Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/100078
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.contributorResearch Institute for Smart Energy-
dc.contributorMainland Development Office-
dc.creatorBodedla, GBen_US
dc.creatorTritton, DNen_US
dc.creatorChen, Xen_US
dc.creatorZhao, Jen_US
dc.creatorGuo, Zen_US
dc.creatorLeung, KCFen_US
dc.creatorWong, WYen_US
dc.creatorZhu, Xen_US
dc.date.accessioned2023-08-08T01:51:57Z-
dc.date.available2023-08-08T01:51:57Z-
dc.identifier.urihttp://hdl.handle.net/10397/100078-
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 ACS Applied Energy Materials, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsaem.1c00318.en_US
dc.subjectCocatalyst-freeen_US
dc.subjectIridium(III) complexen_US
dc.subjectPhotocatalytic hydrogen evolutionen_US
dc.subjectPhotostability and reductive quenchingen_US
dc.titleCocatalyst-free photocatalytic hydrogen evolution with simple heteroleptic iridium(III) complexesen_US
dc.typeJournal/Magazine Articleen_US
dc.description.otherinformationTitle in author's file: Co-catalyst-free Photocatalytic Hydrogen Evolution with Simple Heteroleptic Iridium(III) Complexesen_US
dc.identifier.spage3945en_US
dc.identifier.epage3951en_US
dc.identifier.volume4en_US
dc.identifier.issue4en_US
dc.identifier.doi10.1021/acsaem.1c00318en_US
dcterms.abstractA simple heteroleptic iridium(III) photosensitizer, Ir-1, containing two ligands 5-(trifluoromethyl)-2-phenylpyridine (CN-CF3) and bipyridine (NN) has for the first time been studied for cocatalyst-free photocatalytic hydrogen evolution (PHE). The complex Ir-1 produces a hydrogen production rate (ηH2) of 3.2 mmol g-1 h-1, which is over 3.6-fold higher than that of the control complex Ir-2 (0.9 mmol g-1 h-1) containing bipyridine and 2-phenylpyridine ligands without CF3 groups. The higher ηH2 of Ir-1 could be ascribed to the high light-harvesting property, longer triplet electron lifetime, and more appropriate driving force for accepting electrons from the sacrificial donor, which enable efficient charge separation and transfer of electrons for hydrogen evolution. Additionally, the photostability issues of Ir-1 and Ir-2 are addressed by the selection of suitable organic solvent/water photocatalytic systems.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationACS applied energy materials, 26 Apr. 2021, v. 4, no. 4, p. 3945-3951en_US
dcterms.isPartOfACS applied energy materialsen_US
dcterms.issued2021-04-26-
dc.identifier.scopus2-s2.0-85104928457-
dc.identifier.eissn2574-0962en_US
dc.description.validate202308 bckw-
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberABCT-0120-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextState Key Laboratory of Environmental and Biological Analysis; President’s Award for Outstanding Performance in Research Supervision; NSFC; Hong Kong Polytechnic University; Clarea Au for the Endowed Professorship in Energy; Research Institute for Smart Energy (RISE)en_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS52398257-
dc.description.oaCategoryGreen (AAM)en_US
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