Successive Reactions of Trimethylgermanium Chloride to Achieve > 26% Efficiency MA‐Free Perovskite Solar Cell With 3000‐Hour Unattenuated Operation

The rapidly increased efficiency of perovskite solar cells (PSCs) indicates their broad commercial prospects, but the commercialization of perovskite faces complex optimization processes and stability issues. In this work, a simple optimized strategy is developed by the addition of trimethylgermanium chloride (TGC) into FACsPbI<sub>3</sub> precursor solution. TGC triggers the successive interactions in perovskite solution and film, involving the hydrolysis of vulnerable Ge─Cl bond forming Ge─OH group, then forming the hydrogen bonds (O─H···N and O─H···I) with FAI. These successive interactions effectively safeguard FA<sup>+</sup> from decomposition, accelerate crystallization, restrict ion migration, and passivate film defects. Thus, a high-quality perovskite is obtained with the super-hydrophobic surface, maintaining the light-active phase (α-phase) even after exposure to high-humidity air (RH: 85%) for 10 days. Consequently, the TGC-treated conventional (n-i-p) and inverted (p-i-n) FACsPbI<sub>3</sub> PSCs achieve 26.03%- and 26.38%- efficiencies, respectively, retaining unattenuated operation initial efficiency after tracking at the maximum power point (MPP) under illumination for 3000 h.

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Publication Details

Journal
Advanced Materials
Published
2024-12-26
DOI
https://doi.org/10.1002/adma.202414354
Citations
41
Primary Topic
Perovskite Materials and Applications
Type
article
Field-Weighted Citation Impact
8.56

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article

Successive Reactions of Trimethylgermanium Chloride to Achieve > 26% Efficiency MA‐Free Perovskite Solar Cell With 3000‐Hour Unattenuated Operation

Hongjie Lei, Chunbo Su, Zhuang Xie, Qiang Peng et al.
41 citations
Advanced Materials
Perovskite Materials and Applications
8.56
article

Successive Reactions of Trimethylgermanium Chloride to Achieve > 26% Efficiency MA‐Free Perovskite Solar Cell With 3000‐Hour Unattenuated Operation

Hongjie Lei, Chunbo Su, Zhuang Xie, Qiang Peng, Ming Cheng, H.F. Wang, Rui Sun, Yuwei Duan, Zhike Liu, Shengzhong Frank Liu, Yifan Wang, Yong Li, Hongxiang Li, Ke Zhang, Yongzhe Li, Dongfang Xu, Yiqiao Sun, Kunpeng Guo
article en
41 citations

Abstract

The rapidly increased efficiency of perovskite solar cells (PSCs) indicates their broad commercial prospects, but the commercialization of perovskite faces complex optimization processes and stability issues. In this work, a simple optimized strategy is developed by the addition of trimethylgermanium chloride (TGC) into FACsPbI<sub>3</sub> precursor solution. TGC triggers the successive interactions in perovskite solution and film, involving the hydrolysis of vulnerable Ge─Cl bond forming Ge─OH group, then forming the hydrogen bonds (O─H···N and O─H···I) with FAI. These successive interactions effectively safeguard FA<sup>+</sup> from decomposition, accelerate crystallization, restrict ion migration, and passivate film defects. Thus, a high-quality perovskite is obtained with the super-hydrophobic surface, maintaining the light-active phase (α-phase) even after exposure to high-humidity air (RH: 85%) for 10 days. Consequently, the TGC-treated conventional (n-i-p) and inverted (p-i-n) FACsPbI<sub>3</sub> PSCs achieve 26.03%- and 26.38%- efficiencies, respectively, retaining unattenuated operation initial efficiency after tracking at the maximum power point (MPP) under illumination for 3000 h.

Advanced MaterialsVol. 37(7)
Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN), Sichuan University (CN), Chengdu University of Technology (CN), University of Chinese Academy of Sciences (CN), Shaanxi Normal University (CN), Taiyuan University of Technology (CN)
National Natural Science Foundation of China, Higher Education Discipline Innovation Project, National University Research Fund of China, Natural Science Foundation of Sichuan Province, National Key Research and Development Program of China, Dalian National Laboratory for Clean Energy
Openalex Percentile: Top 2%
Perovskite Materials and Applications
8.56
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