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Study of the Lithium Storage Mechanism of N‐Doped Carbon‐Modified Cu(2)S Electrodes for Lithium‐Ion Batteries
Owing to their high specific capacity and abundant reserve, Cu( x )S compounds are promising electrode materials for lithium‐ion batteries (LIBs). Carbon compositing could stabilize the Cu( x )S structure and repress capacity fading during the electrochemical cycling, but the corresponding Li(+) sto...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9400886/ https://www.ncbi.nlm.nih.gov/pubmed/34318954 http://dx.doi.org/10.1002/chem.202101818 |
Sumario: | Owing to their high specific capacity and abundant reserve, Cu( x )S compounds are promising electrode materials for lithium‐ion batteries (LIBs). Carbon compositing could stabilize the Cu( x )S structure and repress capacity fading during the electrochemical cycling, but the corresponding Li(+) storage mechanism and stabilization effect should be further clarified. In this study, nanoscale Cu(2)S was synthesized by CuS co‐precipitation and thermal reduction with polyelectrolytes. High‐temperature synchrotron radiation diffraction was used to monitor the thermal reduction process. During the first cycle, the conversion mechanism upon lithium storage in the Cu(2)S/carbon was elucidated by operando synchrotron radiation diffraction and in situ X‐ray absorption spectroscopy. The N‐doped carbon‐composited Cu(2)S (Cu(2)S/C) exhibits an initial discharge capacity of 425 mAh g(−1) at 0.1 A g(−1), with a higher, long‐term capacity of 523 mAh g(−1) at 0.1 A g(−1) after 200 cycles; in contrast, the bare CuS electrode exhibits 123 mAh g(−1) after 200 cycles. Multiple‐scan cyclic voltammetry proves that extra Li(+) storage can mainly be ascribed to the contribution of the capacitive storage. |
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