Advanced Science,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 11, 2024
Oxygen
evolution
reaction
(OER)
is
an
indispensable
anode
for
sustainable
hydrogen
production
from
water
electrolysis,
yet
overreliance
on
metal-based
catalysts
featured
with
vibrant
d-electrons.
It
still
has
notable
gap
between
metal-free
and
electrocatalysts,
due
to
lacking
accurate
efficient
p-band
regulation
methods
non-metal
atoms.
Herein,
a
molecular
modularization
strategy
proposed
fine-tuning
the
p-orbital
states
of
series
covalent
organic
frameworks
(COFs)
realizing
OER
performance
beyond
benchmark
precious
metal
catalysts.
Optimized
combination
benzodioxazole/benzodiimide-based
building
blocks
achieves
impressive
applied
potential
1.670
±
0.004
V
versus
reversible
electrode
(RHE)
1.735
0.006
RHE
deliver
enhanced
current
densities
0.5
1.0
A
cm
eScience,
Journal Year:
2024,
Volume and Issue:
unknown, P. 100295 - 100295
Published: July 1, 2024
The
development
of
low-cost
and
efficient
electrocatalysts
for
oxygen
evolution
reaction
(OER)
in
acid
electrolytes
is
critical
to
the
widespread
implementation
proton
electrolyte
membrane
water
electrolyzers
(PEMWE)
towards
carbon
neutralization.
Noble
metal
Ir-
Ru-based
materials
are
state-of-the-art
catalysts
but
still
suffer
from
prohibitive
price
scarcity.
In
this
context,
a
variety
noble
metal-free
have
been
developed
decrease
cost
PEMWE.
review,
we
first
summarize
activity
expression
mechanism
stability
issues
non-precious
catalysts,
highlighting
origins
performance
degradation
possible
mitigation
strategies.
Then,
systematically
review
several
recently
focusing
on
design
rationale
structure-performance
relation.
Finally,
prospects
non-noble
prospected,
with
potential
challenges
practical
applications
presented.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 7, 2024
Abstract
Developing
high‐activity
non‐noble
metal
catalysts
for
improving
the
ability
of
water
dissociation
and
H*
adsorption/desorption
in
hydrogen
evolution
reaction
(HER)
process
alkaline
neutral
electrolytes
is
essential
but
remains
challenging.
Herein,
a
Mo‐doped
NiCoCu
alloy
with
tuned
tensile
strain
localized
electrons
designed
synthesized
by
combining
solvothermal
annealing
methods
achieving
ampere‐level
HER
performance.
Theoretical
calculation
results
prove
that
Mo
doping
induces
lattice
(electrons
from
to
Ni/Co/Cu
atoms),
promoting
adsorption
O*
H
2
O
molecules
on
Co
sites
accelerating
dissociation.
Therefore,
NiCoCu‐Mo
0.078
/CF
(CF
=
copper
foam)
shows
low
energy,
providing
sufficient
during
process.
Meanwhile,
its
Gibbs
free
energy
value
near
zero,
implying
rapid
Electrochemical
show
achieves
better
intrinsic
activity
both
1.0
m
KOH
(
η
−10
/η
−1000
35/212
mV)
phosphate
buffer
solution
24/256
compared
0
0.163
/CF,
it
can
continuously
operate
100
h
at
mA
cm
−2
.
This
work
sustainable
way
design
high‐performance
electrolysis
proposes
well‐performing
catalyst.
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 3, 2025
Abstract
Fine
control
over
the
Ir
precursor
to
Nickel‐based
layered
double
hydroxides
(LDHs)
is
significant
for
decorating
both
single
atoms
(SA)
and
nanoclusters
(NC),
thus
modulating
catalytic
kinetics
improving
overall
performance.
In
this
study,
NiMn‐LDH
synthesized
co‐decorated
it
with
Iridium,
introducing
a
new
pathway
developing
efficient
bifunctional
electrocatalysts
in
water‐splitting
technologies.
Additionally,
typical
fibrous
material
has
developed
by
immobilizing.
onto
PAN
(polyacrylonitrile)
nanofibers
()
using
feasible
electrospinning
technique.
Notably,
catalyst
exhibits
low
overpotentials
of
249
110
mV
oxygen
(OER)
hydrogen
evolution
reactions
(HER)
at
10
mA
cm
−
2
,
cell
voltage
1.65
V
total
water
splitting
(TWS).
remained
stable
effective
alkaline
OER,
HER,
TWS
50
h.
Furthermore,
X‐ray
adsorption
near‐edge
spectrum
(XANES)
experiments,
together
theoretical
calculations,
show
that
synergistic
effect
SA
which
helps
enhance
activity,
promoting
electron
rearrangement
lowering
reaction
energy
barrier.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(48)
Published: Aug. 22, 2024
Abstract
The
development
of
electricity‐driven
oxygen
evolution
reaction
(OER)
is
a
potent
solution
for
energy
storage
applications.
