Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 10, 2024
Abstract
This
study
reports
an
effective
strategy
for
designing
3D
electrocatalyst
via
the
deposition
of
ZIF67‐derived
Co–CN
shell
layer
over
CuO
nanoarrays
to
form
a
CuO@Co–CN
hybrid,
followed
by
incorporation
with
p
‐block
Sb
single
atoms
(CuO@Co–CN/Sb)
obtain
highly
activated
catalytic
behaviors.
Inheriting
both
excellent
intrinsic
activity
components
and
their
synergy,
CuO@Co–CN/Sb
material
serves
as
high‐efficiency
multifunctional
catalyst
overall
water
splitting
zinc
(Zn)–air
batteries.
The
yields
current
density
10
mA
cm
−2
at
low
overpotential
72
250
mV
hydrogen
evolution
reaction
oxygen
reaction,
respectively.
Furthermore,
electrolyzer
based
on
shows
remarkable
performance
derived
0.5
A
cell
voltage
2.67
V
good
stability
50
h
continuous
operation
high
.
Simultaneously,
Zn–air
battery
using
air
cathode
open
circuit
1.455
discharge
power
131.07
mW
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(47)
Published: Aug. 29, 2024
Abstract
Direct
electrochemical
seawater
splitting
is
a
renewable,
scalable,
and
potentially
economic
approach
for
green
hydrogen
production
in
environments
where
ultra‐pure
water
not
readily
available.
However,
issues
related
to
low
durability
caused
by
complex
ions
pose
great
challenges
its
industrialization.
In
this
review,
mechanistic
analysis
of
electrolytic
discussed.
We
critically
analyze
the
development
electrolysis
identify
at
both
anode
cathode.
Particular
emphasis
given
elucidating
rational
strategies
designing
electrocatalysts/electrodes/interfaces
with
long
lifetimes
realistic
including
inducing
passivating
anion
layers,
preferential
OH
−
adsorption,
employing
anti‐corrosion
materials,
fabricating
protective
immobilizing
Cl
on
surface
electrocatalysts,
tailoring
adsorption
sites,
inhibition
binding
Mg
2+
Ca
,
hydroxide
precipitation
adherence,
co‐electrosynthesis
nano‐sized
hydroxides.
Synthesis
methods
electrocatalysts/electrodes
innovations
electrolyzer
are
also
Furthermore,
prospects
developing
technologies
clean
generation
summarized.
found
that
researchers
have
rethought
role
ions,
as
well
more
attention
cathodic
reaction
electrolyzers,
which
conducive
accelerate
commercialization
electrolysis.
Nano-Micro Letters,
Journal Year:
2024,
Volume and Issue:
17(1)
Published: Sept. 26, 2024
Abstract
Anion-exchange
membrane
water
electrolyzers
(AEMWEs)
for
green
hydrogen
production
have
received
intensive
attention
due
to
their
feasibility
of
using
earth-abundant
NiFe-based
catalysts.
By
introducing
a
third
metal
into
catalysts
construct
asymmetrical
M-NiFe
units,
the
d
-orbital
and
electronic
structures
can
be
adjusted,
which
is
an
important
strategy
achieve
sufficient
oxygen
evolution
reaction
(OER)
performance
in
AEMWEs.
Herein,
ternary
NiFeM
(M:
La,
Mo)
featured
with
distinct
units
varying
-orbitals
are
reported
this
work.
Experimental
theoretical
calculation
results
reveal
that
doping
La
leads
optimized
hybridization
between
orbital
2
p
oxygen,
resulting
enhanced
adsorption
strength
intermediates,
reduced
rate-determining
step
energy
barrier,
responsible
OER
performance.
More
critically,
obtained
NiFeLa
catalyst
only
requires
1.58
V
reach
1
A
cm
−2
anion
exchange
electrolyzer
demonstrates
excellent
long-term
stability
up
600
h.
Chemical Communications,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 1, 2024
Nickel
is
integrated
into
self-supported
FeMoO
4
nanosheet
arrays
by
a
spontaneous
redox
reaction,
which
shows
significantly
enhanced
electrocatalytic
OER
performance
and
long-term
durability
under
both
alkaline
seawater
conditions.
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 10, 2025
Abstract
Identification
of
electrocatalysts
with
suitable
electronic
and
hydrophilic
properties
is
indispensable
for
boosting
the
alkaline
oxygen
evolution
reaction
(OER).
The
incorporation
bismuth
(Bi)
into
Nickel
oxide
hydroxides
presented
to
simultaneously
tune
these
catalyst
toward
enhanced
OER.
