Hydrazine Oxidation in Aqueous Solutions II: N4H4 Decomposition
Martin Breza,
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A. Gatial
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ChemistrySelect,
Journal Year:
2024,
Volume and Issue:
9(40)
Published: Oct. 1, 2024
Abstract
The
reaction
mechanism
for
the
N
2
H
4
homogeneous
oxidation
in
aqueous
solutions
is
more
complex
than
its
heterogeneous
electrochemical
on
electrode
surfaces.
Homogenous
of
a
mixture
non‐labeled
(
14
)
and
15
N‐labeled
hydrazine
produces
N,
indicating
intermediate
existence
6
or
intermediates
with
subsequent
hydrogen
transfers
splitting
lateral
N─N
bonds.
To
explain
key
part
reaction,
structures,
thermodynamics,
electron
characteristics
solution
are
investigated.
Unlike
,
we
have
not
found
any
spontaneous
bond
between
nitrogens
.
most
probable
products
disproportionation
N─NH
which
obtained
by
central
nitrogen
atoms,
so
only
molecules
formed.
Additionally,
formation
3
also
preferred
to
structures
without
fissions.
N═N
HN═NH
energetically
less
advantageous.
Cyclo‐N
stable,
fissions,
but
their
energies
indicate
vanishing
abundance
solution,
involvement
highly
improbable.
cannot
be
explained
intermediates.
Language: Английский
Constructing Pdo Reinforced Cuo/Al2o3 Mesoporous Nanostructures as Highefficiency Catalysts for Hydrazine Oxidation Reaction (Hzor)
Published: Jan. 1, 2024
Language: Английский
Boosting the Hydrogen Evolution Performance of Ultrafine Ruthenium Electrocatalysts by a Hierarchical Phosphide Array Promoter
Jing Wang,
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Yuzhe Cao,
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Mingyang Wei
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et al.
Catalysts,
Journal Year:
2024,
Volume and Issue:
14(8), P. 491 - 491
Published: July 31, 2024
Tuning
the
chemical
and
structural
environment
of
Ru-based
nanomaterials
is
a
major
challenge
for
achieving
active
stable
hydrogen
evolution
reaction
(HER)
electrocatalysis.
Here,
we
anchored
ultrafine
Ru
nanoparticles
(with
size
~4.2
nm)
on
hierarchical
Ni2P
array
(Ru/Ni2P)
to
enable
highly
efficient
HER.
The
promoter
weakened
adsorption
proton
sites
by
accepting
electrons
from
nanoparticles.
Moreover,
endowed
catalysts
with
large
surface
area
open
structure.
Consequently,
as-fabricated
Ru/Ni2P
electrode
displayed
low
overpotential
57
164
mV
at
HER
current
densities
10
50
mA
cm−2,
respectively,
comparable
state-of-the-art
Pt
catalysts.
can
operate
stably
96
h
cm−2
without
performance
degradation.
After
pairing
commercial
RuO2
anode,
anode
catalyzed
overall
water
splitting
1.73
V
density
which
was
0.16
lower
than
its
Ni
counterpart.
In
situ
Raman
studies
further
revealed
optimized
Ru-active
promoter,
thus
enhancing
electrocatalytic
performance.
Language: Английский
Advancing Green Hydrogen Purity with Iron-Based Self-Cleaning Oxygen Carriers in Chemical Looping Hydrogen
Catalysts,
Journal Year:
2024,
Volume and Issue:
14(8), P. 515 - 515
Published: Aug. 9, 2024
Green
hydrogen
is
central
to
the
energy
transition,
but
its
production
often
requires
expensive
materials
and
poses
environmental
risks
due
perfluorinated
substances
used
in
electrolysis.
This
study
introduces
a
transformative
approach
green
via
chemical
looping,
utilizing
an
iron-based
oxygen
carrier
with
yttrium-stabilized
zirconium
oxide
(YSZ).
A
significant
innovation
replacement
of
Al2O3
SiO2
as
inert
support
pellet,
enhancing
process
efficiency
reducing
CO2
contamination
by
minimizing
carbon
deposition
up
700%.
The
major
findings
include
achieving
remarkable
purity
99.994%
without
need
for
additional
purification
methods.
Fe-YSZ
possesses
significantly
higher
pore
volume
323
mm³/g
surface
area
18.3
m²/g,
increasing
iron
matrix
50%,
further
improving
efficiency.
catalytic
system
exhibits
unique
self-cleaning
effect,
substantially
contamination.
Fe-YSZ-SiO2
demonstrated
levels
below
100
ppm,
which
particularly
noteworthy.
research
advances
our
understanding
looping
mechanisms
offers
practical,
sustainable
solutions
production,
highlighting
crucial
synergy
between
pellets
carriers.
These
underscore
potential
(CLH)
technology
use
efficient
environmentally
friendly
contributing
transition
cleaner
sources.
Language: Английский