Nanoscale,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 1, 2024
Hydrogen
production
by
proton
exchange
membrane
water
electrolysis
requires
an
anode
with
low
overpotential
for
oxygen
evolution
reaction
(OER)
and
robustness
in
acidic
solution.
While
exploring
new
electrode
materials
to
improve
the
performance
durability,
optimizing
morphology
of
typical
using
methods
is
a
big
challenge
science.
RuO
ACS Sustainable Chemistry & Engineering,
Journal Year:
2024,
Volume and Issue:
12(11), P. 4551 - 4564
Published: March 1, 2024
A
metal–organic
framework
(MOF)
embedded
by
transition
metal
sulfide
(TMS)
particles
is
one
of
the
promising
electrocatalyst
candidates
for
overall
water
splitting
(OWS)
due
to
large
surface
area
and
abundant
active
sites
from
MOF
precursor,
as
well
tunable
electronic
structure
higher
intrinsic
conductivity
TMS.
More
importantly,
its
self-restructuring
under
alkaline
conditions
will
lead
chemical
composition
phase
evolution
catalyst
surface,
which
source
further
enhanced
catalytic
activity.
semi-MOF
(labeled
Co@Ni/Fe-MS/MOF)
with
semisacrificial
template
a
TMS
particle
guest
was
designed
exercisable
universal
heteroatomic
Co
doping
partial
vulcanization.
The
TMS/MOF
heterostructure
establishes
an
ideal
bridge
electron
transfer.
Simultaneously,
dopant
synergistic
effect
multiple
also
effectively
regulate
charge
environment
around
sites,
jointly
improve
adsorption/desorption
kinetics
reaction
intermediates.
As
result,
Co@Ni/Fe-MS/MOF
exhibits
distinguished
overpotential
(η10
=
229
mV
OER,
η10
174
HER)
Tafel
slope
(52.37/114.35
dec–1
OER/HER),
unrivaled
long-term
durability
(80
h
OWS).
Moreover,
two-electrode
∥
cell
illustrates
small
voltage
1.54
V
achieve
power
10
mA
cm–2.
Impressively,
this
superior
OER
property
comes
three-layer
sandwich
restructured
hybrid
semi-MOFs
in
true
sites.
This
work
aspired
catalyst,
induce
effects,
shed
light
on
preparation
materials
heterogeneous
interface
engineering,
evolution.
Nano Letters,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 13, 2024
Electrochemical
acidic
oxygen
evolution
reaction
(OER)
is
an
important
part
for
water
electrolysis
utilizing
a
proton
exchange
membrane
(PEM)
apparatus
industrial
H
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 23, 2025
Abstract
The
oxygen
evolution
reaction
(OER)
in
proton
exchange
membrane
water
electrolyzers
(PEMWE)
has
long
stood
as
a
formidable
challenge
for
green
hydrogen
sustainable
production,
hindered
by
sluggish
kinetics,
high
overpotentials,
and
poor
durability.
Here,
these
barriers
are
transcended
through
novel
material
design:
strategic
engineering
of
high‐density
grain
boundaries
within
solid‐solution
Ru
0.8
Ir
0.2
O
x
ultrathin
nanosheets.
These
carefully
tailored
synergistic
Ir─Ru
interactions,
reduce
the
coordination
atoms
optimize
distribution
charge,
thereby
enhancing
both
catalytic
activity
stability
nanosheets,
verified
merely
requiring
an
overpotential
189
mV
to
achieve
10
mA
cm
−2
acidic
electrolyte.
In
situ
electrochemical
techniques,
complemented
theoretical
calculations,
reveal
that
OER
follows
adsorption
mechanism,
demonstrating
pivotal
role
boundary
electronic
modulation
accelerating
kinetics.
Most
notably,
exhibits
outstanding
industrial‐scale
performance
PEMWE,
reaching
4.0
A
at
2
V
maintaining
>1000
h
500
.
This
efficiency
reduces
production
costs
$0.88
kg
−1
work
marks
transformative
step
forward
designing
efficient,
durable
catalysts,
offering
promising
pathway
toward
technologies
advancing
global
transition
energy.
ACS Sustainable Chemistry & Engineering,
Journal Year:
2024,
Volume and Issue:
12(6), P. 2313 - 2323
Published: Jan. 27, 2024
The
proton
exchange
membrane
(PEM)
water
hydrolyzer
is
crucial
to
promoting
the
sustainable
development
of
hydrogen
energy
and
facilitating
large-scale
transformation.
However,
achieving
sustained
stable
oxygen
evolution
reaction
(OER)
in
acidic
solutions
presents
a
significant
challenge
for
noniridium
based
electrocatalysts.
Herein,
we
develop
Co3O4-supported
RuO2
electrocatalyst
with
optimized
catalyst–support
interface
interactions
breaking
activity–stability
trade-off
relationship
OER.
Through
detailed
electrochemical
experiments
characterization
analysis,
demonstrate
that
crystal
growth
Co3O4
support
can
be
precisely
regulated
by
modifying
ligand
layer-confined
domain
cobalt-based
metal–organic
frameworks
(Co-MOF)
precursor,
thereby
optimizing
RuO2/Co3O4
interface.
Due
weakened
self-sacrifice
effect
Co3O4,
active
heterogeneous
electron
interaction
impeccable
coating
effect,
OER
stability
RuO2/Co3O4–B3DC
significantly
improved
compared
while
preserving
intrinsic
activity.
Theoretical
modeling
suggests
formation
optimizes
adsorption
intermediates,
process.
