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:
2023,
Volume and Issue:
11(50), P. 17564 - 17594
Published: Dec. 6, 2023
Proton
exchange
membrane
water
electrolysis
(PEMWE)
is
considered
the
most
compatible
technology
with
intermittent
renewable
energies
for
clean
hydrogen
generation.
More
than
that,
compared
alkaline
electrolyzers,
totality
of
practicality
enhances
due
to
obvious
advantages
such
as
efficiency,
high
purity,
low
operation
pressure,
etc.
However,
sluggish
four-electron-transfer
reaction
oxygen
evolution
(OER),
which
involves
complex
intermediates
and
multiple
steps,
significantly
impacts
overall
efficiency
PEMWE.
Therefore,
developing
highly
efficient,
stable,
low-cost
high-tech
electrocatalysts
acidic
OER
crucial.
In
comparison
expensive
commercial
iridium
or
oxide
electrocatalyst,
Ru
oxides
are
much
cheaper
alternatives
that
demonstrate
superior
catalytic
performance
OER.
this
perspective,
generally
accepted
mechanisms
including
AEM
LOM
introduced
corresponding
pathways.
Then,
Ru-based
explicated
on
performances
OER,
include
metal
metal-based
alloys,
RuO2-based
catalysts,
solid
solutions,
perovskites,
pyrochlores,
single
atoms,
other
catalysts.
Finally,
challenges
future
research
perspectives
catalysts
discussed.
Energy Reviews,
Journal Year:
2024,
Volume and Issue:
3(4), P. 100103 - 100103
Published: July 16, 2024
This
article
presents
a
strategy
for
enhancing
the
catalytic
performance
and
stability
of
anodic
electrocatalysts
in
proton
exchange
membrane
(PEM)
water
splitting.
PEM
splitting
is
sustainable
method
producing
hydrogen
oxygen
from
utilizing
electrocatalysts.
However,
employed
this
process
are
crucial
its
commercialization
due
to
harsh
condition
causing
low
stability.
The
main
focus
review
strategies
improving
as
well
electrocatalysts,
such
doping
with
heteroatoms,
alloying
other
metals.
results
demonstrate
that
these
modifications
can
significantly
enhance
These
open
new
possibilities
development
efficient
stable
splitting,
paving
way
widespread
use
clean
energy
applications.
Green Energy & Environment,
Journal Year:
2023,
Volume and Issue:
9(6), P. 937 - 948
Published: Dec. 13, 2023
RuO2
has
been
considered
a
potential
alternative
to
commercial
IrO2
for
the
oxygen
evolution
reaction
(OER)
due
its
superior
intrinsic
activity.
However,
inherent
structure
dissolution
in
acidic
environments
restricts
applications.
In
this
study,
we
report
novel
Pd-doped
ruthenium
oxide
(Pd-RuO2)
nanosheet
catalyst
that
exhibits
improved
activity
and
stability
through
synergistic
effect
of
Pd
modulation
Ru
electronic
two-dimensional
structure.
The
excellent
performance,
achieving
an
overpotential
only
204
mV
at
current
density
10
mA
cm-2.
Impressively,
after
undergoing
8000
cycles
cyclic
voltammetry
testing,
merely
decreased
by
5
mV.
PEM
electrolyzer
with
Pd0.08Ru0.92O2
as
anode
survived
almost
130
h
operation
200
To
elucidate
underlying
mechanisms
responsible
enhanced
stability,
conducted
X-ray
photoelectron
spectroscopy
(XPS)
analysis,
which
reveals
electron
transfer
from
effectively
circumvents
over-oxidation
Ru,
thus
playing
crucial
role
enhancing
catalyst's
stability.
Furthermore,
functional
theory
(DFT)
calculations
provide
compelling
evidence
introduction
into
modulates
correlations
facilitates
thereby
preventing
Ru.
Additionally,
application
inhibited
aggregation
growth
nanoparticles,
further
bolstering
structural
integrity
catalyst.
ACS Catalysis,
Journal Year:
2024,
Volume and Issue:
15(2), P. 768 - 779
Published: Dec. 25, 2024
Effective
local
electron
regulation
in
ruthenium-based
catalysts
acidic
oxygen
evolution
reactions
(OER)
remains
a
key
challenge.
The
lack
of
unified
understanding
catalyst
activity
and
stability
based
on
limits
the
further
development
proton
exchange
membrane
water
electrolysis
(PEMWE).
In
this
study,
we
develop
concept
coordination
unsaturated
Ti
(TiOCU)
sites.
Based
constructed
dual-oxide
heterojunction
interface
Ru/TiOx
catalyst,
achieve
precise
modulation
d-electron
orbitals
Ru
charge
redistribution
between
Ru–Obridge–TiOCU
units
strengthened
Ru–O
bonds
suppresses
formation
high-valence
species
deactivation
catalyst.
