{"title":"Fabricating self-standing argyrodite electrolyte sheets containing SiO2 fibers for all-solid-state batteries","authors":"Reiko Matsuda, Irine Yunhafita Malya, Takuya Matsushita, Kazuhiro Hikima, Atsunori Matsuda","doi":"10.1016/j.ssi.2024.116684","DOIUrl":null,"url":null,"abstract":"<div><p>Due to their high ionic conductivities, sulfide-based solid electrolytes (SEs)—such as argyrodite Li<sub>6</sub>PS<sub>5</sub>Cl—are good candidates for all-solid-state lithium-ion batteries (ASSLIBs). For adequate energy density, the thinner SE layers of ASSLIBs, the better, but it must also be durable to avoid short circuits. Using SiO<sub>2</sub> fibers in the SE layer as a support, we used a liquid process to produce all-inorganic, self-standing-sheet argyrodite-SEs with a thickness of approximately 60 μm, without resorting to organofluorine compounds such as polytetrafluoroethylene (PTFE) or polyvinylidene difluoride (PVDF). The ionic conductivity of a sheet containing 20 % SiO<sub>2</sub> fibers was 4.2 × 10<sup>−4</sup> S cm<sup>−1</sup> at 25 °C. We also prepared graphite composites as anodes using argyrodite SE containing SiO<sub>2</sub> fibers. In addition, we fabricated ASSLIB cells using these SE sheets, Ni<sub>1/3</sub>Mn<sub>1/3</sub>Co<sub>1/3</sub>O<sub>2</sub>-composite positive, and graphite-composite negative electrodes and evaluated their charge–discharge characteristics.</p></div>","PeriodicalId":431,"journal":{"name":"Solid State Ionics","volume":"417 ","pages":"Article 116684"},"PeriodicalIF":3.0000,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Solid State Ionics","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0167273824002327","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Due to their high ionic conductivities, sulfide-based solid electrolytes (SEs)—such as argyrodite Li6PS5Cl—are good candidates for all-solid-state lithium-ion batteries (ASSLIBs). For adequate energy density, the thinner SE layers of ASSLIBs, the better, but it must also be durable to avoid short circuits. Using SiO2 fibers in the SE layer as a support, we used a liquid process to produce all-inorganic, self-standing-sheet argyrodite-SEs with a thickness of approximately 60 μm, without resorting to organofluorine compounds such as polytetrafluoroethylene (PTFE) or polyvinylidene difluoride (PVDF). The ionic conductivity of a sheet containing 20 % SiO2 fibers was 4.2 × 10−4 S cm−1 at 25 °C. We also prepared graphite composites as anodes using argyrodite SE containing SiO2 fibers. In addition, we fabricated ASSLIB cells using these SE sheets, Ni1/3Mn1/3Co1/3O2-composite positive, and graphite-composite negative electrodes and evaluated their charge–discharge characteristics.
由于硫化物基固体电解质(SE)具有很高的离子导电性,因此是全固态锂离子电池(ASSLIB)的理想候选材料。为了获得足够的能量密度,全固态锂离子电池的SE层越薄越好,但也必须耐用,以避免短路。我们利用SE层中的二氧化硅纤维作为支撑,采用液态工艺生产出厚度约为60微米的全无机自立片状箭石SE,而无需借助聚四氟乙烯(PTFE)或聚偏二氟乙烯(PVDF)等有机氟化合物。含有 20% SiO2 纤维的薄片在 25 °C 时的离子导电率为 4.2 × 10-4 S cm-1。我们还利用含有二氧化硅纤维的箭石 SE 制备了石墨复合材料作为阳极。此外,我们还利用这些 SE 片、Ni1/3Mn1/3Co1/3O2 复合正极和石墨复合负极制作了 ASSLIB 电池,并评估了它们的充放电特性。
期刊介绍:
This interdisciplinary journal is devoted to the physics, chemistry and materials science of diffusion, mass transport, and reactivity of solids. The major part of each issue is devoted to articles on:
(i) physics and chemistry of defects in solids;
(ii) reactions in and on solids, e.g. intercalation, corrosion, oxidation, sintering;
(iii) ion transport measurements, mechanisms and theory;
(iv) solid state electrochemistry;
(v) ionically-electronically mixed conducting solids.
Related technological applications are also included, provided their characteristics are interpreted in terms of the basic solid state properties.
Review papers and relevant symposium proceedings are welcome.