Additionally,
anode
demonstrates
promising
potential
application
PEM
electrolyzers
variety
renewable
energy-driven
electrolytic
cells.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 3, 2024
Abstract
Polymetallic
oxides
with
extraordinary
electrons/geometry
structure
ensembles,
trimmed
electron
bands,
and
way‐out
coordination
environments,
built
by
an
isomorphic
substitution
strategy,
may
create
unique
contributing
to
concertedly
catalyze
water
oxidation,
which
is
of
great
significance
for
proton
exchange
membrane
electrolysis
(PEMWE).
Herein,
well‐defined
rutile
InSnRuO
2
density‐controllable
oxygen
vacancy
(Ov)‐free
polarons
are
firstly
fabricated
in
situ
substitution,
using
trivalent
In
species
as
Ov
generators
the
adjacent
metal
ions
donors
form
orderly
concerted
In‐Ov‐Ru‐O‐Sn
substructures
tetravalent
oxides.
For
acidic
obtained
displays
ultralow
overpotential
183
mV
(versus
RHE)
a
mass
activity
(MA)
103.02
A
mg
Ru
−1
,
respectively.
long‐term
stability
test
PEMWE,
it
can
run
at
low
unchangeable
cell
potential
(1.56
V)
200
h
50
mA
cm
−2
far
exceeding
current
IrO
||Pt/C
assembly
0.5
m
H
SO
4
.
Accelerated
degradation
testing
results
PEMWE
pure
electrolyte
show
no
significant
increase
voltage
even
when
gradually
increased
from
1
5
The
remarkably
improved
performance
associated
stabilized
dense
Ov‐electron
polarons,
synergistically
activates
band
sites
then
boosting
evolution
kinetics.
More
importantly,
self‐trapped
polaron
induces
decrease
entropy
enthalpy,
efficiently
hinder
atoms
leaching
increasing
lattice
atom
diffusion
energy
barrier,
achieves
oxide.
This
work
open
door
design
next‐generation
Ru‐based
catalysts
asymmetric
active
efficient
electrocatalysis
application.
Journal of Materials Science,
Journal Year:
2024,
Volume and Issue:
59(23), P. 10193 - 10206
Published: June 1, 2024
Abstract
An
amphiphilic
block
copolymer,
poly
(styrene-2-polyvinyl
pyridine-ethylene
oxide),
was
used
as
a
structure-directing
and
stabilizing
agent
to
synthesize
TiO
2
/RuO
nanocomposite.
The
strong
interaction
of
polymers
with
metal
precursors
led
formation
porous
heterointerface
.
It
acted
bridge
for
electron
transport,
which
can
accelerate
the
water
splitting
reaction.
Scanning
microscopy,
energy-dispersive
X
-ray
spectroscopy,
transmission
diffraction
analysis
samples
revealed
successful
fabrication
nanocomposites.
nanocomposites
were
measure
electrochemical
in
three-electrode
systems
0.1-M
KOH.
Electrochemical
activities
unveil
that
-150
displayed
superior
oxygen
evolution
reaction
activity,
having
low
overpotential
260
mV
Tafel
slope
80
mVdec
−1
Graphical
abstract
Energy & Fuels,
Journal Year:
2024,
Volume and Issue:
38(13), P. 11521 - 11540
Published: June 18, 2024
Proton
exchange
membrane
water
electrolysis
(PEMWE)
technology
is
seen
as
the
most
compatible
hydrogen
production
with
renewable
energy
generation.
However,
sluggish
kinetics
of
anodic
oxygen
evolution
reaction
(OER)
and
scarcity
acid-resistant,
high-activity,
low-cost
catalysts
have
seriously
hindered
overall
efficiency
manufacturing
costs
PEMWE.
Recently,
ruthenium
(Ru)-based
materials
gradually
attracted
attention
due
to
their
suitable
binding
strength
toward
intermediates
lowest
price
in
noble
metal
family.
Herein,
great
achievements
progress
Ru-based
acidic
OER
electrocatalysts
are
comprehensively
reviewed,
which
started
a
general
description
mechanisms
situ
characterization
techniques
understand
structure–activity
relationships.
Subsequently,
some
typical
strategies
enhance
activity
stability
highlighted.
Insights
from
synthesis
methods,
advanced
characterizations,
intermediate
evolution,
theoretical
calculations
provided,
together
our
viewpoints
on
daunting
challenges
future
endeavors
for
practical
employment.
Advanced Sustainable Systems,
Journal Year:
2024,
Volume and Issue:
8(11)
Published: July 9, 2024
Abstract
Spinel
metal
oxides
are
extensively
studied
for
supercapacitors
(SCs)
in
alkaline
electrolytes,
where
charge
storage
capacity
is
limited
by
surface
site
availability
due
to
reconstruction
forming
hydroxides/oxyhydroxides.
The
use
of
an
acidic
medium,
which
can
boost
the
spinel
offering
additional
channel
intercalation‐deintercalation
protons,
underexplored.
Moreover,
impact
chemical
compositions
and
cationic
distributions
crucial
on
electrocatalysis
performance
oxides,
however,
such
a
correlation
first
time
reported
properties
ferrite
NiFe
2
O
4
nanoparticles
(NFO
NPs).
Besides,
low‐cost
scalable
synthesis
NFO
NPs
involving
thermal
decomposition
Ni‐Fe
glycolate,
followed
controlled
air‐calcination
reported.
Thus
crafted
NPs‐based
device
shows
impressive
specific
capacitance
(2112
F
g
−1
at
10
A
)
half‐cell
configuration.
flexible
all‐solid‐state
asymmetric
(full‐cell)
configuration
depicts
energy
density
(20.7
Wh
kg
),
power
(4000
W
gravimetric
(140
retention
its
(≈75%
after
10,000
charging/discharging
cycles).
results
depict
new
insight
toward
tuning
electronic
NFO,
otherwise
predominately
attributed
only
crystallite
size
morphological
effects.