Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/96944
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorYin, Jen_US
dc.creatorYin, Zen_US
dc.creatorJin, Jen_US
dc.creatorSun, Men_US
dc.creatorHuang, Ben_US
dc.creatorLin, Hen_US
dc.creatorMa, Zen_US
dc.creatorMuzzio, Men_US
dc.creatorShen, Men_US
dc.creatorYu, Cen_US
dc.creatorZhang, Hen_US
dc.creatorPeng, Yen_US
dc.creatorXi, Pen_US
dc.creatorYan, CHen_US
dc.creatorSun, Sen_US
dc.date.accessioned2023-01-04T06:11:48Z-
dc.date.available2023-01-04T06:11:48Z-
dc.identifier.issn0002-7863en_US
dc.identifier.urihttp://hdl.handle.net/10397/96944-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2021 American Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of the American Chemical Society, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://dx.doi.org/10.1021/jacs.1c06877.en_US
dc.rightsJournal of the American Chemical Society is available at https://pubs.acs.org/journal/jacsat.en_US
dc.titleA new hexagonal cobalt nanosheet catalyst for selective CO2 conversion to ethanalen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage15335en_US
dc.identifier.epage15343en_US
dc.identifier.volume143en_US
dc.identifier.issue37en_US
dc.identifier.doi10.1021/jacs.1c06877en_US
dcterms.abstractWe report a new form of catalyst based on ferromagnetic hexagonal-close-packed (hcp) Co nanosheets (NSs) for selective CO2RR to ethanal, CH3CHO. In all reduction potentials tested from −0.2 to −1.0 V (vs RHE) in 0.5 M KHCO3 solution, the reduction yields ethanal as a major product and ethanol/methanol as minor products. At −0.4 V, the Faradaic efficiency (FE) for ethanal reaches 60% with current densities of 5.1 mA cm–2 and mass activity of 3.4 A g–1 (total FE for ethanal/ethanol/methanol is 82%). Density functional theory (DFT) calculations suggest that this high CO2RR selectivity to ethanal on the hcp Co surface is attributed to the unique intralayer electron transfer, which not only promotes [OC–CO]* coupling but also suppresses the complete hydrogenation of the coupling intermediates to ethylene, leading to highly selective formation of CH3CHO.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of the American Chemical Society, 22 Sept. 2021, v. 143, no. 37, p. 15335-15343en_US
dcterms.isPartOfJournal of the American Chemical Societyen_US
dcterms.issued2021-09-22-
dc.identifier.isiWOS:000700883200047-
dc.identifier.pmid34519488-
dc.identifier.eissn1520-5126en_US
dc.description.validate202301 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumbera1775-
dc.identifier.SubFormID45938-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryGreen (AAM)en_US
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