Combined
with
density
functional
theory
(DFT)
calculations
situ
spectroscopic
experiments,
confirm
that
dz2
orbital
significantly
optimizes
deprotonation
process
interfacial
hydroxyl-rich
interface,
thereby
enhancing
OER
kinetics
dominance
adsorbed
mechanism
(AEM).
Consequently,
exhibits
superior
performance,
achieving
current
10
mA/cm2
at
an
overpotential
only
237
mV
0.5
M
H2SO4,
demonstrates
for
over
160
h.
This
work
reveals
application
TiOCU,
providing
perspective
transition
metal
defect
materials
electrolysis.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 1, 2025
Green
hydrogen
production
via
proton
exchange
membrane
water
electrolysis
(PEMWE)
faces
economic
feasibility
challenges,
primarily
due
to
its
reliance
on
noble
metal
catalysts.
While
cost-effective
Ru-based
catalysts
show
promise
as
alternatives
expensive
Ir-based
for
an
anodic
oxygen
evolution
reaction,
their
long-term
performance
is
compromised
by
overoxidation
at
high
current
densities.
In
addressing
this
challenge,
we
present
a
cooperative
dual-site
strategy
atomic-scale
incorporation
of
high-valent
d0-metal
cations
into
RuO2.
This
synthesis
results
in
uniformly
distributed
Ru-O-d0metal
bonds,
effectively
reconciling
the
activity
and
stability
trade-off.
Leveraging
these
effects,
our
optimized
Ta1/RuO2
catalyst
demonstrates
exceptional
performance,
with
low
overpotential
164
±
2
mV
stable
operation
1000
h
100
mA
cm-2.
practical
PEMWE
systems,
achieves
1.58
V
A
cm-2,
surpassing
2026
Department
Energy
target,
maintains
remarkable
over
650
500
breakthrough
offers
highly
active
durable
system
suitable
industrial-scale
applications.
Applied Physics Reviews,
Journal Year:
2024,
Volume and Issue:
11(2)
Published: May 22, 2024
The
utilization
of
water
electrolysis
for
green
hydrogen
(H2)
production,
powered
by
renewable
energy,
is
a
promising
avenue
sustainable
development.
Proton-exchange-membrane
(PEMWE)
stands
out
as
one
the
most
efficient
H2
production
technologies.
However,
implementing
it
on
an
industrial
scale
faces
substantial
challenges,
particularly
regarding
oxygen
evolution
reaction
(OER).
OER,
critical
process
with
inherently
slow
kinetics
requiring
additional
potential,
significantly
influences
overall
water-splitting
efficiency.
Most
OER
electrocatalysts
in
PEMWE
struggle
poor
stability
harsh
acidic
environments
at
high
oxidative
potentials.
While
rare-earth
metal
oxides,
such
iridium
or
ruthenium
offer
commercial
oxygen-evolving
(OECs),
their
use
depends
achieving
economically
and
sustainably
viable
operations.
An
alternative
approach
involves
developing
low-
non-noble
metal-based
OECs
sustaining
activity
long-term
durability.
Although
materials
currently
exhibit
lower
than
noble-based
OECs,
notable
progress
has
been
made
enhancing
performance.
This
review
provides
overview
recent
advancements
designing
acidic-stable
based
low
without
noble
contents.
It
delves
into
thermodynamics
degradation
mechanisms
media,
evaluation
parameters
stability,
strategies
active
acid-stable
challenges
opportunities
acid
electrolysis.
Through
detailed
analysis
these
aspects,
aims
to
identify
engineering
actively
durable
OECs.
ACS Applied Energy Materials,
Journal Year:
2024,
Volume and Issue:
7(3), P. 941 - 950
Published: Jan. 12, 2024
Developing
an
active,
affordable,
and
stable
catalyst
for
efficient
oxygen
evolution
during
water
electrolysis
remains
a
formidable
task
in
contemporary
research.
The
sluggish
kinetics
of
the
reaction
(OER)
continues
to
impede
overall
efficiency
process.
A
comprehensive
approach
is
demonstrated
here
develop
multiple
catalytic
active
components
into
single
system
by
means
integrating
bimetallic
hydroxide
(NiFe(OH)x)
with
amorphous
molybdenum
sulfide
(MoSx)
heterostructure
using
rational
strategies.
This
proposed
fabrication
strategy
enables
activity
be
enhanced
fast
electron
transfer,
resulting
OER
strong
alkaline
media
through
synergistic
effects
effective
modulation
electronic
interactions.
Moreover,
composite
electrode
(MoSx/NiFe(OH)x/NF)
displayed
lowest
overpotential
Tafel
slope
298
mV
at
50
mA
cm–2
47.25
dec–1,
respectively,
as
well
good
stability
under
large
currents
over
prolonged
period
48
h
without
degradation.
found
dynamically
reform
surface
layer's
phase
after
catalyzing
reactions
serve
oxidation.
These
results
have
not
only
led
development
robust
electrocatalyst
but
also
opened
up
several
possibilities
developing
multicomponent
electrocatalytic
systems
one
material
that
can
integrated
conventional
designs.