Reconstruction of Ni-based catalyst for electrocatalytic urea oxidation reaction
Xuena Gao,
No information about this author
Jianguo Dong,
No information about this author
Huimin Yang
No information about this author
et al.
Journal of Alloys and Compounds,
Journal Year:
2025,
Volume and Issue:
1012, P. 178477 - 178477
Published: Jan. 1, 2025
Language: Английский
Progress on electrochemical and photoelectrochemical urea and ammonia conversion from urine for sustainable wastewater treatment
Applied Catalysis B Environment and Energy,
Journal Year:
2024,
Volume and Issue:
362, P. 124718 - 124718
Published: Oct. 20, 2024
Language: Английский
High‐Performance Electrocatalysts of Potassium Lactate Oxidation for Hydrogen and Solid Potassium Acetate Production
Jun Hu,
No information about this author
Xin Gao,
No information about this author
Shanqing Li
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et al.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 13, 2025
Abstract
With
the
increasing
use
of
polylactic
acid
(PLA),
more
attention
is
turning
to
its
post‐treatment.
Current
methods
such
as
natural
decomposition,
composting,
and
incineration
are
limited
by
significant
carbon
dioxide
emissions
resource
waste.
Here,
an
efficient
electrocatalytic
conversion
approach
presented
transform
PLA
waste
into
high‐value
chemicals,
particularly
potassium
acetate
(AA‐K).
By
combining
experimental
theoretical
calculation,
a
high‐performance
catalyst
Ni(Co)OOH
developed,
which
exhibits
current
density
403
mA
cm⁻
2
at
1.40
V
(vs
RHE)
with
96%
Faraday
efficiency
for
AA‐K
in
electrooxidation
lactate
(LA‐K,
product
degradation
KOH).
Through
situ
spectroscopy
techniques
functional
theory
calculations,
structural
regulation
catalyst,
reaction
pathways
elucidated.
Further
experiments
demonstrate
superior
catalytic
performance
industrial‐scale
tandem
system.
In
h
electrolysis,
320
g
produces
232
L
H₂,
yielding
1200
97%
purity
after
neutralization
drying.
The
system
demonstrates
high
(approaching
97%)
diverse
real
forms,
including
powder,
cups,
fibers,
cloth.
This
research
provides
scalable
sustainable
upcycling.
Language: Английский
Strategies for Modulating Ni-based Layered Double Hydroxides for Boosting Urea Electrooxidation
Chang‐Hyeon Ji,
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Jipeng Wang,
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Sheng Feng
No information about this author
et al.
Journal of Alloys and Compounds,
Journal Year:
2025,
Volume and Issue:
unknown, P. 179306 - 179306
Published: Feb. 1, 2025
Language: Английский
Sulfhydryl group modified layered double hydroxide accelerates the formation of NiOOH active phase for enhanced urea oxidation reaction
Mingqiang Chen,
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Wenda Zhang,
No information about this author
Qingna Gong
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et al.
Journal of Power Sources,
Journal Year:
2025,
Volume and Issue:
641, P. 236834 - 236834
Published: March 21, 2025
Language: Английский
Electron Shuttling of Iron‐Oxygen‐Cobalt Bridging in Cobalt Assembled Iron Oxyhydroxide Catalyst Boosts the Urea Oxidation Stability and Activity
Guizeng Liang,
No information about this author
Rongrong Zhang,
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C. S. Ji
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et al.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 21, 2025
Abstract
Iron
(Fe)‐based
materials
hold
great
potential
as
urea
oxidation
reaction
(UOR)
catalysts,
however,
the
deactivation
of
active
Fe‐oxyhydroxide
(FeOOH)
species
induced
by
its
dissolution
during
catalytic
process
under
high
current
densities
is
still
significant
challenge.
Herein,
cobalt
(Co)
assembled
FeOOH
constructed,
and
formation
Iron‐Oxygen‐Cobalt
(Fe‐O‐Co)
bridging
triggers
electron
transfer
from
Co
to
Fe
sites.
