A novel high-performance BiOBr@graphene (BiOBr@G) photocatalyst
with a new assembly structure had been demonstrated using a facile
hydrothermal method through chemical bonding of reduced graphene oxide
and structure-defined BiOBr flakes for improving charge separation
and transfer performance, which were first synthesized at room temperature
in immiscible solvents without corrosive acids. The prepared samples
were characterized, and the BiOBr@G composite realized an efficient
assembly portfolio of graphene and BiOBr flakes with defined structures,
verified by scanning electron microscopy (SEM), transmission electron
microscopy (TEM), X-ray diffraction (XRD), and Raman and X-ray photoelectron
spectroscopy (XPS), in which BiOBr flakes were covalently linked with
the assembled graphene sheets through the Bi–C bond. This composite
exhibited remarkable visible light absorbance and efficient photoinduced
charge splitting characteristics in comparison with those of pure
BiOBr, as established by DRS absorption, photoluminescence radiation,
and photocurrent study. Hence, a very small amount (5 mg) of the BiOBr@G
composite displayed a complete photodegradation effect on the rhodamine
B dye under only 15 min of visible light excitation, which was three
times faster than that of pure BiOBr and extremely superior to that
of commercial P25. This was probably ascribed to the well-defined
BiOBr structure itself, elevated light absorbance, and Bi–C
chemical bond inducing quick charge separation and transfer in the
BiOBr@G composite. Additionally, investigations on the photocatalytic
mechanism displayed that the photogenerated holes in the BiOBr valence
band and derivative superoxide radicals played vital roles in the
photodegradation of RhB dyes, as reinforced by the electron spin resonance
method, where the covalent linking of BiOBr and graphene served as
an effective pathway for charge transportation.