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High-Voltage Aqueous Magnesium Ion Batteries
[Image: see text] Nonaqueous rechargeable magnesium (Mg) batteries suffer from the complicated and moisture-sensitive electrolyte chemistry. Besides electrolytes, the practicality of a Mg battery is also confined by the absence of high-performance electrode materials due to the intrinsically slow Mg...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658756/ https://www.ncbi.nlm.nih.gov/pubmed/29104929 http://dx.doi.org/10.1021/acscentsci.7b00361 |
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author | Wang, Fei Fan, Xiulin Gao, Tao Sun, Wei Ma, Zhaohui Yang, Chongyin Han, Fudong Xu, Kang Wang, Chunsheng |
author_facet | Wang, Fei Fan, Xiulin Gao, Tao Sun, Wei Ma, Zhaohui Yang, Chongyin Han, Fudong Xu, Kang Wang, Chunsheng |
author_sort | Wang, Fei |
collection | PubMed |
description | [Image: see text] Nonaqueous rechargeable magnesium (Mg) batteries suffer from the complicated and moisture-sensitive electrolyte chemistry. Besides electrolytes, the practicality of a Mg battery is also confined by the absence of high-performance electrode materials due to the intrinsically slow Mg(2+) diffusion in the solids. In this work, we demonstrated a rechargeable aqueous magnesium ion battery (AMIB) concept of high energy density, fast kinetics, and reversibility. Using a superconcentration approach we expanded the electrochemical stability window of the aqueous electrolyte to 2.0 V. More importantly, two new Mg ion host materials, Li superconcentration approach we expanded the electrochemical stability window of the aqueous electrolyte to 2.0 V. More importantly, two new Mg ion host materials, Li(3)V(2)(PO(4))(3) and poly pyromellitic dianhydride, were developed and employed as cathode and anode electrodes, respectively. Based on comparisons of the aqueous and nonaqueous systems, the role of water is identified to be critical in the Mg ion mobility in the intercalation host but remaining little detrimental to its non-diffusion controlled process. Compared with the previously reported Mg ion cell delivers an unprecedented high power density of 6400 W kg ion cell delivers an unprecedented high power density of 6400 W kg while retaining 92% of the initial capacity after 6000 cycles, pushing the Mg ion cell to a brand new stage. |
format | Online Article Text |
id | pubmed-5658756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-56587562017-11-04 High-Voltage Aqueous Magnesium Ion Batteries Wang, Fei Fan, Xiulin Gao, Tao Sun, Wei Ma, Zhaohui Yang, Chongyin Han, Fudong Xu, Kang Wang, Chunsheng ACS Cent Sci [Image: see text] Nonaqueous rechargeable magnesium (Mg) batteries suffer from the complicated and moisture-sensitive electrolyte chemistry. Besides electrolytes, the practicality of a Mg battery is also confined by the absence of high-performance electrode materials due to the intrinsically slow Mg(2+) diffusion in the solids. In this work, we demonstrated a rechargeable aqueous magnesium ion battery (AMIB) concept of high energy density, fast kinetics, and reversibility. Using a superconcentration approach we expanded the electrochemical stability window of the aqueous electrolyte to 2.0 V. More importantly, two new Mg ion host materials, Li superconcentration approach we expanded the electrochemical stability window of the aqueous electrolyte to 2.0 V. More importantly, two new Mg ion host materials, Li(3)V(2)(PO(4))(3) and poly pyromellitic dianhydride, were developed and employed as cathode and anode electrodes, respectively. Based on comparisons of the aqueous and nonaqueous systems, the role of water is identified to be critical in the Mg ion mobility in the intercalation host but remaining little detrimental to its non-diffusion controlled process. Compared with the previously reported Mg ion cell delivers an unprecedented high power density of 6400 W kg ion cell delivers an unprecedented high power density of 6400 W kg while retaining 92% of the initial capacity after 6000 cycles, pushing the Mg ion cell to a brand new stage. American Chemical Society 2017-10-04 2017-10-25 /pmc/articles/PMC5658756/ /pubmed/29104929 http://dx.doi.org/10.1021/acscentsci.7b00361 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Wang, Fei Fan, Xiulin Gao, Tao Sun, Wei Ma, Zhaohui Yang, Chongyin Han, Fudong Xu, Kang Wang, Chunsheng High-Voltage Aqueous Magnesium Ion Batteries |
title | High-Voltage Aqueous Magnesium Ion Batteries |
title_full | High-Voltage Aqueous Magnesium Ion Batteries |
title_fullStr | High-Voltage Aqueous Magnesium Ion Batteries |
title_full_unstemmed | High-Voltage Aqueous Magnesium Ion Batteries |
title_short | High-Voltage Aqueous Magnesium Ion Batteries |
title_sort | high-voltage aqueous magnesium ion batteries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658756/ https://www.ncbi.nlm.nih.gov/pubmed/29104929 http://dx.doi.org/10.1021/acscentsci.7b00361 |
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