Abstract
Oxygen vacancies and Ti3+ defects in anatase TiO2 have attracted great attention to address the insufficient optical absorption and photoinduced charge-carrier separation in photocatalysis. In this study, we demonstrate a superficial and innovative approach for synthesizing anatase TiO2 nanoparticles with abundant oxygen vacancies via γ-ray irradiation reduction at room temperature. X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance (EPR) confirm that oxygen vacancies and Ti3+ defects can be quantitatively and extensively obtained by merely regulating the irradiation dosage. Photoelectrochemical measurements suggest that oxygen vacancies and Ti3+ defects promoted the separation of electron-hole pairs and then enhanced the photocatalytic degradation performance for organic pollutant. In comparison with TiO2 (no irradiation), the sample (49.5 kGy irradiation) exhibited a 20.0-fold enhancement in visible-light decomposition of phenol. In addition, the results of scavenge experiments and mechanism analysis revealed that O2− are the dominant active species. The excited electrons generated at the conduction band and oxygen vacancy level of TiO2−x-49.5 conspicuously contributes to generate much more ·O2− species. This novel study shows at room temperature, the γ-ray approach of irradiation leads to faster formation and quantification of oxygen vacancies in the semiconductor materials.
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