Experimental and DFT study of the degradation of 4-chlorophenol on hierarchical micro-/nanostructured oxide films

0441382 - ÚFCH JH 2016 RIV NL eng J - Článek v odborném periodiku
Guerin, V. M. - Žouželka, Radek - Bíbová-Lipšová, Hana - Jirkovský, Jaromír - Rathouský, Jiří - Pauporté, T.
Experimental and DFT study of the degradation of 4-chlorophenol on hierarchical micro-/nanostructured oxide films.
Applied Catalysis B - Environmental. Roč. 168, JUN 01 (2015), s. 132-140. ISSN 0926-3373. E-ISSN 1873-3883
Grant CEP: GA MK(CZ) DF11P01OVV012
Klíčová slova: 4-Chlorophenol degradation * DFT modeling * ZnO hierarchical nanostructures
Kód oboru RIV: CF - Fyzikální chemie a teoretická chemie
Impakt faktor: 8.328, rok: 2015

Hierarchical ZnO architectures were prepared by a facile electrochemical technique.Photocatalytic activity of hierarchical ZnO was enhanced by its micro/nanostructure.The DFT modeling of the photocatalytic degradation of 4-chlorophenol by OH radicals. Hierarchical ZnO nanoporous/nanowire architectures immobilized on a substrate were prepared by a facile two-step electrochemical technique. The layer optical properties have been characterized by absorption spectroscopy and photoluminescence measurements. The structures strongly absorbed UV light and had a high structural quality. The porosity of the hierarchical layers could be tuned by changing the duration of the second growth step. The photocatalytic activity of ZnO films was higher than that of arrayed ZnO nanowire layers and mesoporous ZnO films. The photocatalytic activity for 4-chlorophenol degradation could be enhanced by developing hierarchical structures with a high percentage exposure of polar (0001) facets, high specific surface area and good accessibility of the pollutant to the oxide surface. The modeling by density functional theory (DFT) of the degradation of 4-chlorophenol molecules by OH radicals lead to several important results, namely that the hydroxylation of the aromatic ring and its opening can occur in parallel releasing hydroperoxyl radical and hydroxyl radical, respectively. The restored OH radical can either further oxidize the primary ring opening product or attack another molecule of 4-chlorophenol. These computational results are in good agreement with the photocatalytic degradation observations made using both ZnO and TiO2 photocatalysts.
Trvalý link: http://hdl.handle.net/11104/0244619