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Structure and particle surface analysis of Li2S–P2S5–LiI-type solid electrolytes synthesized by liquid-phase shaking

材料科学 快离子导体 粒子(生态学) 电解质 相(物质) 电化学 化学工程 类型(生物学) 物理化学 化学 电极 有机化学 海洋学 工程类 地质学 生物 生态学
作者
Kazuhiro Hikima,Kaito Ogawa,Radian Febi Indrawan,Hirofumi Tsukasaki,Satoshi Hiroi,Koji Ohara,Kazutaka Ikeda,Toshiki Watanabe,Toshiyuki Matsunaga,Kentaro Yamamoto,Shigeo Mori,Yoshiharu Uchimoto,Atsunori Matsuda
出处
期刊:Journal of Solid State Electrochemistry [Springer Science+Business Media]
卷期号:28 (12): 4377-4387 被引量:2
标识
DOI:10.1007/s10008-024-05898-3
摘要

Abstract Li 2 S–P 2 S 5 –LiI-type solid electrolytes, such as Li 4 PS 4 I, Li 7 P 2 S 8 I, and Li 10 P 3 S 12 I, are promising candidates for anode layers in all-solid-state batteries because of their high ionic conductivity and stability toward Li anodes. However, few studies have been conducted on their detailed local structure and particle surface state. In this study, Li 7 P 2 S 8 I (Li 2 S: P 2 S 5 :LiI = 3:1:1) solid electrolytes as the chemical composition were synthesized by mechanical milling and liquid-phase shaking, and their local structures were analyzed by transmission electron microscopy. The particle surface states were analyzed by X-ray photoelectron spectroscopy, high-energy X-ray scattering measurements, and neutron total scattering experiments. The results showed that Li 7 P 2 S 8 I solid electrolytes are composed of nanocrystals, such as Li 4 PS 4 I, LiI, Li 10 P 3 S 12 I and an amorphous area as the main region, indicating that the crystalline components alone do not form ionic conductive pathways, with both the amorphous and crystalline regions contributing to the high ionic conductivity. Moreover, the ionic conductivity of the crystalline/amorphous interface of the glass-ceramic was higher than that of the Li 2 S–P 2 S 5 –LiI glass. Finally, an organic-solvent-derived stable surface layer, which was detected in the liquid-phase shaking sample, served as one of the factors that contributed to its high stability (which surpassed that of the mechanically milled sample) toward lithium anodes. We expect these findings to enable the effective harnessing of particle surface states to develop enhanced sulfide solid electrolytes.
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