ACS electrochemistry.,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 5, 2024
Designing
multifunctional
electrocatalysts
that
combine
high
efficiency,
durability,
and
affordability
for
energy
storage
represents
a
significant
challenge.
Here,
we
introduce
novel
trifunctional
electrocatalyst
synthesized
by
doping
self-supported
surface
electrochemically
functionalized
carbon
sphere
chains/MnO2
nanorods
with
Co
or
Ni
(Func
CSCs-2M/Co0.25
(or
Ni0.25)
MnOx).
These
demonstrate
exceptional
electroactivity
the
oxygen
evolution
reaction,
reduction
hydrogen
along
durability
comparable
to
of
commercial
Pt/C
IrO2
catalysts.
Two
Zn-air
batteries
(ZABs)
equipped
Func
CSCs-2M/Co0.25MnOx
cathodes,
connected
in
series,
have
capability
power
39
red
light-emitting
diodes
continuously
an
impressive
duration
200
h.
Moreover,
self-sustaining
water
splitting
system,
powered
ZABs,
is
showcased,
utilizing
as
exclusive
catalyst.
This
system
sustains
consistent
voltage
up
20
h
under
applied
current
density
reaching
30
mA
cm–2.
performance
rivals
noble
catalyst
systems,
showcasing
its
competitive
edge.
The
study
emphasizes
cost-effectiveness
materials
utilization
low-carbon,
renewable
rechargeable
ZAB
combined
electrolysis.
Such
integration
has
potential
make
substantial
impact
addressing
long-term
environmental
challenges,
easing
pressure
on
these
critical
fronts.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 25, 2025
Abstract
To
overcome
the
challenges
of
low
catalytic
activity
and
instability,
a
molecular
weight
engineering
strategy
coupled
with
oxidative
ammonolysis
is
developed
to
synthesize
CoRu‐based
alloy
catalysts
distinct
morphologies
properties
from
biorefinery
lignin.
This
approach
effectively
modulates
intrinsic
active
sites
exposes
unsaturated
nitrogen‐oxygen
structures,
thereby
tailoring
morphology
defect
structure
carbon
layers
in
catalysts.
The
as‐synthesized
CoRu
lignin
precursors
varying
weights
are
designated
as
CoRu@OALC‐EtOAC,
CoRu@OALC‐EtOH,
CoRu@OALC‐Residual.
featuring
defect‐rich
graphitic
carbon‐coated
structure,
exhibited
exceptional
overall
water‐splitting
performance
(1.48
V
at
10
mA
cm
−2
),
significantly
surpassing
Pt/C
||
Ru/C
(1.58
).
In
contrast,
CoRu@OALC‐Residual,
its
amorphous
demonstrated
remarkable
stability
(350
h
100
vastly
outperforming
(6
In‐situ
Raman
spectroscopy
DFT
calculations
revealed
that
adsorb
*
H
intermediates,
accelerating
process.
strong
adsorption
also
induces
layer
rearrangement,
leading
dissolution
oxidation
metal
particles.
provides
universal
method
for
biomass‐derived
catalysts,
establishing
direct
relationship
between
weight,
catalyst
morphology,
electrocatalytic
performance.
ACS Energy Letters,
Journal Year:
2025,
Volume and Issue:
10(1), P. 571 - 578
Published: Jan. 2, 2025
The
utilization
of
anion
exchange
membrane
(AEM)
electrolyzers
presents
an
opportunity
for
commercial
production
2,5-furandicarboxylic
acid
(FDCA)
through
electrochemical
oxidation
5-hydroxymethylfurfural
(HMF).
Consequently,
developing
facile
synthesis
techniques
scaled-up
electrocatalysts
HMF
reaction
(HMFOR)
is
a
crucial
step.
Herein,
we
developed
one-step
soaking
method
preparing
100
cm2
NiCu-based
catalyst
on
Ni
foam
(NiCuOx/NF)
in
10
s.
