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In-situ Functionalization of Metal Electrodes for Advanced Asymmetric Supercapacitors
Nanostructured metal-based compound electrodes with excellent electrochemical activity and electrical conductivity are promising for high-performance energy storage applications. In this paper, we report an asymmetric supercapacitor based on Ti and Cu coated vertical-aligned carbon nanotube electrod...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646466/ https://www.ncbi.nlm.nih.gov/pubmed/31380354 http://dx.doi.org/10.3389/fchem.2019.00512 |
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author | Sun, Leimeng Wang, Xinghui Wang, Yurong Xiao, Dongyang Cai, Weifan Jing, Yuan Wang, Yanrong Hu, Fangjing Zhang, Qing |
author_facet | Sun, Leimeng Wang, Xinghui Wang, Yurong Xiao, Dongyang Cai, Weifan Jing, Yuan Wang, Yanrong Hu, Fangjing Zhang, Qing |
author_sort | Sun, Leimeng |
collection | PubMed |
description | Nanostructured metal-based compound electrodes with excellent electrochemical activity and electrical conductivity are promising for high-performance energy storage applications. In this paper, we report an asymmetric supercapacitor based on Ti and Cu coated vertical-aligned carbon nanotube electrodes on carbon cloth. The active material is achieved by in-situ functionalization using a high-temperature annealing process. Scanning and transmission electron microscopy and Raman spectroscopy confirm the detailed nanostructures and composition of the electrodes. The TiC@VCC and Cu(x)S@VCC electrodes show a high specific capacity of 200.89 F g(−1) and 228.37 F g(−1), respectively, and good capacitive characteristics at different scan speeds. The excellent performance can be attributed to a large surface area to volume ratio and high electrical conductivity of the electrodes. Furthermore, an asymmetric supercapacitor is assembled with TiC@VCC as anode and Cu(x)S@VCC as cathode. The full device can operate within the 0–1.4 V range, and shows a maximum energy density of 9.12 Wh kg(−1) at a power density of 46.88 W kg(−1). These findings suggest that the metal-based asymmetric electrodes have a great potential for supercapacitor applications. |
format | Online Article Text |
id | pubmed-6646466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66464662019-08-02 In-situ Functionalization of Metal Electrodes for Advanced Asymmetric Supercapacitors Sun, Leimeng Wang, Xinghui Wang, Yurong Xiao, Dongyang Cai, Weifan Jing, Yuan Wang, Yanrong Hu, Fangjing Zhang, Qing Front Chem Chemistry Nanostructured metal-based compound electrodes with excellent electrochemical activity and electrical conductivity are promising for high-performance energy storage applications. In this paper, we report an asymmetric supercapacitor based on Ti and Cu coated vertical-aligned carbon nanotube electrodes on carbon cloth. The active material is achieved by in-situ functionalization using a high-temperature annealing process. Scanning and transmission electron microscopy and Raman spectroscopy confirm the detailed nanostructures and composition of the electrodes. The TiC@VCC and Cu(x)S@VCC electrodes show a high specific capacity of 200.89 F g(−1) and 228.37 F g(−1), respectively, and good capacitive characteristics at different scan speeds. The excellent performance can be attributed to a large surface area to volume ratio and high electrical conductivity of the electrodes. Furthermore, an asymmetric supercapacitor is assembled with TiC@VCC as anode and Cu(x)S@VCC as cathode. The full device can operate within the 0–1.4 V range, and shows a maximum energy density of 9.12 Wh kg(−1) at a power density of 46.88 W kg(−1). These findings suggest that the metal-based asymmetric electrodes have a great potential for supercapacitor applications. Frontiers Media S.A. 2019-07-16 /pmc/articles/PMC6646466/ /pubmed/31380354 http://dx.doi.org/10.3389/fchem.2019.00512 Text en Copyright © 2019 Sun, Wang, Wang, Xiao, Cai, Jing, Wang, Hu and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Sun, Leimeng Wang, Xinghui Wang, Yurong Xiao, Dongyang Cai, Weifan Jing, Yuan Wang, Yanrong Hu, Fangjing Zhang, Qing In-situ Functionalization of Metal Electrodes for Advanced Asymmetric Supercapacitors |
title | In-situ Functionalization of Metal Electrodes for Advanced Asymmetric Supercapacitors |
title_full | In-situ Functionalization of Metal Electrodes for Advanced Asymmetric Supercapacitors |
title_fullStr | In-situ Functionalization of Metal Electrodes for Advanced Asymmetric Supercapacitors |
title_full_unstemmed | In-situ Functionalization of Metal Electrodes for Advanced Asymmetric Supercapacitors |
title_short | In-situ Functionalization of Metal Electrodes for Advanced Asymmetric Supercapacitors |
title_sort | in-situ functionalization of metal electrodes for advanced asymmetric supercapacitors |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646466/ https://www.ncbi.nlm.nih.gov/pubmed/31380354 http://dx.doi.org/10.3389/fchem.2019.00512 |
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