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Lithium intercalation mechanism into FeF(3)·0.5H(2)O as a highly stable composite cathode material
The growing demand for lithium-ion batteries (LIBs) requires investigation of high-performance electrode materials with the advantages of being environmentally friendly and cost-effective. In this study, a nanocomposite of open-pyrochlore-structured FeF(3)·0.5H(2)O and reduced graphene oxide (RGO) i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294459/ https://www.ncbi.nlm.nih.gov/pubmed/28169373 http://dx.doi.org/10.1038/srep42237 |
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author | Ali, Ghulam Lee, Ji–Hoon Chang, Wonyoung Cho, Byung-Won Jung, Hun-Gi Nam, Kyung-Wan Chung, Kyung Yoon |
author_facet | Ali, Ghulam Lee, Ji–Hoon Chang, Wonyoung Cho, Byung-Won Jung, Hun-Gi Nam, Kyung-Wan Chung, Kyung Yoon |
author_sort | Ali, Ghulam |
collection | PubMed |
description | The growing demand for lithium-ion batteries (LIBs) requires investigation of high-performance electrode materials with the advantages of being environmentally friendly and cost-effective. In this study, a nanocomposite of open-pyrochlore-structured FeF(3)·0.5H(2)O and reduced graphene oxide (RGO) is synthesized for use as a high-performance cathode in LIBs, where RGO provides high electrical conductivity to the composite material. The morphology of the composite shows that FeF(3)·0.5H(2)O spheres are embedded into RGO layers and high-resolution TEM image shows that those spheres are composed of primary nanoparticles with a size of ~5 nm. The cycling performance indicates that the composite electrode delivers an initial high discharge capacity of 223 mAh g(−1) at 0.05 C, a rate capability up to a high C-rate of 10 C (47 mAh g(−1)) and stable cycle performance at 0.05 C (145 mAh g(−1) after 100 cycles) and 0.2 C (93 mAh g(−1) after 100 cycles) while maintaining high electrochemical reversibility. Furthermore, the responsible electrochemical reaction is investigated using in-situ XRD and synchrotron-based X-ray absorption spectroscopy (XAS), and the XRD results show that FeF(3)·0.5H(2)O transitions to an amorphous-like phase through a lithiation process. However, a reversible oxidation change of Fe(3+) ↔ Fe(2+) is identified by the XAS results. |
format | Online Article Text |
id | pubmed-5294459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52944592017-02-10 Lithium intercalation mechanism into FeF(3)·0.5H(2)O as a highly stable composite cathode material Ali, Ghulam Lee, Ji–Hoon Chang, Wonyoung Cho, Byung-Won Jung, Hun-Gi Nam, Kyung-Wan Chung, Kyung Yoon Sci Rep Article The growing demand for lithium-ion batteries (LIBs) requires investigation of high-performance electrode materials with the advantages of being environmentally friendly and cost-effective. In this study, a nanocomposite of open-pyrochlore-structured FeF(3)·0.5H(2)O and reduced graphene oxide (RGO) is synthesized for use as a high-performance cathode in LIBs, where RGO provides high electrical conductivity to the composite material. The morphology of the composite shows that FeF(3)·0.5H(2)O spheres are embedded into RGO layers and high-resolution TEM image shows that those spheres are composed of primary nanoparticles with a size of ~5 nm. The cycling performance indicates that the composite electrode delivers an initial high discharge capacity of 223 mAh g(−1) at 0.05 C, a rate capability up to a high C-rate of 10 C (47 mAh g(−1)) and stable cycle performance at 0.05 C (145 mAh g(−1) after 100 cycles) and 0.2 C (93 mAh g(−1) after 100 cycles) while maintaining high electrochemical reversibility. Furthermore, the responsible electrochemical reaction is investigated using in-situ XRD and synchrotron-based X-ray absorption spectroscopy (XAS), and the XRD results show that FeF(3)·0.5H(2)O transitions to an amorphous-like phase through a lithiation process. However, a reversible oxidation change of Fe(3+) ↔ Fe(2+) is identified by the XAS results. Nature Publishing Group 2017-02-07 /pmc/articles/PMC5294459/ /pubmed/28169373 http://dx.doi.org/10.1038/srep42237 Text en Copyright © 2017, The Author(s) 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 to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ali, Ghulam Lee, Ji–Hoon Chang, Wonyoung Cho, Byung-Won Jung, Hun-Gi Nam, Kyung-Wan Chung, Kyung Yoon Lithium intercalation mechanism into FeF(3)·0.5H(2)O as a highly stable composite cathode material |
title | Lithium intercalation mechanism into FeF(3)·0.5H(2)O as a highly stable composite cathode material |
title_full | Lithium intercalation mechanism into FeF(3)·0.5H(2)O as a highly stable composite cathode material |
title_fullStr | Lithium intercalation mechanism into FeF(3)·0.5H(2)O as a highly stable composite cathode material |
title_full_unstemmed | Lithium intercalation mechanism into FeF(3)·0.5H(2)O as a highly stable composite cathode material |
title_short | Lithium intercalation mechanism into FeF(3)·0.5H(2)O as a highly stable composite cathode material |
title_sort | lithium intercalation mechanism into fef(3)·0.5h(2)o as a highly stable composite cathode material |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294459/ https://www.ncbi.nlm.nih.gov/pubmed/28169373 http://dx.doi.org/10.1038/srep42237 |
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