In situ conversion reaction of magnesium fluoride to boost the performance of the sulfide-based electrolyte Li 6 PS 5 Cl for all-solid-state lithium metal batteries
Among the solid electrolytes of all-solid-state lithium metal batteries being pursued globally, Li 6 PS 5 Cl is one of the most promising candidates owing to its high ionic conductivity and easy processibility. However, Li 6 PS 5 Cl is vulnerable to the lithium anode because lithium can not only red...
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Veröffentlicht in: | Inorganic chemistry frontiers 2025-01, Vol.12 (3), p.1010-1020 |
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container_title | Inorganic chemistry frontiers |
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creator | Zhang, Yuzhe Chang, Haolong Hu, Xiaohu Xu, Shijie Wang, Xinyu Yang, Shunjin Sun, Yujiang Sun, Xiao Ren, Dehang Chen, Xing Cheng, Fangyi Yang, Yongan |
description | Among the solid electrolytes of all-solid-state lithium metal batteries being pursued globally, Li 6 PS 5 Cl is one of the most promising candidates owing to its high ionic conductivity and easy processibility. However, Li 6 PS 5 Cl is vulnerable to the lithium anode because lithium can not only reduce Li 6 PS 5 Cl to generate passive interfaces but can also lead to the growth of lithium dendrites, which could penetrate the Li 6 PS 5 Cl bulk and eventually short-circuit the battery. Herein, we report that the electrochemical performance of Li 6 PS 5 Cl could be greatly enhanced by compositing it with MgF 2 , which was the most effective metal fluoride among five studied materials. Specifically, critical current density was increased by 4.7 times, cycling durability in Li|electrolyte|Li symmetric cells was extended by 19 times, capacity retention in Li|electrolyte|LiNi 0.7 Co 0.2 Mn 0.1 O 2 full cells was enhanced from 76% to 86%, and rate capability was boosted from 0.2C to 1C. Combination studies involving experimental characterizations and theoretical computations revealed that the performance-improving mechanism involved a sustained-release effect of capsule medicines, meaning during the charging/discharging cycles, MgF 2 could timely scavenge lithium dendrites to generate Li x Mg alloy and LiF, wherein Li x Mg could reversibly release/uptake Li and LiF could suppress the nucleation of lithium dendrites. |
doi_str_mv | 10.1039/D4QI02717E |
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However, Li 6 PS 5 Cl is vulnerable to the lithium anode because lithium can not only reduce Li 6 PS 5 Cl to generate passive interfaces but can also lead to the growth of lithium dendrites, which could penetrate the Li 6 PS 5 Cl bulk and eventually short-circuit the battery. Herein, we report that the electrochemical performance of Li 6 PS 5 Cl could be greatly enhanced by compositing it with MgF 2 , which was the most effective metal fluoride among five studied materials. Specifically, critical current density was increased by 4.7 times, cycling durability in Li|electrolyte|Li symmetric cells was extended by 19 times, capacity retention in Li|electrolyte|LiNi 0.7 Co 0.2 Mn 0.1 O 2 full cells was enhanced from 76% to 86%, and rate capability was boosted from 0.2C to 1C. Combination studies involving experimental characterizations and theoretical computations revealed that the performance-improving mechanism involved a sustained-release effect of capsule medicines, meaning during the charging/discharging cycles, MgF 2 could timely scavenge lithium dendrites to generate Li x Mg alloy and LiF, wherein Li x Mg could reversibly release/uptake Li and LiF could suppress the nucleation of lithium dendrites.