Nano Letters,
Journal Year:
2024,
Volume and Issue:
24(3), P. 1015 - 1023
Published: Jan. 12, 2024
Ru-related
catalysts
have
shown
excellent
performance
for
the
hydrogen
evolution
reaction
(HER)
and
oxidation
(HOR);
however,
a
deep
understanding
of
Ru-active
sites
on
nanoscale
heterogeneous
support
catalysis
is
still
lacking.
Herein,
click
chemistry
strategy
proposed
to
design
Ru
cluster-decorated
nanometer
RuxFe3–xO4
heterointerfaces
(Ru/RuxFe3–xO4)
as
highly
effective
bifunctional
catalysts.
It
found
that
introducing
into
nanometric
Fe3O4
species
breaks
symmetry
configuration
optimizes
active
site
in
Ru/RuxFe3–xO4
HER
HOR.
As
expected,
catalyst
displays
prominent
alkaline
HOR
with
mass
activity
much
higher
than
commercial
Pt/C
well
robust
stability
during
because
strong
interaction
between
cluster
support,
optimized
adsorption
intermediate
(Had
OHad).
This
work
sheds
light
promsing
approach
improving
electrocatalysis
by
breaking
atomic
dimension
symmetry.
ACS Nano,
Journal Year:
2024,
Volume and Issue:
18(14), P. 9942 - 9957
Published: March 29, 2024
Highly
efficient,
cost-effective,
and
durable
electrocatalysts,
capable
of
accelerating
sluggish
reaction
kinetics
attaining
high
performance,
are
essential
for
developing
sustainable
energy
technologies
but
remain
a
great
challenge.
Here,
we
leverage
facile
heterostructure
design
strategy
to
construct
atomically
thin
Os@Pd
metallenes,
with
atomic-scale
Os
nanoclusters
varying
geometries
confined
on
the
surface
layer
Pd
lattice,
which
exhibit
excellent
bifunctional
properties
catalyzing
both
hydrogen
evolution
(HER)
oxygen
reduction
reactions
(ORR).
Importantly,
Os5%@Pd
metallenes
manifest
low
η10
overpotential
only
11
mV
in
1.0
M
KOH
electrolyte
as
well
highly
positive
E1/2
potential
0.92
V
0.1
(ORR),
along
superior
mass
activities
electrochemical
durability.
Theoretical
investigations
reveal
that
strong
electron
redistribution
between
elements
renders
precise
fine-tuning
respective
d-band
centers,
thereby
guiding
adsorption
intermediates
an
appropriate
binding
optimal
HER
ORR.
Materials Advances,
Journal Year:
2023,
Volume and Issue:
5(6), P. 2238 - 2252
Published: Dec. 21, 2023
The
increasing
energy
demands
have
led
modern
societies
to
search
for
green
and
renewable
alternatives.
For
this
purpose,
we
synthesized
highly
active
MXene
supported
catalysts
(Pd@Ti
3
C
2
T
x
–TiO
).
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 16, 2024
Abstract
The
commercialization
of
water‐splitting
technology
strongly
relies
on
the
stable
and
high‐performance
electrocatalyst
for
hydrogen
oxygen
evolution
reactions
(HER‐OER).
In
this
work,
nickel
dopants
in
IrRu
alloyed
acidic
water
splitting
activity
are
investigated.
incorporation
induces
more
atoms
coordinating
with
Ir/Ru
facilitating
formation
*OOH
species
via
nucleophilic
attack
by
H
2
O.
Additionally,
a
fast
surface
reconstruction
is
achieved
due
to
electrochemical
dissolution
Ni
dopants;
as
result,
incorporated,
evidenced
situ
Raman
spectroscopy
impedance
spectroscopy.
Therefore,
mass
Ni@IrRu
enhanced
threefold
than
commercial
IrO
OER
catalysis.
Moreover,
balance
binding
strength;
only
609
mV
overpotential
demanded
reach
1
A
cm
−2
HER
polymer
electrolyte
membrane
electrolyzer
(PEMWE)
test
indicates
1.87
V
required
attain
,
160
lower
Pt/C‐IrO
revealing
its
potential
application
PEMWE.
Small,
Journal Year:
2024,
Volume and Issue:
20(48)
Published: Aug. 25, 2024
Abstract
The
oxygen
evolution
reaction
(OER)
plays
a
pivotal
role
in
diverse
renewable
energy
storage
and
conversion
technologies,
including
water
electrolysis,
electrochemical
CO
2
reduction,
nitrogen
fixation,
metal‐air
batteries.
Among
various
electrolysis
techniques,
proton
exchange
membrane
(PEM)‐based
devices
offer
numerous
advantages,
high
current
densities,
exceptional
chemical
stability,
excellent
conductivity,
high‐purity
H
.
Nevertheless,
the
prohibitive
cost
associated
with
Ir/Ru‐based
OER
electrocatalysts
poses
significant
barrier
to
broad‐scale
application
of
PEM‐based
splitting.
Consequently,
it
is
crucial
advance
development
non‐noble
metal
catalysis
substance
acid‐activity
thereby
fostering
their
widespread
integration
into
PEM
electrolyzers
(PEMWEs).
