Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 16, 2025
Abstract
High
entropy
oxides
(HEOs)
have
gained
increasing
attention
as
lithium‐ion
battery
anodes,
owing
to
their
multi‐principal
synergistic
effect
and
structural
stability.
However,
the
conversion
type
HEOs
also
suffer
from
low
intrinsic
conductivity,
volume
expansion,
slow
kinetics
traditional
metal
oxide.
Herein,
a
(FeCoNiCrMn)
2
O
3
HEO
with
hollow
multishelled
structure
Al‐doping
(Al‐HEO‐HoMS)
is
successfully
prepared
by
thermal
diffusion‐assisted
template
method.
The
effectively
accommodates
changes
mitigates
strains,
resulting
in
excellent
electrochemical
Most
importantly,
inserted
Al
dopant
Al‐HEO‐HoMS
serves
pegging
points,
securely
fastening
other
metallic
elements
Al─O
bonds
maintain
stability
of
anodes
during
repeated
lithiation/delithiation.
Additionally,
abundant
oxygen
vacancies
optimized
electronic
brought
doping
been
validated
accelerate
lithiation
kinetics.
Consequently,
anode
exhibits
high
reversible
capacity
1540
mAh
g
−1
after
500
cycles
at
1
A
.
combination
inert
regulation
expected
alleviate
expansion
problem,
offering
universal
strategy
for
designing
advanced
batteries.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 25, 2024
Abstract
Catalysts
play
a
crucial
role
in
water
electrolysis
by
reducing
the
energy
barriers
for
hydrogen
and
oxygen
evolution
reactions
(HER
OER).
Research
aims
to
enhance
intrinsic
activities
of
potential
catalysts
through
material
selection,
microstructure
design,
various
engineering
techniques.
However,
consumption
has
often
been
overlooked
due
intricate
interplay
among
catalyst
microstructure,
dimensionality,
catalyst–electrolyte–gas
dynamics,
surface
chemistry,
electron
transport
within
electrodes,
transfer
electrode
components.
Efficient
development
high‐current‐density
applications
is
essential
meet
increasing
demand
green
hydrogen.
This
involves
transforming
with
high
into
electrodes
capable
sustaining
current
densities.
review
focuses
on
improvement
strategies
mass
exchange,
charge
transfer,
resistance
decrease
consumption.
It
bridge
gap
between
laboratory‐developed,
highly
efficient
industrial
regarding
structural
catalyst‐electrode
interplay,
outlining
roadmap
hierarchically
structured
electrode‐based
minimizing
loss
electrocatalysts
splitting.
Chemical Reviews,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 11, 2024
Gas
bubbles
generated
by
the
hydrogen
evolution
reaction
and
oxygen
during
water
electrolysis
influence
energy
conversion
efficiency
of
production.
Here,
we
survey
what
is
known
about
interaction
gas
electrode
surfaces
on
practicable
devices
used
for
electrolysis.
We
outline
physical
processes
occurring
life
cycle
a
bubble,
summarize
techniques
to
characterize
phenomena
in
situ
practical
device
environments,
discuss
ways
that
electrodes
can
be
tailored
facilitate
removal
at
high
current
densities.
Lastly,
review
efforts
model
behavior
individual
multiphase
flows
produced
gas-evolving
electrodes.
conclude
our
with
short
summary
outstanding
questions
could
answered
future
electrochemical
environments
or
improved
simulations
flows.
Science,
Journal Year:
2025,
Volume and Issue:
387(6735), P. 791 - 796
Published: Jan. 2, 2025
The
future
deployment
of
terawatt-scale
proton
exchange
membrane
water
electrolyzer
(PEMWE)
technology
necessitates
development
an
efficient
oxygen
evolution
catalyst
with
low
cost
and
long
lifetime.
Currently,
the
stability
most
active
iridium
(Ir)
catalysts
is
impaired
by
dissolution,
redeposition,
detachment,
agglomeration
Ir
species.
Here
we
present
a
ripening-induced
embedding
strategy
that
securely
embeds
in
cerium
oxide
support.
Cryogenic
electron
tomography
all-atom
kinetic
Monte
Carlo
simulations
reveal
synchronizing
growth
rate
support
nucleation
Ir,
regulated
sonication,
pivotal
for
successful
synthesis.
A
PEMWE
using
this
achieves
cell
voltage
1.72
volts
at
current
density
3
amperes
per
square
centimeter
loading
just
0.3
milligrams
degradation
1.33
microvolts
hour,
as
demonstrated
6000-hour
accelerated
aging
test.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 2, 2025
The
sluggish
anodic
oxygen
evolution
reaction
(OER)
in
proton
exchange
membrane
(PEM)
electrolysis
necessitates
applied
bias
to
facilitate
electron
transfer
as
well
bond
cleavage
and
formation.
Traditional
electrocatalysis
focuses
on
analyzing
the
effects
of
transfer,
while
role
charge
accumulation
induced
by
overpotential
has
not
been
thoroughly
investigated.
To
explore
influence
mechanism
bias-driven
accumulation,
capacitive
Mn
is
incorporated
into
IrO
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 7, 2024
Abstract
The
design
of
a
low‐iridium‐loading
anode
catalyst
layer
with
high
activity
and
durability
is
key
challenge
for
proton
exchange
membrane
water
electrolyzer
(PEMWE).
