The electrocatalytic oxygen evolution reaction (OER)
is important
for many renewable energy technologies. Developing cost-effective
electrocatalysts with high performance remains a great challenge.
Here, we successfully demonstrate our novel interface catalyst comprised
of Ni3Fe1-based layered double hydroxides (Ni3Fe1-LDH) vertically immobilized on a two-dimensional
MXene (Ti3C2T
x
)
surface. The Ni3Fe1-LDH/Ti3C2T
x
yielded an anodic OER current
of 100 mA cm–2 at 0.28 V versus reversible hydrogen
electrode (RHE), nearly 74 times lower than that of the pristine Ni3Fe1-LDH. Furthermore, the Ni3Fe1-LDH/Ti3C2T
x
catalyst requires an overpotential of only 0.31 V versus RHE to
deliver an industrial-level current density as high as 1000 mA cm–2. Such excellent OER activity was attributed to the
synergistic interface effect between Ni3Fe1-LDH
and Ti3C2T
x
. Density
functional theory (DFT) results further reveal that the Ti3C2T
x
support can efficiently
accelerate the electron extraction from Ni3Fe1-LDH and tailor the electronic structure of catalytic sites, resulting
in enhanced OER performance.