This
shuttling
induces
low
valence
state
sites
in
FeOOH.
Co‐FeOOH
catalyst
achieves
a
density
1000
mA
cm
−2
at
voltage
merely
1.59
V,
showing
substantial
improvement
compared
pure
(1.97
V).
Meanwhile,
urea‐assisted
anion
exchange
membrane
electrolyzer,
after
24
h
continuous
operation
,
fluctuation
12.4%,
significantly
lower
than
that
(49.9%).
The
situ
experiments
theoretical
calculations
demonstrate
Fe‐O‐Co
endows
suppressive
Fe‐segregation,
fast
charge
Fe(Co)OOH
phase
negative‐shifted
d‐band
center
metal
sites,
boosting
UOR
stability
activity.
Language: Английский
Delamination of NiFe layered double hydroxides into perforated monolayers for efficient water splitting
Huanran Li,
No information about this author
Hong Pang,
No information about this author
Wei Ma
No information about this author
et al.
Journal of Colloid and Interface Science,
Journal Year:
2025,
Volume and Issue:
unknown, P. 137478 - 137478
Published: March 1, 2025
Language: Английский
Formaldehyde oxidation reaction enhanced by interface engineering of Cu/Cu2O/Co(OH)2 composite electrocatalyst for bipolar hydrogen production
Zi Qiang,
No information about this author
Chang Bao Han,
No information about this author
Wen Kang Zhao
No information about this author
et al.
Chemical Engineering Journal,
Journal Year:
2025,
Volume and Issue:
unknown, P. 162568 - 162568
Published: April 1, 2025
Language: Английский
Superhydrophilicity and Electronic Modulation on Self‐Supported Lignin‐Derived Carbon Coupled with NiO@MoNi4 for Enhancing Urea Electrolysis
Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 18, 2024
Developing
highly
efficient
biomass-derived
carbon-based
electrocatalysts
remains
challenging
for
urea
electrolysis
because
most
of
these
show
powder
morphology,
which
can
lead
to
Ostwald
ripening
during
the
reaction
process,
and
its
mechanism
should
be
further
verified.
Herein,
self-supported
lignin-derived
carbon
coupling
NiO@MoNi
Language: Английский
Mediating Self‐Oxidation and Competitive Adsorption for Achieving High‐Selective Urea Oxidation Catalysis at Industrial‐Level Current Densities
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 23, 2024
Abstract
Inhibiting
the
deactivation
of
nickel‐based
catalysts
caused
by
self‐oxidation
and
competitive
adsorption
behavior
is
still
a
major
challenge
for
urea
oxidation
reaction
(UOR),
especially
under
industrial‐level
current
densities.
In
this
study,
crystalline
NiSe
2
/amorphous
NiFe‐LDH
(NiSe
/NiFe‐LDH)
heterojunction
catalyst
rationally
constructed
selective
electrocatalytic
UOR.
situ
Raman
spectra
ex
characterization
results
reveal
that
such
structure
can
tailor
impede
accumulation
NiOOH
species
during
UOR
process.
Density
function
theory
simulations
disclose
self‐driven
charge
transport
from
electron‐deficient
region
to
electron‐rich
would
induce
formation
local
electrophilic/nucleophilic
adsorb
electron‐donating
‐NH
electron‐withdrawing
C
=
O
groups,
respectively.
This
optimizes
molecules
hinders
overaccumulation
OH
−
ions
on
surface
/NiFe‐LDH,
which
beneficial
priority
occurrence
over
oxygen
evolution
(OER)
realization
high
selectivity.
Benefiting
tailored
favorable
adsorption,
/NiFe‐LDH
could
act
as
high‐selective
anode
achieve
ultrahigh
800
mAcm
−2
only
at
1.447
V.
Besides,
UV–vis
spectrophotometry
also
unveiled
has
capability
electrochemically
degrade
urea,
offering
great
promise
practical
application
potentials.
Language: Английский