Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 19, 2024
Abstract
Liquid
crystalline
elastomers
(LCEs)
are
promising
candidates
for
the
development
of
soft,
environmentally‐responsive
actuators
and
have
recently
been
explored
application
in
smart
textiles
soft
robotics.
To
realize
potential
LCEs
within
these
systems,
fast,
scalable,
continuous
production
LCE
filaments
at
controlled
diameters
is
critical.
Here,
a
wet‐spinning
method
presented
scalable
manufacturing
graphene/LCE
composite
filaments.
Through
double
diffusion
mechanism,
precursors
rapidly
crosslink
into
tangible
without
use
UV
light,
instead
taking
advantage
solvent
exchange
high
catalyst
influx.
The
polydomain
can
achieve
speeds
up
to
4500
m
h
−1
.
π−π
interactions
between
graphene
matrix,
across
broad
range
(137
1128
µm)
be
obtained
with
integrity,
achieving
actuation
stresses
strains
3.66
MPa
44%,
respectively,
3
s.
showcased
as
artificial
muscles,
where
both
thin
thick
filament
sizes
interest.
will
open
new
opportunities
design
robotics
from
fibers
sizes.
Polymer Journal,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 27, 2025
Abstract
Stable,
tough,
and
functional
adhesion
systems
are
urgently
needed
for
a
sustainable
society.
As
resolution,
supramolecular
scientists
have
introduced
reversible
movable
crosslinked
materials
into
systems.
Reversible
crosslinks
can
repeatedly
associate
dissociate.
Therefore,
show
self-healing
stimuli-responsive
properties.
Moreover,
topological
in
which
the
polymer
chains
penetrate
cavities
of
cyclic
molecules.
The
sliding
with
deformation
enabled
achievement
showing
high
toughness
self-relaxation.
Adhesion
improved
cohesion,
stability,
functionality.
This
novel
concept
design
is
expected
to
increase
lifetime
adhesives
ameliorate
environmental
problems.
Macromolecules,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 8, 2025
A
liquid
crystal
polymer
(LCP)
is
synthesized
by
the
functionalization
of
polybutadiene
with
side-group
mesogens
and
methacrylate
cross-linker
used
to
investigate
stretching-induced
orientation
chain
backbone.
Unusual
behaviors
two
constituents
coupled
through
spacer
are
revealed
X-ray
diffraction
(XRD)
polarized
infrared
spectroscopic
measurements.
When
a
polydomain
LCP
film
stretched
in
nematic
phase,
backbone
mesogenic
side
groups
oriented
along
perpendicular
stretching
direction
(SD),
respectively;
at
large
strain
(500%),
tilted
plane.
By
contrast,
when
isotropic
phase
cooled
under
into
peculiar
state
observed
where
both
aligned
SD.
photo-cross-linking
films
strain,
different
macroscopic
states
locked
resulting
monodomain
elastomer
(LCE)
films.
Restretching
such
LCE
induce
their
reorientation,
an
auxetic
response
observed,
thickness
increasing
upon
restretching
over
small
range.
Polarized
optical
microscopic
(POM)
observation
UV–vis
absorption
measurement
show
unambiguously
that
behavior
associated
mechanically
induced
reorientation
from
in-plane
homogeneous
out-of-plane
homeotropic
alignment.
The
onset
magnitude
auxeticity
as
well
range
for
its
manifestation
(increased
respect
initial
before
restretching)
affected
relative
orientational
film.
Polymer
materials
that
show
macroscopic
deformation
upon
irradiation
with
light
are
feasible
as
soft
actuators.
However,
previous
photomobile
systems
typically
required
artificial
sources
for
actuation.
Herein,
we
develop
polymer
can
be
deformed
by
natural
sunlight.
Azobenzenes
functionalized
electron-donating
and
-withdrawing
groups
(push–pull
azobenzenes)
trans–cis
photoisomerization
sunlight
cis–trans
thermal
back
isomerization
after
the
cessation
of
irradiation.
Push–pull
azobenzenes
incorporated
into
crosslinked
liquid-crystalline
polymers,
in
which
azobenzene
moieties
uniaxially
aligned.
Upon
simulated
sunlight,
films
exhibit
bending
toward
incident
revert
to
initial
shapes
discontinuation
The
time
scales
unbending
consistent
those
behaviors
moieties.
This
result
indicates
is
induced
through
photochemical
processes
rather
than
photothermal
processes.
development
sunlight-driven
would
lead
creation
autonomous
ecofriendly
photoresponsive
without
need
optical
elements,
such
sources,
lenses,
filters.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 7, 2025
Abstract
High
value-added
azobenzene
liquid
crystal
elastomers
(AZO-LCEs)
derived
from
styrene-butadiene-styrene
triblock
copolymer
(SBS)
are
herein
developed.
