Surface plasma Ag-decorated single-crystalline TiO2-x(B) nanorod/defect-rich g-C3N4 nanosheet ternary superstructure 3D heterojunctions as enhanced visible-light-driven photocatalyst

J Colloid Interface Sci. 2019 Apr 15:542:63-72. doi: 10.1016/j.jcis.2019.01.124. Epub 2019 Jan 30.

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.

Keywords: Heterojunction; Single-crystalline TiO(2)(B) nanorod; Surface engineering; Visible-light-driven photocatalysis; g-C(3)N(4) sheet.