Repozitorij Univerze v Novi Gorici

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Naslov:Effects of Different Copper Loadings on the Photocatalytic Activity of TiO2-SiO2 Prepared at a Low Temperature for the Oxidation of Organic Pollutants in Water
Avtorji:ID Čižmar, T., UNG (Avtor)
ID Arčon, Iztok, UNG (Avtor)
ID Fanetti, Mattia, UNG (Avtor)
ID Lavrenčič Štangar, Urška, UNG, FKKT (Avtor)
Datoteke: Gradivo nima datotek, ki so prostodostopne za javnost. Gradivo je morda fizično dosegljivo v knjižnici fakultete, zalogo lahko preverite v COBISS-u. Povezava se odpre v novem oknu
Jezik:Angleški jezik
Vrsta gradiva:Delo ni kategorizirano
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:UNG - Univerza v Novi Gorici
Opis:The objective of this research is to examine how Cu modification can improve the photocatalytic activity of TiO2-SiO2, to explainthe correlation between the Cu concentration and the chemical state of Cu cations in the TiO2-SiO2 matrix, and the photocatalytic activity under UV/solar irradiation. The Cu-modified TiO2-SiO2 photocatalysts were prepared by a low-temperature sol–gel method from organic Cu, Si and Ti precursors with various Cu concentrations (0.05–3 mol %). The sol–gels were dried at 150 8C to obtain the photocatalysts in a powder form. The photocatalytic activity was determined by using a fluorescence- based method of terephthalic acid decomposition. An up to three times increase in photocatalytic activity is obtained if the TiO2-SiO2 matrix is modified with Cu in a narrow concentration range from 0.05 to 0.1 mol%. At higher Cu loadings, the photocatalytic activity of the Cu-modified photocatalysts is lower than that of the un-modified reference TiO2-SiO2 photocatalyst. XRD was used to show that all Cu-modified TiO2-SiO2 composites with different Cu concentrations have the same crystalline structure as un-modified TiO2-SiO2 composites. The addition of Cu does not change the relative ratio between the anatase and brookite phases or unit cell parameters of the two TiO2 crystalline structures. We used Cu K-edge X-ray absorption near edge structure and extended X-ray absorption fine structure analyses to determine the valence state and local structure of Cu cations in the Cu-modified TiO2-SiO2 photocatalysts. The results elucidate the mechanism responsible for the improved photocatalytic activity. In samples with a low Cu content, which exhibit the highest activity, Cu@O@Ti connections are formed, which suggests that the activity enhancement is caused by the attachment of CuII cations on the surface of the photocatalytically active TiO2 nanoparticles, so CuII cations may act as free-electron traps, which reduce the intensity of recombination between electrons and holes at the TiO2 photocatalyst surface. At higher Cu loadings no additional Cu@O@Ti connections are formed, instead only Cu@O@Cu connections are established. This indicates the formation of amorphous or nanocrystalline copper oxide, which hinders the photocatalytic activity of TiO2.
Ključne besede:Cu modified TiO2-SiO2 photocatalyst Cu EXAFS, XANES, Organic pollutants
Verzija publikacije:Objavljena publikacija
Leto izida:2018
Št. strani:2982-2993
Številčenje:10, 0
PID:20.500.12556/RUNG-4045-e19616e2-9dbb-767a-399d-580d5c03c14d Novo okno
COBISS.SI-ID:5203963 Novo okno
DOI:10.1002/cctc.201800249 Novo okno
NUK URN:URN:SI:UNG:REP:HZU8DJ2A
Datum objave v RUNG:30.08.2018
Število ogledov:4489
Število prenosov:0
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:ChemCatChem
Založnik:Wiley: 12 months
Leto izida:2018
ISSN:1867-3880

Gradivo je financirano iz projekta

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P1-0112
Naslov:Raziskave atomov, molekul in struktur s fotoni in delci

Licence

Licenca:CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by-nc-nd/4.0/deed.sl
Opis:Najbolj omejujoča licenca Creative Commons. Uporabniki lahko prenesejo in delijo delo v nekomercialne namene in ga ne smejo uporabiti za nobene druge namene.
Začetek licenciranja:30.08.2018

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