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A dual-function liquid electrolyte additive for high-energy non-aqueous lithium metal batteries
Engineering the formulation of non-aqueous liquid electrolytes is a viable strategy to produce high-energy lithium metal batteries. However, when the lithium metal anode is combined with a Ni-rich layered cathode, the (electro)chemical stability of both electrodes could be compromised. To circumvent...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8917126/ https://www.ncbi.nlm.nih.gov/pubmed/35277497 http://dx.doi.org/10.1038/s41467-022-28959-5 |
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author | Zhang, Yuji Wu, Yuan Li, Huiyi Chen, Jinghao Lei, Danni Wang, Chengxin |
author_facet | Zhang, Yuji Wu, Yuan Li, Huiyi Chen, Jinghao Lei, Danni Wang, Chengxin |
author_sort | Zhang, Yuji |
collection | PubMed |
description | Engineering the formulation of non-aqueous liquid electrolytes is a viable strategy to produce high-energy lithium metal batteries. However, when the lithium metal anode is combined with a Ni-rich layered cathode, the (electro)chemical stability of both electrodes could be compromised. To circumvent this issue, we report a combination of aluminum ethoxide (0.4 wt.%) and fluoroethylene carbonate (5 vol.%) as additives in a conventional LiPF(6)-containing carbonate-based electrolyte solution. This electrolyte formulation enables the formation of mechanically robust and ionically conductive interphases on both electrodes’ surfaces. In particular, the alumina formed at the interphases prevents the formation of dendritic structures on the lithium metal anode and mitigate the stress-induced cracking and phase transformation in the Ni-rich layered cathode. By coupling a thin (i.e., about 40 μm) lithium metal anode with a high-loading (i.e., 21.5 mg cm(−2)) LiNi(0.8)Co(0.1)Mn(0.1)O(2)-based cathode in coin cell configuration and lean electrolyte conditions, the engineered electrolyte allows a specific discharge capacity retention of 80.3% after 130 cycles at 60 mA g(−1) and 30 °C which results in calculated specific cell energy of about 350 Wh kg(−1). |
format | Online Article Text |
id | pubmed-8917126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89171262022-04-01 A dual-function liquid electrolyte additive for high-energy non-aqueous lithium metal batteries Zhang, Yuji Wu, Yuan Li, Huiyi Chen, Jinghao Lei, Danni Wang, Chengxin Nat Commun Article Engineering the formulation of non-aqueous liquid electrolytes is a viable strategy to produce high-energy lithium metal batteries. However, when the lithium metal anode is combined with a Ni-rich layered cathode, the (electro)chemical stability of both electrodes could be compromised. To circumvent this issue, we report a combination of aluminum ethoxide (0.4 wt.%) and fluoroethylene carbonate (5 vol.%) as additives in a conventional LiPF(6)-containing carbonate-based electrolyte solution. This electrolyte formulation enables the formation of mechanically robust and ionically conductive interphases on both electrodes’ surfaces. In particular, the alumina formed at the interphases prevents the formation of dendritic structures on the lithium metal anode and mitigate the stress-induced cracking and phase transformation in the Ni-rich layered cathode. By coupling a thin (i.e., about 40 μm) lithium metal anode with a high-loading (i.e., 21.5 mg cm(−2)) LiNi(0.8)Co(0.1)Mn(0.1)O(2)-based cathode in coin cell configuration and lean electrolyte conditions, the engineered electrolyte allows a specific discharge capacity retention of 80.3% after 130 cycles at 60 mA g(−1) and 30 °C which results in calculated specific cell energy of about 350 Wh kg(−1). Nature Publishing Group UK 2022-03-11 /pmc/articles/PMC8917126/ /pubmed/35277497 http://dx.doi.org/10.1038/s41467-022-28959-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhang, Yuji Wu, Yuan Li, Huiyi Chen, Jinghao Lei, Danni Wang, Chengxin A dual-function liquid electrolyte additive for high-energy non-aqueous lithium metal batteries |
title | A dual-function liquid electrolyte additive for high-energy non-aqueous lithium metal batteries |
title_full | A dual-function liquid electrolyte additive for high-energy non-aqueous lithium metal batteries |
title_fullStr | A dual-function liquid electrolyte additive for high-energy non-aqueous lithium metal batteries |
title_full_unstemmed | A dual-function liquid electrolyte additive for high-energy non-aqueous lithium metal batteries |
title_short | A dual-function liquid electrolyte additive for high-energy non-aqueous lithium metal batteries |
title_sort | dual-function liquid electrolyte additive for high-energy non-aqueous lithium metal batteries |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8917126/ https://www.ncbi.nlm.nih.gov/pubmed/35277497 http://dx.doi.org/10.1038/s41467-022-28959-5 |
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