Abstract

Nanosized NiO–Ti0.94V0.06O1.94B0.06 p–n junction (70–90 nm) with enhanced photocatalytic activity under visible light was prepared by a two-step sol–gel method. In order to simulate the density of state and band structure, the supercells (2 × 2 × 1) of pure TiO2 and doped TiO2 were calculated by first-principles with the plane-wave ultrasoft pseudopotentials method. The obtained samples were characterized by differential thermal analysis, X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy, UV–vis diffuse reflectance spectroscopy, and photoluminescence emission. It was revealed that the sample was highly crystalline anatase and formed a p–n junction with NiO phase. B atoms incorporated into the TiO2 lattice in the form of interstitial B and substitutional B. V atoms substituted Ti sites in the form of V3+ and V4+. The photocatalytic activity was evaluated by the degradation of Rhodamine B under visible light. Compared with TiO2, TiO1.94B0.06, Ti0.94V0.06O2, and Ti0.94V0.06O1.94B0.06, the NiO–Ti0.94V0.06O1.94B0.06 exhibited much higher photocatalytic activity (12.38 × 10−3 min−1), which can be ascribed to the synergistic effects of the V/B co-doping by narrowing the band gap (2.36 eV) and the p–n junction heterostructures by reducing the possibility of recombination of photogenerated electron–hole pairs.

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