Electrochemical characteristics and charge-discharge mechanisms of Co-substituted Li5AlO4 as a novel positive electrode material

Modern and future products such as electric vehicles and hybrid electric vehicles require batteries with higher energy densities than that of conventional batteries. Anion redox-type active materials are proposed as a new high-capacity positive electrode material for Li-ion batteries with high energ...

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Veröffentlicht in:Solid state ionics 2020-10, Vol.353, p.115374, Article 115374
Hauptverfasser: Okuda, Daisuke, Kobayashi, Hiroaki, Ishikawa, Masashi
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Ishikawa, Masashi
description Modern and future products such as electric vehicles and hybrid electric vehicles require batteries with higher energy densities than that of conventional batteries. Anion redox-type active materials are proposed as a new high-capacity positive electrode material for Li-ion batteries with high energy density. We developed Li5AlO4 as an anion redox-type active material with a higher stability than that of Co-substituted Li2O. Li5AlO4 was substituted with Co by mechanical alloying with LiCoO2 to enhance its conductivity and its reactivity as an oxide anion. Co-substituted Li5AlO4 showed a slightly higher electron conductivity and a remarkably higher oxide anion reactivity than the as-prepared Li5AlO4. From electrochemical analysis, it was shown that Co-substituted Li5AlO4 had a reversible capacity of approximately 140 mAh g−1, while the as-prepared Li5AlO4 had no reversible capacity. According to the atomic valence of Co and Al and the partial structure for Co-substituted Li5AlO4 during the first charge-discharge cycle, we found that the charge capacity of Co-substituted Li5AlO4 is derived from the oxidation of oxide anions, the formation of peroxide and superoxide, and the fact that the partial structure of Co-substituted Li5AlO4 remains unchanged. These results indicate that the charge-discharge reaction of Co-substituted Li5AlO4 proceeds reversibly. Co-substituted Li5AlO4 demonstrates a relatively high specific capacity and good reversibility during the charge-discharge process. •Co-substituted Li5AlO4 has a higher capacity than does Li5AlO4.•Li5AlO4 has a characteristic bonding state of oxygen, yielded by Co substitution.•The bonding state of oxygen varies during the charge-discharge process.
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Anion redox-type active materials are proposed as a new high-capacity positive electrode material for Li-ion batteries with high energy density. We developed Li5AlO4 as an anion redox-type active material with a higher stability than that of Co-substituted Li2O. Li5AlO4 was substituted with Co by mechanical alloying with LiCoO2 to enhance its conductivity and its reactivity as an oxide anion. Co-substituted Li5AlO4 showed a slightly higher electron conductivity and a remarkably higher oxide anion reactivity than the as-prepared Li5AlO4. From electrochemical analysis, it was shown that Co-substituted Li5AlO4 had a reversible capacity of approximately 140 mAh g−1, while the as-prepared Li5AlO4 had no reversible capacity. According to the atomic valence of Co and Al and the partial structure for Co-substituted Li5AlO4 during the first charge-discharge cycle, we found that the charge capacity of Co-substituted Li5AlO4 is derived from the oxidation of oxide anions, the formation of peroxide and superoxide, and the fact that the partial structure of Co-substituted Li5AlO4 remains unchanged. These results indicate that the charge-discharge reaction of Co-substituted Li5AlO4 proceeds reversibly. Co-substituted Li5AlO4 demonstrates a relatively high specific capacity and good reversibility during the charge-discharge process. •Co-substituted Li5AlO4 has a higher capacity than does Li5AlO4.•Li5AlO4 has a characteristic bonding state of oxygen, yielded by Co substitution.•The bonding state of oxygen varies during the charge-discharge process.