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Highly Stable Gully-Network Co(3)O(4) Nanowire Arrays as Battery-Type Electrode for Outstanding Supercapacitor Performance

3D transition metal oxides, especially constructed from the interconnected nanowires directly grown on conductive current collectors, are considered to be the most promising electrode material candidates for advanced supercapacitors because 3D network could simultaneously enhance the mechanical and...

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Autores principales: Guo, Chunli, Yin, Minshuai, Wu, Chun, Li, Jie, Sun, Changhui, Jia, Chuankun, Li, Taotao, Hou, Lifeng, Wei, Yinghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308209/
https://www.ncbi.nlm.nih.gov/pubmed/30622941
http://dx.doi.org/10.3389/fchem.2018.00636
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author Guo, Chunli
Yin, Minshuai
Wu, Chun
Li, Jie
Sun, Changhui
Jia, Chuankun
Li, Taotao
Hou, Lifeng
Wei, Yinghui
author_facet Guo, Chunli
Yin, Minshuai
Wu, Chun
Li, Jie
Sun, Changhui
Jia, Chuankun
Li, Taotao
Hou, Lifeng
Wei, Yinghui
author_sort Guo, Chunli
collection PubMed
description 3D transition metal oxides, especially constructed from the interconnected nanowires directly grown on conductive current collectors, are considered to be the most promising electrode material candidates for advanced supercapacitors because 3D network could simultaneously enhance the mechanical and electrochemical performance. The work about design, fabrication, and characterization of 3D gully-network Co(3)O(4) nanowire arrays directly grown on Ni foam using a facile hydrothermal procedure followed by calcination treatment will be introduced. When evaluated as a binder-free battery-type electrode for supercapacitor, a high specific capacity of 582.8 C g(−1) at a current density of 1 A g(−1), a desirable rate capability with capacity retention about 84.8% at 20 A g(−1), and an outstanding cycle performance of 93.1% capacity retention after 25,000 cycles can be achieved. More remarkably, an energy density of 33.8 W h kg(−1) at a power density of 224 W kg(−1) and wonderful cycling stability with 74% capacity retention after 10,000 cycles can be delivered based on the hybrid-supercapacitor with the as-prepared Co(3)O(4) nanowire arrays as a positive electrode and active carbon as negative electrode. All the unexceptionable supercapacitive behaviors illustrates that our unique 3D gully-network structure Co(3)O(4) nanowire arrays hold a great promise for constructing high-performance energy storage devices.
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spelling pubmed-63082092019-01-08 Highly Stable Gully-Network Co(3)O(4) Nanowire Arrays as Battery-Type Electrode for Outstanding Supercapacitor Performance Guo, Chunli Yin, Minshuai Wu, Chun Li, Jie Sun, Changhui Jia, Chuankun Li, Taotao Hou, Lifeng Wei, Yinghui Front Chem Chemistry 3D transition metal oxides, especially constructed from the interconnected nanowires directly grown on conductive current collectors, are considered to be the most promising electrode material candidates for advanced supercapacitors because 3D network could simultaneously enhance the mechanical and electrochemical performance. The work about design, fabrication, and characterization of 3D gully-network Co(3)O(4) nanowire arrays directly grown on Ni foam using a facile hydrothermal procedure followed by calcination treatment will be introduced. When evaluated as a binder-free battery-type electrode for supercapacitor, a high specific capacity of 582.8 C g(−1) at a current density of 1 A g(−1), a desirable rate capability with capacity retention about 84.8% at 20 A g(−1), and an outstanding cycle performance of 93.1% capacity retention after 25,000 cycles can be achieved. More remarkably, an energy density of 33.8 W h kg(−1) at a power density of 224 W kg(−1) and wonderful cycling stability with 74% capacity retention after 10,000 cycles can be delivered based on the hybrid-supercapacitor with the as-prepared Co(3)O(4) nanowire arrays as a positive electrode and active carbon as negative electrode. All the unexceptionable supercapacitive behaviors illustrates that our unique 3D gully-network structure Co(3)O(4) nanowire arrays hold a great promise for constructing high-performance energy storage devices. Frontiers Media S.A. 2018-12-21 /pmc/articles/PMC6308209/ /pubmed/30622941 http://dx.doi.org/10.3389/fchem.2018.00636 Text en Copyright © 2018 Guo, Yin, Wu, Li, Sun, Jia, Li, Hou and Wei. 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
Guo, Chunli
Yin, Minshuai
Wu, Chun
Li, Jie
Sun, Changhui
Jia, Chuankun
Li, Taotao
Hou, Lifeng
Wei, Yinghui
Highly Stable Gully-Network Co(3)O(4) Nanowire Arrays as Battery-Type Electrode for Outstanding Supercapacitor Performance
title Highly Stable Gully-Network Co(3)O(4) Nanowire Arrays as Battery-Type Electrode for Outstanding Supercapacitor Performance
title_full Highly Stable Gully-Network Co(3)O(4) Nanowire Arrays as Battery-Type Electrode for Outstanding Supercapacitor Performance
title_fullStr Highly Stable Gully-Network Co(3)O(4) Nanowire Arrays as Battery-Type Electrode for Outstanding Supercapacitor Performance
title_full_unstemmed Highly Stable Gully-Network Co(3)O(4) Nanowire Arrays as Battery-Type Electrode for Outstanding Supercapacitor Performance
title_short Highly Stable Gully-Network Co(3)O(4) Nanowire Arrays as Battery-Type Electrode for Outstanding Supercapacitor Performance
title_sort highly stable gully-network co(3)o(4) nanowire arrays as battery-type electrode for outstanding supercapacitor performance
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308209/
https://www.ncbi.nlm.nih.gov/pubmed/30622941
http://dx.doi.org/10.3389/fchem.2018.00636
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