Urea-assisted synthesis of carbon-doped BiNbO4 with oxygen vacancies and visible light photocatalytic applications†
Abstract
Although carbon doping in simple metal oxides like TiO2 and ZnO has been proven to increase photocatalytic dye degradation in visible light, it's unclear if carbon doping in complex BiNbO4 would have the same effect. For the first time, carbon doped BiNbO4 (U-BiNbO4) has been synthesized with urea as the carbon source utilizing a simple sol–gel process. The creation of oxygen vacancies and their energy levels in BiNbO4's electronic band structure are controlled by the decomposition of urea. X-Ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and carrier scavenging tests verified the presence of surface oxygen vacancies and carbon doping. Both pure BiNbO4 and U-BiNbO4 are multi-crystalline structures with orthorhombic and triclinic phases. When compared to pure BiNbO4, U-BiNbO4 degraded cationic methylene blue (MB, 75.7 ± 3.5%) and brilliant green dyes (BG, 86.3 3.5%) more efficiently. The creation of carbon modulated oxygen vacancies and the lowering of the bandgap (from 3.19 eV to 2.95 eV for BiNbO4 and U-BiNbO4) were also postulated as dye degradation mechanisms. By employing a synthesis method of alternate low- and high-oxygen partial pressures, this novel process might be exploited to construct high-performance Bi-based photocatalysts.