A Series of Ternary Metal Chloride Superionic Conductors for High‐Performance All‐Solid‐State Lithium Batteries
Understanding the relationship between structure, ionic conductivity, and synthesis is the key to the development of superionic conductors. Here, a series of Li3‐3xM1+xCl6 (−0.14 < x ≤ 0.5, M = Tb, Dy, Ho, Y, Er, Tm) solid electrolytes with orthorhombic and trigonal structures are reported. The o...
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| Veröffentlicht in: | Advanced energy materials 2022-06, Vol.12 (21), p.n/a |
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| creator | Liang, Jianwen Maas, Eveline Luo, Jing Li, Xiaona Chen, Ning Adair, Keegan R. Li, Weihan Li, Junjie Hu, Yongfeng Liu, Jue Zhang, Li Zhao, Shangqian Lu, Shigang Wang, Jiantao Huang, Huan Zhao, Wenxuan Parnell, Steven Smith, Ronald I. Ganapathy, Swapna Wagemaker, Marnix Sun, Xueliang |
| description | Understanding the relationship between structure, ionic conductivity, and synthesis is the key to the development of superionic conductors. Here, a series of Li3‐3xM1+xCl6 (−0.14 < x ≤ 0.5, M = Tb, Dy, Ho, Y, Er, Tm) solid electrolytes with orthorhombic and trigonal structures are reported. The orthorhombic phase of Li–M–Cl shows an approximately one order of magnitude increase in ionic conductivities when compared to their trigonal phase. Using the Li–Ho–Cl components as an example, their structures, phase transition, ionic conductivity, and electrochemical stability are studied. Molecular dynamics simulations reveal the facile diffusion in the z‐direction in the orthorhombic structure, rationalizing the improved ionic conductivities. All‐solid‐state batteries of NMC811/Li2.73Ho1.09Cl6/In demonstrate excellent electrochemical performance at both 25 and −10 °C. As relevant to the vast number of isostructural halide electrolytes, the present structure control strategy guides the design of halide superionic conductors.
A favorable orthorhombic phase in various Li–M–Cl (M = Dy, Ho, Y, Er, Tm) systems which triggers a significant increase in Li+ diffusivity and reduces the activation energy barrier for diffusion is revealed. The findings are expected to aid the discovery of fundamental chemical theories relating to the activity of rare earth metal halides and exploration of new materials with high Li+ conductivity. |
| doi_str_mv | 10.1002/aenm.202103921 |
| format | Article |
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A favorable orthorhombic phase in various Li–M–Cl (M = Dy, Ho, Y, Er, Tm) systems which triggers a significant increase in Li+ diffusivity and reduces the activation energy barrier for diffusion is revealed. The findings are expected to aid the discovery of fundamental chemical theories relating to the activity of rare earth metal halides and exploration of new materials with high Li+ conductivity.</description><identifier>ISSN: 1614-6832</identifier><identifier>EISSN: 1614-6840</identifier><identifier>DOI: 10.1002/aenm.202103921</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>all‐solid‐state Li batteries ; Conductors ; Dynamic stability ; Electrochemical analysis ; Electrolytes ; energy storage ; Erbium ; halides ; Ion currents ; Ions ; Lithium batteries ; Metal chlorides ; Molecular dynamics ; Molten salt electrolytes ; Orthorhombic phase ; Phase transitions ; Solid electrolytes ; solid‐state electrolytes ; superionic conductors ; Yttrium</subject><ispartof>Advanced energy materials, 2022-06, Vol.12 (21), p.n/a</ispartof><rights>2022 