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dc.contributor.authorIrvine, John T. S.
dc.contributor.authorWilson, Stephy
dc.contributor.authorAmnuaypanich, Sujitra
dc.contributor.authorIrvine, Gavin J.
dc.contributor.authorVerbraeken, Maarten Christiaan
dc.contributor.authorNowicki, Kamil Macie J
dc.contributor.authorCarins, George M.
dc.date.accessioned2023-05-09T11:30:03Z
dc.date.available2023-05-09T11:30:03Z
dc.date.issued2023-07-01
dc.identifier284055423
dc.identifierd1bf1d17-9c1e-4443-9aa4-63082f859435
dc.identifier85158830650
dc.identifier.citationIrvine , J T S , Wilson , S , Amnuaypanich , S , Irvine , G J , Verbraeken , M C , Nowicki , K M J & Carins , G M 2023 , ' Hydrogen ionic conductors and ammonia conversions ' , Faraday Discussions , vol. 243 , pp. 296-306 . https://doi.org/10.1039/D3FD00012Een
dc.identifier.issn1359-6640
dc.identifier.otherORCID: /0000-0002-8394-3359/work/133727430
dc.identifier.urihttps://hdl.handle.net/10023/27537
dc.description.abstractElectrochemical and catalytic conversion to and from ammonia is strongly enhanced by appropriate choice of hydrogen conducting electrolyte or substrate. Here we explore both protonic and hydride ionic conductors in relation to ammonia conversions. Protonic conductors tend to require too high a temperature to achieve sufficient hydrogen flux for ammonia synthesis as thermal decomposition competes stromgly. Coversely protonic conductors are well suited to direct ammonia fuel cell use. Hydride ions can be very mobile and are strongly reducing. Alakaline hydride lattices can exhibit facile H and N mobility and exchange and offer a very promising basis for ammonia conversion and synthesis.
dc.format.extent11
dc.format.extent904697
dc.language.isoeng
dc.relation.ispartofFaraday Discussionsen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subjectMCCen
dc.subject.lccQDen
dc.titleHydrogen ionic conductors and ammonia conversionsen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. Centre for Energy Ethicsen
dc.contributor.institutionUniversity of St Andrews. Centre for Designer Quantum Materialsen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1039/D3FD00012E
dc.description.statusPeer revieweden


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