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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...

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Autores principales: Tian, Guiying, Huang, Chuanfeng, Luo, Xianlin, Zhao, Zijian, Peng, Yong, Gao, Yuqin, Tang, Na, Dsoke, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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
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author Tian, Guiying
Huang, Chuanfeng
Luo, Xianlin
Zhao, Zijian
Peng, Yong
Gao, Yuqin
Tang, Na
Dsoke, Sonia
author_facet Tian, Guiying
Huang, Chuanfeng
Luo, Xianlin
Zhao, Zijian
Peng, Yong
Gao, Yuqin
Tang, Na
Dsoke, Sonia
author_sort Tian, Guiying
collection PubMed
description 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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spelling pubmed-94008862022-08-26 Study of the Lithium Storage Mechanism of N‐Doped Carbon‐Modified Cu(2)S Electrodes for Lithium‐Ion Batteries Tian, Guiying Huang, Chuanfeng Luo, Xianlin Zhao, Zijian Peng, Yong Gao, Yuqin Tang, Na Dsoke, Sonia Chemistry Full Papers 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. John Wiley and Sons Inc. 2021-08-31 2021-10-01 /pmc/articles/PMC9400886/ /pubmed/34318954 http://dx.doi.org/10.1002/chem.202101818 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Tian, Guiying
Huang, Chuanfeng
Luo, Xianlin
Zhao, Zijian
Peng, Yong
Gao, Yuqin
Tang, Na
Dsoke, Sonia
Study of the Lithium Storage Mechanism of N‐Doped Carbon‐Modified Cu(2)S Electrodes for Lithium‐Ion Batteries
title Study of the Lithium Storage Mechanism of N‐Doped Carbon‐Modified Cu(2)S Electrodes for Lithium‐Ion Batteries
title_full Study of the Lithium Storage Mechanism of N‐Doped Carbon‐Modified Cu(2)S Electrodes for Lithium‐Ion Batteries
title_fullStr Study of the Lithium Storage Mechanism of N‐Doped Carbon‐Modified Cu(2)S Electrodes for Lithium‐Ion Batteries
title_full_unstemmed Study of the Lithium Storage Mechanism of N‐Doped Carbon‐Modified Cu(2)S Electrodes for Lithium‐Ion Batteries
title_short Study of the Lithium Storage Mechanism of N‐Doped Carbon‐Modified Cu(2)S Electrodes for Lithium‐Ion Batteries
title_sort study of the lithium storage mechanism of n‐doped carbon‐modified cu(2)s electrodes for lithium‐ion batteries
topic Full Papers
url 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
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