TY - JOUR
T1 - Improvement of lithium ionic conductivity of Li3PS4 through suppression of crystallization using low-boiling-point solvent in liquid-phase synthesis
AU - Takahashi, Masakuni
AU - Yang, Seunghoon
AU - Yamamoto, Kentaro
AU - Ohara, Koji
AU - Phuc, Nguyen Huu Huy
AU - Watanabe, Toshiki
AU - Uchiyama, Tomoki
AU - Sakuda, Atsushi
AU - Hayashi, Akitoshi
AU - Tatsumisago, Masahiro
AU - Muto, Hiroyuki
AU - Matsuda, Atsunori
AU - Uchimoto, Yoshiharu
N1 - Funding Information:
This work was partially supported by the New Energy and Industrial Technology Development Organization (NEDO), Japan. The synchrotron radiation experiments were performed using BL08W at SPring-8 with the approval of the Japan Synchrotron Radiation Research Institute (JASRI) (proposals 2017A1023, 2018A1023, 2018B1030, 2019A1017, and 2019B1021).
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/3
Y1 - 2021/3
N2 - 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 Li3PS4 to 1.85 × 10−4 S cm−1 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 Li3PS4 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.
AB - 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 Li3PS4 to 1.85 × 10−4 S cm−1 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 Li3PS4 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.
KW - All-solid-state battery
KW - Liquid phase synthesis
KW - Pair distribution function analysis
KW - Solid electrolyte
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U2 - 10.1016/j.ssi.2021.115568
DO - 10.1016/j.ssi.2021.115568
M3 - Article
AN - SCOPUS:85099886906
SN - 0167-2738
VL - 361
JO - Solid State Ionics
JF - Solid State Ionics
M1 - 115568
ER -