Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 23, 2024
Abstract
The
exploration
of
a
new
conceptual
strategy
for
improving
the
oxygen
evolution
reaction
(OER)
earth‐abundant
electrocatalysts
is
critical.
In
this
study,
chiral
copper
oxide
nanoflower
explored
by
self‐assembly
method.
characterization
suggests
structure
originates
from
crystal
plane‐level
helical
stack
secondary
nanosheets.
Of
note,
assembly
illustrates
record‐high
degree
spin
polarization
96%,
indicating
ideal
alignment
electron
spin.
Moreover,
density
function
theory
calculations
show
reducing
energy
barrier
(REB)
while
switching
potential‐determining
step
*O→*OOH
to
*OH→*O.
Together
with
enhanced
electrochemical
active
surface
area
and
accelerated
charge
transfer,
production
ground‐state
triplet
O
2
improved
via
spin‐forbidden
route
that
involves
singlet
H
O/OH•.
Consequently,
shows
overpotential
308
mV
at
10
mA
cm
−2
Tafel
slope
93.5
dec
−1
,
which
even
superior
commercial
RuO
(310
mV,
101
).
This
study
presents
OER
activity
simultaneously
enhancing
electronic
properties
lowering
REB
an
non‐noble
electrocatalyst
chirality
engineering.
Chemical Reviews,
Journal Year:
2024,
Volume and Issue:
124(4), P. 1950 - 1991
Published: Feb. 16, 2024
Since
the
initial
landmark
study
on
chiral
induced
spin
selectivity
(CISS)
effect
in
1999,
considerable
experimental
and
theoretical
efforts
have
been
made
to
understand
physical
underpinnings
mechanistic
features
of
this
interesting
phenomenon.
As
first
formulated,
CISS
refers
innate
ability
materials
act
as
filters
for
electron
transport;
however,
more
recent
experiments
demonstrate
that
displacement
currents
arising
from
charge
polarization
molecules
lead
without
need
net
flow.
With
its
identification
a
fundamental
connection
between
symmetry
materials,
promises
profound
ubiquitous
implications
existing
technologies
new
approaches
answering
age
old
questions,
such
homochiral
nature
life.
This
review
begins
with
discussion
different
methods
measuring
then
provides
comprehensive
overview
known
exhibit
CISS-based
phenomena
before
proceeding
identify
structure-property
relations
delineate
leading
models
effect.
Next,
it
identifies
some
physics,
chemistry,
biology.
The
ends
critical
assessment
field
comments
future
outlook.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Anion
dimerization
poses
a
significant
challenge
for
the
application
of
Li-rich
cathode
materials
(LCMs)
in
high-energy-density
Li-ion
batteries
because
its
deleterious
effects,
including
rapid
capacity
and
voltage
decay,
sluggish
reaction
kinetics,
large
hysteresis.
Herein,
we
propose
metal–ligand
spin-lock
strategy
to
inhibit
anion
dimerization,
which
involves
introducing
an
Fe–Ni
couple
having
antiferromagnetic
superexchange
interaction
into
LCM
lock
spin
orientations
unpaired
electrons
anions
same
direction.
As
proof
concept,
applied
this
intralayer
disordered
Li2TiS3
(ID-LTS)
S–S
dimerization.
Electrochemical
characterization
using
galvanostatic
charge/discharge
intermittent
titration
technique
demonstrated
considerably
enhanced
anionic
redox
activity,
reduced
hysteresis,
improved
kinetics
Fe–Ni-couple-incorporated
ID-LTS.
Fe
L2,3-edge
X-ray
absorption
spectroscopy
magnetic
susceptibility
measurements
revealed
that
effect
consequent
suppression
involve
ligand-to-metal
charge
transfer
between
S
Fe.
Further
electrochemical
tests
on
layered
oxide
(Li0.7Li0.1Fe0.2Ni0.1Mn0.6O2)
indicated
importance
π
backbond
enhancing
from
These
findings
demonstrate
potential
our
development
high-performance
LCMs.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(18), P. 12819 - 12827
Published: April 26, 2024
Chirality
evolution
from
molecule
levels
to
the
nanoscale
in
an
achiral
system
is
a
fundamental
issue
that
remains
undiscovered.
Here,
we
report
assembly
of
polyoxometalate
(POM)
clusters
into
chiral
subnanostructures
systems
by
programmable
single-molecule
interactions.
Driven
competing
binding
Ca2+
and
surface
ligands,
POM
assemblies
would
twist
helical
nanobelts,
nanorings,
nanotubes
with
tunable
helicity.
