Unravelling the anionic stability of an ether-based electrolyte with a hard carbon or metallic sodium anode for high-performance sodium-ion batteries

[Display omitted] •The performance and stability of different anionic salts in 2G for HC/Na half-cells are investigated.•The interfacial chemistry, interphasial properties and electrochemical kinetics are comprehensively studies.•The underlying side reaction and mechanism of different anionic salts...

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Veröffentlicht in:Journal of colloid and interface science 2025-01, Vol.678 (Pt C), p.515-525
Hauptverfasser: He, Jiarong, Fu, Yuling, Xie, Zhangyating, Xia, Zhiyong, Chen, Yili, Deng, Yingkang, Guo, Jinyan, Lin, Jizheng, Kuai, Yutong, Li, Weishan
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container_end_page 525
container_issue Pt C
container_start_page 515
container_title Journal of colloid and interface science
container_volume 678
creator He, Jiarong
Fu, Yuling
Xie, Zhangyating
Xia, Zhiyong
Chen, Yili
Deng, Yingkang
Guo, Jinyan
Lin, Jizheng
Kuai, Yutong
Li, Weishan
description [Display omitted] •The performance and stability of different anionic salts in 2G for HC/Na half-cells are investigated.•The interfacial chemistry, interphasial properties and electrochemical kinetics are comprehensively studies.•The underlying side reaction and mechanism of different anionic salts with Na metal is elucidated. In hard carbon (HC) anodes, elucidating the relationship between the solid electrolyte interphase formation and the solvated Na+ co-intercalation mechanism is crucial, particularly considering different anionic salts in ether-based electrolytes. Here, we comprehensively explore the impact of different anionic salts on the electrochemical performance of HC/Na half-cell and elucidate the underlying mechanism through experimental studies and theoretical calculations. The surface morphology of the HC anode and its interphasial property are further investigated to evaluate the differences endowed by the presence of various anionic salts in diglyme (2G). The HC/Na half-cells with NaPF6-2G and sodium trifluoromethanesulfonate (NaCF3SO3)-2G display superior electrochemical performance with faster kinetics and lower interfacial resistance than those with NaClO4-2G, sodium bis-(fluorosulfonyl) imide (NaFSI)-2G and sodium bis-(trifluoromethanesulfonyl) imide (NaTFSI)-2G. NaClO4-2G forms a relatively thick interphase layer with high resistance at the electrode/electrolyte interface owing to its insufficient stability. NaFSI-2G and NaTFSI-2G exhibit severe side reactions with Na metal, producing a thick interphase layer on the HC surface with high interfacial resistance from excess electrolyte decomposition, thus deteriorating the electrochemical performance. In summary, the study on the stability of different anionic salts in ether-based electrolyte for the HC anode with the intercalation mechanism provides valuable insights for screening appropriate conductive salts for high-performance sodium-ion batteries, especially when considering Na metal counter/reference electrodes.
doi_str_mv 10.1016/j.jcis.2024.09.141
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In hard carbon (HC) anodes, elucidating the relationship between the solid electrolyte interphase formation and the solvated Na+ co-intercalation mechanism is crucial, particularly considering different anionic salts in ether-based electrolytes. Here, we comprehensively explore the impact of different anionic salts on the electrochemical performance of HC/Na half-cell and elucidate the underlying mechanism through experimental studies and theoretical calculations. The surface morphology of the HC anode and its interphasial property are further investigated to evaluate the differences endowed by the presence of various anionic salts in diglyme (2G). The HC/Na half-cells with NaPF6-2G and sodium trifluoromethanesulfonate (NaCF3SO3)-2G display superior electrochemical performance with faster kinetics and lower interfacial resistance than those with NaClO4-2G, sodium bis-(fluorosulfonyl) imide (NaFSI)-2G and sodium bis-(trifluoromethanesulfonyl) imide (NaTFSI)-2G. NaClO4-2G forms a relatively thick interphase layer with high resistance at the electrode/electrolyte interface owing to its insufficient stability. NaFSI-2G and NaTFSI-2G exhibit severe side reactions with Na metal, producing a thick interphase layer on the HC surface with high interfacial resistance from excess electrolyte decomposition, thus deteriorating the electrochemical performance. 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In hard carbon (HC) anodes, elucidating the relationship between the solid electrolyte interphase formation and the solvated Na+ co-intercalation mechanism is crucial, particularly considering different anionic salts in ether-based electrolytes. Here, we comprehensively explore the impact of different anionic salts on the electrochemical performance of HC/Na half-cell and elucidate the underlying mechanism through experimental studies and theoretical calculations. The surface morphology of the HC anode and its interphasial property are further investigated to evaluate the differences endowed by the presence of various anionic salts in diglyme (2G). The HC/Na half-cells with NaPF6-2G and sodium trifluoromethanesulfonate (NaCF3SO3)-2G display superior electrochemical performance with faster kinetics and lower interfacial resistance than those with NaClO4-2G, sodium bis-(fluorosulfonyl) imide (NaFSI)-2G and sodium bis-(trifluoromethanesulfonyl) imide (NaTFSI)-2G. NaClO4-2G forms a relatively thick interphase layer with high resistance at the electrode/electrolyte interface owing to its insufficient stability. NaFSI-2G and NaTFSI-2G exhibit severe side reactions with Na metal, producing a thick interphase layer on the HC surface with high interfacial resistance from excess electrolyte decomposition, thus deteriorating the electrochemical performance. In summary, the study on the stability of different anionic salts in ether-based electrolyte for the HC anode with the intercalation mechanism provides valuable insights for screening appropriate conductive salts for high-performance sodium-ion batteries, especially when considering Na metal counter/reference electrodes.