</description><identifier>ISSN: 0167-2738</identifier><identifier>EISSN: 1872-7689</identifier><identifier>DOI: 10.1016/j.ssi.2020.115374</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Anions ; Batteries ; Cathode ; Conductivity ; Densification ; Discharge ; Electric vehicles ; Electrochemical analysis ; Electrode materials ; Electrodes ; Electron conductivity ; Flux density ; Hybrid electric vehicles ; Li5AlO4 ; Lithium ; Lithium oxides ; Lithium-ion batteries ; Mechanical alloying ; Oxidation ; Oxygen redox ; Rechargeable batteries ; Substitutes ; XAFS</subject><ispartof>Solid state ionics, 2020-10, Vol.353, p.115374, Article 115374</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright Elsevier BV Oct 1, 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-63a8040d75c3efa0f34d72c2e6a3745c8a2ae051d63dc0b92f045b969ebe9af13</citedby><cites>FETCH-LOGICAL-c391t-63a8040d75c3efa0f34d72c2e6a3745c8a2ae051d63dc0b92f045b969ebe9af13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0167273820301594$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Okuda, Daisuke</creatorcontrib><creatorcontrib>Kobayashi, Hiroaki</creatorcontrib><creatorcontrib>Ishikawa, Masashi</creatorcontrib><title>Electrochemical characteristics and charge-discharge mechanisms of Co-substituted Li5AlO4 as a novel positive electrode material</title><title>Solid state ionics</title><description>Modern and future products such as electric vehicles and hybrid electric vehicles require batteries with higher energy densities than that of conventional batteries. Anion redox-type active materials are proposed as a new high-capacity positive electrode material for Li-ion batteries with high energy density. We developed Li5AlO4 as an anion redox-type active material with a higher stability than that of Co-substituted Li2O. Li5AlO4 was substituted with Co by mechanical alloying with LiCoO2 to enhance its conductivity and its reactivity as an oxide anion. Co-substituted Li5AlO4 showed a slightly higher electron conductivity and a remarkably higher oxide anion reactivity than the as-prepared Li5AlO4. From electrochemical analysis, it was shown that Co-substituted Li5AlO4 had a reversible capacity of approximately 140 mAh g−1, while the as-prepared Li5AlO4 had no reversible capacity. According to the atomic valence of Co and Al and the partial structure for Co-substituted Li5AlO4 during the first charge-discharge cycle, we found that the charge capacity of Co-substituted Li5AlO4 is derived from the oxidation of oxide anions, the formation of peroxide and superoxide, and the fact that the partial structure of Co-substituted Li5AlO4 remains unchanged. These results indicate that the charge-discharge reaction of Co-substituted Li5AlO4 proceeds reversibly. Co-substituted Li5AlO4 demonstrates a relatively high specific capacity and good reversibility during the charge-discharge process. •Co-substituted Li5AlO4 has a higher capacity than does Li5AlO4.•Li5AlO4 has a characteristic bonding state of oxygen, yielded by Co substitution.•The bonding state of oxygen varies during the charge-discharge process.</description><subject>Anions</subject><subject>Batteries</subject><subject>Cathode</subject><subject>Conductivity</subject><subject>Densification</subject><subject>Discharge</subject><subject>Electric vehicles</subject><subject>Electrochemical analysis</subject><subject>Electrode materials</subject><subject>Electrodes</subject><subject>Electron conductivity</subject><subject>Flux density</subject><subject>Hybrid electric vehicles</subject><subject>Li5AlO4</subject><subject>Lithium</subject><subject>Lithium oxides</subject><subject>Lithium-ion batteries</subject><subject>Mechanical alloying</subject><subject>Oxidation</subject><subject>Oxygen redox</subject><subject>Rechargeable batteries</subject><subject>Substitutes</subject><subject>XAFS</subject><issn>0167-2738</issn><issn>1872-7689</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9UMtOwzAQtBBIlMcHcLPEOcWvJI44VVV5SJV6gbPl2BvqKImLnVTixqfjEs6cdnY1s7M7CN1RsqSEFg_tMka3ZISlnua8FGdoQWXJsrKQ1TlaJE6ZsZLLS3QVY0sIKbgsFuh704EZgzd76J3RHTZ7HbQZIbg4OhOxHuzv7AMy6-KMcA8JDC72EfsGr30WpzrRx2kEi7cuX3U7gXUS48EfocMHH93ojoBhdrNphT556O4GXTS6i3D7V6_R-9Pmbf2SbXfPr-vVNjO8omNWcC2JILbMDYdGk4YLWzLDoNDp2dxIzTSQnNqCW0PqijVE5HVVVFBDpRvKr9H9vPcQ_OcEcVStn8KQLBUTQgouc5EnFp1ZJvgYAzTqEFyvw5eiRJ2CVq1KQatT0GoOOmkeZw2k848OgorGwWDAupC-Vda7f9Q_lRaIPw</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Okuda, Daisuke</creator><creator>Kobayashi, Hiroaki</creator><creator>Ishikawa, Masashi</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20201001</creationdate><title>Electrochemical