Catalysis Science & Technology,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
The
enhancement
of
electrocatalytic
performance
by
using
carbon
materials
as
cathodes
in
acidic
solutions
is
a
critical
research
direction
the
electrochemical
synthesis
hydrogen
peroxide.
ACS Applied Nano Materials,
Год журнала:
2023,
Номер
7(1), С. 1138 - 1145
Опубликована: Дек. 20, 2023
Integrating
metal-based
species
with
a
carbon
matrix
is
promising
approach
for
fabricating
inexpensive,
durable,
and
efficient
electrocatalysts.
Herein,
NiSe2-decorated
N-doped
polyhedra
(NC)
are
prepared
as
electrocatalysts
hydrogen
evolution
reaction
(HER)
by
template-assisted
approach.
The
optimal
NC-NiSe2
delivers
extraordinary
catalytic
activities
toward
HER
in
wide
pH
range,
overpotentials
of
127
mV
0.5
M
H2SO4,
226
1
PBS,
205
KOH
to
drive
current
density
10
mA
cm–2.
In
addition,
this
catalyst
undergoes
fast
kinetics
via
Volmer–Heyrovsky
mechanism
exhibits
excelent
long-term
durability
48
h
the
full
media.
During
electrocatalysis,
when
electrons
pass
through
NC
surface
NiSe2
particles,
water
molecules
at
active
sites
reduced,
then
released.
excellent
activity
mainly
benefit
from
hierarchically
porous
architecture
well
synergistic
interaction
nanoparticles
matrix,
which
not
only
significantly
boost
electronic
conductivity
generate
plentiful
but
also
guarantee
chemical
structural
stabilities
species.
This
work
unravels
deep
insights
into
exploration
carbon-supported
metal
chalcogenides
highly
full-pH
values.
Energy & Environmental Science,
Год журнала:
2024,
Номер
17(5), С. 1725 - 1755
Опубликована: Янв. 1, 2024
This
article
summarizes
the
regulation
strategies
of
Fe-based
MOFs-derived
electrocatalysts
for
ZABs,
and
provides
a
prospect
their
future
development.
Journal of the American Chemical Society,
Год журнала:
2024,
Номер
146(11), С. 7575 - 7583
Опубликована: Март 11, 2024
Electrocatalytic
reactions
taking
place
at
the
electrified
electrode–electrolyte
interface
involve
processes
of
proton-coupled
electron
transfer.
Interfacial
protons
are
delivered
to
electrode
surface
via
a
H2O-dominated
hydrogen-bond
network.
Less
efforts
made
regulate
interfacial
proton
transfer
from
perspective
Here,
we
present
quaternary
ammonium
salt
cationic
surfactants
as
electrolyte
additives
for
enhancing
H2O2
selectivity
oxygen
reduction
reaction
(ORR).
Through
in
situ
vibrational
spectroscopy
and
molecular
dynamics
calculation,
it
is
revealed
that
irreversibly
adsorbed
on
response
given
bias
potential
range,
leading
weakening
This
decreases
kinetics,
particularly
high
potentials,
thus
suppressing
4-electron
ORR
pathway
achieving
highly
selective
2-electron
toward
H2O2.
These
results
highlight
opportunity
steering
H2O-involved
electrochemical
modulating
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Июль 19, 2024
Abstract
The
electrochemical
oxygen
reduction
reaction
(ORR)
to
produce
hydrogen
peroxide
(H
2
O
)
is
appealing
due
its
sustainability.
However,
efficiency
compromised
by
the
competing
4e
−
ORR
pathway.
In
this
work,
we
report
a
hierarchical
carbon
nanosheet
array
electrode
with
single-atom
Ni
catalyst
synthesized
using
organic
molecule-intercalated
layered
double
hydroxides
as
precursors.
exhibits
excellent
2e
performance
under
alkaline
conditions
and
achieves
H
yield
rates
of
0.73
mol
g
cat
−1
h
in
H-cell
5.48
flow
cell,
outperforming
most
reported
catalysts.
experimental
results
show
that
atoms
selectively
adsorb
,
while
nanosheets
generate
reactive
species,
synergistically
enhancing
production.
