4.8 Article

Ultrafine Bi3TaO7 Nanodot-Decorated V, N Codoped TiO2 Nanoblocks for Visible-Light Photocatalytic Activity: Interfacial Effect and Mechanism Insight

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 11, Issue 13, Pages 13011-13021

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b00903

Keywords

Bi3TaO7 nanodots; V/N-TiO2 nanoblocks; electronic interaction; Z-scheme; degradation pathways

Funding

  1. Major Science and Technology Program for Water Pollution Control and Treatment [2017ZX07204004]
  2. National Natural Science Foundation of China [21876078, 51878331, 21707066]
  3. Jiangsu Key RD Plan [BE2017711]
  4. Scientific Research Foundation of Graduate School of Nanjing University [2018CW08]

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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, OD 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)-O-center dot and O-center dot(2)- 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)-O-center dot and O-center dot(2)- generation, thus improving the photocatalytic activity.

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