Bismuth oxybromide (BiOBr) is a promising photocatalytic
semiconductor
material due to its unique hierarchical structure and band structure.
However, its photocatalytic applications are restricted due to its
narrow visible-light absorption range and poor photooxidation capability.
In this study, BiOBr1–x
I
x–y
with rich surface Br vacancies
(BrVs-rich BiOBr1–x
I
x–y
) was created via a facile
indirect substitution strategy. Benefiting from the broadened visible-light
response range and reduced recombination rate of photogenerated carriers,
BiOBr1–x
I
x–y
shows excellent visible-light photodegradation
ability for high-concentration refractory contaminants, such as phenol,
tetracycline, bisphenol A, rhodamine B, methyl orange, and even real
wastewater. At the same time, the Br vacancies can regulate the band
structure of BiOBr1–x
I
x–y
and serve as trap states
to promote charge separation, thus facilitating surface photoredox
reactions. An in-depth investigation of the Br vacancy effect and
photodegradation mechanism was conducted. This novel study revealed
the significance of Br vacancies in enhancing the photocatalytic performance
of BiOBr under visible light, providing a promising strategy for improving
the utilization efficiency of sunlight in wastewater treatment.