The atificial Z-scheme is a promising and rational strategy
for solar-to-chemical energy conversion such as water-splitting. In
the Z-scheme, backward redox processes are an essential drawback that
should be overcome to increase its efficiency. Here, we demonstrate
that the simple co-loading of Fe/Ru oxide, (Fe,Ru)O
x
, onto various photocatalysts effectively improves the efficiency
of water oxidation by suppressing the undesirable backward oxidation
of the redox reagent Fe2+. The (Fe,Ru)O
x
co-loading on Bi4TaO8Cl afforded the
highest water-splitting activity (apparent quantum efficiency of 1.6%
at 420 nm) among the Z-scheme systems employing mixed-anion compounds
as O2-evolving photocatalysts. The results of photoelectrochemical
and electrochemical measurements along with time-resolved spectroscopy
clarified the key roles of Fe/Ru oxide; the Ru oxide component functions
as a “collector” of photogenerated carriers and active
sites for surface redox reactions, while the Fe oxide component acts
as a “blocker” against unfavorable Fe2+ oxidation.
The versatile availability of Fe/Ru oxide has been demonstrated for
other visible-light-responsive photocatalysts.