Compared with the
well-known Pt cocatalyst, molybdenum sulfide
is one of the most prospective alternatives for developing highly
efficient photocatalytic H2-evoultion materials. To further
improve its H2-evoultion activity, it is highly required
to further optimize the electronic and surface structures of molybdenum
sulfide cocatalyst. Herein, a novel amorphous molybdenum-based bimetallic
sulfide (a-CoMoS
x
) was prepared and loaded
on the CdS surface by a photoinduced electron-reduction method to
promote the interfacial H2-production rate of CdS. It is
found that loading a-CoMoS
x
cocatalyst
can markedly enhance the H2-generation activity of CdS
photocatalyst, which is significantly higher than that of pure CdS
and a-MoS2/CdS by a factor of 26.3 and 3.1 times. More
importantly, in addition to CdS, the a-CoMoS
x
can also serve as the general electron cocatalyst to obviously
promote the H2-production activity of well-known TiO2 (typical UV-responsive titanium dioxide) and g-C3N4 (novel visible light-responsive organic semiconductors).
According to the present results, an electron-cocatalyst mechanism
of a-CoMoS
x
is proposed to explain the
enhanced photocatalytic H2-production performance, namely,
amorphous CoMoS
x
can rapidly capture electrons
and then quickly transfer the electrons to the active sites (its unsaturated
S atoms and defect sites) to effectively enhance the interfacial H2-production reaction. In consideration of its facile synthesis,
low cost, and superior performance, the amorphous CoMoS
x
appears to be one of the most prospective cocatalysts
for photocatalytic water splitting.