Chiral
molecules
can
be
used
differentiate
formation
energies
isomers
immobilize
homochiral
isomer,
where
strong
circular
dichroism
(CD)
signals
are
obtained
both
solutions
films.
nanobelts
as
circularly
polarized
light
(CPL)
photodetectors
due
their
distinct
chiroptic
responsivity
for
right
left
CPL.
By
fine-tuning
interactions
at
levels,
morphology
CD
spectra
precisely
controlled,
providing
atomic
precision
model
investigation
structure–chirality
relationship
chirality
manipulation
nanoscale.
Chemical Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Intrinsically
chiral
oxides
show
enhanced
activity
towards
the
oxygen
evolution
reaction
in
full
cell
electrolysers.
Enantiopure
active
sites
were
detected
operando
by
circular
dichroism-spectro-electrochemical
data.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 23, 2024
Subnanometer
materials
(SNMs)
refer
to
nanomaterials
with
a
feature
size
close
1
nm,
similar
the
diameter
of
single
polymer,
DNA
strand,
and
cluster/unit
cell.
The
growth
assembly
subnanometer
building
blocks
can
be
controlled
by
interactions
at
atomic
levels,
representing
limit
for
precise
manipulation
materials.
size,
geometry,
flexibility
1D
SNMs
inorganic
backbones
are
polymer
chains,
bringing
excellent
gelability,
adhesiveness,
processability
different
from
nanocrystals.
ultrahigh
surface
atom
ratio
results
in
significantly
increased
energy,
leading
significant
rearrangement
atoms.
Unconventional
phases,
immiscible
metal
alloys,
high
entropy
few
layers
stabilized,
spontaneous
twisting
may
induce
intrinsic
structural
chirality.
Electron
delocalization
also
emerge
subnanoscale,
giving
rise
enhanced
catalytic
activity.
In
this
perspective,
we
summarized
recent
progress
on
SNMs,
including
their
synthesis,
polymer-like
properties,
metastable
chirality,
toward
energy
conversion.
As
critical
region
nanoscience,
development
functional
fuse
boundary
polymers
conduce
manufacturing
levels.
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(22), P. 28517 - 28525
Published: May 20, 2024
Effective
catalytic
performance
of
the
transition
metal
oxide
is
attributed
to
high
specific
surface
areas,
abundant
oxygen
atoms,
and
balanced
valence
ratios.
Although
chirality
has
attracted
attention,
most
studies
have
focused
on
optical
application.
A
few
chiral
oxides
were
used
as
electrocatalysts
photocatalysts.
The
influence
catalysts
thermal
catalysis
process
been
less
explored.
In
this
study,
Mn-loaded
(M/l-CuO
M/d-CuO)
achiral
CuO
(M/a-CuO)
synthesized
compared
in
oxidization
toluene.
Spectrally
analyzed
Mn
was
well-dispersed
both
CuO.
l-CuO
d-CuO
showed
nanoflower-like
chirality.
angles
between
each
(001)
plane
source
toluene
turnover
frequency
(TOF)
samples
order
Mn/d-CuO
(5.6
×
10–5
s–1)
>
Mn/l-CuO
(4.4
Mn/a-CuO
(3.2
at
240
°C,
consistent
with
replenishment
rate.
as-prepared
had
similar
ratios
lattice
oxygen/surface
adsorbed
oxygen,
Mn3+/Mn4+,
Cu+/Cu2+.
higher
TOF
chirality,
which
increased
speed
from
gaseous
phase
solid
surface.
Our
study
indicates
gas–solid
a
structure–activity
viewpoint.
National Science Review,
Journal Year:
2024,
Volume and Issue:
11(9)
Published: July 18, 2024
ABSTRACT
The
spin
of
electrons
plays
a
vital
role
in
chemical
reactions
and
processes,
the
excited
state
generated
by
absorption
photons
shows
abundant
spin-related
phenomena.
However,
importance
electron
photochemistry
studies
has
been
rarely
mentioned
or
summarized.
In
this
review,
we
briefly
introduce
concept
based
on
multiplicity
state,
which
leads
to
observation
various
photophysical
properties
photochemical
reactivities.
Then,
focus
recent
advances
terms
light-induced
magnetic
properties,
excited-state
magneto-optical
effects
spin-dependent
reactions.
review
aims
provide
comprehensive
overview
utilize
manipulating
above
processes.
Finally,
discuss
existing
challenges
emerging
field
future
opportunities
such
as
smart
materials,
optical
information
technology
spin-enhanced
photocatalysis.