Pure H – conduction in oxyhydrides

Author:

Kobayashi Genki12,Hinuma Yoyo3,Matsuoka Shinji4,Watanabe Akihiro14,Iqbal Muhammad4,Hirayama Masaaki4,Yonemura Masao5,Kamiyama Takashi5,Tanaka Isao3,Kanno Ryoji4

Affiliation:

1. Research Center of Integrative Molecular Systems (CIMoS), Institute for Molecular Science, 38 Nishigonaka, Myodaiji, Okazaki, Aichi 444-8585, Japan.

2. Japan Science and Technology Agency (JST), Precursory Research for Embryonic Science and Technology (PRESTO), 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan.

3. Department of Materials Science and Engineering, Kyoto University, Sakyo, Kyoto 606-8501, Japan.

4. Department of Electronic Chemistry, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta, Midori, Yokohama 226-8502, Japan.

5. Neutron Science Laboratory (KENS), Institute of Materials Structure Science, High Energy Accelerator Research Organization (KEK), 203-1, Shirakata, Tokai, Ibaraki 319-1106, Japan.

Abstract

Transporting the hydrogen anion Hydrogen cation (H + ) transport is common in both biological systems and engineered ones such as fuel cells. In contrast, the transport of hydrogen anions (H ) is far less common and is usually coupled with or compromised by the parallel transport of electrons. Kobayashi et al. examined the transport of H in a series of rare-earth lithium oxyhydrides (see the Perspective by Yamaguchi). They prevented electronic conduction by using Li + as a countercation. In an electrochemical cell, the oxyhydride material acted as a solid-state electrolyte for H , which suggests an alternative avenue for developing energy storage devices. Science , this issue p. 1314 ; see also p. 1262

Funder

JST

PRESTO

Japan Society for the Promotion of Science

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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