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Designed hybrid nanostructure with catalytic effect: beyond the theoretical capacity of SnO(2) anode material for lithium ion batteries

Transition metal cobalt (Co) nanoparticle was designed as catalyst to promote the conversion reaction of Sn to SnO(2) during the delithiation process which is deemed as an irreversible reaction. The designed nanocomposite, named as SnO(2)/Co(3)O(4)/reduced-graphene-oxide (rGO), was synthesized by a...

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Autores principales: Wang, Ye, Huang, Zhi Xiang, Shi, Yumeng, Wong, Jen It, Ding, Meng, Yang, Hui Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361932/
https://www.ncbi.nlm.nih.gov/pubmed/25776280
http://dx.doi.org/10.1038/srep09164
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author Wang, Ye
Huang, Zhi Xiang
Shi, Yumeng
Wong, Jen It
Ding, Meng
Yang, Hui Ying
author_facet Wang, Ye
Huang, Zhi Xiang
Shi, Yumeng
Wong, Jen It
Ding, Meng
Yang, Hui Ying
author_sort Wang, Ye
collection PubMed
description Transition metal cobalt (Co) nanoparticle was designed as catalyst to promote the conversion reaction of Sn to SnO(2) during the delithiation process which is deemed as an irreversible reaction. The designed nanocomposite, named as SnO(2)/Co(3)O(4)/reduced-graphene-oxide (rGO), was synthesized by a simple two-step method composed of hydrothermal (1(st) step) and solvothermal (2(nd) step) synthesis processes. Compared to the pristine SnO(2)/rGO and SnO(2)/Co(3)O(4) electrodes, SnO(2)/Co(3)O(4)/rGO nanocomposites exhibit significantly enhanced electrochemical performance as the anode material of lithium-ion batteries (LIBs). The SnO(2)/Co(3)O(4)/rGO nanocomposites can deliver high specific capacities of 1038 and 712 mAh g(−1) at the current densities of 100 and 1000 mA g(−1), respectively. In addition, the SnO(2)/Co(3)O(4)/rGO nanocomposites also exhibit 641 mAh g(−1) at a high current density of 1000 mA g(−1) after 900 cycles, indicating an ultra-long cycling stability under high current density. Through ex-situ TEM analysis, the excellent electrochemical performance was attributed to the catalytic effect of Co nanoparticles to promote the conversion of Sn to SnO(2) and the decomposition of Li(2)O during the delithiation process. Based on the results, herein we propose a new method in employing the catalyst to increase the capacity of alloying-dealloying type anode material to beyond its theoretical value and enhance the electrochemical performance.
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spelling pubmed-43619322015-03-19 Designed hybrid nanostructure with catalytic effect: beyond the theoretical capacity of SnO(2) anode material for lithium ion batteries Wang, Ye Huang, Zhi Xiang Shi, Yumeng Wong, Jen It Ding, Meng Yang, Hui Ying Sci Rep Article Transition metal cobalt (Co) nanoparticle was designed as catalyst to promote the conversion reaction of Sn to SnO(2) during the delithiation process which is deemed as an irreversible reaction. The designed nanocomposite, named as SnO(2)/Co(3)O(4)/reduced-graphene-oxide (rGO), was synthesized by a simple two-step method composed of hydrothermal (1(st) step) and solvothermal (2(nd) step) synthesis processes. Compared to the pristine SnO(2)/rGO and SnO(2)/Co(3)O(4) electrodes, SnO(2)/Co(3)O(4)/rGO nanocomposites exhibit significantly enhanced electrochemical performance as the anode material of lithium-ion batteries (LIBs). The SnO(2)/Co(3)O(4)/rGO nanocomposites can deliver high specific capacities of 1038 and 712 mAh g(−1) at the current densities of 100 and 1000 mA g(−1), respectively. In addition, the SnO(2)/Co(3)O(4)/rGO nanocomposites also exhibit 641 mAh g(−1) at a high current density of 1000 mA g(−1) after 900 cycles, indicating an ultra-long cycling stability under high current density. Through ex-situ TEM analysis, the excellent electrochemical performance was attributed to the catalytic effect of Co nanoparticles to promote the conversion of Sn to SnO(2) and the decomposition of Li(2)O during the delithiation process. Based on the results, herein we propose a new method in employing the catalyst to increase the capacity of alloying-dealloying type anode material to beyond its theoretical value and enhance the electrochemical performance. Nature Publishing Group 2015-03-17 /pmc/articles/PMC4361932/ /pubmed/25776280 http://dx.doi.org/10.1038/srep09164 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wang, Ye
Huang, Zhi Xiang
Shi, Yumeng
Wong, Jen It
Ding, Meng
Yang, Hui Ying
Designed hybrid nanostructure with catalytic effect: beyond the theoretical capacity of SnO(2) anode material for lithium ion batteries
title Designed hybrid nanostructure with catalytic effect: beyond the theoretical capacity of SnO(2) anode material for lithium ion batteries
title_full Designed hybrid nanostructure with catalytic effect: beyond the theoretical capacity of SnO(2) anode material for lithium ion batteries
title_fullStr Designed hybrid nanostructure with catalytic effect: beyond the theoretical capacity of SnO(2) anode material for lithium ion batteries
title_full_unstemmed Designed hybrid nanostructure with catalytic effect: beyond the theoretical capacity of SnO(2) anode material for lithium ion batteries
title_short Designed hybrid nanostructure with catalytic effect: beyond the theoretical capacity of SnO(2) anode material for lithium ion batteries
title_sort designed hybrid nanostructure with catalytic effect: beyond the theoretical capacity of sno(2) anode material for lithium ion batteries
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361932/
https://www.ncbi.nlm.nih.gov/pubmed/25776280
http://dx.doi.org/10.1038/srep09164
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