Conversion-intercalation competing behaviour of halogen storage on graphite electrode from fluid ZnCl/ZnBr hydrates
Zinc-based aqueous dual-ion batteries (ADIBs) with halogen-graphite intercalation compound positive electrodes are among the most competitive candidates for next-generation electrochemical energy storage systems. However, most of the electrolytes employed have been gel-like electrolytes; hence, a fu...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2024-01, Vol.6 (8), p.127-13 |
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description | Zinc-based aqueous dual-ion batteries (ADIBs) with halogen-graphite intercalation compound positive electrodes are among the most competitive candidates for next-generation electrochemical energy storage systems. However, most of the electrolytes employed have been gel-like electrolytes; hence, a fundamental understanding of the halogen storage process using fluid hydrates will be essential for constructing efficient Zn-based ADIBs. Herein, the halogen storage mechanism on a graphite electrode from fluid ZnCl
2
/ZnBr
2
hydrates is studied by experimental and computational methods. The results indicate that the halogen storage mechanism is a competition between conversion and intercalation. Moreover, the macroscopic electrode reaction is determined by both the ion-pair solvation state at the graphite-electrolyte interface and the subsequent reactant supply is influenced by the electrode reaction rate.
The macroscopic electrode reaction depends on both the ion-pair solvation state at the graphite-electrolyte interface and the subsequent reactant supply influenced by the electrode reaction rate. |
doi_str_mv | 10.1039/d3cc04755e |
format | Article |
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2
/ZnBr
2
hydrates is studied by experimental and computational methods. The results indicate that the halogen storage mechanism is a competition between conversion and intercalation. Moreover, the macroscopic electrode reaction is determined by both the ion-pair solvation state at the graphite-electrolyte interface and the subsequent reactant supply is influenced by the electrode reaction rate.
The macroscopic electrode reaction depends on both the ion-pair solvation state at the graphite-electrolyte interface and the subsequent reactant supply influenced by the electrode reaction rate.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/d3cc04755e</identifier><ispartof>Chemical communications (Cambridge, England), 2024-01, Vol.6 (8), p.127-13</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27928,27929</link.rule.ids></links><search><creatorcontrib>Xu, Shiguan</creatorcontrib><creatorcontrib>Shen, Lin</creatorcontrib><creatorcontrib>Wang, Xiaoxu</creatorcontrib><creatorcontrib>Gu, Shaonan</creatorcontrib><creatorcontrib>Sun, Wei</creatorcontrib><creatorcontrib>Huang, Yuhao</creatorcontrib><title>Conversion-intercalation competing behaviour of halogen storage on graphite electrode from fluid ZnCl/ZnBr hydrates</title><title>Chemical communications (Cambridge, England)</title><description>Zinc-based aqueous dual-ion batteries (ADIBs) with halogen-graphite intercalation compound positive electrodes are among the most competitive candidates for next-generation electrochemical energy storage systems. However, most of the electrolytes employed have been gel-like electrolytes; hence, a fundamental understanding of the halogen storage process using fluid hydrates will be essential for constructing efficient Zn-based ADIBs. Herein, the halogen storage mechanism on a graphite electrode from fluid ZnCl
2
/ZnBr
2
hydrates is studied by experimental and computational methods. The results indicate that the halogen storage mechanism is a competition between conversion and intercalation. Moreover, the macroscopic electrode reaction is determined by both the ion-pair solvation state at the graphite-electrolyte interface and the subsequent reactant supply is influenced by the electrode reaction rate.
The macroscopic electrode reaction depends on both the ion-pair solvation state at the graphite-electrolyte interface and the subsequent reactant supply influenced by the electrode reaction rate.</description><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFj8FqwzAQREVpoGnSS--F_QHXNrKa5FqT0g_oIeQSNvLaVpG1ZqUE8vdxINBj5zLzmLmMUq9l8V4WepM32tqiWhlDD2pe6o8qM9V693jLZpOtdGWe1HOMv8Wk0qznKtYcziTRcchcSCQWPaaJwPIwUnKhgyP1eHZ8EuAWevTcUYCYWLAjmJad4Ni7RECebBJuCFrhAVp_cg3sQ-3zffgU6C-NYKK4VLMWfaSXuy_U29f2p_7OJNrDKG5AuRz-nuj_-itqTk7n</recordid><startdate>20240123</startdate><enddate>20240123</enddate><creator>Xu, Shiguan</creator><creator>Shen, Lin</creator><creator>Wang, Xiaoxu</creator><creator>Gu, Shaonan</creator><creator>Sun, Wei</creator><creator>Huang, Yuhao</creator><scope/></search><sort><creationdate>20240123</creationdate><title>Conversion-intercalation competing behaviour of halogen storage on graphite electrode from fluid ZnCl/ZnBr hydrates</title><author>Xu, Shiguan ; Shen, Lin ; Wang, Xiaoxu ; Gu, Shaonan ; Sun, Wei ; Huang, Yuhao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_d3cc04755e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Shiguan</creatorcontrib><creatorcontrib>Shen, Lin</creatorcontrib><creatorcontrib>Wang, Xiaoxu</creatorcontrib><creatorcontrib>Gu, Shaonan</creatorcontrib><creatorcontrib>Sun, Wei</creatorcontrib><creatorcontrib>Huang, Yuhao</creatorcontrib><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Shiguan</au><au>Shen, Lin</au><au>Wang, Xiaoxu</au><au>Gu, Shaonan</au><au>Sun, Wei</au><au>Huang, Yuhao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Conversion-intercalation competing behaviour of halogen storage on graphite electrode from fluid ZnCl/ZnBr hydrates</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><date>2024-01-23</date><risdate>2024</risdate><volume>6</volume><issue>8</issue><spage>127</spage><epage>13</epage><pages>127-13</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>Zinc-based aqueous dual-ion batteries (ADIBs) with halogen-graphite intercalation compound positive electrodes are among the most competitive candidates for next-generation electrochemical energy storage systems. However, most of the electrolytes employed have been gel-like electrolytes; hence, a fundamental understanding of the halogen storage process using fluid hydrates will be essential for constructing efficient Zn-based ADIBs. Herein, the halogen storage mechanism on a graphite electrode from fluid ZnCl
2
/ZnBr
2
hydrates is studied by experimental and computational methods. The results indicate that the halogen storage mechanism is a competition between conversion and intercalation. Moreover, the macroscopic electrode reaction is determined by both the ion-pair solvation state at the graphite-electrolyte interface and the subsequent reactant supply is influenced by the electrode reaction rate.
The macroscopic electrode reaction depends on both the ion-pair solvation state at the graphite-electrolyte interface and the subsequent reactant supply influenced by the electrode reaction rate.</abstract><doi>10.1039/d3cc04755e</doi><tpages>4</tpages></addata></record> |
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title | Conversion-intercalation competing behaviour of halogen storage on graphite electrode from fluid ZnCl/ZnBr hydrates |
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