Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 23, 2024
Abstract
As
the
demand
for
cleaner
energy
becomes
a
paramount
objective
of
sustainable
development,
advancement
cutting‐edge
engineered
materials
wide
range
applications
increasingly
vital.
Tailoring
catalyst
properties
through
precise
design
and
electronic
state
tuning
is
essential
adapting
these
to
large‐scale
applications.
Given
this,
an
effective
fine‐tuning
(EFT)
strategy
presented
optimize
structures
single‐atom
Zn
site
Ru
species,
synergistically
enhancing
both
electrocatalytic
oxygen
reduction
reaction
(ORR)
hydrogen
evolution
(HER).
Benefiting
from
interaction
between
species
anchored
on
hierarchically
layered
nanosheets
isolated
atoms
(Ru@Zn‐SAs/N‐C),
exhibits
superior
ORR
HER
activities
compared
benchmark
Pt/C
catalyst.
X‐ray
absorption
spectroscopy
density
functional
theory
(DFT)
calculations
confirm
novel
EFT
effect
single
that
enables
Ru@Zn‐SAs/N‐C
approaches
optimal
scaling
relation
*
OOH
OH,
breaking
universal
limitation.
Additionally,
G
H*
value
positions
near
apex
theoretical
volcano
model.
This
work
provides
innovative
avenue
regulating
localization
catalytic
active
centers
by
virtue
carbon
substrate
offers
valuable
insights
designing
high‐efficiency
electrocatalysts.
Advanced Powder Materials,
Journal Year:
2024,
Volume and Issue:
3(5), P. 100214 - 100214
Published: June 13, 2024
Water
electrolysis
via
alkaline
hydrogen
evolution
reaction
(HER)
is
a
promising
approach
for
large-scale
production
of
high-purity
at
low
cost,
utilizing
renewable
and
clean
energy.
However,
the
sluggish
kinetics
derived
from
high
energy
barrier
water
dissociation
impedes
seriously
its
practical
application.
Herein,
series
hybrid
Pt
nanoclusters/Ru
nanowires
(Pt/Ru
NWs)
catalysts
are
demonstrated
to
accelerate
HER.
And
optimized
Pt/Ru
NWs
(10
%
wt
Pt)
exhibits
exceptional
performance
with
an
ultralow
overpotential
(24
mV
10
mA
cm−2),
small
Tafel
slope
(26.3
dec−1),
long-term
stability,
outperforming
benchmark
commercial
Pt/C-JM-20
catalyst.
This
amazing
also
occurred
in
anion-exchange
membrane
devices,
where
it
delivered
cell
voltage
about
1.9
V
1
A
cm−2
outstanding
stability
(more
than
100
h).
The
calculations
have
revealed
such
superior
exhibited
by
stems
formed
heterointerfaces,
which
significantly
reduce
decisive
rate
step
cooperative-action
between
cluster
Ru
substance.
work
provides
valuable
perspectives
designing
advanced
materials
toward
HER
beyond.
Analytical Chemistry,
Journal Year:
2024,
Volume and Issue:
96(26), P. 10686 - 10695
Published: June 17, 2024
Exploiting
the
multiple
properties
of
nanozymes
for
multimode
lateral
flow
assay
(LFA)
is
urgently
required
to
improve
accuracy
and
versatility.
Herein,
we
developed
a
novel
plasmonic
Au
nanostar@PtOs
nanocluster
(Au@PtOs)
as
signal
tag
LFA
detection.
Based
on
PtOs
bimetallic
doping
strategy,
Au@PtOs
can
indicate
both
excellent
SERS
enhancement
nanozyme
catalytic
activity.
Meanwhile,
displays
better
photothermal
effect
than
that
nanostars.
Therefore,
colorimetric/SERS/temperature
three-mode
signals
be
read
out
based
nanocomposite.
The
was
combined
with
applied
breast
cancer
exosome
detection
limit
mode
2.6
×
103/4.1
101/4.6
102
exosomes/μL,
respectively,
which
much
superior
common
nanoparticles
(∼105
exosomes/μL).
Moreover,
fingerprint
molecular
recognition
ability
mode,
phenotypes
derived
from
different
cell
lines
discriminated
easily.
convenient
visual
colorimetric
sensitive
SERS/temperature
quantitative
modes,
driven
satisfy
requirements
accurate
flexible
multimodal
sensing
in
application
scenarios.
Journal of Materials Chemistry A,
Journal Year:
2024,
Volume and Issue:
12(31), P. 19720 - 19756
Published: Jan. 1, 2024
This
review,
for
the
first
time,
provides
concise
insights
into
synthetic
methods,
material
characterization,
and
recent
strategies
boosting
OER
activity
of
various
sol–gel-derived
composites
paving
way
subsequent
research.
Small,
Journal Year:
2024,
Volume and Issue:
20(43)
Published: June 27, 2024
Abstract
Developing
high
electroactivity
ruthenium
(Ru)‐based
electrocatalysts
for
pH‐universal
hydrogen
evolution
reaction
(HER)
is
challenging
due
to
the
strong
bonding
strengths
of
key
Ru─H/Ru─OH
intermediates
and
sluggish
water
dissociation
rates
on
active
Ru
sites.
Herein,
a
semi‐ionic
F‐modified
N‐doped
porous
carbon
implanted
with
nanoclusters
(Ru/FNPC)
introduced
by
hydrogel
sealing‐pyrolying‐etching
strategy
toward
highly
efficient
generation.
