ACS Applied Materials & Interfaces,
Год журнала:
2025,
Номер
17(19), С. 28256 - 28266
Опубликована: Апрель 30, 2025
The
rechargeable
Zn-nitrate
battery
presents
a
promising
strategy
for
renewable
energy
conversion,
ammonia
production,
and
sewage
treatment.
Despite
achieving
excellent
performance
with
transition
metal-based
electrocatalysts,
the
structure
evolution
of
electrocatalyst
during
charging/discharging
corresponding
reaction
mechanism
on
nitrate
reduction
(NO3RR)
are
still
unclear.
Inspired
by
structural
reconstruction
in
charging
process,
nanoporous
Co2P/CoOOH
prepared
dealloying
anodic
oxidation
is
reported
as
an
NO3RR,
remarkable
catalytic
(ammonia
yield
rate:
1.93
mmol
h-1
cm-2,
Faradaic
efficiency:
94.18%)
high
cathodic
efficiency
34.51%.
Additionally,
assembled
delivers
power
density
31.99
mW
cm-2
charge-discharge
stability.
In-situ
spectroscopy
investigation
reveals
generation
Co2P/Co3O4
heterosturcture
through
synergetic
redox
involving
cobalt
species
ions
which
enhances
approach
potassium-ionized
water
improves
kinetics
regulating
NO2-
*NH2
generation.
Density
functional
theoretical
calculation
further
illustrates
that
heterostructure
optimizes
adsorption
*NO
intermediate
enables
energetically
favorable
rate-limiting
*NOH
formation
step.
unique
activation
mode
cobalt-based
would
provide
new
insights
designing
efficient
electrocatalysts
battery.
Advanced Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Июль 24, 2024
Abstract
Supramolecular
assemblies,
formed
through
electronic
charge
transfer
between
two
or
more
entities,
represent
a
rich
class
of
compounds
dubbed
as
charge‐transfer
complexes
(CTCs).
Their
distinctive
formation
pathway,
rooted
in
processes
at
the
interface
CTC‐forming
components,
results
delocalization
along
molecular
stacks,
rendering
CTCs
intrinsic
conductors.
Since
discovery
CTCs,
intensive
research
has
explored
their
unique
properties
including
magnetism,
conductivity,
and
superconductivity.
recently
recognized
semiconducting
functionality
inspired
recent
developments
applications
requiring
organic
semiconductors.
In
this
context,
offer
tuneable
energy
gap,
charge‐transport
properties,
tailorable
physicochemical
interactions,
photoresponsiveness,
potential
for
scalable
manufacturing.
Here,
an
updated
viewpoint
on
is
provided,
presenting
them
emerging
To
end,
chemical
alongside
synthesis
methods
are
reviewed.
The
that
benefit
various
related
realms
optoelectronics,
catalysts,
gas
sensors
discussed.
Insights
future
existing
limitations
described.
Advanced Energy Materials,
Год журнала:
2024,
Номер
14(42)
Опубликована: Сен. 25, 2024
Abstract
Using
low
and
optimized
magnetic
field
along
with
electric
is
a
novel
strategy
to
facilitate
electrochemical
nitrite
reduction
reaction
(NO
2
RR).
Herein,
the
assisted
electrocatalytic
ammonia
synthesis
employing
spin‐thrusted
β‐MnPc
at
95
mT
explored.
The
calculated
rate
of
generation
16603.4
µg
h
−1
mg
cat
,
which
almost
twice
that
nonpolarized
manganese
phthalocyanine
(MnPc)
catalyst.
Additionally,
Faradaic
efficiency
(FE)
–0.9
V
versus
RHE
found
be
92.9%,
significantly
higher
compared
MnPc
In
presence
external
field,
catalysts
provide
better
electron
transfer
channel
results
in
lower
charge
resistance
hence
performances.
Density
functional
theory
(DFT)
result
further
verifies
induced
has
potential
barrier
(0.51
eV)
for
protonation
NO*
than
(1.08
eV),
confirms
enhanced
ammonia.
Chemical Science,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
The
orientation
of
β-CuPc
favours
the
overlap
central
Cu
with
N
parallel
molecules,
which
is
reason
behind
high
electrical
conductivity
and
selectivity
in
NH
3
production
via
nitrate
reduction,
impossible
other
polymorphs.
Abstract
Electrocatalysis
performs
a
vital
role
in
numerous
energy
transformation
and
repository
mechanics,
including
power
cells,
Electric
field‐assisted
catalysis,
batteries.
It
is
crucial
to
investigate
new
methods
improve
electrocatalytic
performance
if
effective
long‐lasting
systems
are
developed.