</description><subject>Anionic stability</subject><subject>Diglyme-based electrolyte</subject><subject>Hard carbon</subject><subject>Sodium-ion batteries</subject><subject>Solid electrolyte interphase</subject><issn>0021-9797</issn><issn>1095-7103</issn><issn>1095-7103</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><recordid>eNp9kctuFDEQRS0EIpPAD7BAXrLpxo9x25bYoCgQpEhsyNryozrtUXd7sD1B8yH8Lx7NwJJVWVW3Tsn3IvSOkp4SOnzc9TsfS88I2_ZE93RLX6ANJVp0khL-Em0IYbTTUssrdF3KjhBKhdCv0RXXnIiB6g36_bhm-wzzHNcnXCfAdo1pjR6Xal2cYz3iNLYmhjbMnbMFAoYZfM1pPlbAv2KdsMWTzQF7m11accp4gWobs2FSiIelAVIAPLbJFJ-mbg-5vRe7ergounYVO1sr5AjlDXo12rnA20u9QY9f7n7c3ncP379-u_380HnGZe0C2YJzXAZm1QBacsc5c1wJp5Ty1jExekcVYQyEGtQgwij4OIyKbK2WUvIb9OHM3ef08wClmiUW39ywK6RDMZwSKZXQTDcpO0t9TqVkGM0-x8Xmo6HEnOIwO3OKw5ziMESbFkdben_hH9wC4d_KX_-b4NNZAO2XzxGyKT5CsyXE3Dw2IcX_8f8ASeWemQ</recordid><startdate>20250115</startdate><enddate>20250115</enddate><creator>He, Jiarong</creator><creator>Fu, Yuling</creator><creator>Xie, Zhangyating</creator><creator>Xia, Zhiyong</creator><creator>Chen, Yili</creator><creator>Deng, Yingkang</creator><creator>Guo, Jinyan</creator><creator>Lin, Jizheng</creator><creator>Kuai, Yutong</creator><creator>Li, Weishan</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20250115</creationdate><title>Unravelling the anionic stability of an ether-based electrolyte with a hard carbon or metallic sodium anode for high-performance sodium-ion batteries</title><author>He, Jiarong ; Fu, Yuling ; Xie, Zhangyating ; Xia, Zhiyong ; Chen, Yili ; Deng, Yingkang ; Guo, Jinyan ; Lin, Jizheng ; Kuai, Yutong ; Li, Weishan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c237t-d04ebb37d2a86e973b332b385b888cab25fcb18022e586865df53f6f804a97773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Anionic stability</topic><topic>Diglyme-based electrolyte</topic><topic>Hard carbon</topic><topic>Sodium-ion batteries</topic><topic>Solid electrolyte interphase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>He, Jiarong</creatorcontrib><creatorcontrib>Fu, Yuling</creatorcontrib><creatorcontrib>Xie, Zhangyating</creatorcontrib><creatorcontrib>Xia, Zhiyong</creatorcontrib><creatorcontrib>Chen, Yili</creatorcontrib><creatorcontrib>Deng, Yingkang</creatorcontrib><creatorcontrib>Guo, Jinyan</creatorcontrib><creatorcontrib>Lin, Jizheng</creatorcontrib><creatorcontrib>Kuai, Yutong</creatorcontrib><creatorcontrib>Li, Weishan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of colloid and interface science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>He, Jiarong</au><au>Fu, Yuling</au><au>Xie, Zhangyating</au><au>Xia, Zhiyong</au><au>Chen, Yili</au><au>Deng, Yingkang</au><au>Guo, Jinyan</au><au>Lin, Jizheng</au><au>Kuai, Yutong</au><au>Li, Weishan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unravelling the anionic stability of an ether-based electrolyte with a hard carbon or metallic sodium anode for high-performance sodium-ion batteries</atitle><jtitle>Journal of colloid and interface science</jtitle><addtitle>J Colloid Interface Sci</addtitle><date>2025-01-15</date><risdate>2025</risdate><volume>678</volume><issue>Pt C</issue><spage>515</spage><epage>525</epage><pages>515-525</pages><issn>0021-9797</issn><issn>1095-7103</issn><eissn>1095-7103</eissn><abstract>[Display omitted] •The performance and stability of different anionic salts in 2G for HC/Na half-cells are investigated.•The interfacial chemistry, interphasial properties and electrochemical kinetics are comprehensively studies.•The underlying side reaction and mechanism of different anionic salts with Na metal is elucidated. In hard carbon (HC) anodes, elucidating the relationship between the solid electrolyte interphase formation and the solvated Na+ co-intercalation mechanism is crucial, particularly considering different anionic salts in ether-based electrolytes. Here, we comprehensively explore the impact of different anionic salts on the electrochemical performance of HC/Na half-cell and elucidate the underlying mechanism through experimental studies and theoretical calculations. The surface morphology of the HC anode and its interphasial property are further investigated to evaluate the differences endowed by the presence of various anionic salts in diglyme (2G). The HC/Na half-cells with NaPF6-2G and sodium trifluoromethanesulfonate (NaCF3SO3)-2G display superior electrochemical performance with faster kinetics and lower interfacial resistance than those with NaClO4-2G, sodium bis-(fluorosulfonyl) imide (NaFSI)-2G and sodium bis-(trifluoromethanesulfonyl) imide (NaTFSI)-2G. 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subjects Anionic stability
Diglyme-based electrolyte
Hard carbon
Sodium-ion batteries
Solid electrolyte interphase
title Unravelling the anionic stability of an ether-based electrolyte with a hard carbon or metallic sodium anode for high-performance sodium-ion batteries
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