Co-catalytic metal–support interactions in single-atom electrocatalysts

dc.contributor.authorGloag, Lucyen
dc.contributor.authorSomerville, Samuel V.en
dc.contributor.authorGooding, J. Justinen
dc.contributor.authorTilley, Richard D.en
dc.date.accessioned2025-06-03T07:30:10Z
dc.date.available2025-06-03T07:30:10Z
dc.date.issued2024en
dc.description.abstractSingle-atom catalysts (SACs) are advantageous because every active atom is exposed at the surface, ensuring maximum utilization of catalytically active metals. To optimize the effectiveness of SACs, every atomic site needs to contribute to an accelerated reaction and retain this performance over extended use. The state-of-the-art approach for optimizing the catalytic properties of these atomic sites is through metal–support interactions. In this Review, we present the concept of co-catalytic interactions, in which both the single atom and the support are directly involved in catalysis by binding intermediates to enhance and alter the reaction mechanism. The power of this concept is highlighted for a range of important electrocatalytic reactions. First, we investigate the role of single atoms and supports in the reaction mechanism and explore the SAC designs that have successfully enhanced performance. We then discuss the synthetic targets and strategies for producing SACs that achieve co-reactant, functional group or intermediate binding for co-catalyst metal–support interactions. Finally, we offer a perspective on the future of SAC research and on the opportunities in co-catalytic metal–support interactions to further elevate electrocatalytic performance.en
dc.description.sponsorshipThe authors acknowledge funding under the Australian Research Council's Discovery Project (R.D.T., DP200100143 and DP230100596; J.J.G., DP210102698), Centre of Excellence (R.D.T., CE230100032) and Training Centre IC210100056 and National Health and Medical Research Council Investigator grant (J.J.G., GNT1196648). S.V.S. acknowledges support from the Australian Government Research Training Program (RTP) Scholarship. They also acknowledge support from Microscopy Australia and the Mark Wainwright Analytical Centre and Electron Microscope Unit at the University of New South Wales.en
dc.description.statusPeer-revieweden
dc.format.extent17en
dc.identifier.otherWOS:001139773100001en
dc.identifier.otherORCID:/0000-0001-7548-1521/work/172102534en
dc.identifier.scopus85182155211en
dc.identifier.urihttp://www.scopus.com/inward/record.url?scp=85182155211&partnerID=8YFLogxKen
dc.identifier.urihttps://hdl.handle.net/1885/733756520
dc.language.isoenen
dc.rightsPublisher Copyright: © Springer Nature Limited 2024.en
dc.sourceNature Reviews Materialsen
dc.subjectElectrodesen
dc.subjectReductionen
dc.subjectDual sitesen
dc.subjectPlatinumen
dc.subjectMethanol electrooxidationen
dc.subjectHydrogen oxidationen
dc.subjectEvolutionen
dc.subjectElectroreductionen
dc.subjectCarbonen
dc.subjectSurfaceen
dc.titleCo-catalytic metal–support interactions in single-atom electrocatalystsen
dc.typeJournal articleen
dspace.entity.typePublicationen
local.bibliographicCitation.lastpage189en
local.bibliographicCitation.startpage173en
local.contributor.affiliationGloag, Lucy; University of Technology Sydneyen
local.contributor.affiliationSomerville, Samuel V.; University of New South Walesen
local.contributor.affiliationGooding, J. Justin; University of New South Walesen
local.contributor.affiliationTilley, Richard D.; University of New South Walesen
local.identifier.citationvolume9en
local.identifier.doi10.1038/s41578-023-00633-2en
local.identifier.pure58104837-492d-4f5d-9149-229e32daf514en
local.identifier.urlhttps://www.scopus.com/pages/publications/85182155211en
local.type.statusPublisheden

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