The
modulation
of
catalytic
activity
selectivity
by
external
magnetic
fields
over
electrochemical
processes
has
received
lot
interest
lately.
How
the
use
various
electrocatalysis
great
promise
for
building
selective
catalysts,
opening
door
advancement
sophisticated
conversion
discussed.
Furthermore,
challenges
possibilities
incorporating
into
suggestions
future
research
areas
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
unknown
Опубликована: Сен. 30, 2024
Abstract
Glycine
as
one
of
the
most
abundant
amino
acids
in
human
proteins,
with
extensive
applications
both
life
and
industry,
is
conventionally
synthesized
through
complex
procedures
or
toxic
feedstocks.
In
this
study,
we
present
a
facile
benign
electrochemical
pathway
for
synthesis
glycine
reductive
coupling
glyoxylic
acid
nitrate
over
copper‐bismuth
bimetal
catalyst
derived
from
metal–organic
framework
(MOF)
array
on
copper
foam
(Cu/Bi−C@CF).
Remarkably,
Cu/Bi−C@CF
achieves
fantastic
selectivity
89
%,
corresponding
high
Faraday
efficiency
65.9
%.
From
control
experiments,
introduction
Bi
caused
binding
energy
Cu
shift
to
lower
state,
which
leads
towards
formation
key
intermediate
hydroxylamine
rather
than
ammonia
product,
facilitating
oxime
providing
additional
sites
subsequent
hydrogenation
reaction
way
glycine.
Moreover,
derivation
MOF
arrays
ensures
effective
dispersion
enhances
stability
Cu/Bi−C@CF.
This
innovative
approach
not
only
presents
sustainable
pathways
production
value‐added
organonitrogen
compounds
utilizing
readily
available
carbon
nitrogen
sources,
but
also
provides
novel
insights
into
design
multistage
structural
catalysts
sequential
reactions.
Abstract
Crystalline
γ‐FeO(OH)
dominantly
possessing
─
OH
terminals
(𝛾‐FeO(OH)
c
),
polycrystalline
containing
multiple
O,
OH,
and
Fe
pc
α‐Fe
2
O
3
majorly
surface
are
used
as
electrocatalysts
to
study
the
effect
of
on
electrocatalytic
nitrate
reduction
reaction
(eNO
RR)
selectivity
stabilization
intermediates.
Brunauer‐Emmett‐Teller
analysis
electrochemically
determined
area
suggest
a
high
active
117.79
m
g
−1
(ECSA:
0.211
cm
)
for
𝛾‐FeO(OH)
maximizing
accessibility
adsorption
exhibiting
selective
eNO
RR
NH
at
pH
7
with
yield
rate
18.326
mg
h
−2
,
>85%
Faradaic
efficiency
(FE),
least
nine‐times
catalyst‐recyclability.
15
N‐
D‐labeling
combined
in
situ
IR
Raman
studies
validate
ions
generation
nitrite
hydroxyl
amine
A
kinetic
isotope
(KIE)
value
2.1
indicates
H
proton
source
proton‐coupled
electron
transfer
rate‐limiting
step.
The
rotating‐ring
disk
electrochemical
(RRDE)
subsequent
Koutecký‐Levich
reveal
electron‐transfer
constant
(k)
2e‐
is
5.7
×
10
−6
s
.
This
provides
direct
evidence
formation
dominant
pathway
γ‐FeO(OH).
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 10, 2025
Abstract
Electrochemically
promoted
nitrate
reduction
reaction
(NITRR)
holds
great
potential
for
the
“green”
synthesis
of
ammonia
(NH
3
).
However,
NITRR
in
neutral
media,
though
close
to
practical
scenario,
is
often
limited
by
an
insufficient
supply
active
hydrogen
(*H)
due
sluggish
water
cleavage.
In
this
work,
it
demonstrated
that
a
bimetallic
alloy
FeIr
can
optimize
trade‐off
between
and
*H
formation
media.
As
result,
exhibits
excellent
catalytic
performance
toward
with
Faradaic
efficiency
NH
up
97.3%
high
yield
rate
11.67
mg
h
−1
cm
−2
at
low
working
−0.6
V
(versus
reversible
electrode
(RHE)),
surpassing
monometallic
catalysts
as
well
majority
Fe‐based
state‐of‐the‐art.
It
also
found
displays
remarkable
electron
rearrangement
hetero‐atoms
their
significant
orbital
hybridization,
which
benefits
not
only
but
process.
Moreover,
coupling
FeIr‐based
methanol
oxidation
(MOR)
results
sustainable
productions
formate
combined
FE
nearly
200%
cell‐voltage
2
V.
This
work
thus
demonstrates
promising
strategy
designing
efficient
NITRR.