To obtain efficient photocatalytic activity on a hybrid composite,
facile transfer of photogenerated carriers at the hybrid interface
and their rapid reaction with redox species on different components
of a photocatalyst play two significant roles. Here, titanium hydroxide
as a precursor instead of synthesized TiO2 was mixed with
g-C3N4 first, and then, the TiO2/g-C3N4 composite with a strongly coupling (Ti)2–N–C bond at the interface was synthesized by
a simple hydrothermal method to efficiently realize both roles. According
to the transmission electron microscopy, X-ray photoelectron spectroscopy,
and nuclear magnetic resonance results, the closely coupled TiO2/g-C3N4 composite not only improves
the separation and transfer of the photogenerated carriers at the
hybrid interface of the composites but also constrains abundant H2O at the interface of the TiO2/g-C3N4 catalyst to accelerate the H2O reaction with photogenerated
carriers on g-C3N4. All of these lead to the
highly efficient photocatalytic activity for H2 evolution
on the TiO2/g-C3N4 composite by factors
of 9.0 and 4.7 compared to that on pure g-C3N4 under solar light and visible light, respectively.