In
single-pass
25
AEM
electrolyzer
assembled
by
the
obtained
catalyst,
high
yield
≥95.0%
and
selectivity
≥99.9%
were
achieved
to
produce
FDCA
continuously
with
200
mM
electrolyte.
After
h
stable
operation
at
A,
207.28
g
was
attained
purity
over
99%.
This
work
provides
valuable
insights
into
industrial-scale
commercialization
biomass
upgrading
electrolyzers.
Small Methods,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 16, 2025
Abstract
Electrocatalytic
water
splitting
for
hydrogen
generation
plays
a
crucial
role
in
promoting
the
energy
transition
and
achieving
goals
of
carbon
neutrality.
Nevertheless,
context
electrolysis,
generated
bubbles
have
an
adverse
impact
on
consumption
mass
transfer
efficiency.
To
address
this
challenge,
variety
strategies
are
investigated
to
accelerate
bubble
detachment
transport.
It
is
utmost
significance
summarize
those
facilitating
advancement
electrolysis
performance.
In
review,
comprehensive
account
presented
enhancing
performance
through
behavior
management.
First,
electrolyte
discussed.
Then,
optimized
interactions
between
electrode
surface
introduced,
which
focus
reducing
adhesion
forces
implementing
other
forces.
Next,
dynamic
bubbling
deformable
catalysts
discussed,
such
as
fern‐
caterpillar‐like
catalysts.
Following
that,
bubble‐bubble
coalescence
proved
be
beneficial
earlier
departure
compared
buoyancy
effect
alone.
Finally,
outlooks
future
development
efficient
removal
enhanced
The
review
aims
deepen
comprehension
stimulate
management
strategies,
thereby
further
electrolysis.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 5, 2025
Abstract
Enhancing
critical
heat
flux
(CHF)
and
transfer
coefficient
(HTC)
by
promoting
the
nucleation,
growth,
departure
of
boiling
bubbles
has
drawn
significant
attention
owing
to
its
wide
applications.
However,
in‐depth
understanding
comprehensive
manipulation
under‐liquid
bubble
dynamics
from
in
situ
microscale
perspectives
remain
challenging.
Herein,
observations
analyses
microsized
ultra‐low
surface
tension
fluorinated
liquids
(FLs)
are
conducted
on
superaerophobic
silicon
surfaces
with
crisscross
microchannels
selective
nanowires.
It
is
revealed
that
deep
yet
short
nanowires
enable
ultrafast
liquid
spreading
(<549.6
ms)
ultralow
adhesion
(≈1.1
µN),
while
an
appropriate
spacing
(240–600
µm)
between
minimizes
time
(<20.6
due
timely
coalescence.
By
verifying
above
principles
through
collaborative
enhancement
CHF
HTC,
optimized
structure
(microchannel
depth
≈52.9
µm,
microchannel
≈362.9
nanowire
length
≈0
nm)
obtained
further
implemented
onto
exposed
Si
a
commercial
CPU
chip.
Cooled
phase‐change
FLs,
average
temperature
maintains
≈64.9
°C
even
under
extreme
power
loads
(≈130
W),
far
below
than
those
conventional
air‐cooling
water‐cooling
operations.
Langmuir,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 10, 2025
Water
electrolysis
recognizes
nickel
foam
(NF)
as
an
effective
current
collector
due
to
its
excellent
conductivity.
However,
recent
studies
highlighted
NF's
effect
on
the
efficacy
of
various
electrocatalytic
reactions,
primarily
presence
electroactive
chemical
species
at
interface.
In
contrast,
numerous
reports
suggested
that
NF
has
a
negligible
impact
overall
activity.
When
evaluated
against
other
collectors,
NF-supported
catalysts
demonstrate
better
electrochemical
activity,
predominantly
interfacial
design.
This
study
presents
electrochemically
relevant
with
flexible
design,
supported
by
case
and
insights
into
promising
future
directions.
Perspective
reveals
advantages,
challenges,
applicability
design
context
water
splitting
in
mind.
