The
synthesis
of
three
poly(dithienofluorene-alt-dithienodiketopyrrolopyrrole)
polymers,
PDTFDPP-H
with
an
average
molecular
weight
(Mn)
77
kg
mol–1,
PDTFDPP-M
Mn
28
and
PDTFDPP-L
11
has
been
accomplished.
UV–vis
spectroscopy
reveals
a
shoulder
at
780
nm
for
PDTFDPP-H,
indicating
potential
polymer
aggregation.
Solvent-
temperature-variable
absorption
spectra,
coupled
DFT
calculations,
support
this
observation.
Hole
mobility
(μh)
follows
the
sequence
(0.305
cm2
V–1
s–1)
>
(1.88
×
10–3
(5.19
10–4
s–1).
Grazing
incidence
X-ray
scattering
that
primarily
exhibit
edge-on
crystallites,
while
displays
both
face-on
all
demonstrating
short-range
π-order.
formation
or
crystallites
seems
to
correlate
weight.
Transmission
electron
microscopy
analysis
chain
entanglement.
Overall,
results
suggest
aggregates
are
interconnected
help
one-dimensional
chains,
achieving
μh
higher
than
0.1
s–1.
SusMat,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 17, 2025
ABSTRACT
All‐polymer
solar
cells
(all‐PSCs)
are
of
interest
owing
to
their
unique
advantages,
including
remarkably
improved
device
stability
and
exceptional
mechanical
stretchability.
Over
recent
years,
there
has
been
a
notable
increase
in
the
power
conversion
efficiency
(PCE)
all‐PSCs,
largely
attributed
advancements
morphology
control
active
layer.
Notably,
domain
size
is
paramount
importance
as
it
impacts
critical
factors
such
exciton
dissociation,
charge
transport,
collection.
However,
low
glass
transition
temperature
conjugated
polymers,
coupled
with
minimal
change
mixing
entropy,
often
results
an
excessive
degree
phase
separation.
Consequently,
essential
comprehend
evolution
separation
develop
strategies
regulate
size.
In
this
review,
we
elucidate
key
parameters
that
contribute
enhancement
present
qualitative
quantitative
characterization
techniques
for
Building
on
foundation,
introduce
principles
regulating
sizes,
encompassing
crystallinity,
miscibility,
molecular
conformation
from
thermodynamic
perspective,
well
film‐forming
kinetics
crystallization
sequence
kinetic
perspective.
Lastly,
offer
insights
into
current
challenges
potential
future
prospects
all‐PSCs.
Accounts of Chemical Research,
Journal Year:
2024,
Volume and Issue:
57(9), P. 1360 - 1371
Published: April 26, 2024
ConspectusNonradiative
processes
with
the
determined
role
in
excited-state
energy
conversion,
such
as
internal
conversion
(IC),
vibrational
relaxation
(VR),
intersystem
crossing
(ISC),
and
or
electron
transfer
(ET
eT),
have
exerted
a
crucial
effect
on
biological
functions
nature.
Inspired
by
these,
nonradiative
process
manipulation
has
been
extensively
utilized
to
develop
organic
functional
materials
fields
of
biomedicine.
Therefore,
comprehensive
knowledge
effective
sophisticated
for
achieving
high-efficiency
are
quintessential.
So
far,
many
strategies
focused
molecular
engineering
demonstrated
tremendous
potential
manipulating
tailor
conversion.
Besides,
aggregation
considerably
affects
due
their
ultrasensitivity,
thus
providing
us
another
essential
approach
processes,
famous
aggregation-induced
emission.
However,
weak
interactions
established
upon
aggregation,
namely,
microenvironment
(AME),
possess
hierarchical,
dynamic,
systemic
characteristics
extremely
complicated
elucidate.
Revealing
relationship
between
AME
employing
it
customize
would
greatly
promote
advanced
utilization,
biomedicine,
etc.,
but
remain
huge
challenge.
Our
group
devoted
much
effort
this
goal.In
Account,
we
focus
our
recent
developments
based
AME.
First,
provide
insight
into
terms
its
steric
electronic
regulation,
illustrating
possibility
through
modulation.
