Potassium-rich antiperovskites K3HTe and K3FTe and their structural relation to lithium and sodium counterparts

Author:

Okada Koji1ORCID,Fujii Susumu23ORCID,Tassel Cédric1,Gao Shenghan1,Ubukata Hiroki1ORCID,Pan Wenli4,Yamamoto Kentaro45ORCID,Uchimoto Yoshiharu4ORCID,Kuwabara Akihide2ORCID,Kageyama Hiroshi1ORCID

Affiliation:

1. Department of Energy and Hydrocarbon Chemistry, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Kyoto 615-8510, Japan

2. Nanostructures Research Laboratory, Japan Fine Ceramics Center, Nagoya 456-8587, Japan

3. Division of Materials and Manufacturing Science, Graduate School of Engineering, Osaka University, Osaka 565-0871, Japan

4. Graduate School of Human and Environment Studies, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan

5. Faculty of Engineering, Nara Women's University, Kitauoyanishimachi, Nara 630-8506, Japan

Abstract

Unlike perovskite oxides, antiperovskites M3HCh and M3FCh (M = Li, Na; Ch = S, Se, Te) mostly retain their ideal cubic structure owing to anionic size flexibility and low-energy phonon modes that promote their ionic conductivity.

Funder

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

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