Zobrazit minimální záznam

dc.contributor.authorPřech, Jan
dc.contributor.authorSzaniawska, Ewelina
dc.contributor.authorKočí, Kamila
dc.contributor.authorČejka, Jiří
dc.contributor.authorBarrocas, Beatriz Trindade
dc.contributor.authorFilip Edelmannová, Miroslava
dc.date.accessioned2022-07-13T11:49:35Z
dc.date.available2022-07-13T11:49:35Z
dc.date.issued2022
dc.identifier.citationApplied Materials Today. 2022, vol. 26, art. no. 101392.cs
dc.identifier.issn2352-9407
dc.identifier.urihttp://hdl.handle.net/10084/146376
dc.description.abstractIn this study, we aimed to correlate the structural properties of mesoporous zeolites with their photo catalytic performance. We prepared three types of titanosilicate zeolite photocatalysts and characterized them in detail. Titanosilicate photocatalysts showed significantly higher selectivity to CO2 reduction products, i.e., CH4 and CO, than a commercial TiO2, P25. Among them, the photocatalysts TS-1-V and Lam-TS 1, which consist of unit-cell-thick nanosheets with MFI zeolite topology, had the highest photoreduction quantum efficiency. The TPD-CO2 results showed that Lam-TS-1 and TS-1-V samples have stronger interactions with both CO2 and H2O than TS-1-C. Furthermore, the amount of CO2 chemisorbed/ desorbed on Lam-TS-1 and TS-1-V was higher, indicating a higher number of interaction sites. Therefore, the key factors in photocatalytic CO2 reduction with titanosilicate catalysts are not only the strength and number of CO2 adsorption sites but also the hydrophilicity of the photocatalysts, which strongly affects their efficiency and selectivity.cs
dc.language.isoencs
dc.publisherElseviercs
dc.relation.ispartofseriesApplied Materials Todaycs
dc.relation.urihttps://doi.org/10.1016/j.apmt.2022.101392cs
dc.rights© 2022 Elsevier Ltd. All rights reserved.cs
dc.subjectCO2 photo-reductioncs
dc.subjectphotocatalysiscs
dc.subjecttitanosilicate zeolitecs
dc.subjectcarbon dioxidecs
dc.subjectTS-1cs
dc.titleTitanosilicates enhance carbon dioxide photocatalytic reductioncs
dc.typearticlecs
dc.identifier.doi10.1016/j.apmt.2022.101392
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume26cs
dc.description.firstpageart. no. 101392cs
dc.identifier.wos000790303700006


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