</description><identifier>ISSN: 2052-1553</identifier><identifier>EISSN: 2052-1553</identifier><identifier>DOI: 10.1039/D4QI02717E</identifier><language>eng</language><ispartof>Inorganic chemistry frontiers, 2025-01, Vol.12 (3), p.1010-1020</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-crossref_primary_10_1039_D4QI02717E3</cites><orcidid>0000-0002-1223-298X ; 0000-0002-9400-1500 ; 0000-0002-4252-4924 ; 0000-0003-1451-2923</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Zhang, Yuzhe</creatorcontrib><creatorcontrib>Chang, Haolong</creatorcontrib><creatorcontrib>Hu, Xiaohu</creatorcontrib><creatorcontrib>Xu, Shijie</creatorcontrib><creatorcontrib>Wang, Xinyu</creatorcontrib><creatorcontrib>Yang, Shunjin</creatorcontrib><creatorcontrib>Sun, Yujiang</creatorcontrib><creatorcontrib>Sun, Xiao</creatorcontrib><creatorcontrib>Ren, Dehang</creatorcontrib><creatorcontrib>Chen, Xing</creatorcontrib><creatorcontrib>Cheng, Fangyi</creatorcontrib><creatorcontrib>Yang, Yongan</creatorcontrib><title>In situ conversion reaction of magnesium fluoride to boost the performance of the sulfide-based electrolyte Li 6 PS 5 Cl for all-solid-state lithium metal batteries</title><title>Inorganic chemistry frontiers</title><description>Among the solid electrolytes of all-solid-state lithium metal batteries being pursued globally, Li 6 PS 5 Cl is one of the most promising candidates owing to its high ionic conductivity and easy processibility. However, Li 6 PS 5 Cl is vulnerable to the lithium anode because lithium can not only reduce Li 6 PS 5 Cl to generate passive interfaces but can also lead to the growth of lithium dendrites, which could penetrate the Li 6 PS 5 Cl bulk and eventually short-circuit the battery. Herein, we report that the electrochemical performance of Li 6 PS 5 Cl could be greatly enhanced by compositing it with MgF 2 , which was the most effective metal fluoride among five studied materials. Specifically, critical current density was increased by 4.7 times, cycling durability in Li|electrolyte|Li symmetric cells was extended by 19 times, capacity retention in Li|electrolyte|LiNi 0.7 Co 0.2 Mn 0.1 O 2 full cells was enhanced from 76% to 86%, and rate capability was boosted from 0.2C to 1C. Combination studies involving experimental characterizations and theoretical computations revealed that the performance-improving mechanism involved a sustained-release effect of capsule medicines, meaning during the charging/discharging cycles, MgF 2 could timely scavenge lithium dendrites to generate Li x Mg alloy and LiF, wherein Li x Mg could reversibly release/uptake Li and LiF could suppress the nucleation of lithium dendrites.</description><issn>2052-1553</issn><issn>2052-1553</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><recordid>eNqVkEFLw0AQhRexYLG9-AvmLER3k6bFc61Y8KDoPWySWbsyyZSdidD_4w81AUGvnt7j8T0ePGOunL1xtri7vV-97G2-cZvdmZnntswzV5bF-R9_YZYiH9Za51bWre3cfO17kKgDNNx_YpLIPST0jU6GA3T-vUeJQweBBk6xRVCGmlkU9IBwxBQ4db5vcMKnSAYKI5fVXrAFJGw0MZ0U4SnCGp5foYQtwVgDT5QJU2wzUT8CFPUwbXWonqD2qpgiysLMgifB5Y9emuuH3dv2MWsSiyQM1THFzqdT5Ww1XVH9XlH8C_4Gf3Bmww</recordid><startdate>20250128</startdate><enddate>20250128</enddate><creator>Zhang, Yuzhe</creator><creator>Chang, Haolong</creator><creator>Hu, Xiaohu</creator><creator>Xu, Shijie</creator><creator>Wang, Xinyu</creator><creator>Yang, Shunjin</creator><creator>Sun, Yujiang</creator><creator>Sun, Xiao</creator><creator>Ren, Dehang</creator><creator>Chen, Xing</creator><creator>Cheng, Fangyi</creator><creator>Yang, Yongan</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-1223-298X</orcidid><orcidid>https://orcid.org/0000-0002-9400-1500</orcidid><orcidid>https://orcid.org/0000-0002-4252-4924</orcidid><orcidid>https://orcid.org/0000-0003-1451-2923</orcidid></search><sort><creationdate>20250128</creationdate><title>In situ conversion reaction of magnesium fluoride