Rapid Outgassing of Hydrophilic TiO2 Electrodes Achieves Long-Term Stability of Anion Exchange Membrane Water Electrolyzers
Nano-Micro Letters,
Journal Year:
2025,
Volume and Issue:
17(1)
Published: March 13, 2025
Abstract
The
state-of-the-art
anion-exchange
membrane
water
electrolyzers
(AEMWEs)
require
highly
stable
electrodes
for
prolonged
operation.
stability
of
the
electrode
is
closely
linked
to
effective
evacuation
H
2
or
O
gas
generated
from
surface
during
electrolysis.
In
this
study,
we
prepared
a
super-hydrophilic
by
depositing
porous
nickel–iron
nanoparticles
on
annealed
TiO
nanotubes
(NiFe/ATNT)
rapid
outgassing
such
nonpolar
gases.
NiFe/ATNT
exhibited
an
overpotential
235
mV
at
10
mA
cm
−2
oxygen
evolution
reaction
in
1.0
M
KOH
solution,
and
was
utilized
as
anode
AEMWE
achieve
current
density
1.67
A
1.80
V.
addition,
with
electrode,
which
enables
outgassing,
showed
record
1500
h
0.50
under
harsh
temperature
conditions
80
±
3
°C.
Language: Английский
Tuning the eg* band broadening of the in-situ NiOOH by W doping for efficient biomass electrooxidation
Jinlv Wei,
No information about this author
Jianlong Zhang,
No information about this author
Huan Fei Wen
No information about this author
et al.
Chinese Journal of Structural Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown, P. 100541 - 100541
Published: Feb. 1, 2025
Language: Английский
The synergistic effect of Ni–NiMo4N5 heterointerface construction and Fe-doping enables active and durable alkaline water splitting at industrial current density
Journal of Materials Chemistry A,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
The
synergistic
effect
of
heterogeneous
interfaces
and
doping
optimizes
electronic
structure
accelerates
charge
transfer,
significantly
boosting
alkaline
water
electrolysis
performance.
Language: Английский
Recent advances in lanthanide-based materials for oxygen evolution reaction: Challenges and future prospects
Sheraz Muhammad,
No information about this author
Lixia Wang,
No information about this author
Zhiyang Huang
No information about this author
et al.
Coordination Chemistry Reviews,
Journal Year:
2025,
Volume and Issue:
534, P. 216573 - 216573
Published: March 4, 2025
Language: Английский
Cation (Cr3+, Zn2+, Cu2+ and Mn3+) doping to construct high entropy spinel oxide nanocrystals for modulation of oxygen evolution reaction
Bingxuan Zhai,
No information about this author
Jian Gong,
No information about this author
Leping Liu
No information about this author
et al.
Fuel,
Journal Year:
2025,
Volume and Issue:
393, P. 134992 - 134992
Published: March 9, 2025
Language: Английский
Bifunctional barium cerate catalyst doped with Fe for enhanced electrochemical stability during oxygen reduction and evolution reactions
International Journal of Hydrogen Energy,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 1, 2025
Language: Английский
Enhancing Oxygen Evolution Electrocatalysis in Heazlewoodite: Unveiling the Critical Role of Entropy Levels and Surface Reconstruction
Hangning Liu,
No information about this author
Xinghang Liu,
No information about this author
Anbang Sun
No information about this author
et al.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 7, 2025
Abstract
Entropy
engineering
has
proven
effective
in
enhancing
catalyst
electrochemical
properties,
particularly
for
the
oxygen
evolution
reaction
(OER).
Challenges
persist,
however,
modulating
entropy
and
understanding
dynamic
reconfiguration
of
high‐entropy
sulfides
during
OER.
In
this
study,
an
innovative
situ
corrosion
method
is
introduced
to
convert
low‐valent
nickel
on
a
foam
substrate
into
heazlewoodite
(HES/NF),
significantly
boosting
OER
performance.
By
synthesizing
series
low‐,
medium‐,
heazlewoodites,
intrinsic
factors
influence
surface
electrocatalytic
activity
systematically
explored.
Employing
combination
ex
characterization
techniques,
it
observed
that
HES/NF
dynamically
transforms
stable
hydroxide
oxide
(MOOH)‐sulfide
composite
under
conditions.
