Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
14(38)
Published: July 14, 2024
Abstract
Replacing
the
slow
protonation
process
of
oxygen
evolution
reaction
(OER)
with
fast
alcohol
electro‐oxidation
can
decrease
driving
potentials,
thus
improving
overall
efficiency
electrochemical
devices.
However,
formation
effective
catalytic
sites
for
oxidation
remains
challenging
in
accelerating
to
inhibit
metal
leaching
and
improve
catalyst
stability.
Herein,
asymmetric
Ni‐O‐Cr
are
constructed
by
alloying
Cr
into
NiO
matrix
optimize
coordination
environments,
showing
significantly
enhanced
stability
during
electro‐oxidation.
The
maintain
constant
valence
states
Ni
oxidation,
efficiently
suppressing
dissolution
even
at
high
potentials.
In
situ
characterizations
combined
theoretical
calculations
indicate
that
adsorption
activation
OH*
molecules
compared
pure
NiO,
increasing
anodic
kinetics.
results
also
smaller
gap
3
d
‐O
2
p
strengthens
charge
transfer,
leading
This
work
gives
insights
boosting
using
sites‐enriched
solid‐solution
electrocatalysts.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(21)
Published: April 15, 2024
Abstract
Mn‐based
mullite
oxides
AMn
2
O
5
(A
=
lanthanide,
Y,
Bi)
is
a
novel
type
of
ternary
catalyst
in
terms
their
electronic
and
geometric
structures.
The
coexistence
pyramid
Mn
3+
–O
octahedral
4+
makes
the
d‐orbital
selectively
active
toward
various
catalytic
reactions.
alternative
edge‐
corner‐sharing
stacking
configuration
constructs
confined
sites
abundant
oxygen
species.
As
result,
they
tend
to
show
superior
behaviors
thus
gain
great
attention
environmental
treatment
energy
conversion
storage.
In
applications,
mullites
have
been
demonstrated
be
highly
low‐temperature
oxidization
CO,
NO,
volatile
organic
compounds
(VOCs),
etc.
Recent
research
further
shows
that
decompose
3
ozonize
VOCs
from
−20
°C
room
temperature.
Moreover,
enhance
reduction
reactions
(ORR)
sulfur
(SRR),
critical
kinetic
steps
air‐battery
Li–S
batteries,
respectively.
Their
distinctive
structures
also
facilitate
applications
gas‐sensitive
sensing,
ionic
conduction,
high
mobility
dielectrics,
storage,
piezoelectricity,
dehydration,
H
decomposition,
beyond.
A
comprehensive
review
basic
physicochemical
properties
application
certainly
not
only
gains
full
picture
but
provides
new
insights
into
designing
heterogeneous
catalysts.
Small,
Journal Year:
2024,
Volume and Issue:
20(46)
Published: Aug. 3, 2024
Abstract
Electrochemical
conversion
of
nitrate
(NO
3
−
)
to
ammonia
(NH
is
an
effective
approach
reduce
pollutants
in
the
environment
and
also
a
promising
low‐temperature,
low‐pressure
method
for
synthesis.
However,
adequate
H
*
intermediates
are
highly
expected
NO
hydrogenation,
while
suppressing
competitive
hydrogen
evolution.
Herein,
effect
coverage
on
RR
synthesis
by
Cu
electrocatalysts
investigated.
The
can
be
adjusted
changing
Pd
nanoparticle
sizes.
optimized
Pd@Cu
with
average
size
2.88
nm
shows
best
activity
RR,
achieving
maximum
Faradaic
efficiency
97%
(at
−0.8
V
vs
RHE)
NH
yield
21
mg
h
−1
cm
2
,
from
industrial
wastewater
level
500
ppm
–
.
In
situ
electrochemical
experiments
indicate
that
particles
promote
hydrogenation
via
well‐modulated
adsorbed
species.
Coupling
anodic
glycerol
oxidation
reaction,
ammonium
formate
successfully
obtained
as
value‐added
products
membrane
electrode
assembly
electrolyzer.
This
work
provides
feasible
strategy
obtaining
size‐dependent
hydrogenation.
Small,
Journal Year:
2024,
Volume and Issue:
20(34)
Published: April 10, 2024
Abstract
Single‐component
electrocatalysts
generally
lead
to
unbalanced
adsorption
of
OH
−
and
urea
during
oxidation
reaction
(UOR),
thus
obtaining
low
activity
selectivity
especially
when
oxygen
evolution
(OER)
competes
at
high
potentials
(>1.5
V).
Herein,
a
cross‐alignment
strategy
in
situ
vertically
growing
Ni(OH)
2
nanosheets
on
2D
semiconductor
g‐C
3
N
4
is
reported
form
hetero‐structured
electrocatalyst.