Here,
the
synthesis
novel
supported
IrO
2
nanocatalyst
tri‐layered
structure,
dubbed
@TaO
x
@TaB
that
composed
ultrasmall
nanoparticles
anchored
on
amorphous
TaO
overlayer
TaB
nanorods
reported.
composite
electrocatalyst
shows
great
stability
toward
oxygen
evolution
reaction
(OER)
in
acid,
thanks
to
its
dual‐interface
structural
feature.
electronic
interaction
/TaO
interface
can
regulate
coverage
surface
hydroxyl
groups,
Ir
3+
/
4+
ratio,
redox
peak
potential
enhancing
OER
activity,
while
dense
prevent
further
oxidation
substrate
stabilize
catalytic
layers
improving
during
OER.
be
used
fabricate
an
PEMWE
iridium‐loading
as
low
0.26
mg
cm
−2
.
delivers
current
densities
at
cell
voltages
(e.g.,
3.9
A
@2.0
V),
gives
excellent
retention
more
than
1500
h
2.0
density.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(35)
Published: May 21, 2024
Abstract
Interstitial
filling
of
light
atoms
strongly
affects
the
electronic
structure
and
adsorption
properties
parent
catalyst
due
to
ligand
ensemble
effects.
Different
from
conventional
doping
surface
modification,
constructing
ordered
intermetallic
structures
is
more
promising
overcome
dissolution
reconstruction
active
sites
through
strong
interactions
generated
by
atomic
periodic
arrangement,
achieving
joint
improvement
in
catalytic
activity
stability.
However,
for
tightly
arranged
metal
lattices,
such
as
iridium
(Ir),
obtaining
further
unveiling
their
interstitial
effects
are
still
limited
highly
activated
processes.
Herein,
we
report
a
high‐temperature
molten
salt
assisted
strategy
form
Ir−B
compounds
(IrB
1.1
)
with
boron
(B)
atoms.
The
B
residing
lattice
Ir
constitutes
favorable
surfaces
donor‐acceptor
architecture,
which
has
an
optimal
free
energy
uphill
rate‐determining
step
(RDS)
oxygen
evolution
reaction
(OER),
resulting
enhanced
activity.
Meanwhile,
coupling
structural
units
suppresses
demetallation
behavior
Ir,
ensuring
Such
B‐induced
endow
IrB
higher
OER
performance
than
commercial
IrO
2
,
validated
proton
exchange
membrane
water
electrolyzers
(PEMWEs).
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 20, 2024
Abstract
Achieving
robust
long‐term
durability
with
high
catalytic
activity
at
low
iridium
loading
remains
one
of
great
challenges
for
proton
exchange
membrane
water
electrolyzer
(PEMWE).
Herein,
we
report
the
low‐temperature
synthesis
oxide
foam
platelets
comprising
edge‐sharing
IrO
6
octahedral
honeycomb
framework,
and
demonstrate
structural
advantages
this
material
multilevel
tuning
anodic
catalyst
layer
across
atomic‐to‐microscopic
scales
PEMWE.
The
integration
foam‐like
texture
platelet
morphology
into
a
single
system
assures
generation
exposure
highly
active
stable
sites
oxygen
evolution
reaction
(OER),
while
facilitating
reduction
both
mass
transport
loss
electronic
resistance
layer.
As
proof
concept,
electrode
assembly
in
single‐cell
PEMWE
based
on
honeycomb‐structured
x
platelets,
(~0.3
mg
Ir
/cm
2
),
is
demonstrated
to
exhibit
ampere‐level
current
densities
remain
more
than
2000
hours.
Materials Horizons,
Journal Year:
2025,
Volume and Issue:
12(6), P. 1757 - 1795
Published: Jan. 1, 2025
Noble
metal-based
oxide
electrocatalysts
are
essential
for
the
development
of
H
2
production
technology
by
water
electrolysis,
and
this
review
summarises
recent
research
progress
noble
metal
oxides
in
field
electrolysis.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 16, 2025
Abstract
Engineering
nanomaterials
at
single‐atomic
sites
can
enable
unprecedented
catalytic
properties
for
broad
applications,
yet
it
remains
challenging
to
do
so
on
RuO
2
‐based
electrocatalysts
proton
exchange
membrane
water
electrolyzer
(PEMWE).
Herein,
the
rational
design
and
construction
of
Bi‐RuO
single‐atom
alloy
oxide
(SAAO)
are
presented
boost
acidic
oxygen
evolution
reaction
(OER),
via
phase
engineering
a
novel
hexagonal
close
packed
(
hcp
)
RuBi
alloy.
This
SAAO
electrocatalyst
exhibits
low
overpotential
192
mV
superb
stability
over
650
h
10
mA
cm
−2
,
enabling
practical
PEMWE
that
needs
only
1.59
V
reach
1.0
A
under
industrial
conditions.
Operando
differential
electrochemical
mass
spectroscopy
analysis,
coupled
with
density
functional
theory
studies,
confirmed
adsorbate‐evolving
mechanism
incorporation
Bi
1
improves
activity
by
electronic
optimization
hindering
surface
Ru
demetallation.
work
not
introduces
new
strategy
fabricate
high‐performance
atomic‐level,
but
also
demonstrates
their
potential
use
in
electrolyzers.