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4231-b50feb15d856a4b40df9281beb15d20c8441960698159f6371aea144bed625563</citedby><cites>FETCH-LOGICAL-c4231-b50feb15d856a4b40df9281beb15d20c8441960698159f6371aea144bed625563</cites><orcidid>0000-0003-0374-1245 ; 0000-0001-6713-2997 ; 0000-0003-4055-1301</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Faenm.202103921$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Faenm.202103921$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids></links><search><creatorcontrib>Liang, Jianwen</creatorcontrib><creatorcontrib>Maas, Eveline</creatorcontrib><creatorcontrib>Luo, Jing</creatorcontrib><creatorcontrib>Li, Xiaona</creatorcontrib><creatorcontrib>Chen, Ning</creatorcontrib><creatorcontrib>Adair, Keegan R.</creatorcontrib><creatorcontrib>Li, Weihan</creatorcontrib><creatorcontrib>Li, Junjie</creatorcontrib><creatorcontrib>Hu, Yongfeng</creatorcontrib><creatorcontrib>Liu, Jue</creatorcontrib><creatorcontrib>Zhang, Li</creatorcontrib><creatorcontrib>Zhao, Shangqian</creatorcontrib><creatorcontrib>Lu, Shigang</creatorcontrib><creatorcontrib>Wang, Jiantao</creatorcontrib><creatorcontrib>Huang, Huan</creatorcontrib><creatorcontrib>Zhao, Wenxuan</creatorcontrib><creatorcontrib>Parnell, Steven</creatorcontrib><creatorcontrib>Smith, Ronald I.</creatorcontrib><creatorcontrib>Ganapathy, Swapna</creatorcontrib><creatorcontrib>Wagemaker, Marnix</creatorcontrib><creatorcontrib>Sun, Xueliang</creatorcontrib><title>A Series of Ternary Metal Chloride Superionic Conductors for High‐Performance All‐Solid‐State Lithium Batteries</title><title>Advanced energy materials</title><description>Understanding the relationship between structure, ionic conductivity, and synthesis is the key to the development of superionic conductors. Here, a series of Li3‐3xM1+xCl6 (−0.14 < x ≤ 0.5, M = Tb, Dy, Ho, Y, Er, Tm) solid electrolytes with orthorhombic and trigonal structures are reported. The orthorhombic phase of Li–M–Cl shows an approximately one order of magnitude increase in ionic conductivities when compared to their trigonal phase. Using the Li–Ho–Cl components as an example, their structures, phase transition, ionic conductivity, and electrochemical stability are studied. Molecular dynamics simulations reveal the facile diffusion in the z‐direction in the orthorhombic structure, rationalizing the improved ionic conductivities. All‐solid‐state batteries of NMC811/Li2.73Ho1.09Cl6/In demonstrate excellent electrochemical performance at both 25 and −10 °C. As relevant to the vast number of isostructural halide electrolytes, the present structure control strategy guides the design of halide superionic conductors.
A favorable orthorhombic phase in various Li–M–Cl (M = Dy, Ho, Y, Er, Tm) systems which triggers a significant increase in Li+ diffusivity and reduces the activation energy barrier for diffusion is revealed. The findings are expected to aid the discovery of fundamental chemical theories relating to the activity of rare earth metal halides and exploration of new materials with high Li+ conductivity.</description><subject>all‐solid‐state Li batteries</subject><subject>Conductors</subject><subject>Dynamic stability</subject><subject>Electrochemical analysis</subject><subject>Electrolytes</subject><subject>energy storage</subject><subject>Erbium</subject><subject>halides</subject><subject>Ion currents</subject><subject>Ions</subject><subject>Lithium batteries</subject><subject>Metal chlorides</subject><subject>Molecular dynamics</subject><subject>Molten salt electrolytes</subject><subject>Orthorhombic phase</subject><subject>Phase