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Direct Visualization of the Interfacial Degradation of Cathode Coatings in Solid State Batteries: A Combined Experimental and Computational Study
The interfacial instability between a thiophosphate solid electrolyte and oxide cathodes results in rapid capacity fade and has driven the need for cathode coatings. In this work, the stability, evolution, and performance of uncoated, Li2ZrO3‐coated, and Li3B11O18‐coated LiNi0.5Co0.2Mn0.3O2 cathodes...
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Published in: | Advanced energy materials 2020-07, Vol.10 (27), p.n/a |
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creator | Zhang, Ya‐Qian Tian, Yaosen Xiao, Yihan Miara, Lincoln J. Aihara, Yuichi Tsujimura, Tomoyuki Shi, Tan Scott, M. C. Ceder, Gerbrand |
description | The interfacial instability between a thiophosphate solid electrolyte and oxide cathodes results in rapid capacity fade and has driven the need for cathode coatings. In this work, the stability, evolution, and performance of uncoated, Li2ZrO3‐coated, and Li3B11O18‐coated LiNi0.5Co0.2Mn0.3O2 cathodes are compared using first‐principles computations and electron microscopy characterization. Li3B11O18 is identified as a superior coating that exhibits excellent oxidation/chemical stability, leading to substantially improved performance over cells with Li2ZrO3‐coated or uncoated cathodes. The chemical and structural origin of the different performance is interpreted using different microscopy techniques which enable the direct observation of the phase decomposition of the Li2ZrO3 coating. It is observed that Li is already extracted from the Li2ZrO3 in the first charge, leading to the formation of ZrO2 nanocrystallites with loss of protection of the cathode. After 50 cycles separated (Co, Ni)‐sulfides and Mn‐sulfides can be observed within the Li2ZrO3‐coated material. This work illustrates the severity of the interfacial reactions between a thiophosphate electrolyte and oxide cathode and shows the importance of using coating materials that are absolutely stable at high voltage.
This work compares the stability, evolution, and performance of uncoated, Li2ZrO3‐coated, and Li3B11O18‐coated oxide cathodes using first‐principles computation and electron microscopy characterization. A lack of oxidation stability and O/S exchange are identified as critical failure modes of cathode coatings in thiophosphate‐based solid‐state batteries and strong oxygen bonding is suggested for creating highly stable cathode coatings. |
doi_str_mv | 10.1002/aenm.201903778 |
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This work compares the stability, evolution, and performance of uncoated, Li2ZrO3‐coated, and Li3B11O18‐coated oxide cathodes using first‐principles computation and electron microscopy characterization. A lack of oxidation stability and O/S exchange are identified as critical failure modes of cathode coatings in thiophosphate‐based solid‐state batteries and strong oxygen bonding is suggested for creating highly stable cathode coatings.</description><identifier>ISSN: 1614-6832</identifier><identifier>EISSN: 1614-6840</identifier><identifier>DOI: 10.1002/aenm.201903778</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>all‐solid‐state batteries ; cathode coatings ; Cathodes ; Cathodic protection ; DFT calculations ; Electrolytes ; Electrolytic cells ; Interface reactions ; Interface stability ; interfacial stability ; Manganese ; Microscopy ; microscopy observations ; Nickel ; Oxidation ; Oxide coatings ; Phase decomposition ; Protective coatings ; Solid electrolytes ; Sulfides ; Zirconium dioxide</subject><ispartof>Advanced energy materials, 2020-07, Vol.10 (27), p.n/a</ispartof><rights>2020 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2020. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4898-bdd7987ba78f4755f20f9e40f3dec747aa9411e58d58422455850844225f5afa3</citedby><cites>FETCH-LOGICAL-c4898-bdd7987ba78f4755f20f9e40f3dec747aa9411e58d58422455850844225f5afa3</cites><orcidid>0000-0002-4692-3033 ; 0000000246923033</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/1632018$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Ya‐Qian</creatorcontrib><creatorcontrib>Tian, Yaosen</creatorcontrib><creatorcontrib>Xiao, Yihan</creatorcontrib><creatorcontrib>Miara, Lincoln J.