characteristics and charge-discharge mechanisms of Co-substituted Li5AlO4 as a novel positive electrode material</title><author>Okuda, Daisuke ; Kobayashi, Hiroaki ; Ishikawa, Masashi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-63a8040d75c3efa0f34d72c2e6a3745c8a2ae051d63dc0b92f045b969ebe9af13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Anions</topic><topic>Batteries</topic><topic>Cathode</topic><topic>Conductivity</topic><topic>Densification</topic><topic>Discharge</topic><topic>Electric vehicles</topic><topic>Electrochemical analysis</topic><topic>Electrode materials</topic><topic>Electrodes</topic><topic>Electron conductivity</topic><topic>Flux density</topic><topic>Hybrid electric vehicles</topic><topic>Li5AlO4</topic><topic>Lithium</topic><topic>Lithium oxides</topic><topic>Lithium-ion batteries</topic><topic>Mechanical alloying</topic><topic>Oxidation</topic><topic>Oxygen redox</topic><topic>Rechargeable batteries</topic><topic>Substitutes</topic><topic>XAFS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Okuda, Daisuke</creatorcontrib><creatorcontrib>Kobayashi, Hiroaki</creatorcontrib><creatorcontrib>Ishikawa, Masashi</creatorcontrib><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Solid state ionics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Okuda, Daisuke</au><au>Kobayashi, Hiroaki</au><au>Ishikawa, Masashi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrochemical characteristics and charge-discharge mechanisms of Co-substituted Li5AlO4 as a novel positive electrode material</atitle><jtitle>Solid state ionics</jtitle><date>2020-10-01</date><risdate>2020</risdate><volume>353</volume><spage>115374</spage><pages>115374-</pages><artnum>115374</artnum><issn>0167-2738</issn><eissn>1872-7689</eissn><abstract>Modern and future products such as electric vehicles and hybrid electric vehicles require batteries with higher energy densities than that of conventional batteries. Anion redox-type active materials are proposed as a new high-capacity positive electrode material for Li-ion batteries with high energy density. We developed Li5AlO4 as an anion redox-type active material with a higher stability than that of Co-substituted Li2O. Li5AlO4 was substituted with Co by mechanical alloying with LiCoO2 to enhance its conductivity and its reactivity as an oxide anion. Co-substituted Li5AlO4 showed a slightly higher electron conductivity and a remarkably higher oxide anion reactivity than the as-prepared Li5AlO4. From electrochemical analysis, it was shown that Co-substituted Li5AlO4 had a reversible capacity of approximately 140 mAh g−1, while the as-prepared Li5AlO4 had no reversible capacity. According to the atomic valence of Co and Al and the partial structure for Co-substituted Li5AlO4 during the first charge-discharge cycle, we found that the charge capacity of Co-substituted Li5AlO4 is derived from the oxidation of oxide anions, the formation of peroxide and superoxide, and the fact that the partial structure of Co-substituted Li5AlO4 remains unchanged. These results indicate that the charge-discharge reaction of Co-substituted Li5AlO4 proceeds reversibly. Co-substituted Li5AlO4 demonstrates a relatively high specific capacity and good reversibility during the charge-discharge process. •Co-substituted Li5AlO4 has a higher capacity than does Li5AlO4.•Li5AlO4 has a characteristic bonding state of oxygen, yielded by Co substitution.•The bonding state of oxygen varies during the charge-discharge process.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.ssi.2020.115374</doi></addata></record>
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subjects Anions
Batteries
Cathode
Conductivity
Densification
Discharge
Electric vehicles
Electrochemical analysis
Electrode materials
Electrodes
Electron conductivity
Flux density
Hybrid electric vehicles
Li5AlO4
Lithium
Lithium oxides
Lithium-ion batteries
Mechanical alloying
Oxidation
Oxygen redox
Rechargeable batteries
Substitutes
XAFS
title Electrochemical characteristics and charge-discharge mechanisms of Co-substituted Li5AlO4 as a novel positive electrode material
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