2021年3月
Improvement of lithium ionic conductivity of Li<inf>3</inf>PS<inf>4</inf> through suppression of crystallization using low-boiling-point solvent in liquid-phase synthesis
Solid State Ionics
- 巻
- 361
- 号
- 記述言語
- 英語
- 掲載種別
- 研究論文(学術雑誌)
- DOI
- 10.1016/j.ssi.2021.115568
- 出版者・発行元
- ELSEVIER
Liquid-phase synthesis for solid electrolytes has received considerable attention owing to its shape control, with the potential to produce particles easily on a large scale, and its low cost and energy consumption. However, solid electrolytes prepared through liquid-phase synthesis have been shown to have lower ionic conductivity than solid electrolytes prepared through the mechanical milling method. Recently, following various efforts, our group found that the crystallinity and remaining intermediate are the reasons for the low ionic conductivity of these materials. By using tetrahydrofuran (THF), we successfully improved the ionic conductivity of Li PS to 1.85 × 10 S cm at 25 °C, higher than that afforded by ethyl propionate, which was reported to produce the highest ionic conductivity among the solvents used for liquid-phase synthesis. High-energy X-ray diffraction (XRD) measurements coupled with pair distribution function (PDF) analysis were employed to analyze the synthesized materials in order to determine why the ionic conductivity was higher than that of a sample prepared using ethyl propionate. The PDF analysis revealed that the crystallization of Li PS can be suppressed using THF, which has a lower boiling point than ethyl propionate. Moreover, it was revealed that the solvent could not be removed completely when the material has an amorphous structure, and thus, the ionic conductivity was lower than that of a material prepared using the solid-phase synthesis method. 3 4 3 4 −4 −1
- リンク情報
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- DOI
- https://doi.org/10.1016/j.ssi.2021.115568
- Web of Science
- https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000648719900013&DestApp=WOS_CPL
- Scopus
- https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85099886906&origin=inward
- Scopus Citedby
- https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85099886906&origin=inward
- ID情報
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- DOI : 10.1016/j.ssi.2021.115568
- ISSN : 0167-2738
- eISSN : 1872-7689
- SCOPUS ID : 85099886906
- Web of Science ID : WOS:000648719900013