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dc.contributor.authorShunichi Fukuzumi-
dc.date.accessioned2016-08-28T10:08:10Z-
dc.date.available2016-08-28T10:08:10Z-
dc.date.issued2012-
dc.identifier.issn0004-9425-
dc.identifier.otherOAK-9543-
dc.identifier.urihttp://dspace.ewha.ac.kr/handle/2015.oak/223255-
dc.description.abstractPhotocatalytic hydrogen evolution has been performed by photoirradiation (λ>420nm) of a mixed solution of a phthalate buffer and acetonitrile (MeCN) (1:1 (v/v)) containing EDTA disodium salt (EDTA), [RuII(bpy) 3]2+ (bpy=2,2′-bipyiridine), 9-phenyl-10- methylacridinium ion (Ph-Acr+-Me), and Pt nanoparticles (PtNPs) as a sacrificial electron donor, a photosensitiser, an electron mediator, and a hydrogen-evolution catalyst, respectively. The hydrogen-evolution rate of the reaction system employing Ph-Acr+-Me as an electron mediator was more than 10 times higher than that employing a conventional electron mediator of methyl viologen. In this reaction system, ruthenium nanoparticles (RuNPs) also act as a hydrogen-evolution catalyst as well as the PtNPs. The immobilization of the efficient electron mediator on the surface of a hydrogen-evolution catalyst is expected to enhance the hydrogen-evolution rate. The methyl group of Ph-Acr+-Me was chemically modified with a carboxy group (Ph-Acr +-CH2COOH) to interact with metal oxide surfaces. In the photocatalytic hydrogen-evolution system using Ph-Acr+-CH2COOH and Pt-loaded ruthenium oxide nanoparticles (Pt/RuO2NPs) as electron donor and hydrogen-evolution catalyst, respectively, the hydrogen-evolution rate was 1.5-2 times faster than the reaction system using Ph-Acr+-Me as an electron mediator. On the other hand, no enhancement in the hydrogen-evolution rate was observed in the reaction system using Ph-Acr +-CH2COOH with PtNPs. Thus, the enhancement of hydrogen-evolution rate originated from the favourable interaction between Ph-Acr +-CH2COOH and RuO2NPs. These results suggest that the use of Ph-Acr+-Me as an electron mediator enables the photocatalytic hydrogen evolution using PtNPs and RuNPs as hydrogen-evolution catalysts, and the chemical modification of Ph-Acr+-Me with a carboxy group paves the way to utilise a supporting catalyst, Pt loaded on a metal oxide, as a hydrogen-evolution catalyst. © 2012 CSIRO.-
dc.languageEnglish-
dc.titlePhotocatalytic hydrogen evolution using 9-phenyl-10-methyl-acridinium ion derivatives as efficient electron mediators and Ru-based catalysts-
dc.typeConference Paper-
dc.relation.issue12-
dc.relation.volume65-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage1573-
dc.relation.lastpage1581-
dc.relation.journaltitleAustralian Journal of Chemistry-
dc.identifier.doi10.1071/CH12294-
dc.identifier.wosidWOS:000312163400003-
dc.identifier.scopusid2-s2.0-84871595695-
dc.author.googleYamada Y.-
dc.author.googleYano K.-
dc.author.googleFukuzumi S.-
dc.contributor.scopusidShunichi Fukuzumi(35430038100)-
dc.date.modifydate20200403081004-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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