge, Ziyi
Format Journal Article
LanguageEnglish
Published 02.08.2024
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Summary:Efficiencies of all-perovskite tandem solar cells are dominantly constrained by the challenges pertaining to defects and stability within tin–lead (Sn–Pb) perovskite sub-cells. On top of the well-studied oxygen oxidation, defects related to iodide and the consequent generation of I 2 upon light illumination pose significant degradation risks, leading to Sn 2+ → Sn 4+ oxidation. To address this, we screen phenylhydrazine cation (PEH + )-based additives of varying polarities, which strongly coordinate with Sn for reinforcing the Sn–I bond, and interacting electrostatically with negatively charged defects (V Sn , V FA , I Sn , and I−i). The synergistic effects suppress the photo-induced formation of I 2 and the subsequent oxidation of Sn–Pb perovskites, circumventing the stability concerns of narrow bandgap (NBG) perovskite solar cells (PSCs) under operational conditions. The reducing agent 2-mercaptobenzimidazole (MBI) was further introduced into the precursor solution, which not only demonstrates strong resistance to oxygen erosion, but also reduces the deep-level defect density of the Sn–Pb perovskites. Consequently, single-junction Sn–Pb cells achieve a champion efficiency of 23.0%. The enhanced light stability allows these cells to retain 89.4% of their initial efficiency after 400 hours of continuous operation, as assessed by tracking the maximum power point (MPP). We further integrated the Sn–Pb perovskite into a two-terminal (2T) monolithic all-perovskite tandem cell and achieved a PCE of 27.9% (27.2% certified). Meanwhile, the encapsulated tandem device maintained 90.3% of its initial PCE after 300 h through MPP tracking. The work offers new ideas for tackling the stability issues related to light-triggered oxidation.
ISSN:1754-5692
1754-5706
DOI:10.1039/D4EE02427C