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Reversible Electrochemical Energy Storage Based on Zinc-Halide Chemistry
[Image: see text] The development of rechargeable Zinc-ion batteries (ZIBs) has been hindered by the lack of efficient cathode materials due to the strong binding of divalent zinc ions with the host lattice. Herein, we report a strategy that eliminates the participation of Zn(2+) within the cathode...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041251/ https://www.ncbi.nlm.nih.gov/pubmed/33724772 http://dx.doi.org/10.1021/acsami.0c20622 |
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author | Ejigu, Andinet Le Fevre, Lewis W. Dryfe, Robert A. W. |
author_facet | Ejigu, Andinet Le Fevre, Lewis W. Dryfe, Robert A. W. |
author_sort | Ejigu, Andinet |
collection | PubMed |
description | [Image: see text] The development of rechargeable Zinc-ion batteries (ZIBs) has been hindered by the lack of efficient cathode materials due to the strong binding of divalent zinc ions with the host lattice. Herein, we report a strategy that eliminates the participation of Zn(2+) within the cathode chemistry. The approach involves the use of composite cathode materials that contain Zn halides (ZnCl(2), ZnBr(2), and ZnI(2)) and carbon (graphite or activated carbon), where the halide ions act both as charge carriers and redox centers while using a Zn(2+)-conducting water-in-salt gel electrolyte. The use of graphite in the composite electrode produced batterylike behavior, where the voltage plateau was related to the standard potential of the halogen species. When activated carbon was used in the composite, however, the cell acted as a hybrid Zn-ion capacitor due to the fast, reversible halide ion electrosorption/desorption in the carbon pores. The ZnX(2)-activated carbon composite delivers a capacity of over 400 mAh g(–1) and cell energy density of 140 Wh kg(–1) while retaining over 95% of its capacity after 500 cycles. The halogen reaction mechanism has been elucidated using combinations of electrochemical and in situ spectroscopic techniques. |
format | Online Article Text |
id | pubmed-8041251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-80412512021-04-13 Reversible Electrochemical Energy Storage Based on Zinc-Halide Chemistry Ejigu, Andinet Le Fevre, Lewis W. Dryfe, Robert A. W. ACS Appl Mater Interfaces [Image: see text] The development of rechargeable Zinc-ion batteries (ZIBs) has been hindered by the lack of efficient cathode materials due to the strong binding of divalent zinc ions with the host lattice. Herein, we report a strategy that eliminates the participation of Zn(2+) within the cathode chemistry. The approach involves the use of composite cathode materials that contain Zn halides (ZnCl(2), ZnBr(2), and ZnI(2)) and carbon (graphite or activated carbon), where the halide ions act both as charge carriers and redox centers while using a Zn(2+)-conducting water-in-salt gel electrolyte. The use of graphite in the composite electrode produced batterylike behavior, where the voltage plateau was related to the standard potential of the halogen species. When activated carbon was used in the composite, however, the cell acted as a hybrid Zn-ion capacitor due to the fast, reversible halide ion electrosorption/desorption in the carbon pores. The ZnX(2)-activated carbon composite delivers a capacity of over 400 mAh g(–1) and cell energy density of 140 Wh kg(–1) while retaining over 95% of its capacity after 500 cycles. The halogen reaction mechanism has been elucidated using combinations of electrochemical and in situ spectroscopic techniques. American Chemical Society 2021-03-16 2021-03-31 /pmc/articles/PMC8041251/ /pubmed/33724772 http://dx.doi.org/10.1021/acsami.0c20622 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Ejigu, Andinet Le Fevre, Lewis W. Dryfe, Robert A. W. Reversible Electrochemical Energy Storage Based on Zinc-Halide Chemistry |
title | Reversible
Electrochemical Energy Storage Based on
Zinc-Halide Chemistry |
title_full | Reversible
Electrochemical Energy Storage Based on
Zinc-Halide Chemistry |
title_fullStr | Reversible
Electrochemical Energy Storage Based on
Zinc-Halide Chemistry |
title_full_unstemmed | Reversible
Electrochemical Energy Storage Based on
Zinc-Halide Chemistry |
title_short | Reversible
Electrochemical Energy Storage Based on
Zinc-Halide Chemistry |
title_sort | reversible
electrochemical energy storage based on
zinc-halide chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041251/ https://www.ncbi.nlm.nih.gov/pubmed/33724772 http://dx.doi.org/10.1021/acsami.0c20622 |
work_keys_str_mv | AT ejiguandinet reversibleelectrochemicalenergystoragebasedonzinchalidechemistry AT lefevrelewisw reversibleelectrochemicalenergystoragebasedonzinchalidechemistry AT dryferobertaw reversibleelectrochemicalenergystoragebasedonzinchalidechemistry |