transitions</subject><subject>Solid electrolytes</subject><subject>solid‐state electrolytes</subject><subject>superionic conductors</subject><subject>Yttrium</subject><issn>1614-6832</issn><issn>1614-6840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkEFPwyAUx4nRxGXu6pnEcydQytpjbaYz2dRk80xoSx0LLRNozG5-BD-jn0S2mXmUy4OX3_-98APgGqMxRojcCtm1Y4IIRnFG8BkYYIZpxFKKzk_3mFyCkXMbFA7NAhkPQJ_DpbRKOmgauJK2E3YHF9ILDYu1NlbVEi77bUBMpypYmK7uK2-sg42xcKbe1t-fXy_ShlcrukrCXOvQWRqt6n31wks4V36t-hbeCe8Py67ARSO0k6PfOgSv99NVMYvmzw-PRT6PKkpiHJUJamSJkzpNmKAlRXWTkRSXhx5BVUopzhhiWYqTrGHxBAspMKWlrBlJEhYPwc1x7taa9146zzemD3_UjhM2IYSwoCZQ4yNVWeOclQ3fWtUGERwjvrfL93b5yW4IZMfAh9Jy9w_N8-nT4i_7AwrhgNM</recordid><startdate>20220601</startdate><enddate>20220601</enddate><creator>Liang, Jianwen</creator><creator>Maas, Eveline</creator><creator>Luo, Jing</creator><creator>Li, Xiaona</creator><creator>Chen, Ning</creator><creator>Adair, Keegan R.</creator><creator>Li, Weihan</creator><creator>Li, Junjie</creator><creator>Hu, Yongfeng</creator><creator>Liu, Jue</creator><creator>Zhang, Li</creator><creator>Zhao, Shangqian</creator><creator>Lu, Shigang</creator><creator>Wang, Jiantao</creator><creator>Huang, Huan</creator><creator>Zhao, Wenxuan</creator><creator>Parnell, Steven</creator><creator>Smith, Ronald I.</creator><creator>Ganapathy, Swapna</creator><creator>Wagemaker, Marnix</creator><creator>Sun, Xueliang</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7TB</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0003-0374-1245</orcidid><orcidid>https://orcid.org/0000-0001-6713-2997</orcidid><orcidid>https://orcid.org/0000-0003-4055-1301</orcidid></search><sort><creationdate>20220601</creationdate><title>A Series of Ternary Metal Chloride Superionic Conductors for High‐Performance All‐Solid‐State Lithium Batteries</title><author>Liang, Jianwen ; Maas, Eveline ; Luo, Jing ; Li, Xiaona ; Chen, Ning ; Adair, Keegan R. ; Li, Weihan ; Li, Junjie ; Hu, Yongfeng ; Liu, Jue ; Zhang, Li ; Zhao, Shangqian ; Lu, Shigang ; Wang, Jiantao ; Huang, Huan ; Zhao, Wenxuan ; Parnell, Steven ; Smith, Ronald I. ; Ganapathy, Swapna ; Wagemaker, Marnix ; Sun, Xueliang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4231-b50feb15d856a4b40df9281beb15d20c8441960698159f6371aea144bed625563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>all‐solid‐state Li batteries</topic><topic>Conductors</topic><topic>Dynamic stability</topic><topic>Electrochemical analysis</topic><topic>Electrolytes</topic><topic>energy storage</topic><topic>Erbium</topic><topic>halides</topic><topic>Ion currents</topic><topic>Ions</topic><topic>Lithium batteries</topic><topic>Metal chlorides</topic><topic>Molecular dynamics</topic><topic>Molten salt electrolytes</topic><topic>Orthorhombic phase</topic><topic>Phase transitions</topic><topic>Solid electrolytes</topic><topic>solid‐state electrolytes</topic><topic>superionic conductors</topic><topic>Yttrium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liang, Jianwen</creatorcontrib><creatorcontrib>Maas, Eveline</creatorcontrib><creatorcontrib>Luo, Jing</creatorcontrib><creatorcontrib>Li, Xiaona</creatorcontrib><creatorcontrib>Chen, Ning</creatorcontrib><creatorcontrib>Adair, Keegan R.</creatorcontrib><creatorcontrib>Li, Weihan</creatorcontrib><creatorcontrib>Li, Junjie</creatorcontrib><creatorcontrib>Hu, Yongfeng</creatorcontrib><creatorcontrib>Liu, Jue</creatorcontrib><creatorcontrib>Zhang, Li</creatorcontrib><creatorcontrib>Zhao, Shangqian</creatorcontrib><creatorcontrib>Lu, Shigang</creatorcontrib><creatorcontrib>Wang, Jiantao</creatorcontrib><creatorcontrib>Huang, Huan</creatorcontrib><creatorcontrib>Zhao, Wenxuan</creatorcontrib><creatorcontrib>Parnell, Steven</creatorcontrib><creatorcontrib>Smith, Ronald I.