ACS electrochemistry.,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 7, 2025
Anion
exchange
membrane
water
electrolysis
(AEMWE)
is
an
emerging
technology
for
the
low-cost
production
of
hydrogen.
However,
efficiency
and
durability
AEMWE
devices
currently
insufficient
to
compete
with
other
low-temperature
technologies.
The
porous
transport
layer
(PTL)
a
critical
cell
component
that
remains
relatively
unoptimized
AEMWE.
In
this
study,
we
demonstrate
device
performance
significantly
affected
by
morphology
composition
PTL.
For
Ni
fiber-based
PTLs
∼2
μm
Co3O4
oxygen
evolution
reaction
catalyst
layer,
decreasing
pore
size
porosity
resulted
in
20%
increase
current
density
at
2
V
1
M
KOH
supporting
electrolyte.
Alloy
even
lower
had
higher
performance;
particular,
stainless
steel
PTL
gave
80%
relative
Ni.
Without
Co3O4,
alloy
still
demonstrated
high
activity,
indicating
material
was
catalytically
active.
characterization
electrode
electrolyte
after
testing
indicated
also
underwent
restructuring
corrosion
processes
may
limit
long-term
stability.
This
study
demonstrates
design
improved
important
area
focus
achieve
targets.
Nanoscale,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Rice
leaves
inspired
the
development
of
an
anisotropic
microstructured
gas
conduction
electrode
featuring
rapid
desorption
and
transfer
bubbles
to
achieve
highly
efficient
hydrogen
production.
Industrial & Engineering Chemistry Research,
Journal Year:
2025,
Volume and Issue:
64(9), P. 5087 - 5098
Published: Feb. 21, 2025
Gas
bubble
adhesion,
a
ubiquitous
phenomenon
in
electrochemical
gas-evolving
reactions,
reduces
the
hydrogen
evolution
reaction
(HER)
activity
water
electrolysis.
Understanding
dynamics
of
gas
detachment
and
its
dependence
on
force
balance
is
crucial
for
manipulating
departure,
but
it
remains
insufficiently
investigated.
Here,
we
found
that
differ
markedly
between
fluidizable
stationary
electrocatalysts,
with
electrocatalysts
minimizing
adhesion
showing
37-fold
increase
HER
rate
constant.
This
enhancement
attributed
to
accelerated
driven
by
fluidization
effect
electrocatalyst
particles.
Specifically,
transition
from
marks
shift
flat
particulate
model,
introducing
promoting
effects
arising
particle
movement
spin-induced
centrifugal
collision-triggered
coalescence.
Consequently,
measured
approaches
intrinsic
value.
work
highlights
as
an
effective
strategy
eliminate
thereby
exposing
nearly
all
active
sites
electrocatalytic
reactions.
Electrochemical
alkyne
reduction
with
H2O
as
a
hydrogen
source
represents
sustainable
route
for
value-added
olefin
production.
However,
the
reaction
efficiency
is
hampered
by
high
voltage
and
low
activity
of
Cu
electrodes
due
to
their
weak
adsorbed
(*H)
generation
property.
In
this
article,
we
present
enhanced
electrocatalysis
phenylacetylene
styrene
over
highly
dispersive
Cr-doped
Cu2O
nanowire
(Cr-Cu2O)
cathode.
The
Cr-Cu2O
demonstrates
improved
catalytic
compared
pure
Cu2O,
achieving
conversion
about
94.7%
selectivity
87.9%
Faraday
64.5%
at
potential
−1.15
V
vs
Hg/HgO.
combination
electrochemical
characterization
techniques
theoretical
calculations
demonstrated
key
role
introduced
Cr
atoms
in
lowering
activation
energy
barrier
surface
water
electrolysis
*H
facilitating
adsorption
phenylacetylene,
which
promotes
effective
hydrogenation
via
an
electrocatalytic
mechanism.
short,
work
provides
feasible
strategy
enrich
interfacial
*H,
thus
improving
semihydrogenation
performance
phenylacetylene.