Iridium (Ir) nanostructures with
well-defined shapes, and particularly,
highly active surface, are attractive for the application of electrocatalytic
oxygen evolution reaction (OER), yet they have had very limited success
to date because of challenges in their synthesis. Here, we report
the synthesis of Ir nanocrystals, in the form of Pd@Ir core–shell
structures and with well-defined high-index {331} facets, by a robust
seed-mediated process. The success relies on the precise control over
the deposition of ultrathin Ir layer on Pd trioctahedral nanocrystals.
The Pd@Ir nanocatalyst with such unique high-index facets delivers
substantially promoted OER activity and durability compared with those
with low-index facets (i.e., {100} and {111} facets), with an overpotential
as low as 300 mV, boosted mass activities up to 1.01 A mgIr
–1 at 1.53 V, and a minimal Tafel slope of 84.9
mV dec–1. Density functional theory (DFT) calculations
suggest that the superior OER performance originates from the easier
hydroxylation of *O to *OOH over high-index facets, along with the
appropriate value of ΔG
O-ΔG
OH and satisfactory adsorption/desorption property.
Moreover, the high-index facets are apt to be electrochemically oxidized
into stable IrO
x
species, leading to an
improved durability. Both theoretical and experimental studies demonstrate
the fascinating property of a high-index Ir shell in facilitating
OER activity and durability.