Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 29, 2024
Abstract
Electrolysis
of
seawater
represents
great
potentials
for
sustainable
hydrogen
production.
However,
both
competitive
Cl
−
adsorption
and
catalysts
corrosion
caused
by
chlorine
oxidation
reaction
(ClOR)
are
major
challenges
in
electrolysis.
Inspired
the
concept
hard
soft
acids
bases
(HSAB),
polyphosphate
oxyanions
(P
3
O
10
5−
)
on
Ni(OH)
2
surface
is
coordinated
to
obtain
harder
acid
Ni
sites,
which
could
160
times
stability
enhancement
compared
pure
oxygen
evolution
(OER)
alkaline
at
800
mA
cm
−2
.
Also,
turnover
frequency
value
‐P
50
that
,
implying
higher
intrinsic
OER
activity
Theoretical
experimental
investigations
show
P
facilitate
transition
3+
>3+
thus
preferring
base
OH
rather
than
This
enhance
selectivity
inhibit
undesirable
ClOR.
Furthermore,
molecular
dynamics
simulations
indicate
concentration
near
electrode
be
reduced
nearly
half
due
electrostatic
repulsion
oxyanions.
When
assembled
into
an
electrolyzer
splitting,
it
operate
2.2
V
with
large
current
up
1.4
A
240
h.
Small,
Journal Year:
2024,
Volume and Issue:
20(33)
Published: April 12, 2024
Limited
by
the
strong
oxidation
environment
and
sluggish
reconstruction
process
in
oxygen
evolution
reaction
(OER),
designing
rapid
self-reconstruction
with
high
activity
stability
electrocatalysts
is
crucial
to
promoting
anion
exchange
membrane
(AEM)
water
electrolyzer.
Herein,
trace
Fe/S-modified
Ni
oxyhydroxide
(Fe/S-NiOOH/NF)
nanowires
are
constructed
via
a
simple
situ
electrochemical
strategy
based
on
precipitation-dissolution
equilibrium.
In
characterization
techniques
reveal
that
successful
introduction
of
Fe
S
leads
lattice
disorder
boosts
favorable
hydroxyl
capture,
accelerating
formation
highly
active
γ-NiOOH.
The
Density
Functional
Theory
(DFT)
calculations
have
also
verified
incorporation
optimizes
electrons
redistribution
d-band
center,
decreasing
energy
barrier
rate-determining
step
(
Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 28, 2024
Abstract
The
design
of
electrocatalysts
for
oxygen
evolution
reaction
(OER)
remains
a
limitation
industrial
hydrogen
production
by
electrolysis
water.
Excellent
and
stable
OER
catalysts
can
be
developed
activating
lattice
changing
the
path.
Herein,
S
FeOOH
on
Co(OH)
2
nanoneedle
arrays
are
introduced
to
construct
heterostructure
(S‐FeOOH/Co(OH)
/NF)
as
proof
concept.
Theoretical
calculations
experimental
suggest
that
Co‐O‐Fe
motif
formed
at
heterogeneous
interface
with
introduction
FeOOH,
inducing
electron
transfer
from
Co
Fe,
enhancing
Co─O
covalency
reducing
intramolecular
charge
energy,
thereby
stimulating
direct
coupling.
Doping
in
further
accelerates
transfer,
improves
activity,
prevents
dissolution
FeOOH.
Consequently,
overpotential
S‐FeOOH/Co(OH)
/NF
is
only
199
mV
10
mA
cm
−2
,
coupled
Pt/C
electrode
up
1
A
under
1.79
V
remain
over
120
h
an
anion
exchange
membrane
water
electrolyzer
(AEMWE).
This
work
proposes
strategy
efficient
promotes
commercialization
AEMWE.