Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 1, 2024
Abstract
Electrocatalytic
technology
is
essential
to
develop
environmentally
friendly
energy
technologies
and
reduce
dependence
on
non‐renewable
resources.
The
construction
of
highly
efficient,
inexpensive,
robust
electrocatalysts
the
primary
prerequisite
large‐scale
application
electrochemical
devices.
In
recent
years,
selenium‐based
catalysts
(SBCs)
have
been
extensively
investigated
emerged
as
a
promising
candidate
for
electrocatalysis
given
their
potential
or
replace
dosage
noble
metals
ability
catalyze
range
critical
processes.
This
Review
minutely
analyses
research
advances
in
SBCs,
highlighting
significant
role
Se
enhancing
catalytic
performance.
First,
it
starts
from
concepts
related
followed
by
classification
SBCs
well
strategies
regulate
activity
are
elaborated.
Then,
techniques
characterizing
systematically
summed
up,
mainly
focusing
morphological
structural
characterization
methods.
Next,
applications
various
energy‐conversion
reactions
(e.g.,
hydrogen
evolution
reaction,
oxygen
reduction
nitrogen
CO
2
reaction)
discussed,
aiming
at
elucidating
association
between
structure–activity
correlations.
Finally,
challenges
future
development
trends
presented.
Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
14(21)
Published: Feb. 2, 2024
Abstract
Metal–support
interaction
(MSI)
is
witnessed
as
an
essential
manner
to
stabilize
active
metals
and
tune
catalytic
activity
for
heterogonous
water
splitting.
Kinetically
driving
the
electrolysis
(WE)
appeals
a
rational
MSI
system
with
coupled
electron‐donating/accepting
(e‐D/A)
characters
hydrogen/oxygen
evolution
reactions
(HER/OER).
However,
metal
stabilization
effect
by
will
in
turn
restrict
deblocking
of
e‐D/A
properties
challenge
full
electrocatalytic
optimization.
This
study
profiles
heterostructure
featuring
metastable
Ru
clusters
on
defective
NiFe
hydroxide
(Ru/d‐NiFe
LDH)
support
low‐precious
(≈2
wt%)
platform
efficient
WE.
It
indicated
that
interfacial
oxygen
vacancies
can
deviate
stable
4d
5
orbit
2+δ
state,
regulate
d‐band
center
levels
toward
facilitated
HER/OER
processes.
Resultantly,
Ru/d‐NiFe
LDH
attains
ultralow
overpotentials
at
10
mA
cm
−2
Pt‐beyond
alkaline
HER
(18
mV)
OER
(220
fast
kinetics
durability.
The
symmetrical
electrolyzer
delivers
promising
voltage
1.49
V
1
m
KOH
seawater
splitting
performance.
work
carries
interesting
opportunities
rationalizing
sophisticated
metal‐support
electrocatalysts
through
metal‐site
metastabilization
engineering.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(22), P. 15515 - 15524
Published: May 24, 2024
The
continuous
dissolution
and
oxidation
of
active
sites
in
Ru-based
electrocatalysts
have
greatly
hindered
their
practical
application
proton
exchange
membrane
water
electrolyzers
(PEMWE).
In
this
work,
we
first
used
density
functional
theory
(DFT)
to
calculate
the
energy
Ru
3d
transition
metal-doped
MRuOx
(M
=
Sc,
Ti,
V,
Cr,
Mn,
Fe,
Co,
Ni,
Cu,
Zn)
evaluate
stability
for
acidic
oxygen
evolution
reaction
(OER)
screen
out
ZnRuOx
as
best
candidate.
To
confirm
theoretical
predictions,
experimentally
synthesized
these
materials
found
that
indeed
displays
robust
OER
with
a
negligible
decay
η10
after
15
000
CV
cycles.
Of
importance,
using
anode,
PEMWE
can
run
stably
120
h
at
200
mA
cm–2.
We
also
further
uncover
mechanism
ZnRuOx,
i.e.,
Zn
atoms
doped
outside
nanocrystal
would
form
"Zn-rich"
shell,
which
effectively
shortened
average
Ru–O
bond
lengths
strengthen
interaction
therefore
boosted
intrinsic
OER.
short,
work
not
only
provides
new
study
paradigm
DFT
calculations
guide
experimental
synthesis
but
offers
proof-of-concept
metal
dopants
RuO2
stabilizer
universal
principle
develop
high-durability
catalysts
PEMWE.
Advanced Materials,
Journal Year:
2023,
Volume and Issue:
36(9)
Published: Dec. 4, 2023
Designing
robust
bifunctional
catalysts
for
oxygen
evolution
reaction
(OER)
and
hydrogen
in
all-pH
conditions
overall
water
splitting
(OWS)
is
an
effective
way
to
achieve
sustainable
development.
