Precious
metals (like Ir, Ru, and Pt) and their derivatives are
the benchmark catalysts for water splitting in acidic media due to
their high stability and activity. However, the high cost and scarcity
of these materials hamper the large-scale applications. To solve this
issue, construction of catalysts containing low content of precious
metals with high intrinsic activity can be an efficient strategy,
which expectedly can decrease the cost but meanwhile preserve the
activity. Herein, we synthesized an IrW/WO3 array catalyst
by in situ formation of IrW alloy on hierarchical
WO3 nanosheet arrays. With extremely low Ir content of
1.25 wt % in 0.5 M H2SO4, this composite catalyst
not only shows superior water oxidation activity (the overpotential
at 10 mA cm–2 is only 229 mV, significantly lower
than that of the commercial IrO2 (358 mV)) but also exhibits
excellent proton reduction performance (the overpotential at −10
mA cm–2 is 49 mV, close to that of commercial Pt/C
catalyst (42 mV)), showing promising bifunctionality for the overall
water splitting. As a result, only 1.5 V is needed to drive the overall
water splitting at 10 mA cm–2 with a good long-term
stability under acidic conditions. These remarkable features can be
ascribed to the abundant active sites exposed by the three-dimensional
nanostructure, and the high intrinsic activity per Ir site. The theoretical
calculation verifies that Ir sites in IrW surface after oxidation
have a higher intrinsic activity than IrO2 for water oxidation.
We believe this research can supply a strategy to design highly active
and stable catalysts with low loading of noble metals for acidic water
splitting.