</creatorcontrib><creatorcontrib>Aihara, Yuichi</creatorcontrib><creatorcontrib>Tsujimura, Tomoyuki</creatorcontrib><creatorcontrib>Shi, Tan</creatorcontrib><creatorcontrib>Scott, M. C.</creatorcontrib><creatorcontrib>Ceder, Gerbrand</creatorcontrib><title>Direct Visualization of the Interfacial Degradation of Cathode Coatings in Solid State Batteries: A Combined Experimental and Computational Study</title><title>Advanced energy materials</title><description>The interfacial instability between a thiophosphate solid electrolyte and oxide cathodes results in rapid capacity fade and has driven the need for cathode coatings. In this work, the stability, evolution, and performance of uncoated, Li2ZrO3‐coated, and Li3B11O18‐coated LiNi0.5Co0.2Mn0.3O2 cathodes are compared using first‐principles computations and electron microscopy characterization. Li3B11O18 is identified as a superior coating that exhibits excellent oxidation/chemical stability, leading to substantially improved performance over cells with Li2ZrO3‐coated or uncoated cathodes. The chemical and structural origin of the different performance is interpreted using different microscopy techniques which enable the direct observation of the phase decomposition of the Li2ZrO3 coating. It is observed that Li is already extracted from the Li2ZrO3 in the first charge, leading to the formation of ZrO2 nanocrystallites with loss of protection of the cathode. After 50 cycles separated (Co, Ni)‐sulfides and Mn‐sulfides can be observed within the Li2ZrO3‐coated material. This work illustrates the severity of the interfacial reactions between a thiophosphate electrolyte and oxide cathode and shows the importance of using coating materials that are absolutely stable at high voltage.
This work compares the stability, evolution, and performance of uncoated, Li2ZrO3‐coated, and Li3B11O18‐coated oxide cathodes using first‐principles computation and electron microscopy characterization. A lack of oxidation stability and O/S exchange are identified as critical failure modes of cathode coatings in thiophosphate‐based solid‐state batteries and strong oxygen bonding is suggested for creating highly stable cathode coatings.</description><subject>all‐solid‐state batteries</subject><subject>cathode coatings</subject><subject>Cathodes</subject><subject>Cathodic protection</subject><subject>DFT calculations</subject><subject>Electrolytes</subject><subject>Electrolytic cells</subject><subject>Interface reactions</subject><subject>Interface stability</subject><subject>interfacial stability</subject><subject>Manganese</subject><subject>Microscopy</subject><subject>microscopy observations</subject><subject>Nickel</subject><subject>Oxidation</subject><subject>Oxide coatings</subject><subject>Phase decomposition</subject><subject>Protective coatings</subject><subject>Solid electrolytes</subject><subject>Sulfides</subject><subject>Zirconium dioxide</subject><issn>1614-6832</issn><issn>1614-6840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkUFvGyEQhVdVI9VKc-0ZNWc7sAte6M1xnNSSkx7c9orGyxBjrcFdWCXOv8g_Do4r91gujN587wlmiuILoyNGaXkF6LejkjJFq7qWH4oBGzM-HEtOP57qqvxUXMS4oflwxWhVDYrXG9dhk8hvF3to3QskFzwJlqQ1krlP2FloHLTkBh87MKf2FNI6GCTTkCX_GInzZBlaZ8gyQUJyDSl7HcZvZJKh7cp5NGT2vMviFn3KieDNobPr03tqVpapN_vPxZmFNuLF3_u8-HU7-zn9Plz8uJtPJ4thw6WSw5UxtZL1CmppeS2ELalVyKmtDDY1rwEUZwyFNELysuRCSEElz6WwAixU58XXY26IyenYuITNugne53FoNq7yMGWGLo_Qrgt_eoxJb0Lf5bdGXfJScMWpGmdqdKSaLsTYodW7_Evo9ppRfViPPqxHn9aTDepoeHIt7v9D68ns4f6f9w0y_JSB</recordid><startdate>20200701</startdate><enddate>20200701</enddate><creator>Zhang, Ya‐Qian</creator><creator>Tian, Yaosen</creator><creator>Xiao, Yihan</creator><creator>Miara, Lincoln J.</creator><creator>Aihara, Yuichi</creator><creator>Tsujimura, Tomoyuki</creator><creator>Shi, Tan</creator><creator>Scott, M. C.