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dc.contributor.authorO’Mara, Peter B.
dc.contributor.authorWilde, Patrick
dc.contributor.authorBenedetti, Tania M.
dc.contributor.authorAndrones, Corina
dc.contributor.authorCheong, Soshan
dc.contributor.authorGooding, Justin
dc.contributor.authorTilley, Richard D.
dc.contributor.authorSchuhmann, Wolfgang
dc.date.accessioned2022-12-11T21:12:12Z
dc.date.available2022-12-11T21:12:12Z
dc.date.issued2019
dc.identifier.citationO’Mara, P. B., Wilde, P., Benedetti, T. M., Andronescu, C., Cheong, S., Gooding, J. J., ... & Schuhmann, W. (2019). Cascade reactions in nanozymes: Spatially separated active sites inside Ag-Core–Porous-Cu-shell nanoparticles for multistep carbon dioxide reduction to higher organic molecules. Journal of the American Chemical Society, 141(36), 14093-14097. DOI: 10.1021/jacs.9b07310en_US
dc.identifier.other10.1021/jacs.9b07310
dc.identifier.urihttps://nru.uncst.go.ug/handle/123456789/6203
dc.description.abstractEnzymes can perform complex multistep cascade reactions by linking multiple distinct catalytic sites via substrate channeling. We mimic this feature in a generalized approach with an electrocatalytic nanoparticle for the carbon dioxide reduction reaction comprising a Ag core surrounded by a porous Cu shell, providing different active sites in nanoconfined volumes. The architecture of the nanozyme provides the basis for a cascade reaction, which promotes C−C coupling reactions. The first step occurs on the Ag core, and the subsequent steps on the porous copper shell, where a sufficiently high CO concentration due to the nanoconfinement facilitates C−C bond formation. The architecture yields the formation of n-propanol and propionaldehyde at potentials as low as −0.6 V vs RHE.en_US
dc.language.isoenen_US
dc.publisherJournal of the American Chemical Societyen_US
dc.subjectCascade Reactionsen_US
dc.subjectNanozymesen_US
dc.subjectAg-Core−Porous-Cu-Shell Nanoparticlesen_US
dc.subjectCarbon Dioxideen_US
dc.subjectOrganic Moleculesen_US
dc.titleCascade Reactions in Nanozymes: Spatially Separated Active Sites inside Ag-Core−Porous-Cu-Shell Nanoparticles for Multistep Carbon Dioxide Reduction to Higher Organic Moleculesen_US
dc.typeArticleen_US


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