</creatorcontrib><creatorcontrib>Ganapathy, Swapna</creatorcontrib><creatorcontrib>Wagemaker, Marnix</creatorcontrib><creatorcontrib>Sun, Xueliang</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Advanced energy materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liang, Jianwen</au><au>Maas, Eveline</au><au>Luo, Jing</au><au>Li, Xiaona</au><au>Chen, Ning</au><au>Adair, Keegan R.</au><au>Li, Weihan</au><au>Li, Junjie</au><au>Hu, Yongfeng</au><au>Liu, Jue</au><au>Zhang, Li</au><au>Zhao, Shangqian</au><au>Lu, Shigang</au><au>Wang, Jiantao</au><au>Huang, Huan</au><au>Zhao, Wenxuan</au><au>Parnell, Steven</au><au>Smith, Ronald I.</au><au>Ganapathy, Swapna</au><au>Wagemaker, Marnix</au><au>Sun, Xueliang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Series of Ternary Metal Chloride Superionic Conductors for High‐Performance All‐Solid‐State Lithium Batteries</atitle><jtitle>Advanced energy materials</jtitle><date>2022-06-01</date><risdate>2022</risdate><volume>12</volume><issue>21</issue><epage>n/a</epage><issn>1614-6832</issn><eissn>1614-6840</eissn><abstract>Understanding the relationship between structure, ionic conductivity, and synthesis is the key to the development of superionic conductors. Here, a series of Li3‐3xM1+xCl6 (−0.14 < x ≤ 0.5, M = Tb, Dy, Ho, Y, Er, Tm) solid electrolytes with orthorhombic and trigonal structures are reported. The orthorhombic phase of Li–M–Cl shows an approximately one order of magnitude increase in ionic conductivities when compared to their trigonal phase. Using the Li–Ho–Cl components as an example, their structures, phase transition, ionic conductivity, and electrochemical stability are studied. Molecular dynamics simulations reveal the facile diffusion in the z‐direction in the orthorhombic structure, rationalizing the improved ionic conductivities. All‐solid‐state batteries of NMC811/Li2.73Ho1.09Cl6/In demonstrate excellent electrochemical performance at both 25 and −10 °C. As relevant to the vast number of isostructural halide electrolytes, the present structure control strategy guides the design of halide superionic conductors.
A favorable orthorhombic phase in various Li–M–Cl (M = Dy, Ho, Y, Er, Tm) systems which triggers a significant increase in Li+ diffusivity and reduces the activation energy barrier for diffusion is revealed. The findings are expected to aid the discovery of fundamental chemical theories relating to the activity of rare earth metal halides and exploration of new materials with high Li+ conductivity.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/aenm.202103921</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-0374-1245</orcidid><orcidid>https://orcid.org/0000-0001-6713-2997</orcidid><orcidid>https://orcid.org/0000-0003-4055-1301</orcidid><oa>free_for_read</oa></addata></record> |
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| subjects | all‐solid‐state Li batteries Conductors Dynamic stability Electrochemical analysis Electrolytes energy storage Erbium halides Ion currents Ions Lithium batteries Metal chlorides Molecular dynamics Molten salt electrolytes Orthorhombic phase Phase transitions Solid electrolytes solid‐state electrolytes superionic conductors Yttrium |
| title | A Series of Ternary Metal Chloride Superionic Conductors for High‐Performance All‐Solid‐State Lithium Batteries |
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