Visible-light-responsive
photocatalysts used in the highly efficient
hydrogen production exhibit several disadvantages such as photocorrosion
and fast recombination. Because of the potential important applications
of such catalysts, it is crucial that a simple, effective solution
is developed. In this respect, in this study, we combined SiC (β
modification) and TiO
2
with CdS to overcome the challenges
of photocorrosion and fast recombination of CdS. Notably, we found
that when irradiated with visible light, CdS was excited, and the
excited electrons moved to the conduction band of TiO
2
,
thereby increasing the efficiency of charge separation. In addition,
by moving the holes generated on CdS to the valence band of SiC, in
the opposite direction of TiO
2
, photocorrosion and fast
recombination were prevented. As a result, in the sulfide solution,
the CdS/SiC composite catalyst exhibited 4.3 times higher hydrogen
generation ability than pure CdS. Moreover, this effect was enhanced
with the addition of TiO
2
, giving 10.8 times higher hydrogen
generation ability for the CdS/SiC/TiO
2
catalyst. Notably,
the most efficient catalyst, which was obtained by depositing Pt as
a cocatalyst, exhibited 1.09 mmol g
–1
h
–1
hydrogen generation ability and an apparent quantum yield of 24.8%.
Because water reduction proceeded on the TiO
2
surface and
oxidative sulfide decomposition proceeded on the SiC surface, the
exposure of CdS to the solution was unnecessary, and X-ray photoelectron
spectroscopy confirmed that photocorrosion was successfully suppressed.
Thus, we believe that the effective composite photocatalyst construction
method presented herein can also be applied to other visible-light-responsive
powder photocatalysts having the same disadvantages as CdS, thereby
improving the efficiency of such catalysts.