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dc.contributor.authorMASUDA, Yoshihoen
dc.contributor.authorINOO, Akaneen
dc.contributor.authorKONDO, Yasuyukien
dc.contributor.authorYOKOYAMA, Yukoen
dc.contributor.authorMIYAHARA, Yutoen
dc.contributor.authorMIYAZAKI, Koheien
dc.contributor.authorABE, Takeshien
dc.contributor.alternative増田, 佳穂ja
dc.contributor.alternative稲生, 朱音ja
dc.contributor.alternative近藤, 靖幸ja
dc.contributor.alternative横山, 悠子ja
dc.contributor.alternative宮原, 雄人ja
dc.contributor.alternative宮崎, 晃平ja
dc.contributor.alternative安部, 武志ja
dc.date.accessioned2024-02-29T01:38:42Z-
dc.date.available2024-02-29T01:38:42Z-
dc.date.issued2023-09-02-
dc.identifier.urihttp://hdl.handle.net/2433/287126-
dc.description.abstractSolid electrolyte interphase (SEI) layer that forms on the graphite negative electrodes of lithium-ion batteries (LIBs) has a crucial role in inhibiting the excess decomposition of electrolyte solutions. While this passivating ability is essential for improving the durability of LIBs, the relationship between the passivating ability and the surface structure of the graphite is not yet fully understood. In this study, we investigate the solvent co-intercalation behavior in the presence of SEI layers formed on various types of graphite surface structures. The amount of edge sites on each graphite sample is determined using electric double layer capacitance. The co-intercalation reactions of untreated, ethylene-carbonate-treated, and vinylene-carbonate-treated graphite samples in dimethoxyethane-based electrolyte solutions are compared. The co-intercalation reactions commence at approximately 1 V vs. Li/Li⁺ for all untreated samples, but the onset potentials are lowered by the presence of SEI layers, and the extent of this lowering depends on the sample. The SEI layer formed on the edge-rich surface effectively suppresses the co-intercalation reaction, and the additive is also more effective for the edge-rich sample.en
dc.language.isoeng-
dc.publisherThe Electrochemical Society of Japanen
dc.publisher.alternative電気化学会ja
dc.rights© The Author(s) 2023. Published by ECSJ.en
dc.rightsThis is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY), which permits unrestricted reuse of the work in any medium provided the original work is properly cited.en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.subjectLithium-ion Batteryen
dc.subjectSolid Electrolyte Interphaseen
dc.subjectGraphite Anodeen
dc.subjectSolvent Co-intercalationen
dc.titleEffect of Surface Structure of Graphite on the Passivation Ability of Solid Electrolyte Interphasesen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleElectrochemistryen
dc.identifier.volume91-
dc.identifier.issue9-
dc.relation.doi10.5796/electrochemistry.23-00071-
dc.textversionpublisher-
dc.identifier.artnum097002-
dcterms.accessRightsopen access-
dc.identifier.pissn1344-3542-
dc.identifier.eissn2186-2451-
出現コレクション:学術雑誌掲載論文等

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