Second,
distinct
enhanced
is
crystallization
heterogeneous
polymerization
conduct
crystallization-induced
reversal
from
dark
bright
excited
states
dynamic
hardening-triggered
suppression
highly
efficient
luminescence.
Meanwhile,
promoting
ISC
stabilizing
triplet
state
also
manipulated
crystal
polymer
matrix
induce
room-temperature
phosphorescence.
Furthermore,
employed
exploit
photothermy
photosensitization
reviewed.
For
photothermal
besides
weakened
promoted
motions,
new
strategy
involving
introduction
diradicals
narrow
band
gap
enhance
intermolecular
put
forward
facilitate
IC
VR
photosensitization,
both
rigid
regulation
electron-rich
ISC,
ET,
eT
superior
photosensitization.
Finally,
explore
existing
challenges
future
directions
modulation
customized
We
hope
that
Account
will
be
wide
interest
readers
different
disciplines.
Macromolecules,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 8, 2025
Fine-tuning
the
charge
polarity
and
enhancing
electron
transport
in
conjugated
polymers
are
critical
for
developing
high-performance
organic
field-effect
transistors
(OFETs).
Quinoidal
polymers,
characterized
by
planar
backbones
deep-lying
lowest
unoccupied
molecular
orbital
(LUMO)
energy
levels,
offer
distinct
advantages
over
their
aromatic
counterparts
but
face
challenges
achieving
reliable
mobilities
exceeding
1
cm2
V–1
s–1.
Herein,
we
synthesized
a
set
of
novel
quinoid–donor–acceptor
(Q-D-A)
with
various
acceptor
units.
Increasing
strength
narrowed
band
gap,
lowered
LUMO
shifted
from
unipolar
p-type
to
ambipolar
ultimately
dominant
n-type
behavior.
The
electron-to-hole
mobility
ratio
increased
0
40
behavior
observed
Q-D-A
polymer
first
time.
Consequently,
strongest
acceptor-based
exhibited
backbone,
small
effective
mass,
high
crystallinity,
low
disorder,
resulting
1.20
s–1
decent
operational
stability.
This
is
record-high
value
quinoidal
transport.
Our
findings
viable
strategy
tuning
improving
providing
insights
into
structure–property
relationships
essential
advancing
electronics.
Due
to
their
unique
optoelectronic
properties
and
potential
for
high
efficiency,
quantum
dot
(QD)
solar
cells
photodetectors
have
gained
tremendous
attention.
Achieving
efficient
charge
transport
extraction
in
these
devices
is
crucial
enhancing
performance.
Polymer
interlayers
play
a
vital
role
facilitating
improving
the
device
stability.
This
Spotlight
on
Applications
paper
focuses
effective
strategies
employed
tune
microstructure
of
polymer
QD
achieve
efficiency
by
bringing
together
recent
literature.
With
use
advanced
synchrotron
radiation
scattering
microscopic
characterizations,
we
elucidate
impact
properties,
casting
solvents,
physical
blending
methods
microstructures
photodetectors.
Furthermore,
take
detailed
look
at
some
facile
such
as
aggregation-suppressed
synergy
that
enabled
precise
control
over
interlayers.
Finally,
provide
perspectives
future
research
directions
obstacles
field.
Macromolecules,
Journal Year:
2024,
Volume and Issue:
57(12), P. 5902 - 5914
Published: June 5, 2024
Conjugated
polymers
(CPs)
are
pivotal
for
high-mobility
applications,
typically
avoiding
nonconjugated
units
due
to
their
perceived
negative
impact
on
charge
transport.
Contrary
this
belief,
our
study
introduces
a
unit,
DKPDO,
which
when
employed
as
conjugation-break
spacer
(CBS),
significantly
enhances
DKPDO
was
obtained
center-modified
isoindigo
variant
featuring
strongly
electron-withdrawing
amide
groups
that
diminish
the
electron
density
and
foster
multiple
hydrogen-bonding
interactions.
This
results
in
enhanced
deficiency
reinforced
coplanarity
relative
isoindigo.
incorporated
into
polymer
backbone,
comprising
bithiophene,
create
series
of
terpolymers
with
varied
molar
ratios,
allowing
systematic
evaluation
solubilities,
interchain
interactions,
crystallinities,
energy
levels.