to boost the performance of the sulfide-based electrolyte Li 6 PS 5 Cl for all-solid-state lithium metal batteries</title><author>Zhang, Yuzhe ; Chang, Haolong ; Hu, Xiaohu ; Xu, Shijie ; Wang, Xinyu ; Yang, Shunjin ; Sun, Yujiang ; Sun, Xiao ; Ren, Dehang ; Chen, Xing ; Cheng, Fangyi ; Yang, Yongan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-crossref_primary_10_1039_D4QI02717E3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Yuzhe</creatorcontrib><creatorcontrib>Chang, Haolong</creatorcontrib><creatorcontrib>Hu, Xiaohu</creatorcontrib><creatorcontrib>Xu, Shijie</creatorcontrib><creatorcontrib>Wang, Xinyu</creatorcontrib><creatorcontrib>Yang, Shunjin</creatorcontrib><creatorcontrib>Sun, Yujiang</creatorcontrib><creatorcontrib>Sun, Xiao</creatorcontrib><creatorcontrib>Ren, Dehang</creatorcontrib><creatorcontrib>Chen, Xing</creatorcontrib><creatorcontrib>Cheng, Fangyi</creatorcontrib><creatorcontrib>Yang, Yongan</creatorcontrib><collection>CrossRef</collection><jtitle>Inorganic chemistry frontiers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Yuzhe</au><au>Chang, Haolong</au><au>Hu, Xiaohu</au><au>Xu, Shijie</au><au>Wang, Xinyu</au><au>Yang, Shunjin</au><au>Sun, Yujiang</au><au>Sun, Xiao</au><au>Ren, Dehang</au><au>Chen, Xing</au><au>Cheng, Fangyi</au><au>Yang, Yongan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In situ conversion reaction of magnesium fluoride to boost the performance of the sulfide-based electrolyte Li 6 PS 5 Cl for all-solid-state lithium metal batteries</atitle><jtitle>Inorganic chemistry frontiers</jtitle><date>2025-01-28</date><risdate>2025</risdate><volume>12</volume><issue>3</issue><spage>1010</spage><epage>1020</epage><pages>1010-1020</pages><issn>2052-1553</issn><eissn>2052-1553</eissn><abstract>Among the solid electrolytes of all-solid-state lithium metal batteries being pursued globally, Li 6 PS 5 Cl is one of the most promising candidates owing to its high ionic conductivity and easy processibility. However, Li 6 PS 5 Cl is vulnerable to the lithium anode because lithium can not only reduce Li 6 PS 5 Cl to generate passive interfaces but can also lead to the growth of lithium dendrites, which could penetrate the Li 6 PS 5 Cl bulk and eventually short-circuit the battery. Herein, we report that the electrochemical performance of Li 6 PS 5 Cl could be greatly enhanced by compositing it with MgF 2 , which was the most effective metal fluoride among five studied materials. Specifically, critical current density was increased by 4.7 times, cycling durability in Li|electrolyte|Li symmetric cells was extended by 19 times, capacity retention in Li|electrolyte|LiNi 0.7 Co 0.2 Mn 0.1 O 2 full cells was enhanced from 76% to 86%, and rate capability was boosted from 0.2C to 1C. Combination studies involving experimental characterizations and theoretical computations revealed that the performance-improving mechanism involved a sustained-release effect of capsule medicines, meaning during the charging/discharging cycles, MgF 2 could timely scavenge lithium dendrites to generate Li x Mg alloy and LiF, wherein Li x Mg could reversibly release/uptake Li and LiF could suppress the nucleation of lithium dendrites.</abstract><doi>10.1039/D4QI02717E</doi><orcidid>https://orcid.org/0000-0002-1223-298X</orcidid><orcidid>https://orcid.org/0000-0002-9400-1500</orcidid><orcidid>https://orcid.org/0000-0002-4252-4924</orcidid><orcidid>https://orcid.org/0000-0003-1451-2923</orcidid></addata></record> |
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title | In situ conversion reaction of magnesium fluoride to boost the performance of the sulfide-based electrolyte Li 6 PS 5 Cl for all-solid-state lithium metal batteries |
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