TY - JOUR
T1 - Synthesis of Sulfide Solid Electrolytes through the Liquid Phase
T2 - Optimization of the Preparation Conditions
AU - Yamamoto, Kentaro
AU - Takahashi, Masakuni
AU - Ohara, Koji
AU - Phuc, Nguyen Huu Huy
AU - Yang, Seunghoon
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 at BL04B2 and BL08W of SPring-8 with the approval of the Japan Synchrotron Radiation Research Institute (JASRI) (Proposals 2017A1023, 2018A1023, 2018B1027 2018B1030, and 2019A1017).
Funding Information:
This work was partially supported by the New Energy and Industrial Technology Development Organization (NEDO), Japan. The synchrotron radiation experiments were performed at BL04B2 and BL08W of SPring-8 with the approval of the Japan Synchrotron Radiation Research Institute (JASRI) (Proposals 2017A1023, 2018A1023, 2018B1027, 2018B1030, and 2019A1017).
Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/10/13
Y1 - 2020/10/13
N2 - All-solid-state lithium batteries using inorganic sulfide solid electrolytes have good safety properties and high rate capabilities as expected for a next-generation battery. Presently, conventional preparation methods such as mechanical milling and/or solid-phase synthesis need a long time to provide a small amount of the product, and they have difficult in supplying a sufficient amount to meet the demand. Hence, liquid-phase synthesis methods have been developed for large-scale synthesis. However, the ionic conductivity of sulfide solid electrolytes prepared via liquid-phase synthesis is typically lower than that prepared via solid-phase synthesis. In this study, we have controlled three factors: (1) shaking time, (2) annealing temperature, and (3) annealing time. The factors influencing lithium ionic conductivity of Li3PS4 prepared via liquid-phase synthesis were quantitatively evaluated using high-energy X-ray diffraction (XRD) measurement coupled with pair distribution function (PDF) analysis. It was revealed from PDF analysis that the amount of Li2S that cannot be detected by Raman spectroscopy or XRD decreased the ionic conductivity. Furthermore, it was revealed that the ionic conductivity of Li3PS4 is dominated by other parameters, such as remaining solvent in the sample and high crystallinity of the sample.
AB - All-solid-state lithium batteries using inorganic sulfide solid electrolytes have good safety properties and high rate capabilities as expected for a next-generation battery. Presently, conventional preparation methods such as mechanical milling and/or solid-phase synthesis need a long time to provide a small amount of the product, and they have difficult in supplying a sufficient amount to meet the demand. Hence, liquid-phase synthesis methods have been developed for large-scale synthesis. However, the ionic conductivity of sulfide solid electrolytes prepared via liquid-phase synthesis is typically lower than that prepared via solid-phase synthesis. In this study, we have controlled three factors: (1) shaking time, (2) annealing temperature, and (3) annealing time. The factors influencing lithium ionic conductivity of Li3PS4 prepared via liquid-phase synthesis were quantitatively evaluated using high-energy X-ray diffraction (XRD) measurement coupled with pair distribution function (PDF) analysis. It was revealed from PDF analysis that the amount of Li2S that cannot be detected by Raman spectroscopy or XRD decreased the ionic conductivity. Furthermore, it was revealed that the ionic conductivity of Li3PS4 is dominated by other parameters, such as remaining solvent in the sample and high crystallinity of the sample.
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U2 - 10.1021/acsomega.0c04307
DO - 10.1021/acsomega.0c04307
M3 - Article
AN - SCOPUS:85094587614
SN - 2470-1343
VL - 5
SP - 26287
EP - 26294
JO - ACS Omega
JF - ACS Omega
IS - 40
ER -