Catalyst and gas diffusion electrode design toward C–N coupling for urea electrosynthesis
eScience,
Journal Year:
2025,
Volume and Issue:
unknown, P. 100425 - 100425
Published: April 1, 2025
Language: Английский
Electrocatalytic N–H bond transformations: a zero-carbon paradigm for sustainable energy storage and conversion
Kang Ji,
No information about this author
Guixi Wang,
No information about this author
Shiyu Wang
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et al.
Chemical Communications,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Electrocatalytic
zero-carbon
energy
systems
based
on
the
N–H
bond
have
achieved
a
complete
cycle
of
storage
and
conversion,
providing
guidance
for
application
clean
conversion.
Language: Английский
Electrode Materials for NO Electroreduction Based on Dithiolene Metal–Organic Frameworks: A Theoretical Study
Jiake Fan,
No information about this author
Lei Yang,
No information about this author
Lixin Ye
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et al.
Catalysts,
Journal Year:
2024,
Volume and Issue:
14(10), P. 739 - 739
Published: Oct. 21, 2024
To
quickly
and
efficiently
screen
catalytic
materials
with
both
activity
selectivity
for
the
nitric
oxide
reduction
reaction
(NORR),
we
adopted
a
strategy
that
considers
of
side
hydrogen
evolution
(HER)
first.
It
can
be
seen
Fe3(THT)2
(THT
=
triphenylene-2,3,6,7,10,11-hexathiol)
has
extremely
excellent
HER
activity,
Gibbs
free
energy
change
(ΔG)
0.007
eV.
Based
on
relationship
between
ΔG
theoretical
exchange
current
density,
all
TM3(THT)2
divided
into
two
regions:
one
is
absolute
values
greater
than
1
eV,
other
0
eV
less
1eV.
Obviously,
candidates
have
poor
performance,
but
this
precisely
provides
possibility
obtaining
NORR
activity.
Subsequent
calculation
results
show
maximum
rate-determining
step
Ta3(THT)2
unexpectedly
only
0.05
Therefore,
may
regarded
as
material
performance
selectivity.
electron
transfer
partial
density
states
(PDOS)
analysis,
it
Ta
plays
crucial
role
in
activation
stage
NO.
The
approach
first
provide
new
idea
rapidly
screening
highly
selective
active
catalysts.
Language: Английский
Electrochemical Ammonia Synthesis from Dilute Gaseous Nitric Oxide Reduction at Ambient Conditions
Catalysts,
Journal Year:
2024,
Volume and Issue:
14(11), P. 838 - 838
Published: Nov. 20, 2024
Converting
gaseous
nitric
oxide
(NO)
to
ammonia
(NH3)
is
important
because
of
its
environmental
and
industrial
implications.
The
electrochemical
transformation
nitrogen
(N2)
NH3
faces
several
challenges,
including
a
slow
reaction
rate
low
Faradaic
efficiency
(FE).
This
study
presents
an
innovative
approach
by
integrating
NO
elimination
production
reduction
(NORR)
under
ambient
conditions.
Co
Mo-based
catalysts
were
investigated
for
the
continuous
diluted
gas
(1%)
within
proton
exchange
membrane
(PEM)
cell
In
NORR
tests
conducted
without
catholyte,
CoMo-NC
demonstrated
notable
performance,
achieving
yield
23.2
×
10−10
mol
s−1
cm−2
at
−2.2
Vcell
FENH3
94.6%
−1.6
Vcell,
along
with
enhanced
durability.
Notably,
this
performance
represents
one
highest
achievements
gas-phase
room
temperature.
Language: Английский