ACS Applied Materials & Interfaces,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 23, 2025
The
electrocatalytic
urea
oxidation
reaction
(UOR)
is
a
promising
approach
to
lowering
the
energy
barrier
of
anode
half-reaction
in
water
splitting
for
energy-efficient
hydrogen
production
and
remove
excess
from
blood
or
dialysis
fluid.
However,
sluggish
kinetics
large
overpotential
caused
by
scaling
relationships
significantly
limit
development
UOR
technology.
Herein,
bifunctional
amorphous
M-CoS
(M
=
Zr,
Cu,
Mn,
Fe)
nanosheets
were
synthesized
via
one-step
electrodeposition
process.
Among
them,
Zr-CoS
exhibited
exceptional
performance,
achieving
10
mA
cm-2
at
an
1.26
V,
outperforming
recently
reported
catalysts,
while
CoS
demonstrated
evolution
impressively
low
-175
mV.
Density
functional
theory
calculations
revealed
that
doped
Cu
Zr
ions
migrated
adsorption
sites
N
atoms
before
after
C-N
cleavage,
breaking
limitation
relationships.
Meanwhile,
cleavage
step
showed
good
linear
relationship
with
variation
integrated
crystal
orbital
Hamilton
population
(ΔICOHP),
indicating
ΔICOHP
was
descriptor
evaluate
performances.
This
work
not
only
emphasized
outstanding
performances
but
also
offered
innovative
insights
into
role
metal
sulfides
UOR.
Water
dissociation
in
anion
exchange
membrane
water
electrolysis
(AEMWE)
faces
significant
energy
barriers,
posing
a
challenge
for
reducing
cell
voltage.
Herein,
we
engineered
CoP
nanosheets
by
doping
Er
and
hybridizing
with
NiCoP
to
optimize
local
electronic
states
accelerate
H2O
during
the
hydrogen
evolution
reaction.
The
resulting
Er0.1-CoP/NiCoP
catalyst
achieves
low
overpotential
of
154
mV
at
-500
mA
cm-2
1.0
M
KOH.
An
AEM
electrolyzer
comprising
an
Er0.1-CoP/NiCoP@NF
cathode
demonstrates
voltage
1.672
V
stability
exceeding
1000
h
500
(50
°C).
Characterization,
density
functional
theory
(DFT)
calculations,
ab
initio
molecular
dynamics
(AIMD)
simulations
reveal
that
hybridization
synergistically
modulate
charge
distribution
across
multisites,
shifting
p-band
centers
away
from
Fermi
level.
These
adjustments
free
H*
adsorption
(ΔGH*)
improve
OH*/H2O*
adsorption,
thereby
facilitating
H2
evolution.
Journal of the American Chemical Society,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 8, 2025
Electrochemical
H2
production
from
water
favors
low-voltage
molecular
oxidation
to
replace
the
oxygen
evolution
reaction
as
an
energy-saving
and
value-added
approach.
However,
there
exists
a
mismatch
between
high
demand
for
slow
anodic
reactions,
restricting
practical
applications
of
such
hybrid
systems.
Here,
we
propose
bipolar
approach,
with
generation
N–N
oxidatively
coupled
dehydrogenation
(OCD)
3,5-diamino-1H-1,2,4-triazole
(DAT),
in
addition
cathodic
generation.
The
system
requires
relatively
low
potentials
0.872
1.108
V
vs
RHE
reach
10
500
mA
cm–2,
respectively.
H-type
electrolyzer
only
0.946
1.129
deliver
100
respectively,
electricity
consumption
(1.3
kWh
per
m3
H2)
reduced
by
68%,
compared
conventional
splitting.
Moreover,
process
is
highly
appealing
due
absence
traditional
hazardous
synthetic
conditions
azo
compounds
at
anode
crossover/mixing
H2/O2
electrolyzer.
A
flow-type
operates
stably
cm–2
300
h.
Mechanistic
studies
reveal
that
Pt
single
atom
nanoparticle
(Pt1,n)
optimize
adsorption
S
active
sites
over
Pt1,n@VS2
catalysts.
At
anode,
stepwise
−NH2
DAT
then
oxidative
coupling
−N–N–
predominantly
form
while
generating
H2.
present
report
paves
new
way
atom-economical
aminotriazole
green
electrosynthesis
chemicals.
Advanced Sustainable Systems,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 12, 2025
Abstract
Water
electrolysis
represents
the
primary
method
to
produce
green
hydrogen.
Nevertheless,
during
water
electrolysis,
particularly
at
high
current
densities,
a
large
number
of
gas
bubbles
generated
are
difficult
detach
from
electrode,
triggering
series
negative
effects
such
as
active
site
covering,
ionic
conductance
block,
and
catalyst
deactivation,
which
in
turn
reduces
efficiency.
