Production of renewable fuels by the photohydrogenation of CO2: effect of the Cu species loaded onto TiO2 photocatalysts

dc.contributor.authorChen, Bo-Ren
dc.contributor.authorNguyen, Van-Huy
dc.contributor.authorWu, Jeffrey C. S.
dc.contributor.authorKočí, Kamila
dc.contributor.authorReli, Martin
dc.date.accessioned2016-03-30T08:05:16Z
dc.date.available2016-03-30T08:05:16Z
dc.date.issued2016
dc.descriptionPubMed ID: 26807649cs
dc.description.abstractThe efficient gas phase photocatalytic hydrogenation of CO2 into a desirable renewable fuel was achieved using a Cu-loaded TiO2 photocatalyst system. Enhancing the amount of Ti3+ relative to Ti4+ in a Cu-loaded TiO2 photocatalyst provided an excellent opportunity to promote the photohydrogenation of CO2. The coexistence of Cu and Cu+ species during the photoreaction was shown to efficiently enhance the photocatalytic activity by prolonging the lifetime of the electrons. To achieve the best photoactivity, the Cu species must be maintained at an appropriately low concentration (≤1 wt%). The highest CH4 yield obtained was 28.72 μmol g−1. This approach opens a feasible route not only to store hydrogen by converting it into a desirable renewable fuel, but also to reduce the amount of the greenhouse gas CO2 in the atmosphere.cs
dc.description.firstpage4942cs
dc.description.issue6cs
dc.description.lastpage4951cs
dc.description.sourceWeb of Sciencecs
dc.description.volume18cs
dc.identifier.citationPhysical Chemistry Chemical Physics. 2016, vol. 18, issue 6, p. 4942-4951.cs
dc.identifier.doi10.1039/c5cp06999h
dc.identifier.issn1463-9076
dc.identifier.issn1463-9084
dc.identifier.urihttp://hdl.handle.net/10084/111412
dc.identifier.wos000369509100078
dc.language.isoencs
dc.publisherRoyal Society of Chemistrycs
dc.relation.ispartofseriesPhysical Chemistry Chemical Physicscs
dc.relation.urihttp://dx.doi.org/10.1039/c5cp06999hcs
dc.titleProduction of renewable fuels by the photohydrogenation of CO2: effect of the Cu species loaded onto TiO2 photocatalystscs
dc.typearticlecs
dc.type.statusPeer-reviewedcs

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