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Realizing high-capacity all-solid-state lithium-sulfur batteries using a low-density inorganic solid-state electrolyte

Lithium-sulfur all-solid-state batteries using inorganic solid-state electrolytes are considered promising electrochemical energy storage technologies. However, developing positive electrodes with high sulfur content, adequate sulfur utilization, and high mass loading is challenging. Here, to addres...

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Autores principales: Wang, Daiwei, Jhang, Li-Ji, Kou, Rong, Liao, Meng, Zheng, Shiyao, Jiang, Heng, Shi, Pei, Li, Guo-Xing, Meng, Kui, Wang, Donghai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076334/
https://www.ncbi.nlm.nih.gov/pubmed/37019929
http://dx.doi.org/10.1038/s41467-023-37564-z
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author Wang, Daiwei
Jhang, Li-Ji
Kou, Rong
Liao, Meng
Zheng, Shiyao
Jiang, Heng
Shi, Pei
Li, Guo-Xing
Meng, Kui
Wang, Donghai
author_facet Wang, Daiwei
Jhang, Li-Ji
Kou, Rong
Liao, Meng
Zheng, Shiyao
Jiang, Heng
Shi, Pei
Li, Guo-Xing
Meng, Kui
Wang, Donghai
author_sort Wang, Daiwei
collection PubMed
description Lithium-sulfur all-solid-state batteries using inorganic solid-state electrolytes are considered promising electrochemical energy storage technologies. However, developing positive electrodes with high sulfur content, adequate sulfur utilization, and high mass loading is challenging. Here, to address these concerns, we propose using a liquid-phase-synthesized Li(3)PS(4)-2LiBH(4) glass-ceramic solid electrolyte with a low density (1.491 g cm(−3)), small primary particle size (~500 nm) and bulk ionic conductivity of 6.0 mS cm(−1) at 25 °C for fabricating lithium-sulfur all-solid-state batteries. When tested in a Swagelok cell configuration with a Li-In negative electrode and a 60 wt% S positive electrode applying an average stack pressure of ~55 MPa, the all-solid-state battery delivered a high discharge capacity of about 1144.6 mAh g(−1) at 167.5 mA g(−1) and 60 °C. We further demonstrate that the use of the low-density solid electrolyte increases the electrolyte volume ratio in the cathode, reduces inactive bulky sulfur, and improves the content uniformity of the sulfur-based positive electrode, thus providing sufficient ion conduction pathways for battery performance improvement.
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spelling pubmed-100763342023-04-07 Realizing high-capacity all-solid-state lithium-sulfur batteries using a low-density inorganic solid-state electrolyte Wang, Daiwei Jhang, Li-Ji Kou, Rong Liao, Meng Zheng, Shiyao Jiang, Heng Shi, Pei Li, Guo-Xing Meng, Kui Wang, Donghai Nat Commun Article Lithium-sulfur all-solid-state batteries using inorganic solid-state electrolytes are considered promising electrochemical energy storage technologies. However, developing positive electrodes with high sulfur content, adequate sulfur utilization, and high mass loading is challenging. Here, to address these concerns, we propose using a liquid-phase-synthesized Li(3)PS(4)-2LiBH(4) glass-ceramic solid electrolyte with a low density (1.491 g cm(−3)), small primary particle size (~500 nm) and bulk ionic conductivity of 6.0 mS cm(−1) at 25 °C for fabricating lithium-sulfur all-solid-state batteries. When tested in a Swagelok cell configuration with a Li-In negative electrode and a 60 wt% S positive electrode applying an average stack pressure of ~55 MPa, the all-solid-state battery delivered a high discharge capacity of about 1144.6 mAh g(−1) at 167.5 mA g(−1) and 60 °C. We further demonstrate that the use of the low-density solid electrolyte increases the electrolyte volume ratio in the cathode, reduces inactive bulky sulfur, and improves the content uniformity of the sulfur-based positive electrode, thus providing sufficient ion conduction pathways for battery performance improvement. Nature Publishing Group UK 2023-04-05 /pmc/articles/PMC10076334/ /pubmed/37019929 http://dx.doi.org/10.1038/s41467-023-37564-z Text en © The Author(s) 2023 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
Wang, Daiwei
Jhang, Li-Ji
Kou, Rong
Liao, Meng
Zheng, Shiyao
Jiang, Heng
Shi, Pei
Li, Guo-Xing
Meng, Kui
Wang, Donghai
Realizing high-capacity all-solid-state lithium-sulfur batteries using a low-density inorganic solid-state electrolyte
title Realizing high-capacity all-solid-state lithium-sulfur batteries using a low-density inorganic solid-state electrolyte
title_full Realizing high-capacity all-solid-state lithium-sulfur batteries using a low-density inorganic solid-state electrolyte
title_fullStr Realizing high-capacity all-solid-state lithium-sulfur batteries using a low-density inorganic solid-state electrolyte
title_full_unstemmed Realizing high-capacity all-solid-state lithium-sulfur batteries using a low-density inorganic solid-state electrolyte
title_short Realizing high-capacity all-solid-state lithium-sulfur batteries using a low-density inorganic solid-state electrolyte
title_sort realizing high-capacity all-solid-state lithium-sulfur batteries using a low-density inorganic solid-state electrolyte
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076334/
https://www.ncbi.nlm.nih.gov/pubmed/37019929
http://dx.doi.org/10.1038/s41467-023-37564-z
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