ACS Applied Energy Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 7, 2024
The
development
of
highly
efficient
nonprecious
metal
electrocatalysts
for
hydrogen
evolution
reaction
(HER)
is
important
and
urgent.
Herein,
a
heterostructured
electrocatalyst
Mo–CoP/Yb2O3
was
fabricated
between
Mo-doped
CoP
rare-earth
oxide
Yb2O3.
not
only
displays
outstanding
HER
activity
but
also
exhibits
urea
oxidation
hydrazine
activity,
which
the
indicated
by
low
overpotential
values
33
mV
at
10
mA
cm–2
100
cm–2,
performance
with
potential
1.449
V
vs
RHE
0.153
cm–2.
Further,
when
used
as
both
cathode
anode
urea-assisted
production
(cell
voltage
1.513
cm–2)
oxidation-assisted
0.253
cm–2),
it
economically
advantageous.
results
show
that
plays
significant
role
in
catalytic
process,
while
incorporation
Yb2O3
can
enhance
catalyst's
hydrophilicity
increase
water
adsorption,
potentially
aiding
splitting.
Besides,
synergistic
effect
Mo
doping
heterostructure
regulates
electronic
structure
facilitates
electron
transfer,
thus
improving
Mo–CoP/Yb2O3.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 2, 2024
Abstract
Exploring
an
efficient
nonnoble
metal
catalyst
for
hydrogen
evolution
reaction
(HER)
is
critical
industrial
alkaline
water
electrolysis.
However,
it
remains
a
great
challenge
due
to
the
additional
energy
required
H─OH
bond
cleavage
and
lack
of
enough
H
2
O
adsorption
sites
most
catalysts.
Herein,
integration
oxophilic
Eu
3
with
NiCo
alloy
evoked
multisite
synergism
facilitate
dissociation
HER
proposed.
The
optimized
‐NiCo
exhibits
excellent
activity
low
overpotential
only
60
mV
at
10
mA
cm
−2
good
electrochemical
stability,
which
superior
that
‐free
comparable
benchmark
Pt/C.
key
roles
on
enhanced
performance
are
identified
by
in
situ
Raman
spectroscopy
theoretical
calculations.
It
discovered
strong
oxophilicity
facilitates
breakage
bonding
while
evoking
electron
redistribution
/NiCo
interface
accelerating
Volmer
step
HER.
Furthermore,
obtained
as
both
anode
cathode
displays
overall
water‐splitting
stability
1.0
M
KOH
solution.
believed
this
study
provides
important
inspiration
design
high‐performance
electrocatalysts
toward
based
rare‐earth
materials.
Chemical Science,
Journal Year:
2024,
Volume and Issue:
15(30), P. 11890 - 11901
Published: Jan. 1, 2024
Ir
nanoparticles
on
Co
6
Mo
C
nanofibers
bridging
with
a
carbon
layer
have
been
fabricated
as
efficient
bifunctional
electrocatalysts
for
water
splitting,
presenting
ultrahigh
electrocatalytic
performance
at
ampere-level
current
density.
Science,
Journal Year:
2025,
Volume and Issue:
387(6735), P. 791 - 796
Published: Jan. 2, 2025
The
future
deployment
of
terawatt-scale
proton
exchange
membrane
water
electrolyzer
(PEMWE)
technology
necessitates
development
an
efficient
oxygen
evolution
catalyst
with
low
cost
and
long
lifetime.
Currently,
the
stability
most
active
iridium
(Ir)
catalysts
is
impaired
by
dissolution,
redeposition,
detachment,
agglomeration
Ir
species.
Here
we
present
a
ripening-induced
embedding
strategy
that
securely
embeds
in
cerium
oxide
support.
Cryogenic
electron
tomography
all-atom
kinetic
Monte
Carlo
simulations
reveal
synchronizing
growth
rate
support
nucleation
Ir,
regulated
sonication,
pivotal
for
successful
synthesis.
A
PEMWE
using
this
achieves
cell
voltage
1.72
volts
at
current
density
3
amperes
per
square
centimeter
loading
just
0.3
milligrams
degradation
1.33
microvolts
hour,
as
demonstrated
6000-hour
accelerated
aging
test.
Advanced Energy Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 10, 2025
Abstract
Designing
heterogeneous
interface
to
enhance
the
kinetics
for
electrocatalysts
is
a
highly
efficient
but
challenging
pathway
toward
hydrogen
evolution
reaction
(HER)
in
water
electrolysis.
Herein,
coupling
of
CeO
2
quantum
dots
onto
porous
Ru
aerogel
through
interfacial
Ru‐O‐Ce
bridge
proposed
construct
‐Ru
as
superior
HER
electrocatalyst
with
ultra‐low
overpotentials.
In
situ
characterizations
and
theoretical
calculations
reveal
electron
distribution
at
boost
bonding
sites,
faster
adsorption
dissociation
sites
kinetics.
Furthermore,
employed
excellent
cathodes
both
acidic
alkaline
electrolyzers
ampere‐level
current
density
stably
operated
over
500
hours.
Thus,
synergistic
effect
tunes
catalytic
mechanism
reinforces
activity,
realizing
generation
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 22, 2024
Abstract
Reconstruction
of
catalysts
is
now
well
recognized
as
a
common
phenomenon
in
electrocatalysis.
As
the
reconstructed
structure
may
promote
or
hamper
electrochemical
performance,
how
to
achieve
designed
active
surface
for
highly
enhanced
catalytic
activity
through
reconstruction
needs
be
carefully
investigated.
In
this
review,
genesis
and
effects
various
processes,
such
hydrogen
evolution
reaction
(HER),
oxygen
(OER),
carbon
dioxide
reduction
(CO
2
RR),
nitrate
(NO
3
RR)
are
first
described.