It
shown
that
Bi
doping
endows
more
reversibility
Ni,
enhances
lattice
reactivity,
leads
a
weakly
binding
surface
resultant
NiBi(OH)
x
electrocatalyst.
These
can
not
only
accelerate
redox
transformation
OER
intermediates
but
also
enhance
oxygen‐involved
process,
which
collaboratively
boost
kinetics.
Moreover,
manipulates
property
electrode,
facilitates
mass
transfer
by
allowing
facile
diffusion
gaseous
products
electrolytes.
As
result,
optimized
Ni
97
3
(OH)
electrode
delivers
current
density
500
mA
cm
−2
at
an
overpotential
357
mV
without
losing
performance
over
1000
h,
on
par
state‐of‐the‐art
NiFe
anodes.
This
work
provides
effective
strategy
electrocatalytic
in
through
integration
regulation
modification.
As
an
electrocatalyst
for
water
electrolysis,
nickel
oxide
(NiO)
has
received
significant
attention
due
to
its
cost-effectiveness
and
high
reactivity
among
non-noble-metal-based
catalytic
materials.
However,
NiO
still
exhibits
poor
alkaline
hydrogen
evolution
reaction
(HER)
oxygen
(OER)
kinetics
compared
conventional
noble
metal-based
catalysts.
This
is
because
a
strong
interaction
with
protons
the
HER
too
low
free
energy
of
OH*
state,
resulting
in
slower
rate-determining
step
(RDS)
OER.
To
address
these
issues,
adding
dopant
suggested
as
efficient
method
modify
electron
structure
favorably
each
kinetics.
In
this
context,
we
demonstrate
that
Bismuth
(Bi),
higher
electronegativity
than
Nickel
(Ni),
induces
positive
charge
on
Ni
sites.
enhances
activity
by
reducing
number
excessive
cation
interactions
electrocatalyst.
Moreover,
Bi
ratio
increases,
sites
become
more
positively
charged,
changes
electronic
directly
impact
mechanism.
Particularly,
it
confirmed
HER,
additives
increase
proton-adsorbed
toward
near-zero
value
and,
additionally,
decrease
difference
second
considered
RDS
OER,
calculated
density
functional
theory.
The
effects
both
OER
are
demonstrated
practical
electrochemical
evaluations
half/single
cells.
Notably,
Bi-containing
catalysts
Bi05:NiO
Bi02:NiO
exhibit
remarkable
kinetics,
showing
performance
improvements
97.0%
21.9%,
respectively.
Applied Physics Letters,
Journal Year:
2025,
Volume and Issue:
126(7)
Published: Feb. 17, 2025
Magnetic
heating
by
alternating
magnetic
field
(AMF)
is
a
fascinating
solution
to
break
the
bottleneck
in
oxygen
evolution
reaction
(OER)
catalyst
improvement.
However,
practical
applications
of
AMF
electrochemistry
are
always
impeded
inherent
characteristics
(i.e.,
non-magnetic
nature
and
oxidizable
feature).
Here,
self-heating
working
electrode
substrate
C/Fe3O4/C
proposed
be
fabricated,
on
which
Ru
nanoparticles
confined
within
amorphous
carbon
matrix
deposited
as
catalytic
layer.
Under
AMF,
Fe3O4
particle
can
stimulated
generate
associated
with
Néel
relaxation,
improves
OER
efficiency
overpotential
at
10
mA
cm−2
reduced
72
mV.
Together
high
stability
rendered
structure,
exploitation
confirmed,
developed
strategy
offers
general
pathway
advance
performance
future.
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 26, 2025
During
seawater
electrolysis,
chloride
ion
(Cl–)
adsorption
at
the
anode
leads
to
an
inevitable
competitive
oxidation
reaction
(ClOR)
with
oxygen
evolution
(OER),
compromising
long-term
stability
of
electrolysis
process.
Furthermore,
Ni-based
OER
electrocatalysts
are
challenged
by
activity
degradation
due
overoxidation
Ni3+.
In
response,
we
present
a
design
oxygen-vacancy-regulated
asymmetric
Nb–O–Ni
bonds
aimed
selective
oxidation.
The
experimental
and
in
situ
characterization
results
indicate
that
blocking
effect
vacancies
effectively
alleviates
electron
release
Ni3+
enrichment
Nb5+
on
bonds,
achieving
stable
alkaline
seawater.
Density
functional
theory
(DFT)
calculations
reveal
optimize
strength
intermediates
break
up
scaling
relationship
between
*OH
*OOH
intermediates.
constructed
anion
exchange
membrane
cell
achieves
cost
efficiency
$1.07
per
GGE
(gasoline
gallon
equivalent)
for
H2
production
current
density
1000
mA
cm–2,
maintaining
operational
100
h
500
cm–2.