Fabricating efficient bifunctional catalysts for both hydrogen/oxygen
evolution reactions (HER/OER) in an easy and mass-productive way is
highly attractive for alkaline water electrolyzers. Perovskite oxides
show compositional flexibility and high property tunability, while
poor electrical conductivity and relatively low HER activity hamper
their application in overall water splitting. Here, a conductive monoclinic
SrIrO3 perovskite is developed as an excellent alkaline
electrocatalyst with bifunctionality which can be easily synthesized
under normal conditions. Toward the HER, it experiences progressive
surface self-reconstruction during the activation process because
of lattice Sr2+ leaching, eventually leading to a remarkable
apparent activity with an approximately 11-fold enhancement at 200
mV overpotential relative to the fresh sample. Experimental and theoretical
evidence reveals that etching of lattice Sr2+ in relatively
less-stable SrIrO3 compared to IrO2 is crucial
for triggering this self-reconstruction. Toward the OER, no obvious
surface reconstruction occurs, and an overpotential of only 300 mV
is required to realize 10 mA cmgeo–2,
significantly lower than that for most perovskites reported previously
(340–450 mV). The activated SrIrO3 from HER operation
can be used alternatively as an OER electrocatalyst with further improved
performance. A SrIrO3-based two-electrode water-splitting
cell shows exceptional performance, that is, 1.59 V@10 mA cmgeo–2 with negligible performance degradation over
10 h.