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Authors |
Yamaguchi, Kazuki
Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University / Center for Research on Green Sustainable Chemistry, Tottori University
Usui, Hiroyuki
Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University / Center for Research on Green Sustainable Chemistry, Tottori University
Researchers DB
KAKEN
Domi, Yasuhiro
Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University / Center for Research on Green Sustainable Chemistry, Tottori University
Researchers DB
KAKEN
Nishida, Haruka
Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University / Center for Research on Green Sustainable Chemistry, Tottori University
Komura, Takuro
Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University / Center for Research on Green Sustainable Chemistry, Tottori University
Nokami, Toshiki
Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University / Center for Research on Green Sustainable Chemistry, Tottori University
Researchers DB
KAKEN
Itoh, Toshiyuki
Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University / Center for Research on Green Sustainable Chemistry, Tottori University
Researchers DB
KAKEN
Sakaguchi, Hiroki
Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University / Center for Research on Green Sustainable Chemistry, Tottori University
Researchers DB
KAKEN
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Keywords | Tin phosphide
Na-ion battery
Ionic liquid electrolyte
Ether-substitution
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Abstract | We have previously disclosed that the ionic-liquid electrolyte sodium bis(fluorosulfonyl)amide (NaFSA)/1-methyl-1-propylpyrrolidinium bis(fluorosulfonyl)amide (Py13-FSA) can significantly improve the cycling stability of Sn4P3 negative electrodes for Na-ion batteries (NIBs). However, the strong electrostatic interaction between Na+ and FSA− in the electrolyte leads to high viscosity and low conductivity. In this study, we have tried to improve the conductivity of the electrolyte and enhance the rate capability of the Sn4P3 electrode by introducing an ether group in the side-chain of the ionic liquid cation to reduce said electrostatic interaction. Ether-substituted ionic liquid 1-methoxymethyl-1-methylpyrrolidinium (PyMOM)-FSA showed higher conductivity than Py13-FSA and the Sn4P3 electrode exhibited a higher rate capability. The differential capacity vs. potential plots suggest that the reaction between Na+ and Sn or P is promoted in the ether-substituted ionic liquid electrolyte. These results demonstrate that introduction of an ether moiety is an effective approach to improve the rate capability of the Sn4P3 electrode in NIBs.
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Publisher | Elsevier
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Content Type |
Journal Article
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ISSN | 15726657
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Journal Title | Journal of Electroanalytical Chemistry
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Volume | 845
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Start Page | 66
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End Page | 71
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Published Date | 2019-07-15
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Text Version |
Author
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Rights | (C) 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/
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Citation | Yamaguchi, Kazuki. Usui, Hiroyuki. Domi, Yasuhiro. et al. Electrochemical performance of Sn4P3 negative electrode for Na-ion batteries in ether-substituted ionic liquid electrolyte. Journal of Electroanalytical Chemistry. 845. 66-71. 2019-07-15. doi:10.1016/j.jelechem.2019.05.047
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Department |
Faculty of Engineering/Graduate School of Engineering
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Language |
English
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pii | S1572-6657(19)30403-5
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