Ultrafine Bi3TaO7 Nanodot-Decorated V, N Codoped TiO2 Nanoblocks for Visible-Light Photocatalytic Activity: Interfacial Effect and Mechanism Insight
Bi3TaO7 is a potential photocatalyst because of its high chemical stability, defective fluorite-type structure, and superior mobility of photoinduced holes. However, few studies have focused on the interfacial effects of Bi3TaO7-based photocatalysts. In this work, 0D Bi3TaO7 nanodot-hybridized 3D V...
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Veröffentlicht in: | ACS applied materials & interfaces 2019-04, Vol.11 (13), p.13011-13021 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Bi3TaO7 is a potential photocatalyst because of its high chemical stability, defective fluorite-type structure, and superior mobility of photoinduced holes. However, few studies have focused on the interfacial effects of Bi3TaO7-based photocatalysts. In this work, 0D Bi3TaO7 nanodot-hybridized 3D V and N codoped TiO2 nanoblock (B/VNT) composites were first synthesized for the photocatalytic removal of oxytetracycline hydrochloride, 2,4,6-trichlorophenol, and tetrabromobisphenol A. The fabricated B/VNT had a photocatalytic performance superior to that of pristine components, and probable degradation pathways were proposed according to the primary intermediates identified by a gas chromatography–mass spectrometer. Interestingly, on B/VNT, the transfer of interfacial electrons was observed from V/N–TiO2 to Bi3TaO7, and the formed built-in electronic field led to a direct Z-scheme structure, rather than type II, as confirmed by the generated •OH and •O2 – radicals and band structures from the density functional theory calculation. Therefore, the strong interfacial electronic interaction on the B/VNT was significant, which drove faster photogenerated charge transfer, more visible-light adsorption, and active •OH and •O2 – generation, thus improving the photocatalytic activity. |
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ISSN: | 1944-8244 1944-8252 |
DOI: | 10.1021/acsami.9b00903 |