Various
spectroscopy
measurements
including
experiments
indicate
the
existence
enhanced
internal
electric
field
interfaces
vertical
nanosheets,
favorable
for
balancing
intermediates.
This
heterojunction
electrocatalyst
shows
high‐selectivity
UOR
compared
pure
,
even
V)
large
current
density.
The
computational
results
show
could
steer
increase
urea,
efficiently
avoiding
poisoning
strongly
adsorbed
active
sites.
A
membrane
electrode
assembly
(MEA)‐based
electrolyzer
with
anode
operate
an
industrial‐level
density
200
mA
cm
−2
.
work
paves
avenue
designing
high‐performance
by
cross‐alignments
components.
ACS Applied Nano Materials,
Journal Year:
2024,
Volume and Issue:
7(7), P. 7684 - 7693
Published: March 15, 2024
The
exploitation
of
highly
active,
nonprecious
metal
bifunctional
electrodes
to
facilitate
the
hydrogen
evolution
reaction
(HER)
and
oxygen
(OER)
is
essential
for
water
electrolysis
produce
hydrogen,
but
performances
are
still
unsatisfactory.
Herein,
a
facile
strategy
was
proposed
fabricate
three-dimensional
(3D)
bimetallic
phosphide
(NiFeP)
nanoflower
array
on
self-standing
assembled
MXene
nanosheet
film
(denoted
as
NiFeP@MXene)
structurally
integrated
electrode
overall
splitting.
NiFeP@MXene
with
3D
hierarchical
structures
can
be
directly
used
an
without
traditional
polymer
binders,
which
significantly
reduces
contact
resistance
facilitates
electron
transfer
at
interface.
Meanwhile,
interfacial
synergistic
coupling
created
between
conductive
phosphides,
favorable
catalytic
activity.
Moreover,
addition
Fe
improves
intrinsic
activity
simultaneously
formation
flower-like
more
active
sites.
Thus,
demonstrates
excellent
in
alkaline
electrolyte
small
overpotentials
240
122
mV
drive
10
mA
cm–2
current
density
OER
HER,
respectively,
along
superior
performance
compared
commercial
precious
IrO2∥Pt/C
catalyst.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(40)
Published: April 12, 2024
Abstract
Seawater
hydrogen
production,
vital
for
sustainable
energy
solutions
and
freshwater
preservation,
faces
challenges
due
to
seawater
complexity
high
consumption.
A
strategy
modulate
dehydrogenation
kinetics
of
dual‐phase
metal
nitrides
using
low‐loaded
Pt
quantum
dots
(QDs),
achieving
stable
energy‐efficient
generation
is
introduced.
The
QDs@Ni
3
N‐MoN/Ti
catalyst
displays
outstanding
bifunctional
catalytic
performance,
enabling
efficient
production
hydrazine
degradation
in
a
flow
anion
exchange
membrane
water
electrolysis
(AEMWE)
device.
Operating
at
low
voltage
1.41
V,
it
achieves
2
cm
−2
300
h,
circumventing
chlorine
corrosion
yielding
record‐breaking
equivalent
input
(2.68
kWh
m
−3
H
1
),
47.1%
reduction
compared
traditional
methods.
Integration
with
solar
biomass
facilitates
self‐powered
hybrid
highlighting
its
potential
applications.
This
work
marine
resource
conversion
green
offers
viable
insights
into
industrial
hazardous
pollutant
metal‐nitride
electrocatalysts.
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(28)
Published: May 2, 2024
Abstract
Sodium
ion
batteries
(SIBs)
are
considered
as
the
ideal
candidates
for
next
generation
of
electrochemical
energy
storage
devices.
The
major
challenges
anode
lie
in
poor
cycling
stability
and
sluggish
kinetics
attributed
to
inherent
large
Na
+
size.
In
this
work,
Bi
nanosphere
encapsulated
N‐doped
carbon
nanowires
(Bi@N‐C)
is
assembled
by
facile
electrospinning
carbonization.
mitigates
structure
stress/strain
during
alloying/dealloying,
optimizes
ionic/electronic
diffusion,
provides
fast
electron
transfer
structural
stability.
Due
excellent
structure,
Bi@N‐C
shows
performance
SIBs
terms
good
rate
capacity
half
cells
full
cells.
fundamental
mechanism
outstanding
has
been
demonstrated
through
synchrotron
in‐situ
XRD,
atomic
force
microscopy,
ex‐situ
scanning
microscopy
(SEM)
density
functional
theory
(DFT)
calculation.
Importantly,
a
deeper
understanding
underlying
reasons
improvement
elucidated,
which
vital
providing
theoretical
basis
application
SIBs.