In
recent
years,
there
surge
in
interest
designing
transition
metal‐based
catalysts
with
stable
linkages,
presenting
an
efficient
alternative
to
noble
electrocatalysts.
Transition
metal
complexes
linked
by
salen
ligands
garner
considerable
attention
due
their
capacity
chelate
and
stabilize
ions.
This
work
presents
novel
approach
strategically
incorporating
the
metal–salen
core
into
porous
organic
polymer
(POP)
backbone,
thereby
fabricating
highly
effective
electrocatalyst
evolution.
judicious
selection
active
sites,
coupled
intramolecular
free
volume
(IMFV)
triptycene
high
specific
surface
area
salen–POPs,
result
superior
OER
activity.
By
precisely
tuning
structure
through
variation
unit,
deep
insights
are
gained
electrocatalytic
behavior.
Notably,
most
catalyst,
Ni‐DHDA‐TAT,
exhibits
impressively
low
overpotential
(
η
10
)
≈
270
mV
at
current
density
mA
cm
−2
(in
1
m
KOH).
Further,
Ni‐DHDA‐TAT
retains
its
activity
even
after
50
h
chronoamperometry
1000
cyclic
voltammetry
cycles
negligible
degradation
initial
performance.
Small,
Journal Year:
2024,
Volume and Issue:
20(43)
Published: June 28, 2024
As
the
anode
reaction
of
proton
exchange
membrane
water
electrolysis
(PEMWE),
acidic
oxygen
evolution
(OER)
is
one
main
obstacles
to
practical
application
PEMWE
due
its
sluggish
four-electron
transfer
process.
The
development
high-performance
OER
electrocatalysts
has
become
key
improving
kinetics.
To
date,
although
various
excellent
have
been
widely
researched,
Ir-based
nanomaterials
are
still
state-of-the-art
electrocatalysts.
Hence,
a
comprehensive
and
in-depth
understanding
mechanism
crucial
for
precise
optimization
catalytic
performance.
In
this
review,
origin
nature
conventional
adsorbate
(AEM)
derived
volcanic
relationship
on
processes
summarized
some
strategies
based
AEM
introduced.
further
investigate
strategy
electrocatalysts,
several
unconventional
mechanisms
including
dual-site
lattice
mediated
mechanism,
their
applications
introduced
in
detail.
Thereafter,
active
species
at
classified
into
surface
Ir
O
species.
Finally,
future
direction
prospect
put
forward.
ACS Materials Letters,
Journal Year:
2024,
Volume and Issue:
unknown, P. 3625 - 3666
Published: July 15, 2024
Hydrogen
energy,
heralded
as
a
novel,
clean,
and
highly
efficient
energy
source,
stands
at
the
forefront
of
initiatives
aimed
decarbonizing
fostering
sustainable
carbon-neutral
economy.
Recent
strides
in
hydrogen
production
through
water
splitting
have
marked
significant
progress,
leveraging
its
inherent
benefits,
such
zero
carbon
emissions,
safety,
exceptional
product
purity.
Despite
these
advancements,
challenges
persist
surmounting
substantial
barrier
water-splitting
costs.
Many
electrocatalysts
been
innovatively
designed
reported
to
address
hurdles.
However,
translation
advances
into
industrial-scale
applications
faces
multifaceted
obstacles.
Urgent
demands
for
high-performance
meeting
industrial
standards
underscore
imperative
deeper
comprehension
systems.
This
review
delves
latest
developments
electrolysis,
synthesizing
experimental
findings
promising
strategies
with
different
electrochemical
parameters
along
high
entropy
metals,
doping
engineering,
interface
construction,
defect
engineering.
considerable
creating
numerous
recent
investigations,
persist,
impeding
widespread
implementation
electrolytic
splitting.
By
providing
comprehensive
overview,
this
aims
furnish
knowledge-driven
framework
fundamental
science
while
inspiration
technical
engineering
endeavors
craft
tailored
ACS Applied Nano Materials,
Journal Year:
2025,
Volume and Issue:
8(4), P. 1749 - 1761
Published: Jan. 21, 2025
In
recent
years,
the
oxygen
evolution
reaction
(OER)
has
garnered
considerable
attention
as
a
pivotal
process
for
water
electrolysis.
The
progress
of
this
hinges
on
efficacy
catalyst.
present
study,
role
DNA
origami-assembled
gold
nanobipyramid
(Au
NBP)
dimer
structure
was
explored
initiating
electrocatalytic
activity
water-splitting
reaction.
Through
strategic
integration
origami
technology
and
Au
NBPs,
study
aims
to
orchestrate
precise
modulation
electrocatalyst
architecture
achieve
unprecedented
levels
in
OER.
NBP
catalyst
exhibits
lowest
overpotential
146
mV
at
current
density
10
mAcm–2
compared
with
its
various
constituents.
configuration
optimizes
exposure
catalytically
active
sites
promotes
efficient
charge
transfer
pathways
due
presence
origami.
This
endeavors
unlock
new
frontiers
material
design,
paving
way
toward
sustainable
energy
technologies
enhanced
efficiency
scalability.