Benefiting
from
synergistic
effects
between
(Ru
NCs)
hierarchically
F,
N‐codoped
support,
such
synthesized
catalyst
displays
exceptional
HER
reactivity
durability
at
all
pH
levels.
The
optimal
8Ru/FNPC
affords
ultralow
overpotentials
17.8,
71.2,
53.8
mV
current
density
10
mA
cm
−2
in
alkaline,
neutral,
acidic
media,
respectively.
Density
functional
theory
(DFT)
calculations
elucidate
that
F‐doped
substrate
support
NCs
weakens
adsorption
energies
H
OH
sites
reduces
energy
barriers
elementary
steps
HER,
thus
enhancing
intrinsic
activity
accelerating
kinetics.
This
work
provides
new
perspectives
design
advanced
ultrafine
metal
conversion
applications.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
64(1)
Published: Sept. 3, 2024
Dual-atom
catalysts
(DACs)
have
garnered
significant
interest
due
to
their
remarkable
catalytic
reactivity.
However,
achieving
atomically
precise
control
in
the
fabrication
of
DACs
remains
a
major
challenge.
Herein,
we
developed
straightforward
and
direct
sublimation
transformation
synthesis
strategy
for
dual-atom
Fe
(Fe
The Journal of Physical Chemistry Letters,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1899 - 1908
Published: Feb. 17, 2025
Expediting
the
torpid
kinetics
of
acidic
oxygen
reduction
reaction
(ORR)
is
a
crucial
yet
formidable
challenge
toward
advancing
proton
exchange
membrane
fuel
cells
(PEMFCs)
for
commercialization.
The
cutting-edge
Pd-based
nanomaterials
ORR
are
hindered
by
their
low
intrinsic
activities
and
significant
CO
poisoning,
stemming
from
simultaneously
optimizing
surface
adsorption
various
adsorbates.
Herein,
we
introduce
an
ultrathin
PdRhCu
ternary
metallene
(PdRhCu
metallene)
boosting
in
PEMFC.
Mechanistic
studies
have
identified
that
incorporation
Cu
into
PdRh
configuration
could
downshift
d-band
center
on
Pd
to
promote
weakened
key
intermediates,
ensuring
efficient
electron
transfer
between
metal
sites
adsorbates,
thereby
lowering
energy
barriers
rate-determining
step
ORR.
As
proof-of-concept,
optimized
demonstrates
impressive
performance
with
high
half-wave
potential
(0.93
VRHE),
negligible
activity
decay
after
10
000
cycles,
superior
anti-CO-poisoning
capacity
compared
counterparts
commercial
Pt/C
catalysts.
Intriguingly,
metallene-assembled
PEMFC
achieves
maximum
power
density
820
mW
cm–2
electrocatalytic
stability
under
H2/air
conditions,
paving
avenues
further
advancements
electrocatalyst
engineering
practical
implementation
PEMFCs.
Improving
the
electrocatalytic
conversion
of
formate
in
alkaline
solutions
is
crucial
for
commercial
application
fuel
cells.
However,
palladium-based
catalysts
used
oxidation
reactions
(FOR)
face
challenges
due
to
strong
adsorption
hydrogen
intermediates,
resulting
lower
catalytic
efficiency
environments.
Herein,
we
prepared
a
PdZr/C
catalyst
aimed
at
employing
doping-induced
strain
strategy
reduce
binding
energy
palladium
and
release
more
active
sites
formate.
Through
density
functional
theory
calculations
experimental
investigations,
find
that
lattice
compression
induced
by
Zr
doping
regulates
electronic
structure
Pd.
Specifically,
incorporation
dopant
shifts
d-band
center
Pd
downward,
weakening
sites.
This
adjustment
promotes
desorption
thus
accelerating
FOR
kinetics
alleviating
site-blocking
effect.
As
result,
exhibited
2.4-fold
increase
activity
compared
conventional
Pd/C
catalyst.
It
also
achieved
peak
potential
delivered
significantly
higher
current
1917
mA
mg–1.
These
findings
highlight
critical
role
tuning
properties
offer
valuable
insights
into
design
high-performance
electrocatalysts
technologies.
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 17, 2025
Abstract
The
commercial
utilization
of
low‐dimensional
catalysts
has
been
hindered
by
their
propensity
for
agglomeration
and
stacking,
greatly
minimizing
active
sites.
To
circumvent
this
problem,
materials
can
be
assembled
into
systematic
3D
architectures
to
synergistically
retain
the
benefits
constituent
nanomaterials,
with
value‐added
bulk
properties
such
as
increased
surface
area,
improved
charge
transport
pathways,
enhanced
mass
transfer,
leading
higher
catalytic
activity
durability
compared
constituents.
hierarchical
organization
building
blocks
within
structures
also
enables
precise
control
over
catalyst's
morphology,
composition,
chemistry,
facilitating
tailored
design
specific
electrochemical
applications.
Despite
surge
in
metal‐based
assemblies,
there
are
no
reviews
encompassing
different
types
assemblies
from
nanomaterials
electrocatalysis.
Herein,
review
addresses
gap
investigating
various
self‐supported
exploring
how
electrocatalytic
performance
elevated
through
structural
modifications
mechanistic
studies
tailor
them
reactions.