Furthermore,
coupling
system
integrating
ethylene
glycol
oxidation
significantly
enhances
rate
7.30
producing
valuable
glycolic
acid.
Moreover,
convert
electrolyte
containing
directly
into
downstream
product
sodium
perborate
reduce
separation
cost
further.
Techno-economic
analysis
validates
economic
viability
system.
Journal of Materials Chemistry A,
Год журнала:
2024,
Номер
12(14), С. 8420 - 8428
Опубликована: Янв. 1, 2024
Intramolecular
donor–acceptor
conjugated
polymer
was
constructed
in
resorcinol-formaldehyde
resin
by
embedding
benzothiadiazole,
which
can
reduce
the
Gibbs
free
energy
for
two-electron
oxygen
reduction
and
improve
photocatalytic
H
2
O
evolution.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
63(23)
Опубликована: Апрель 3, 2024
Abstract
Two‐electron
oxygen
reduction
reaction
(2e
−
ORR)
is
a
promising
method
for
the
synthesis
of
hydrogen
peroxide
(H
2
O
).
However,
high
energy
barriers
generation
key
*OOH
intermediates
hinder
process
2e
ORR.
Herein,
we
prepared
copper‐supported
indium
selenide
catalyst
(Cu/In
Se
3
)
to
enhance
selectivity
and
yield
ORR
by
employing
an
electronic
metal–support
interactions
(EMSIs)
strategy.
EMSIs‐induced
charge
rearrangement
between
metallic
Cu
In
conducive
intermediate
generation,
promoting
H
production.
Theoretical
investigations
reveal
that
inclusion
significantly
lowers
barrier
impedes
4e
pathway,
thus
favoring
formation
.
The
concentration
produced
Cu/In
~2
times
than
,
shows
applications
in
antibiotic
degradation.
This
research
presents
valuable
approach
future
utilization
EMSIs
Advanced Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Июль 25, 2024
Over
the
last
decade,
carbon-based
metal-free
electrocatalysts
(C-MFECs)
have
become
important
in
electrocatalysis.
This
field
is
started
thanks
to
initial
discovery
that
nitrogen
atom
doped
carbon
can
function
as
a
electrode
alkaline
fuel
cells.
A
wide
variety
of
nanomaterials,
including
0D
dots,
1D
nanotubes,
2D
graphene,
and
3D
porous
carbons,
has
demonstrated
high
electrocatalytic
performance
across
applications.
These
include
clean
energy
generation
storage,
green
chemistry,
environmental
remediation.
The
applicability
C-MFECs
facilitated
by
effective
synthetic
approaches,
e.g.,
heteroatom
doping,
physical/chemical
modification.
methods
enable
creation
catalysts
with
properties
useful
for
sustainable
transformation
storage
(e.g.,
cells,
Zn-air
batteries,
Li-O
Angewandte Chemie International Edition,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 8, 2025
Abstract
The
production
of
hydrogen
peroxide
(H
2
O
)
through
two‐electron
oxygen
reduction
reaction
(2e
−
ORR)
has
emerged
as
a
more
environmentally
friendly
alternative
to
the
traditional
anthraquinone
method.
Although
oxidized
carbon
catalysts
have
intensive
developed
due
their
high
selectivity
and
activity,
yield
conversion
rate
H
under
overpotential
still
limited.
produced
was
rapidly
consumed
by
increased
intensity
reduction,
which
could
ascribe
decomposition
radicals
voltage
in
catalyst.
To
overcome
this
issue,
B
doped
been
catalyze
2e
ORR
with
efficient
suppressing
at
potential.
Thus,
thermal
reducing
containing
groups
(OCGs)
on
graphite
construct
defects
vacancies,
situ
convert
B−C
x
subunits
edge
graphene
sheets.
introduction
effectively
prevented
*O−O
bond
provided
suitable
adsorption
capacity
for
*OOH,
achieving
excellent
across
wide
range.
Finally,
remarkable
7.91
mmol
cm
−2
h
−1
delivered
an
industrial
current
density
600
mA
,
provide
“green”
pathway
scale‐upable
synthesis
.