Silver Nanoparticle-Decorated NiFe-MOFs as Highly Active Electrocatalysts for Overall Water Splitting
Conghui Zhang,
No information about this author
Hao Chen,
No information about this author
Chenyue Zhou
No information about this author
et al.
ACS Applied Nano Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 27, 2025
Language: Английский
Synergistic catalytic mechanism of cyanide-bridged Ni-Fe bimetallic electrocatalyst for highly efficient urea oxidation
Zhanhong Zhao,
No information about this author
Zeng He,
No information about this author
Yitong Zhou
No information about this author
et al.
Applied Catalysis B Environment and Energy,
Journal Year:
2025,
Volume and Issue:
unknown, P. 125414 - 125414
Published: April 1, 2025
Language: Английский
Ultrahigh Pyrrolic Nitrogen Triggers High-Activity Sites in Carbon Catalysts for Selective Oxygen Reduction to Efficient H2O2 Production
Carbon,
Journal Year:
2025,
Volume and Issue:
unknown, P. 120450 - 120450
Published: May 1, 2025
Language: Английский
Heterostructure of Fe3O4 Confined in Hierarchical Porous Carbon for Interface‐Enhanced Medical‐Grade H2O2 Electrosynthesis
Advanced Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 19, 2025
Abstract
The
electrocatalytic
two‐electron
oxygen
reduction
reaction
(2e
−
ORR)
presents
an
environmentally
sustainable
approach
to
produce
hydrogen
peroxide
(H
2
O
).
Heterostructures
coupling
non‐noble
transition
metal
oxides
(TMOs)
with
carbon
materials
hold
promise
for
2e
ORR,
but
face
challenges
in
controlling
morphology,
phase
composition,
and
active
centers.
In
this
study,
a
hierarchically
porous
tremella‐like
heterojunction
characterized
by
ultrafine
cubic
Fe
3
4
nanoparticles
within
the
amorphous
(UFe
@HPAC)
is
obtained
using
integrated
platform
of
green
Fe‐based
deep
eutectic
solvent
via
two‐step
annealing
process.
UFe
@HPAC
exhibits
remarkable
overall
intrinsic
ORR
activity,
delivering
96%
H
selectivity
turnover
frequency
(TOF)
67.5
s
−1
.
Notably,
possesses
superior
production
capabilities,
showing
long‐term
stability
100
h
rate
8.1
g
L
flow‐cell,
while
achieving
various
medical‐grade
concentrations
(3.0–7.8
wt%).
Additionally,
integrating
on‐site
electro‐Fenton
achieved
rapid
decomposition
contaminants.
unique
heterostructure,
synergistic
effect
carbon,
enhances
electronic
conductivity.
Moreover,
redistribution
at
interface
heterostructure
triggers
thermodynamically
favorable
multiple
sites
C
centers
ORR.
This
work
offers
new
perspective
on
metal‐based
production.
Language: Английский
Multiscale Catalyst Engineering for Stable, Selective, and Carbon‐Neutral Industrial Hydrogen Peroxide Electrosynthesis
Mengxue Yang,
No information about this author
Zhiyong Zhao,
No information about this author
Tianyu Zhi
No information about this author
et al.
Carbon Neutralization,
Journal Year:
2025,
Volume and Issue:
4(3)
Published: May 1, 2025
ABSTRACT
The
electrocatalytic
two‐electron
oxygen
reduction
reaction
(2e
−
ORR)
has
emerged
as
a
pivotal
strategy
for
sustainable
hydrogen
peroxide
(H
2
O
)
synthesis,
offering
carbon‐neutral
alternative
to
the
energy‐intensive
anthraquinone
process.
This
review
critically
synthesizes
recent
breakthroughs
in
catalyst
design,
mechanistic
understanding,
and
system
integration
address
persistent
selectivity–stability
trade‐off.
Key
advances
include
atomic‐level
engineering
of
electronic
modulation
surface
functionalization
hydrophobicity
control,
which
achieve
>
95%
H
selectivity
by
precisely
tuning
*OOH
adsorption
energy
suppressing
4e
pathways.
Hierarchical
architectures,
such
flow‐through
electrodes
catalytic
membranes,
extend
operational
stability
beyond
500
h
at
industrial
current
densities
(>
200
mA
cm
through
confinement
effects
interfacial
engineering.
Emerging
operando
characterization
techniques
coupled
with
machine
learning‐accelerated
simulations
now
enable
dynamic
mapping
active‐site
evolution
degradation
mechanisms.
System‐level
innovations
integrating
renewable
input
circular
carbon
strategies
demonstrate
pilot‐scale
feasibility
net‐negative
emission
production.
However,
challenges
scalability,
long‐term
durability
under
fluctuating
loads,
techno‐economic
gaps
between
laboratory
implementations
require
urgent
attention.
We
propose
multidisciplinary
roadmap
combining
materials
genome
initiatives,
modular
reactor
policy‐driven
lifecycle
assessment
frameworks
accelerate
deployment
2e
ORR
systems.
work
provides
actionable
guidance
advancing
chemical
manufacturing
electrochemical
routes
aligned
global
net‐zero
goals.
Language: Английский
Symmetry distortion engineering single-atom catalysts: Exceptional ORR activity and ultra-stable Zn-air batteries
Chemical Engineering Journal,
Journal Year:
2025,
Volume and Issue:
unknown, P. 164156 - 164156
Published: May 1, 2025
Language: Английский
Phase Reconstruction‐Directed Synthesis of Oxalate‐Functionalized Nickel Hydroxide Electrocatalyst for High‐Yield H2O2 Generation at Industrial Currents
Zhiwei Liu,
No information about this author
Weijie Yuan,
No information about this author
Hongyuan Yang
No information about this author
et al.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 22, 2024
Abstract
The
electrochemical
oxygen
reduction
reaction
(2e
−
ORR)
offers
a
promising
approach
for
H
2
O
production,
yet
developing
highly
active,
selective,
and
stable
electrocatalysts
remains
challenge.
In
this
work,
phase
reconstruction
strategy
is
presented
to
synthesize
an
oxalate‐adsorbed
nickel
hydroxide
electrocatalyst
(Ni(OH)
‐C
4
)
through
the
self‐dissociation
of
oxalate
in
alkaline
medium,
leading
notable
enhancement
yield
at
elevated
current
densities.
Remarkably,
Ni(OH)
exhibits
2e
selectivity
exceeding
93%
across
broad
voltage
range
(0.0
0.5
V
vs
RHE)
0.1
M
KOH,
outperforming
pristine
.
When
deployed
as
gas
diffusion
electrode
flow
cell,
catalyst
demonstrates
operation
50
h
200
mA
cm
−2
,
with
Faradaic
efficiency
surpassing
90%
peak
6.2
mol
g
−1
cat
Comprehensive
advanced
characterizations,
including
situ
Raman
spectroscopy,
transient
photovoltage
spectra,
potential
scanning
coupled
post‐ORR
analyses,
reveal
that
surface‐adsorbed
groups
on
enhance
interfacial
kinetics
between
active
Ni
sites
reactants
by
inducing
charge
trapping
effect
forming
hydrogen‐bonded
network,
facilitating
robust
high‐yield
production.
Language: Английский