Bridging gaps between lab- and fab-oriented anode design for proton exchange membrane water electrolyzers
Chem,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 1, 2024
Language: Английский
Progress of Ir/Ru-based catalysts for electrocatalytic oxygen evolution reaction in acidic environments
International Journal of Hydrogen Energy,
Journal Year:
2024,
Volume and Issue:
92, P. 657 - 671
Published: Oct. 30, 2024
Language: Английский
Strong Metal‐Support Interactions in Heterogeneous Oxygen Electrocatalysis
Zhiqian Hou,
No information about this author
Chenghao Cui,
No information about this author
Yanan Yang
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et al.
Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 26, 2024
Molecular
oxygen
redox
electrocatalysis
involves
reduction
and
evolution
as
core
reactions
in
various
energy
conversion
environmental
technology
fields.
Strong
metal-support
interactions
(SMSIs)
based
nanomaterials
are
regarded
desirable
state-of-the-art
heterogeneous
electrocatalysts
due
to
their
exceptional
physicochemical
properties.
Over
the
past
decades,
considerable
advancements
theory
experiment
have
been
achieved
related
studies,
especially
modulating
electronic
structure
geometrical
configuration
of
SMSIs
enable
activity,
selectivity,
stability.
In
this
focuses
on
concept
SMSI,
explore
manifestations
mechanisms
action,
summarizes
recent
advances
for
efficient
applications.
Additionally,
correlation
between
properties
different
metals
supports
is
systematically
elucidated,
potential
structure-activity
relationships
catalytic
performance
outlined
through
theoretical
models.
Finally,
obstacles
confronting
burgeoning
field
comprehensively
concluded,
targeted
recommendations
coping
strategies
proposed,
future
research
perspectives
outlined.
Language: Английский
Advances in Ru-based Acidic OER Electrocatalysts: Addressing the Activity-Stability Trade-off
Published: April 1, 2025
Language: Английский
Research Progress in Structure Evolution and Durability Modulation of Ir‐ and Ru‐Based OER Catalysts under Acidic Conditions
Yunhai Zi,
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Chengxu Zhang,
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Jian-Qiang Zhao
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et al.
Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 6, 2024
Abstract
Green
hydrogen
energy,
as
one
of
the
most
promising
energy
carriers,
plays
a
crucial
role
in
addressing
and
environmental
issues.
Oxygen
evolution
reaction
catalysts,
key
to
water
electrolysis
production
technology,
have
been
subject
durability
constraints,
preventing
large‐scale
commercial
development.
Under
high
current
density
harsh
acid‐base
electrolyte
conditions
reaction,
active
metals
catalysts
are
easily
converted
into
high‐valent
soluble
species
dissolve,
leading
poor
structural
catalysts.
There
is
an
urgent
need
overcome
challenges
under
acidic
develop
electrocatalysts
with
both
catalytic
activity
durability.
In
this
review,
latest
research
results
analyzed
depth
from
thermodynamic
kinetic
perspectives.
First,
comprehensive
summary
deactivation
state
process
noble
metal
oxide
presented.
Second,
structure
possessing
discussed.
Finally,
four
new
strategies
for
preparation
stable
“electron
buffer
(ECB)
strategy”,
combination
strength
control,
strain
surface
coating,
summarized.
The
prospects
also
elaborated
future
synthesis
more
effective
Ru/Ir‐based
boost
their
application.
Language: Английский
IrO2/MnO2 metal oxide-support interaction enables robust acidic water oxidation
Journal of Colloid and Interface Science,
Journal Year:
2024,
Volume and Issue:
683, P. 160 - 169
Published: Dec. 6, 2024
Language: Английский
Porous and B‐site Substituted Y2[Mn0.2Ru0.8]2O7 Pyrochlore for Boosting Acidic Water Oxidation Activity and Stability
Zhan Tian,
No information about this author
Xin Yang,
No information about this author
Hongrui Jia
No information about this author
et al.
ChemCatChem,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 7, 2024
Abstract
Boosting
the
reaction
stability
without
sacrificing
activity
and
cost
is
extremely
important
but
full
of
challenges
for
RuO
2
‐based
oxygen
evolution
catalysts.
Herein,
porous
B‐site
substituted
Y
[Mn
0.2
Ru
0.8
]
O
7
(p‐Y
)
pyrochlore
toward
innovatively
synthesized.
The
formed
meso‐/macroporous
structure
can
increase
specific
surface
area
corresponding
active
sites,
meanwhile,
Mn‐substitution
modulate
electronic
structure,
stabilize
morphology,
reduce
dosage
species.
Interestingly,
p‐Y
performs
50
h
stable
operation,
significantly
outperforming
commercial
(CM)
counterpart
with
less
than
life.
Furthermore,
required
overpotential
to
achieve
10
mA
cm
−2
only
266
mV,
accompanied
favorable
kinetics
catalyst
utilization.
Language: Английский