ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 30, 2025
Traditional
recovery
of
valuable
metals
from
spent
ternary
lithium-ion
batteries
concentrates
on
complicated
pyrometallurgy
and
hydrometallurgy
routes.
Direct
reutilization
these
used
to
catalyze
Li-O2
is
highly
appealing
yet
remains
a
significant
challenge.
Here,
we
report
general
synthesis
ultrafine
αNiCoMn
(α
=
Pt,
Ir,
Ru)
high-entropy
alloy
(HEA)
nanoparticles
anchored
nitrogen-doped
carbon
(N-C)
support
through
facile
one-step
Joule
heating,
which
serves
as
high-efficiency
catalyst
for
batteries.
Solution
alloying
recycled
NiCoMn
with
Pt
group
facilitates
catalytic
efficiency
3d-5d
electronic
interactions
the
assembly
effect.
Both
experimental
calculation
results
reveal
that,
driven
by
rapid,
nonequilibrium
thermal
shock,
electron
transfer
defies
conventional
expectations,
where
electrons
are
inclined
higher
electronegative
surrounding
atoms.
This
interesting
reverse
local
charge
redistribution
orbital
hybridization
endow
an
elevated
d-band
center
optimized
structure.
The
induced
coordination
effects
further
generate
active
catalysis
surfaces,
favoring
adsorption
LiO2
intermediates
facilitating
rapid
decomposition
kinetics
nanoscale
Li2O2
products.
These
advantages
HEA@N-C
superior
bifunctional
activity,
achieving
ultralow
polarization
0.27
V
significantly
enhanced
cycling
life
240
cycles.
We
anticipate
that
this
work
will
provide
insights
into
upcycling
constructing
efficient
HEA
electrocatalysts.
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 26, 2025
Abstract
Near‐infrared
light
response
catalysts
have
received
great
attention
in
renewable
solar
energy
conversion,
production,
and
environmental
purification.
Here,
near‐infrared
photodegradation
is
successfully
achieved
rare
earth
single
atom
anchored
NaYF
4
@g‐C
3
N
heterojunctions
by
the
synergistic
effect
of
Z‐scheme
heterojunction
antenna
atoms.
The
UV–vis
emitted
Tm
3+
can
not
only
be
directly
absorbed
g‐C
to
generate
electron–hole
pairs,
realizing
efficient
transfer,
but
also
substrate,
generating
photo‐generated
electrons
at
its
impurity
level,
transferring
active
charge
valence
band
,
forming
a
further
improving
photocatalytic
efficiency.
Importantly,
atoms
has
multiple
functions
such
as
acting
transfer
channels
facilitate
regulating
critical
distance
prolonging
pair
lifetime.
Under
NIR
light,
it
exhibited
remarkable
performance
degrading
antibiotics
(the
removal
rate
TC
reached
91%
for
6
h)
while
maintaining
excellent
stability.
LC‐MS/MS
technology
used
reveal
reaction
intermediates,
species,
pathways,
complex
mechanism
proposed.
This
study
provides
experimental
theoretical
support
designing
synthesizing
with
characteristics.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
147(6), P. 5398 - 5407
Published: Jan. 31, 2025
Anion-exchange
membrane
fuel
cell
(AEMFC)
is
a
cost-effective
hydrogen-to-electricity
conversion
technology
under
zero-emission
scenario.
However,
the
sluggish
kinetics
of
anodic
hydrogen
oxidation
reaction
(HOR)
impedes
commercial
implementation
AEMFCs.
Here,
we
develop
Pd
single-atom-embedded
Ni3N
catalyst
(Pd1/Ni3N)
with
unconventional
Pd1Ni2
trimer
sites
to
drive
efficient
and
durable
HOR
in
alkaline
media.
Integrating
theoretical
experimental
analyses,
demonstrate
that
dual
achieve
"*H
on
Pd1Ni2-HV
+
*OH
Pd1Ni2-HN"
adsorption
mode,
effectively
weakening
overstrong
*H
adsorptions
pristine
Ni3N.
Owing
unique
coordination
mode
atomically
dispersed
catalytic
sites,
resulting
Pd1/Ni3N
delivers
high
intrinsic
mass
activity
together
excellent
antioxidation
capability
CO
tolerance.
Specifically,
reaches
7.54
A
mgPd-1
at
overpotential
50
mV.
The
AEMFC
employing
as
anode
displays
power
density
31.7
W
an
ultralow
precious
metal
loading
only
0.023
mgPd
cm-2.
This
study
provides
guidance
for
design
high-performance
atomic
level.
ACS Applied Energy Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 13, 2025
The
development
of
efficient
and
durable
hydrogen
evolution
reaction
(HER)
electrocatalysts
is
critical
for
sustainable
energy
conversion.
Although
platinum
(Pt)
serves
as
a
benchmark
HER
catalyst,
its
practical
application
hindered
by
the
high
cost,
limited
durability,
susceptibility
to
CO
poisoning.
In
this
work,
we
report
heterojunction
Pt-based
Pt@NCL-MXene,
synthesized
LiF
etching
MXene
subsequent
NH3
calcination.
This
process
introduces
dual
nitrogen
(N)
fluorine
(F)
doping
yields
nitrogen-doped
carbon
layer
(NCL)
coating
on
Pt
nanoparticles
with
an
average
size
only
3.4
nm.
Compared
conventional
Pt–C
catalysts,
Pt@NCL-MXene
exhibits
larger
specific
surface
area,
enhanced
electron
transfer
efficiency,
optimized
d-band
center,
thereby
facilitating
both
H*
adsorption
desorption.
As
result,
achieves
significantly
lower
overpotential
73
mV
at
current
density
100
mA
cm–2,
alongside
improved
kinetics
stability
under
operational
conditions.
Furthermore,
9
wt
%
F-rich
support
effectively
suppresses
Pt,
reducing
uptake
0.224
mmol
g–1,
which
purportedly
than
that
(0.264
g–1),
mitigating
poisoning
prolonging
catalyst's
service
life.
These
findings
offer
insights
into
rational
design
advanced
CO-resistant
electrocatalysts.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 25, 2025
Abstract
The
development
of
nanocluster
electrocatalysts
is
a
promising
way
to
simultaneously
improve
atomic
utilization
and
catalytic
reactivity
noble
metals.
Although
precisely
controlled
nanocatalysts
with
exact
composition
well‐defined
structures
have
been
widely
investigated
for
various
electrocatalytic
reactions,
the
origin
their
excellent
performance
has
mainly
focused
on
thermodynamic
energetics
key
intermediates.
relationship
between
structure
nanoclusters
electric‐double‐layer
(EDL)
environment
formed
at
interface
electrode
electrolyte
largely
overlooked.
Herein,
MoN‐supported
Pt
catalysts
are
synthesized
remarkable
intrinsic
activity
1.927
mA
cm
−2
toward
alkaline
hydrogen
oxidation
reaction
(HOR).
Electrochemical
experiments,
in
situ
surface‐enhanced
infrared
absorption
spectroscopy,
theoretical
calculations
verify
coordination
environment,
charge
redistribution,
band
conducive
providing
optimized
adsorption
energy
vital
hydroxyl
Furthermore,
it
found
that
adsorbed
species
can
promote
proportion
water
molecules
gap
region
mitigate
discontinuity
hydrogen‐bond
network
EDL,
thereby
more
transfer
channels
accelerate
overall
kinetics.
This
work
uncovers
optimization
interfacial
microenvironment
induced
by
metal
nanoclusters,
shedding
light
rational
design
highly
effective
HOR
catalysts.