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Surface plasma Ag-decorated single-crystalline TiO2-x(B) nanorod/defect-rich g-C3N4 nanosheet ternary superstructure
Junyan Kuang1, Zipeng Xing1, Junwei Yin1
1Department of Environmental Science, School of Chemistry and Materials Science, Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education of the People's Republic of China, Heilongjiang University, Harbin 150080, PR China.
Abstract:
Ag-TiO2-x(B)/g-C3N4 ternary heterojunctions photocatalysts are fabricated by hydrothermal-calcination, photo-deposition procedure, and followed by in-situ solid-state chemical reduction procedure. As-obtained photocatalysts are consisted with heterojunctions between 2D g-C3N4 sheets and 1D TiO2(B) single-crystalline nanorods. The band gap of Ag-TiO2-x(B)/g-C3N4 ternary heterojunctions photocatalysts is reduced to ∼2.23 eV due to plasma Ag and surface engineering. Under visible light irradiation, it has an optimal photocatalytic property for the reduction of Cr6+ (95%) and degradation of NH4+ (93%). The apparent reaction rate constants (k) of ternary heterojunctions photocatalysts for NH4+ and Cr6+ are 25 and 12 folds higher than that of original TiO2(B). Furthermore, Ag-TiO2-x(B)/g-C3N4 also has excellent hydrogen production efficiency, which is up to 410 µmol h-1 g-1. This enhancement can be attributed to the unique heterojunction formed by 1D single-crystalline TiO2(B) nanorods and 2D g-C3N4 sheets, surface plasma resonance effect of plasma Ag nanoparticle, and surface engineering. A possible photocatalytic mechanism is also proposed by analysizing the XPS valence-band spectra and the Mott-Schottky.
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