This
transition,
coupled
with
lattice
distortion,
optimizes
electrostatic
potential
distribution,
ensuring
superior
catalytic
preventing
sulfide
deactivation
through
formation
HES‐MOOH
species.
synergy
enables
achieve
remarkably
low
overpotentials:
172.0
mV
at
100.0
mA
cm
−2
229.0
extreme
current
density
300.0
.
When
paired
Pt/C
cathode,
exhibits
rapid
kinetics,
outstanding
stability,
exceptional
water‐splitting
The
scalable,
cost‐effective
approach
paves
way
advanced
electrocatalyst
design,
promising
breakthroughs
energy
storage
conversion
technologies.
Language: Английский
Optimizing Electron Delocalization in Cobalt Clusters via d‐d Orbital Coupling for Efficient Bifunctional Oxygen Electrocatalysis
Xin Yu Wang,
No information about this author
Sichen Huo,
No information about this author
Yanjie Chen
No information about this author
et al.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 14, 2025
Abstract
Cobalt
atom
cluster
(Co
AC
)‐based
electrocatalysts
usually
exhibit
high
activity
for
oxygen
reduction
reaction
(ORR),
but
display
limited
performance
in
evolution
(OER).
To
enhance
their
bifunctional
catalytic
efficiency,
it
is
crucial
to
tailor
the
d
‐orbital
electronic
structure
of
Co
through
orbital
coupling
effect,
optimizing
chemisorption
O‐intermediates.
Herein,
a
3
‐4
strategy
used
construct
‐molybdenum
carbide/nanocarbon
cake
‐Mo
x
C/CC)
catalyst
with
hollow
ORR/OER
zinc‐air
batteries
(ZABs).
Experimental
and
theoretical
results
confirm
that
4
transition
metal
Mo,
fewer
electrons
more
unfilled
orbitals,
interacts
strongly
sites
‐
coupling,
promoting
electron
enrichment
triggering
delocalization.
This
process
accelerates
rate‐limiting
steps
*OH
desorption
ORR
*OOH
formation
OER,
leading
an
ultra‐low
potential
gap
0.604
V
improved
stability.
Notably,
C/CC‐based
liquid
flexible
all‐solid‐state
ZABs
excellent
open‐circuit
voltages
1.49
1.47
V,
power
densities
146.4
103.4
mW
cm
−2
,
respectively,
highlighting
replace
precious
catalysts.
study
may
open
new
avenues
manipulating
properties
‐based
boosting
strategy.
Language: Английский
Etching Accelerates Reconstruction and Activates Lattice Oxygen of Anion Vacancies‐Enriched Cobalt‐Iron Phosphide/(Oxy)Hydroxide Nanohybrid Frameworks for Enhanced Oxygen Evolution
Jiayao Fan,
No information about this author
Jiadong Jiang,
No information about this author
Yingying Wang
No information about this author
et al.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 14, 2025
Abstract
Transition
metal
phosphides
(TMPs)
nanostructures
are
considered
to
be
promising
pre‐catalysts
for
electrochemical
oxygen
evolution
reaction
(OER).
Nonetheless,
most
TMPs
only
experience
limited
surface
reconstruction
during
OER,
resulting
in
fewer
active
layer,
insufficient
sites
and
thus
unsatisfactory
performance.
Thereby,
finely
control
the
level
is
crucial
but
still
challenging.
Here,
Co
0.7−x
Fe
0.3−y
P/Co
x
y
OOH
nanohybird
frameworks
with
numerous
crystalline/amorphous
interfaces
fabricated
by
alkali
etching
of
hollow
crystalline
0.7
0.3
P
nanocubes,
leading
in‐situ
growth
amorphous
nanosheets
subunits.
Such
nanohybrid
own
abundant
phosphorus
vacancies,
optimal
interface
electronic
structure,
hydrophilic
character,
which
manifest
exceptional
OER
performance
overpotential
256
mV
reach
10
mA
cm
−2
current
alkaline
media,
exceeding
1−x
OOH,
1−y
P/Fe
P,
IrO
2
,
reported
unprecious‐metal‐based
catalysts.
As
revealed
series
ex‐situ
spectroscopic
analyses,
formation
anion
defects
phase
promote
deep
such
catalyst,
triggering
lattice
participation
synergy
adsorbate
mechanism
toward
OER.
This
work
may
spur
development
TMPs‐based
catalysts
integrating
defect,
engineering
via
facile
etching,
their
applications
water
splitting
or
other
clean
energy
options.
Language: Английский