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Research Article

Regulating electrochemical performance of Cu7S4 electrodes via ligand engineering in copper cluster precursors

Zhou WuLu-Fan WangXiao-Fei LiuRen-Wu HuangRui WangGuoqiang Sun( )Shuang-Quan Zang ( )
Henan Key Laboratory of Crystalline Molecular Functional Materials, College of Chemistry, Zhengzhou University, Zhengzhou 450001, China
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Abstract

Cu-based chalcogenide materials exhibit significant promise for the development of Zn-metal-free anode materials for aqueous Zn-ion batteries (AZIBs). Here, we present the establishment of an efficient and universal strategy that capitalizes on the pyrolysis of copper nanoclusters to fabricate conversion-type Cu7S4 anodes engineered for AZIBs, showcasing outstanding electrochemical performance. Furthermore, by exploiting ligand engineering, we enable the precise control of both the type of molecular fragments generated during nanocluster pyrolysis, thus enabling the manipulation of vacancy concentrations and ion/electron migration in the resultant pyrolysis products. In contrast to the direct pyrolysis of metal salts and ligands, the products derived from copper nanoclusters exhibit enhanced specific capacity, rate performance, and overall stability. This research offers valuable insights for the development of novel electrode materials through the pyrolysis of atomically precise nanoclusters.

Graphical Abstract

Atomically precise protected nanoclusters are used as precursors to fabricate copper-based metal sulfides via pyrolysis. The bond energy can be modulated by the ligands, which allows tuning the vacancy concentration and electrochemical performance of the final pyrolysis products.

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Nano Research
Pages 9746-9755

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Cite this article:
Wu Z, Wang L-F, Liu X-F, et al. Regulating electrochemical performance of Cu7S4 electrodes via ligand engineering in copper cluster precursors. Nano Research, 2024, 17(11): 9746-9755. https://doi.org/10.1007/s12274-024-6956-z
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Received: 12 July 2024
Revised: 07 August 2024
Accepted: 08 August 2024
Published: 07 September 2024
© Tsinghua University Press 2024