In
recent
years,
flexible
electrocatalysts
have
been
developed
address
this
issue
well,
with
superior
characteristics
including
mechanical
deformability,
optimization,
mass
transfer
efficiency,
structural
stability.
The
advanced
development
electrocatalyst
engineering
for
is
urgently
needed
be
systematically
reviewed.
Here,
first,
summarized
deeply
understand
their
impact
on
performance.
Second,
strategies
design
based
2D
nanosheets
fern‐like
structure
comprehensively
introduced.
Last
but
not
least,
outlooks
research
presented,
will
provide
preliminary
theoretical
basis
new
ideas
low‐cost,
high‐performance,
long‐life
applied
electrolysis.
Chemical Communications,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
The
development
of
robust
simulation
techniques
is
crucial
for
elucidating
electrochemical
catalytic
mechanisms
and
can
even
provide
guidance
the
tailored
design
regulation
highly
efficient
catalysts.
Advanced Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 24, 2025
Abstract
The
catalytic
activity
and
stability
under
high
current
densities
for
hydrogen
evolution
reactions
(HER)
are
impeded
by
firm
adherence
coverage
of
H
2
bubbles
to
the
sites.
Herein,
we
systematically
synthesize
core/shell
nanoarrays
engineer
bubble
transport
channels,
which
further
remarkably
regulate
interfacial
O
activity,
swift
generation
release.
self‐supported
catalyst
holds
uniform
ultra‐low
Ru
active
sites
0.38
wt%
promotes
rapid
formation
plentiful
small
bubbles,
rapidly
released
upright
mitigating
blockage
avoiding
surface
damage
from
movements.
As
a
result,
these
achieve
ultralow
overpotentials
18
24
mV
reach
10
mA
cm
−2
HER
in
1
M
KOH
freshwater
seawater,
respectively.
Additionally,
assembled
electrolyzer
demonstrates
stable
durability
over
800
hours
with
density
A
seawater.
techno‐economic
analysis
(TEA)
indicates
that
unit
cost
production
system
is
nearly
half
DOE's
(Department
Energy)
2026
target.
Our
work
addresses
challenges
highlights
its
potential
as
sustainable
economically
feasible
solution
large‐scale
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 27, 2025
Abstract
Atomically
precise
supported
nanocluster
catalysts
(APSNCs),
with
well‐defined
metal
active
sites,
unique
geometrical
and
electronic
structures
metal–metal
bonds,
demonstrate
excellent
catalytic
performance.
However,
the
synthesis
of
APSNCs
centers
stable
remains
a
huge
challenge
due
to
uncontrollable
aggregation
during
reactions.
Herein,
Ru
3
uniformly
dispersed
on
oxidized
carbon
nanotubes
(Ru
/OCNT)
is
successfully
synthesized
by
using
rapid
pyrolysis
precursor
strategy.
The
obtained
/OCNT
exhibits
performance
for
alkaline
hydrogen
evolution
reaction
(HER).
catalyst
achieves
an
overpotential
19
mV
at
current
density
10
mA
cm
−2
in
1
m
KOH
solution,
outperforming
commercial
20
wt.%
Pt/C
5
Ru/C.
Moreover,
mass
activity
23.47
11.83
times
higher
than
that
Density
functional
theory
(DFT)
calculations
reveal
interaction
metal–support
effectively
modulate
structure
atoms,
lower
adsorption
energy
site,
promote
H*
desorption.
This
work
offers
new
perspective
design
Two-dimensional
layered
transition
metal
dichalcogenides
(2D
TMDs)
have
emerged
as
promising
candidates
for
supercapacitor
(SCs)
owing
to
their
tunable
electronic
properties,
structures,
and
effective
ion
intercalation
capabilities.
Despite
these
advantages,
challenges
such
low
electrical
conductivity,
the
interlayer
restacking,
oxidation
structural
collapse
hinder
practical
implementation.
This
review
provides
a
comprehensive
overview
of
recent
advances
in
development
2D
TMDs
SCs.
We
begin
by
outlining
charge
storage
mechanisms
design
principles
SCs,
followed
an
in-depth
discussion
synthesis
methods
associated
fabricating
TMD
architectures.
The
subsequent
sections
explore
crystal
structures
reaction
mechanisms,
illustrating
electrochemical
potential
Furthermore,
we
highlight
material
modification
strategies,
including
nanostructuring,
defect
engineering,
phase
control,
surface/interface
modulation,
which
been
proposed
overcome
existing
challenges.
Finally,
address
critical
issues
emerging
opportunities
inspire
SC
technologies.