Ti-doped synergistic hollow thin-walled Bi2O3 nano-microspheres for efficient tetracycline hydrochloride photodegradation

Bismuth oxide (Bi2O3) has been extensively investigated in the fields of environmental photocatalysis, owing to its exceptional charge transport performance and remarkable resistance to photocorrosion. However, the limited absorption spectrum of light and rapid recombination of photogenerated charge results in a low quantum efficiency. Herein, an efficient photocatalytic system for tetracycline hydrochloride (TCH) photodegradation based on titanium (Ti)-doped hollow, thin-walled Bi2O3 with nano-microspheres is fabricated via a facile self-assembly strategy. It is shown that doping Ti in Bi2O3 can generate oxygen vacancies, in addition, the addition of Ti in the solvothermal process inhibits the conversion of Bi3+ to bismuth at high temperature, making the content of each component in the heterostructure controllable. The hybrid catalyst exhibits superior performance in visible-light-driven photocatalytic degradation of TCH (about 95.1 % degradation efficiency after 120 min) and excellent stability (up to 4 cycles) under visible light irradiation. The optimized catalyst exhibits excellent performance in visible light catalytic degradation, owing to the synergistic effect of high specific surface area, Bi plasma resonance effect and charge mobility. Moreover, the photocatalytic mechanism of Ti-Bi2O3 have been deeply analyzed through experimental investigation and DFT theoretical calculations. The findings contribute to the synthesis of efficient visible-light-driven Bi-based photocatalysts and to the understanding of photocatalytic degradation reactions. [Display omitted] ●Ti-doped Bi2O3 with hollow microspheres synthesized by hydrothermal method.●The synergistic effects of Ti enhanced structural and physicochemical properties.●Hollow thin-walled structure displays an importance role in photocatalysis.●Ti-Bi2O3-450℃ exhibited high performance of removal organic pollutant.●The photocatalysis system increases active sites and inhibits e--h+ recombination.