In
this
review,
comprehensive
analysis
acidic
mechanism,
encompassing
adsorbate
mechanism
(AEM),
lattice
(LOM)
oxide
path
(OPM)
offered.
Subsequently,
systematic
summary
recently
reported
noble‐metal‐free
catalysts
transition
metal‐based,
carbon‐based
other
types
provided.
Additionally,
compilation
situ/operando
characterization
techniques
provided,
serving
as
invaluable
tools
for
furnishing
experimental
evidence
comprehend
catalytic
mechanism.
Finally,
present
challenges
future
research
directions
concerning
precious‐metal‐free
are
comprehensively
summarized
discussed
review.
SusMat,
Journal Year:
2024,
Volume and Issue:
4(5)
Published: Aug. 21, 2024
Abstract
The
utilization
of
single
atoms
(SAs)
as
trifunctional
electrocatalyst
for
nitrogen
reduction,
oxygen
and
evolution
reactions
(NRR,
ORR,
OER)
is
still
a
formidable
challenge.
Herein,
we
devise
one‐pot
synthesized
palladium
SAs
stabilized
on
nitrogen‐doped
carbon
SA
(Pd‐SA/NC)
efficient
NRR,
OER.
Pd‐SA/NC
performs
robust
catalytic
activity
toward
NRR
with
faradaic
efficiency
22.5%
at
−0.25
V
versus
reversible
hydrogen
electrode
(RHE),
the
relative
Pd
enhanced
by
17‐fold
than
Pd‐NP/NC.
In
addition,
half‐wave
potential
reaches
0.876
RHE,
amounting
to
58‐time
higher
mass
commercial
Pt/C.
Moreover,
overpotential
10
mA
cm
−2
low
287
mV
Pd‐SA/NC,
outperforming
IrO
2
360
times
in
turnover
frequency
1.6
RHE.
Accordingly,
assembled
rechargeable
zinc‐air
battery
(ZAB)
achieves
maximum
power
density
170
mW
,
boosted
2.3
Pt/C–IrO
.
Two
constructed
ZABs
efficiently
NRR‐OER
system
electrochemically
generate
ammonia
implying
its
superior
trifunctionality.
ACS Applied Nano Materials,
Journal Year:
2024,
Volume and Issue:
7(8), P. 8978 - 8987
Published: April 11, 2024
The
oxygen
evolution
reaction
(OER)
plays
a
pivotal
role
in
the
hydrolysis
process
of
zinc–air
batteries.
Consequently,
it
is
essential
to
develop
cathode
catalysts
with
both
cost-effectiveness
and
high
activity.
In
this
study,
we
synthesized
FeFFIVE-1-Ni
two-dimensional
(2D)
metal–organic
framework
(MOF)
nanosheets
via
straightforward
solvothermal
approach
oxidized
them
an
air
atmosphere.
During
calcination
atmosphere,
heteroatoms
(O,
F)
within
2D
MOF
combine
iron
nickel
metal
ions,
forming
FeOF
NiF2
compounds.
synergy
between
these
compounds
creation
surface
cracks
during
yield
catalytic
active
power
sites
for
reaction.
Notably,
overpotential
calcined
under
alkaline
test
conditions
(η10
=
286
mV)
was
lower
than
that
commercial
RuO2
355
mV).
This
work
presents
effective
strategy
replacing
noble
such
as
by
simply
treating
fluorinated
frameworks.
Energy & Fuels,
Journal Year:
2024,
Volume and Issue:
38(7), P. 6300 - 6313
Published: March 21, 2024
Here,
we
studied
a
simple,
scalable,
and
in
situ
hydrothermal
method
to
prepare
an
Fe–Mn-doped
ZnO
nanowire–nanosheet
on
three-dimensional
(3D)
Ni-foam
substrate
for
electrocatalytic
overall
water
splitting.
Attractively,
the
doping
of
Fe
Mn
plays
significant
role
mobilizing
electron
from
toward
due
different
vacuum
levels
Fe,
Mn,
ZnO,
facilitating
development
more
active
sites
surface
catalyst,
which
crucial
improving
catalytic
performances
during
Consequently,
shows
lowermost
overpotential
230
mV
Tafel
slope
115.2
dec–1
hydrogen
evolution
reaction
(HER)
248
short
109.1
oxygen
(OER)
1.0
M
KOH
electrolyte.
Besides,
depicts
low
charge
transfer
series
resistances
3.7
0.41
Ω
HER
0.36
1.66
OER,
respectively.
Also,
it
elucidates
outstanding
durability
at
−10
mA
cm–2
12
h
10
using
chronopotentiometry
1000
cycles.
In
addition,
Fe–Mn–ZnO||Fe–Mn–ZnO
cell
lower
potential
1.74
V
stability
over
24
deliver
staircase
also
suggests
8.2
current
densities.
Captivatingly,
concept
energy
band
modulation
bimetallic
doped
Fe–Mn–ZnO
catalyst
is
envisaged
explore
insights
into
mechanisms
oxygen.