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dc.contributor.authorTasbihi, Minoo
dc.contributor.authorKočí, Kamila
dc.contributor.authorEdelmannová, Miroslava
dc.contributor.authorTroppová, Ivana
dc.contributor.authorReli, Martin
dc.contributor.authorSchomaecker, Reinhard
dc.date.accessioned2019-01-29T09:29:19Z
dc.date.available2019-01-29T09:29:19Z
dc.date.issued2018
dc.identifier.citationJournal of Photochemistry and Photobiology A: Chemistry. 2018, vol. 366, special issue, p. 72-80.cs
dc.identifier.issn1010-6030
dc.identifier.urihttp://hdl.handle.net/10084/133670
dc.description.abstractPt/TiO2 (PC500) photocatalysts with different amount of Pt (0.5-3.0 wt.%) deposited on commercial support (Al2O3 foam) were-characterized in detail.by-X-ray powder diffrartion, nitrogen physisorption measurement, UV-vis diffuse reflectance spectroscopy, inductively coupled plasma optical emission spectrometry (ICP-OES), photoelectrochemical measurements and tested for CO2 photocatalytic reduction and compared with commercial anatase TiO2 PC500. The main reaction product was methane; however, hydrogen and carbon monoxide were also detected. The highest yields of CH4, H-2 and CO were achieved in the presence of 1.5 wt.% PtiTiO(2). Base on the performed experiments, it was suggested that the key role in the CO2 photocatalytic reduction plays the potentials of electrons and holes within the electronic structure of photocatalyst, which were markedly affected by the Pt loading in such a way that it improved the transformation efficiency of CO2 to methane. Significantly higher yields of CO2 photocatalytic reduction were achieved in the presence of photocatalysts deposited on the commercial support compared to the powder photocatalysts. These findings confirmed the great importance of the supports surface areas on photocatalyst activity in photocatalytic reaction.cs
dc.language.isoencs
dc.publisherElseviercs
dc.relation.ispartofseriesJournal of Photochemistry and Photobiology A: Chemistrycs
dc.relation.urihttp://doi.org/10.1016/j.jphotochem.2018.04.012cs
dc.rights© 2018 Elsevier B.V. All rights reserved.cs
dc.subjectCO2 reductioncs
dc.subjectCH4cs
dc.subjectphotocatalysiscs
dc.subjectPt/TiO2cs
dc.subjectAl2O3 supportcs
dc.subjectdeposition-precipitationcs
dc.titlePt/TiO2 photocatalysts deposited on commercial support for photocatalytic reduction of CO2cs
dc.typearticlecs
dc.identifier.doi10.1016/j.jphotochem.2018.04.012
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume366cs
dc.description.issuespecial issuecs
dc.description.lastpage80cs
dc.description.firstpage72cs
dc.identifier.wos000452577600011


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