Herein,
a
composite
Ru-VO
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(12), P. 14742 - 14749
Published: March 14, 2024
The
sluggish
kinetics
of
the
oxygen
evolution
reaction
(OER)
always
results
in
a
high
overpotential
at
anode
water
electrolysis
and
an
excessive
electric
energy
consumption,
which
has
been
major
obstacle
for
hydrogen
production
through
electrolysis.
In
this
study,
we
present
CoNi-LDH/Fe
MOF/NF
heterostructure
catalyst
with
nanoneedle
array
morphology
OER.
1.0
M
KOH
solution,
only
required
overpotentials
275
305
mV
to
achieve
current
densities
500
1000
mA/cm2
OER,
respectively.
catalytic
activities
are
much
higher
than
those
reference
single-component
CoNi-LDH/NF
Fe
catalysts.
improved
performance
can
be
ascribed
synergistic
effect
CoNi-LDH
MOF.
particular,
when
anodic
OER
is
replaced
urea
oxidation
(UOR),
relatively
lower
thermodynamic
equilibrium
potential
expected
reduce
cell
voltage,
same
reduced
by
80
40
mV,
voltage
drive
overall
splitting
(OUS)
1.55
V
100
Pt/C/NF||CoNi-LDH/Fe
two-electrode
electrolytic
cell.
This
value
60
compared
that
(OWS).
Our
indicate
reasonable
construction
significantly
give
rise
electrocatalytic
performance,
using
UOR
replace
OWS
greatly
consumption.
Journal of Materials Chemistry A,
Journal Year:
2024,
Volume and Issue:
12(30), P. 18832 - 18865
Published: Jan. 1, 2024
This
review
focuses
mainly
on
the
overall
facilitating
effect
of
heterostructures
OER
process.
The
fabrication
heterostructured
electrocatalysts
and
relationship
between
their
structures
electrocatalytic
properties
are
discussed.
Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: May 25, 2024
Developing
low-cost
and
highly
efficient
bifunctional
catalysts
for
both
the
oxygen
evolution
reaction
(OER)
hydrogen
(HER)
is
a
challenging
problem
in
electrochemical
overall
water
splitting.
Here,
iron,
tungsten
dual-doped
nickel
sulfide
catalyst
(Fe/W-Ni
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(34)
Published: March 12, 2024
Abstract
Alkaline
water
electrolysis
is
among
the
most
promising
technologies
to
massively
produce
green
hydrogen.
Developing
highly‐active
and
durable
electrodes
catalyze
oxygen
evolution
reaction
(OER)
hydrogen
(HER)
of
primary
importance.
Here
a
facile,
room‐temperature
synthetic
route
presented
access
heazlewoodite
phase
(Ni,
Fe)
3
S
2
nanosheet
arrays
supported
on
NiFe
foam
(NFF),
whose
production
can
be
easily
scaled
up
meter
size
per
batch
operation.
The
/NFF
electrode
serve
as
high‐performance
electrocatalyst
for
both
HER
OER
in
alkaline
media,
remains
highly
stable
over
1000
h
at
100
mA
cm
−2
current
densities.
When
working
electrocatalyst,
confirmed
catalytic
that
provides
high
density
efficient
active
sites
(e.g.,
Ni─Ni
Ni─Fe
bridge
sites).
During
electrochemical
testing,
nanosheets
totally
transform
into
γ
‐(Fe,
Ni)OOH
OER.
As
consequence,
used
integrate
an
electrolyzer
cathode
anode,
give
excellent
performance
(600
@1.93
V),
which
better
than
based
commercial
Raney
Ni
electrodes.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 10, 2024
Abstract
Transition
metal
chalcogenides
are
an
important
class
of
electrocatalysts
with
broad
application
prospects
in
alkaline
oxygen
evolution
reactions.
Many
researchers
focusing
on
the
situ
conversion
cations
catalysts,
but
have
rarely
considered
contribution
oxidation,
leaching,
and
re‐absorption
to
catalytic
activity.
Herein,
multiple
characterization
approaches
used
monitor
mechanism
origin
CoTe@CoS‐electrocatalyzed
reaction
(OER)
The
research
results
reveal
that
electro‐oxidative
dissolution
Te
S
electrode
surface
forms
TeO
3
2−
SO
,
which
adsorbed
surface.
Moreover,
species
will
further
transform
into
4
.
As
expected,
extra
addition
mixed
tellurite
sulfate
ions
Co
(OH)
2
electrolyte
produces
a
synergistic
effect
can
significantly
boost
OER
Selenites
analogous
effect,
indicating
adsorption
chalcogenates
has
universal
improving
performance.
findings
this
work
provide
unique
insights
materials
enhancing
activity
during
processes.