| Literature DB >> 35027719 |
Fumitaka Takeiri1,2, Akihiro Watanabe1,3, Kei Okamoto1,2, Dominic Bresser4,5,6, Sandrine Lyonnard4, Bernhard Frick7, Asad Ali1,2, Yumiko Imai1, Masako Nishikawa1, Masao Yonemura2,8, Takashi Saito2,8, Kazutaka Ikeda2,8, Toshiya Otomo2,8, Takashi Kamiyama2,8, Ryoji Kanno3,9, Genki Kobayashi10,11.
Abstract
Hydrogen transport in solids, applied in electrochemical devices such as fuel cells and electrolysis cells, is key to sustainable energy societies. Although using proton (H+) conductors is an attractive choice, practical conductivity at intermediate temperatures (200-400 °C), which would be ideal for most energy and chemical conversion applications, remains a challenge. Alternatively, hydride ions (H-), that is, monovalent anions with high polarizability, can be considered a promising charge carrier that facilitates fast ionic conduction in solids. Here, we report a K2NiF4-type Ba-Li oxyhydride with an appreciable amount of hydrogen vacancies that presents long-range order at room temperature. Increasing the temperature results in the disappearance of the vacancy ordering, triggering a high and essentially temperature-independent H- conductivity of more than 0.01 S cm-1 above 315 °C. Such a remarkable H- conducting nature at intermediate temperatures is anticipated to be important for energy and chemical conversion devices.Entities:
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Year: 2022 PMID: 35027719 DOI: 10.1038/s41563-021-01175-0
Source DB: PubMed Journal: Nat Mater ISSN: 1476-1122 Impact factor: 47.656