High H− ionic conductivity in barium hydride
With hydrogen being seen as a key renewable energy vector, the search for materials exhibiting fast hydrogen transport becomes ever more important. Not only do hydrogen storage materials require high mobility of hydrogen in the solid state, but the efficiency of electrochemical devices is also large...
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Veröffentlicht in: | Nature materials 2015-01, Vol.14 (1), p.95-100 |
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Sprache: | eng |
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Zusammenfassung: | With hydrogen being seen as a key renewable energy vector, the search for materials exhibiting fast hydrogen transport becomes ever more important. Not only do hydrogen storage materials require high mobility of hydrogen in the solid state, but the efficiency of electrochemical devices is also largely determined by fast ionic transport. Although the heavy alkaline-earth hydrides are of limited interest for their hydrogen storage potential, owing to low gravimetric densities, their ionic nature may prove useful in new electrochemical applications, especially as an ionically conducting electrolyte material. Here we show that barium hydride shows fast pure ionic transport of hydride ions (H
−
) in the high-temperature, high-symmetry phase. Although some conductivity studies have been reported on related materials previously, the nature of the charge carriers has not been determined. BaH
2
gives rise to hydride ion conductivity of 0.2 S cm
−1
at 630 °C. This is an order of magnitude larger than that of state-of-the-art proton-conducting perovskites or oxide ion conductors at this temperature. These results suggest that the alkaline-earth hydrides form an important new family of materials, with potential use in a number of applications, such as separation membranes, electrochemical reactors and so on.
Heavy alkaline-earth hydrides could be of interest as ionically conducting electrolytes for electrochemical applications. Barium hydride is now shown to exhibit fast ionic transport of hydride ions in a high-temperature and high-symmetry phase. |
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ISSN: | 1476-1122 1476-4660 |
DOI: | 10.1038/nmat4136 |