Universal Solution Synthesis of Sulfide Solid Electrolytes Using Alkahest for All-Solid-State Batteries

© 2022 Wiley-VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 34(2022), 16 vom: 12. Apr., Seite e2200083
1. Verfasser: Lee, Ji Eun (VerfasserIn)
Weitere Verfasser: Park, Kern-Ho, Kim, Jin Chul, Wi, Tae-Ung, Ha, A Reum, Song, Yong Bae, Oh, Dae Yang, Woo, Jehoon, Kweon, Seong Hyeon, Yeom, Su Jeong, Cho, Woosuk, Kim, KyungSu, Lee, Hyun-Wook, Kwak, Sang Kyu, Jung, Yoon Seok
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2022
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article all-solid-state batteries inorganic solid electrolytes solution syntheses sulfides wet-chemical methods
Beschreibung
Zusammenfassung:© 2022 Wiley-VCH GmbH.
The wet-chemical processability of sulfide solid electrolytes (SEs) provides intriguing opportunities for all-solid-state batteries. Thus far, sulfide SEs are wet-prepared either from solid precursors suspended in solvents (suspension synthesis) or from homogeneous solutions using SEs (solution process) with restricted composition spaces. Here, a universal solution synthesis method for preparing sulfide SEs from precursors, not only Li2 S, P2 S5 , LiCl, and Na2 S, but also metal sulfides (e.g., GeS2 and SnS2 ), fully dissolved in an alkahest: a mixture solvent of 1,2-ethylenediamine (EDA) and 1,2-ethanedithiol (EDT) (or ethanethiol). Raman spectroscopy and theoretical calculations reveal that the exceptional dissolving power of EDA-EDT toward GeS2 is due to the nucleophilicity of the thiolate anions that is strong enough to dissociate the GeS bonds. Solution-synthesized Li10 GeP2 S12 , Li6 PS5 Cl, and Na11 Sn2 PS12 exhibit high ionic conductivities (0.74, 1.3, and 0.10 mS cm-1 at 30 °C, respectively), and their application for all-solid-state batteries is successfully demonstrated
Beschreibung:Date Revised 21.04.2022
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.202200083