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dc.contributor.authorXu, Min
dc.contributor.authorCao, Ran
dc.contributor.authorQin, Han
dc.contributor.authorZhang, Nuoxi
dc.contributor.authorYan, Wenle
dc.contributor.authorLiu, Liming
dc.contributor.authorIrvine, John T.S.
dc.contributor.authorChen, Di
dc.identifier.citationXu , M , Cao , R , Qin , H , Zhang , N , Yan , W , Liu , L , Irvine , J T S & Chen , D 2023 , ' Exsolved materials for CO 2 reduction in high-temperature electrolysis cells ' , Materials Reports: Energy , vol. 3 , no. 2 , 100198 .
dc.identifier.otherRIS: urn:3228744B0C250414A38ECEB88642067F
dc.descriptionFunding: This work is supported by the National Key Research and Development Program of China (No. 2021YFA0718900) and the National Natural Science Foundation of China (No. NSCF52102137).en
dc.description.abstractElectrochemical reduction of CO2 into valuable fuels and chemicals has become a contemporary research area, where the heterogeneous catalyst plays a critical role. Metal nanoparticles supported on oxides performing as active sites of electrochemical reactions have been the focus of intensive investigation. Here, we review the CO2 reduction with active materials prepared by exsolution. The fundamental of exsolution was summarized in terms of mechanism and models, materials, and driven forces. The advances in the exsolved materials used in high-temperature CO2 electrolysis were catalogued into tailored interfaces, synergistic effects on alloy particles, phase transition, reversibility and electrochemical switching.
dc.relation.ispartofMaterials Reports: Energyen
dc.subjectCO reductionen
dc.subjectSolid oxide electrolysis cellsen
dc.titleExsolved materials for CO2 reduction in high-temperature electrolysis cellsen
dc.typeJournal itemen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
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. EaSTCHEMen
dc.description.statusPeer revieweden

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