Then,
strategies
optimizing
reconstruction,
valence
states
control,
phase
retention,
engineering,
poisoning
prevention
comprehensively
discussed.
Finally,
general
rules
optimization
summarized
give
perspectives
future
study.
It
believed
that
review
shall
provide
deep
insights
into
electrocatalytic
mechanisms
guide
design
pre‐catalysts
with
improved
activity.
EcoEnergy,
Journal Year:
2024,
Volume and Issue:
2(2), P. 322 - 335
Published: May 25, 2024
Abstract
Photoelectrochemical
(PEC)
water
splitting
offers
a
promising
route
for
harnessing
solar
energy
to
produce
clean
hydrogen
fuel
sustainably.
A
major
hurdle
has
been
boosting
the
performance
of
photoanode
materials
within
acidic
electrolytes—a
critical
aspect
advancing
PEC
technology.
In
response
this
challenge,
we
report
method
augment
efficacy
hematite
photoanodes
under
conditions
by
anchoring
IrO
x
nanoparticles,
replete
with
hydroxyl
groups,
onto
their
surface.
remarkable
and
steady
photocurrent
density
1.71
mA
cm
−2
at
1.23
V
versus
RHE
was
achieved,
marking
significant
leap
in
efficiency
media.
The
introduction
layer
notably
expanded
electrochemically
active
surface
area
more
sites,
fostering
improved
charge
separation
transfer.
It
also
served
as
an
effective
hole
capture
layer,
drawing
photogenerated
holes
from
facilitate
swift
migration
sites
oxidation
process.
This
advancement
potential
fully
harness
capabilities
environments,
thereby
smoothing
path
toward
sustainable
production
through
splitting.
Small Methods,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 4, 2025
Stabilizing
oxidation
state
of
Cu
(Cuδ+,
δ
>
0)
sites
is
the
key-enabling
issue
for
electrocatalytic
carbon
dioxide
(CO2)
reduction
reaction
(eCO2RR)
to
multicarbon
(C2+)
products.
The
present
study
addresses
this
challenge
by
introducing
cerium
(Ce)
doping
into
La2CuO4.
Ce
facilitates
f-d
orbital
coupling
between
4f
and
3d
orbitals,
suppressing
electron
enrichment
around
atoms
transferring
electrons
from
orbitals
via
a
Cu-O-Ce
chain.
These
changes
modulate
electronic
structure
Cu,
reduce
distance
neighboring
atoms,
optimize
binding
energy
surface-adsorbed
CO
(*CO),
lower
barrier
*CO
dimerization.
As
result,
La1.95Ce0.05CuO4
catalyst
achieves
Faradaic
efficiency
up
81%
C2+
products
maintains
high
stability
over
50
h
operation.
This
work
highlights
unique
role
in
stabilizing
Cuδ+
hence
enhancing
C-C
coupling,
providing
pathway
designing
efficient
catalysts
eCO2RR.
ACS Catalysis,
Journal Year:
2024,
Volume and Issue:
14(17)
Published: Aug. 14, 2024
Designing
highly
active
and
durable
electrocatalysts
with
low
noble-metal
mass-loading
to
boost
the
sluggish
oxygen
evolution
reaction
is
crucial
for
hydrogen
production.
Herein,
a
Ru-enriched
surface
oxygen-defective
[email protected]
catalyst
developed
enhanced
activity
robust
stability
through
MnOx
serving
as
an
electron
reservoir.
This
ultralow
of
91.2
μgRu
cm−2
delivers
1645
A
gRu−[email protected]
V
versus
RHE
long-term
operational
exceeding
240
h
high
number
(6.22
×
104)
in
0.5
M
H2SO4.
Characterizations
theoretical
calculations
reveal
that
sacrificial
spaced
Mn
dissolution
makes
adjacent
serve
reservoir
replenish
electrons
on
Ru
sites
suppress
overoxidation
extending
stability.
The
crystalline−amorphous
heterointerfaces,
abundant
vacancies,
stable
Ru−O−Mn
motifs
simultaneously
facilitate
superior
activity.
weaker
adsorption
between
oxo-intermediates
lowers
energy
barrier
from
O*
*OOH
following
adsorbate
mechanism
(AEM)
pathway.
work
provides
promising
perspective
designing
cost-effective
OER
proton
exchange
membrane
water
electrolysis.
Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: May 21, 2024
Abstract
Understanding
the
structure‐activity
correlation
is
an
important
prerequisite
for
rational
design
of
high‐efficiency
electrocatalysts
at
atomic
level.
However,
effect
coordination
environment
on
electrocatalytic
oxygen
evolution
reaction
(OER)
remains
enigmatic.
In
this
work,
regulation
proton
transfer
involved
in
water
oxidation
by
engineering
based
Co
3
(PO
4
)
2
and
CoHPO
reported.
The
HPO
2−
anion
has
intermediate
p
K
a
value
between
Co(II)‐H
O
Co(III)‐H
to
be
served
as
appealing
proton‐coupled
electron
(PCET)
induction
group.
From
theoretical
calculations,
pH‐dependent
OER
properties,
deuterium
kinetic
isotope
effects,
operando
electrochemical
impedance
spectroscopy
(EIS)
Raman
studies,
catalyst
beneficially
reduces
energy
barrier
hopping
modulates
formation
high‐valent
species,
thereby
enhancing
activity.
This
work
demonstrates
promising
strategy
that
involves
tuning
local
optimize
PCET
steps
activities
applications.
addition,
designed
system
offers
motif
understand
structure‐efficiency
relationship
from
those
amino‐acid
residue
with
buffer
ability
natural
photosynthesis.