Understanding
and
tuning
epitaxial
complex
oxide
films
are
crucial
in
controlling
the
behavior
of
devices
catalytic
processes.
Substrate-induced
strain,
doping,
layer
growth
known
to
influence
electronic
magnetic
properties
bulk
film.
In
this
study,
we
demonstrate
a
clear
distinction
between
surface
thin
La0.67Sr0.33MnO3
terms
chemical
composition,
disorder,
morphology.
We
use
combined
experimental
approach
X-ray-based
characterization
methods
scanning
probe
microscopy.
Using
X-ray
diffraction
resonant
reflectivity,
uncover
nonstoichiometry
strontium
lanthanum
alongside
an
accumulation
oxygen
vacancies.
With
tunneling
microscopy,
observed
phase
separation
(EPS)
on
related
nonstoichiometry.
The
EPS
is
likely
driving
temperature-dependent
resistivity
transition
cause
proposed
mixed-phase
ferromagnetic
paramagnetic
states
near
room
temperature
these
films.
Applied Physics Reviews,
Journal Year:
2025,
Volume and Issue:
12(1)
Published: Feb. 3, 2025
Solar
fuel
production
through
water
splitting
and
CO2
reduction
by
employing
photocatalytic
materials
is
a
paradigm
track
to
present
renewable
energy
sources
lessen
global
warming.
Among
these
materials,
layered
double
hydroxides
(LDHs)
have
been
widely
investigated
in
produce
chemical
fuels.
However,
pure
LDHs
suffer
from
sluggish
charge-carrier
transport,
great
electron–hole
recombination
rate
as
well
tend
cause
agglomeration.
Due
the
aforementioned
bottlenecks,
numerous
modification
techniques
considerably
explored
enhance
potential
of
toward
photoreduction.
Therefore,
this
article
presents
thorough
review
developments
made
for
construction
LDH
photocatalyst
properties
aiming
reduction.
The
starts
with
adopted
synthesize
LDH-based
structures
enhanced
structure
morphology.
key
semiconducting,
optical,
electronic
are
studied
understand
conduct
excellent
material.
study
then
deliberates
such
morphological
engineering,
hybridization
conducting
semiconducting
vacancy
creation
defect
components
tuning,
photothermal
catalysis,
heterojunction,
heterostructural
engineering
employed
enrichment
properties.
also
discusses
steps
taken
adsorption
coupling
computational
operando
structural,
optical
investigate
best-performing
photocatalysts.
reviews
recent
advancements
applications
conversion.
Inorganic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(17), P. 5414 - 5434
Published: Jan. 1, 2024
In
this
review,
we
describe
how
external
magnetic
fields
and
the
intrinsic
magnetism
of
catalysts
can
affect
electrocatalytic
reactions
using
select
literature
reports.
Physical Chemistry Chemical Physics,
Journal Year:
2024,
Volume and Issue:
26(34), P. 22620 - 22639
Published: Jan. 1, 2024
Catalysis
is
a
quantum
phenomenon
enthalpically
driven
by
electronic
correlations
with
many-particle
effects
in
all
of
its
branches,
including
electro-photo-catalysis
and
electron
transfer.
This
means
that
only
probability
amplitudes
provide
complete
relationship
between
the
state
catalysis
observations.
Thus,
any
atomic
system
material),
competing
space-time
interactions
coexist
to
define
(related)
properties
such
as
stability,
(super)conductivity,
magnetism
(spin-orbital
ordering),
chemisorption
catalysis.
Catalysts,
reactants,
chemisorbed
transition
states
have
possibility
optimizing
improve
reaction
kinetics.
Active
sites
closed-shell
orbital
configurations
share
maximum
number
spin-paired
electrons,
mainly
coulombic
attractions
covalency
defining
weakly
correlated
(WCCS)
structures.
However,
compositions
open-shell
configurations,
at
least,
spin
exchange
(QSEIopenshells)
arise,
stabilising
unpaired
electrons
less
covalent
bonds
differentiating
non-weakly
(or
strongly)
(NWCOS)
systems.
In
NWCOS
catalysts,
ground
can
diverse
rival
spin-orbital
orderings
well
ferro-,
ferri-
multiple
antiferro-magnetic
textures,
which
deeply
their
activities.
Particularly
inter-atomic
ferromagnetic
(FM)
bonds,
increase
relevance
non-classical
potentials
significantly
optimize
energies,
(TSs),
activation
energies
(overpotential)
spin-dependent
transfer
(conductivity),
overall
implying
need
for
explaining
thermodynamic
kinetic
origin
from
true
energy.
To
do
so,
we
use
connection
Born-Oppenheimer
approximation
Virial
theorem
treatment
potential
energies.
exact
fundamental
decompose
TSs
appear.