The
glassy
polystyrene
(PS)
domains
in
SBS
that
spontaneously
separate
LCEs
can
provide
the
self-supporting
template
during
actuation
and
lock
LC
orientation,
enabling
reprogrammable,
reshapable
recyclable
AZO-LCE
actuators.
decoupling
effect
between
oriented
continuous
polybutadiene
(PB)
phase
leads
to
arrangement
of
side-chain
mesogens
perpendicular
main
chain,
simultaneous
synergistic
them
enables
actuators
exhibit
differentiated
auxetic
behaviours
as
temperature
transition
isotropic
(TLC-I)
varies.
To
achieve
a
large
strain,
bilayer
“Janus”
with
orthogonal
forces
designed
be
driven
synergistically
by
angular
cutting
angles,
bionic
applications
(like
peasecod
morphology
flower
blooming)
superior
designability.
Under
prestored
stresses
inside
aforementioned
actuators,
athletes
perform
vivid
activities.
By
assembling
right-
left-handed
sensitive
TLC-I,
they
selective
actions.
Upon
programming
microscopic
macroscopic
behaviours,
these
easily
implementable
valuable
insights
for
further
development
soft
robots.
Journal of Applied Polymer Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 15, 2025
ABSTRACT
Liquid
crystal
elastomers
(LCEs)
are
liquid
polymers
with
moderate
crosslinking
that
exhibit
elasticity
in
both
their
isotropic
and
states.
These
materials
can
be
programmed
through
chemical
design
geometric
configuration
to
achieve
autonomous
actuation
at
specific
temperatures.
Typically,
the
temperature
of
LCEs
exceeds
phase
transition
states,
most
reported
requiring
temperatures
above
100°C.
Such
high
pose
challenges
for
use
soft
robotics
due
increased
energy
consumption
limited
operational
flexibility.
In
this
study,
we
introduce
a
small
amount
polycaprolactone
(PCL)
into
main
chain
LCEs,
effectively
lowering
while
maintaining
over
90%
reversible
shrinkage
strain
characteristic
pure
LCEs.
By
adjusting
PCL
content,
number
twists,
helix
density,
successfully
obtained
an
LCE‐PCL
actuator
improved
performance
ranging
from
45°C
105°C.
Moreover,
by
modulating
degree
torsion
operating
temperature,
demonstrates
ability
perform
complex
motions,
such
as
reversing
parking.
This
work
offers
new
insights
application
reduced
enhanced
self‐driving
capabilities.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 13, 2025
Abstract
Liquid
crystal
elastomers
(LCEs)
are
highly
promising
soft
actuators
due
to
their
ability
undergo
significant,
rapid,
and
programmable
shape
transformations.
Achieving
this
actuation
requires
precise
mesogen
alignment
before
crosslinking.
Magnetic
field
offers
an
advantage
over
other
techniques
as
it
enables
volumetric
alignment.
However,
magnetic
has
be
performed
in
the
state
where
mesogens
exhibit
anisotropic
diamagnetic
properties
suitable
for
alignment,
typically
nematic
phase.
Therefore,
is
difficult
obtain
a
stable
liquid
crystalline
mixture
crosslinking,
while
preventing
recrystallization.
To
address
challenge,
method
using
assisted
thio‐Michael
polyaddition
followed
by
photo‐crosslinking
of
oligomers
(LCOs)
presented.
This
process
straightforward
allows
synthesis
magnetically
aligned
high
molecular
weight
LCOs,
which
maintain
phase
By
applying
different
orientations
during
polyaddition,
three
distinct
LCE
networks
synthesized,
each
demonstrating
unique
reversible
deformation
behaviors,
including
radial
contraction
expansion,
thickness
contraction,
bending.
The
potential
approach
further
demonstrated
with
LCE‐based
four‐leaf
clovers
exhibiting
selective
large‐angle
bending
deformation,
despite
material.
simple
should
help
researchers
various
fields
looking
practical
versatile
designing
robust
actuators.
Nanomaterials,
Journal Year:
2025,
Volume and Issue:
15(6), P. 443 - 443
Published: March 14, 2025
The
chemical
response
of
liquid
crystal
elastomers
(LCEs)
offers
substantial
potential
for
applications
in
propulsion
systems,
micromechanical
and
active
smart
surfaces.
However,
the
shape-changing
behaviors
LCEs
to
organic
(isotropic)
solvents
remain
scarcely
explored,
with
most
research
focusing
on
(anisotropic)
solvents.
Herein,
we
prepared
a
series
aligned
varying
crosslink
densities
using
surface
alignment
technique
combined
an
aza-Michael
addition
reaction,
aiming
investigate
their
swelling
different
isotropic
We
found
that
rates
shape
volume
variation
modes,
elastic
modulus
LCEs,
polarity
solvent
all
significantly
influence
behavior.
Specifically,
when
swell
acetone,
dimethylformamide
(DMF),
ethyl
acetate,
contraction
occurs
along
direction.
Conversely,
extension
direction
is
observed
toluene,
anisole,
acrylic
acid.
Meanwhile,
perpendicular
noted
nearly
These
changes
can
be
attributed
phase
transitions
LCEs.
This
not
only
provides
valuable
insights
into
mechanisms
but
also
holds
great
promise
development
sensors
gas
sensing
applications.