</creator><creator>Ceder, Gerbrand</creator><general>Wiley Subscription Services, Inc</general><general>Wiley Blackwell (John Wiley & Sons)</general><scope>24P</scope><scope>WIN</scope><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><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0002-4692-3033</orcidid><orcidid>https://orcid.org/0000000246923033</orcidid></search><sort><creationdate>20200701</creationdate><title>Direct Visualization of the Interfacial Degradation of Cathode Coatings in Solid State Batteries: A Combined Experimental and Computational Study</title><author>Zhang, Ya‐Qian ; Tian, Yaosen ; Xiao, Yihan ; Miara, Lincoln J. ; Aihara, Yuichi ; Tsujimura, Tomoyuki ; Shi, Tan ; Scott, M. C. ; Ceder, Gerbrand</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4898-bdd7987ba78f4755f20f9e40f3dec747aa9411e58d58422455850844225f5afa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>all‐solid‐state batteries</topic><topic>cathode coatings</topic><topic>Cathodes</topic><topic>Cathodic protection</topic><topic>DFT calculations</topic><topic>Electrolytes</topic><topic>Electrolytic cells</topic><topic>Interface reactions</topic><topic>Interface stability</topic><topic>interfacial stability</topic><topic>Manganese</topic><topic>Microscopy</topic><topic>microscopy observations</topic><topic>Nickel</topic><topic>Oxidation</topic><topic>Oxide coatings</topic><topic>Phase decomposition</topic><topic>Protective coatings</topic><topic>Solid electrolytes</topic><topic>Sulfides</topic><topic>Zirconium dioxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Ya‐Qian</creatorcontrib><creatorcontrib>Tian, Yaosen</creatorcontrib><creatorcontrib>Xiao, Yihan</creatorcontrib><creatorcontrib>Miara, Lincoln J.</creatorcontrib><creatorcontrib>Aihara, Yuichi</creatorcontrib><creatorcontrib>Tsujimura, Tomoyuki</creatorcontrib><creatorcontrib>Shi, Tan</creatorcontrib><creatorcontrib>Scott, M. 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C.</au><au>Ceder, Gerbrand</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Direct Visualization of the Interfacial Degradation of Cathode Coatings in Solid State Batteries: A Combined Experimental and Computational Study</atitle><jtitle>Advanced energy materials</jtitle><date>2020-07-01</date><risdate>2020</risdate><volume>10</volume><issue>27</issue><epage>n/a</epage><issn>1614-6832</issn><eissn>1614-6840</eissn><abstract>The interfacial instability between a thiophosphate solid electrolyte and oxide cathodes results in rapid capacity fade and has driven the need for cathode coatings. In this work, the stability, evolution, and performance of uncoated, Li2ZrO3‐coated, and Li3B11O18‐coated LiNi0.5Co0.2Mn0.3O2 cathodes are compared using first‐principles computations and electron microscopy characterization. Li3B11O18 is identified as a superior coating that exhibits excellent oxidation/chemical stability, leading to substantially improved performance over cells with Li2ZrO3‐coated or uncoated cathodes. The chemical and structural origin of the different performance is interpreted using different microscopy techniques which enable the direct observation of the phase decomposition of the Li2ZrO3 coating. It is observed that Li is already extracted from the Li2ZrO3 in the first charge, leading to the formation of ZrO2 nanocrystallites with loss of protection of the cathode. After 50 cycles separated (Co, Ni)‐sulfides and Mn‐sulfides can be observed within the Li2ZrO3‐coated material. This work illustrates the severity of the interfacial reactions between a thiophosphate electrolyte and oxide cathode and shows the importance of using coating materials that are absolutely stable at high voltage.
This work compares the stability, evolution, and performance of uncoated, Li2ZrO3‐coated, and Li3B11O18‐coated oxide cathodes using first‐principles computation and electron microscopy characterization. A lack of oxidation stability and O/S exchange are identified as critical failure modes of cathode coatings in thiophosphate‐based solid‐state batteries and strong oxygen bonding is suggested for creating highly stable cathode coatings.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/aenm.201903778</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-4692-3033</orcidid><orcidid>https://orcid.org/0000000246923033</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | all‐solid‐state batteries cathode coatings Cathodes Cathodic protection DFT calculations Electrolytes Electrolytic cells Interface reactions Interface stability interfacial stability Manganese Microscopy microscopy observations Nickel Oxidation Oxide coatings Phase decomposition Protective coatings Solid electrolytes Sulfides Zirconium dioxide |
title | Direct Visualization of the Interfacial Degradation of Cathode Coatings in Solid State Batteries: A Combined Experimental and Computational Study |
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