The
increasing
stabilization
TSs,
due
on
NWCO
opens
simultaneously
reducing
enthalpies
barriers
mechanisms,
implies
anticipation
explanation
positive
deviations
Brønsted-Evans-Polanyi
principle.
Applied Physics Reviews,
Journal Year:
2024,
Volume and Issue:
11(4)
Published: Oct. 8, 2024
Significant
efforts
have
been
dedicated
to
hydrogen
production
through
photocatalytic
water
splitting
(PWS)
over
the
past
five
decades.
However,
achieving
commercially
viable
solar-to-hydrogen
conversion
efficiency
in
PWS
systems
remains
elusive.
These
face
intrinsic
and
extrinsic
challenges,
such
as
inadequate
light
absorption,
insufficient
charge
separation,
limited
redox
active
sites,
low
surface
area,
scalability
issues
practical
designs.
To
address
these
issues,
conventional
strategies
including
heterojunction
engineering,
plasmonics,
hybridization,
lattice
defects,
sensitization,
upconversion
processes
extensively
employed.
More
recently,
innovative
hybrid
like
photonic
crystal-assisted
polarization
field-assisted
emerged,
which
improve
absorption
separation
by
harnessing
slow
photon
effect,
multiple
scattering,
piezoelectric,
pyroelectric,
ferroelectric
properties
of
materials.
This
review
article
aims
provide
a
comprehensive
examination
summary
new
synergistic
approaches,
integrating
plasmonic
effects,
processes,
crystal
photocatalysis.
It
also
explores
role
temperature
suppressing
exciton
recombination
during
photothermic
highlights
emerging
effects
magnetic
fields,
periodic
illumination,
many-body
large-hole
polaron,
anapole
excitations,
hold
significant
potential
advance
technology
facilitate
renewable
generation.
Nano Letters,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 13, 2025
In
situ
studies
of
the
relationship
between
surface
spin
configurations
and
spin-related
electrocatalytic
reactions
are
crucial
for
understanding
how
magnetic
catalysts
enhance
oxygen
evolution
reaction
(OER)
performance
under
fields.
this
work,
2D
Fe7Se8
nanosheets
with
rich
synthesized
via
chemical
vapor
deposition.
force
microscopy
Raman
spectroscopy
reveal
that
a
200
mT
field
eliminates
spin-disordered
domain
walls,
forming
spin-ordered
single-domain
structure,
which
lowers
OER
energy
barrier,
as
confirmed
by
theoretical
calculations.
Electrochemical
tests
show
field,
overpotential
multidomain
at
10
mA
cm–2
decreases
from
346
mV
to
259
mV,
while
has
minimal
effect
on
nanosheets.
These
findings
highlight
critical
role
in
enhancing
performance,
offering
new
insights
into
design
industrial
applications.
ChemElectroChem,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 30, 2025
In
energy
conversion
technologies,
the
electron
spin
effect
in
catalysts
plays
a
crucial
role
overcoming
spin‐forbidden
reactions,
offering
novel
approach
to
overcome
performance
bottlenecks
of
catalysts.
Recently,
with
breakthroughs
magnetic
field–enhanced
catalysis
and
theoretical
predictions,
significant
progress
has
been
made
design
development
this
concept,
several
attractive
inspiring
catalyst
strategies
reported
recently,
particularly
precise
modulation
states/spin
interactions
at
catalytic
sites
through
coordination
modulation,
spin‐pinning
effect,
chirality
induction,
radical
adsorption,
are
outlined.
The
concept
then
explores
advantages
these
enhancing
activity/selectivity,
investigating
selectivity
reaction
pathways,
expanding
systems.
Finally,
proposes
future
directions
for
technologies.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 12, 2025
Manipulating
the
spin
ordering
of
oxygen
evolution
reaction
(OER)
catalysts
through
magnetization
has
recently
emerged
as
a
promising
strategy
to
enhance
performance.
Despite
numerous
experiments
elaborating
on
magnetic
effect
for
improved
OER,
origin
this
phenomenon
remains
largely
unexplored,
primarily
due
difficulty
in
directly
distinguishing
states
electrocatalysts
during
chemical
reactions
at
atomic
level.
X-ray
emission
spectroscopy
(XES),
which
provides
information
sensitive
specific
elements
complex,
may
serve
technique
differentiate
onset
OER
catalytic
activities
from
influence
states.
In
work,
we
employ
situ
XES
technique,
along
with
absorption
(XAS),
investigate
interplay
between
atomic/electronic
structures,
states,
and
CoFe2O4
(CFO)
catalyst
under
an
external
field.
This
enhancement
is
that
facilitates
spin-selective
electron
transfer
adsorbed
OH-
reactants,
strongly
depends
configurations
tetrahedral-(Td)
octahedral-(Oh)
sites
both
Fe
Co
ions.
Our
result
contributes
comprehensive
understanding
field-assisted
electrocatalysis
level
paves
way
designing
highly
efficient
catalysts.