Notably,
incorporating
universal
improvement
hole
mobilities
operational
stabilities
over
DKPDO-free
counterpart.
Remarkably,
terpolymer
containing
2.5%
achieves
high
mobility
4.12
cm2
V–1
s–1,
approximately
6-fold
higher
than
parent
CP
among
highest
CPs
based
center-inserted
units.
The
not
only,
first
time,
realizes
transport
enhancement
CBS
backbones
but
also
sets
precedent
strategic
use
developing
high-performing
CPs.
Journal of Materials Chemistry C,
Journal Year:
2024,
Volume and Issue:
12(11), P. 4142 - 4156
Published: Jan. 1, 2024
PYIT
was
added
to
the
PM6:Y6
system
delay
and
shorten
crystallization
time
of
Y6.
The
ternary
strategy
has
been
successfully
proven
increase
D/A
interface
area
for
faster
exciton
dissociation.
E
loss
decreased
(0.559
eV
0.539
eV),
PCE
increased
(15.40%
17.05%).
Polymers,
Journal Year:
2024,
Volume and Issue:
16(3), P. 396 - 396
Published: Jan. 31, 2024
The
design
of
novel
acceptor
molecular
structures
based
on
classical
building
blocks
is
regarded
as
one
the
efficient
ways
to
explore
application
organic
conjugated
materials
in
conductivity
and
electronics.
Here,
a
moiety,
thiophene-vinyl-diketopyrrolopyrrole
(TVDPP),
was
envisioned
prepared
with
longer
conjugation
length
more
rigid
structure
than
thiophene-diketopyrrolopyrrole
(TDPP).
brominated
TVDPP
can
be
sequentially
bonded
trimethyltin-containing
benzo[c][1,2,5]thiadiazole
units
via
Suzuki
polycondensation
efficiently
prepare
polymer
PTVDPP-BSz,
which
features
high
weight
excellent
thermal
stability.
polymerization
process
takes
only
24
h
eliminates
need
for
chlorinated
solvents
or
toxic
tin-based
reagents.
Density
functional
theory
(DFT)
simulations
film
morphology
analyses
verify
planarity
crystallinity
material,
respectively,
facilitates
achievement
carrier
mobility.
Conductivity
measurements
polymeric
material
transistor
device
show
hole
mobility
0.34
cm2
V−1
s−1,
illustrates
its
potential
functionalized
semiconductor
applications.
Macromolecules,
Journal Year:
2024,
Volume and Issue:
57(9), P. 4141 - 4157
Published: April 18, 2024
Charge
transport
in
conjugated
semiconducting
polymer
films
predominantly
occurs
along
the
intrachain
backbone
as
well
interchain
π–π
stacking
directions.
The
molecular
orientation
significantly
affects
favorable
charge
direction,
since
it
determines
alignment
of
stacking.
Bimodal
texture
exhibited
both
out-of-plane
and
in-plane
directions,
thus
forming
a
continuous
3D
pathway
to
achieve
optimized
electrical
performance.
However,
mechanism
transition
has
not
been
well-defined;
thus,
construction
bimodal
remains
an
issue.
Here,
we
achieved
reorientation
n-type
high-molecular-weight
poly{[N,N′-bis(2-octyldodecyl)-naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5,5′-(2,2′-bithiophene)}
[P(NDI2OD-T2)]
from
predominately
face-on
by
employing
side-chain
selective
solvent
vapor
annealing
(SVA)
post-treatment,
which
could
be
divided
into
two
stages:
film
swelling
process
drying
process.
During
process,
observed
situ
2D-GIWAXS,
side
chains
were
aligned
perpendicular
substrate
due
stronger
solvent–side
chain
interactions
than
that
main
chain;
part
molecules
began
reorient
edge-on.
As
more
selectively
dissolved,
much
greater
free
volume
was
provided
for
further
transition.
Eventually,
intermediate
edge-on
formed.
swollen
crystallites
stable.
following
some
kept
orientation,
while
metastable
ones
reorientated
disappeared
upon
evaporation,
ultimately
leading
texture.
Consequently,
mobility
SVA-treated
improved
0.092
(pristine
film)
0.155
cm2
V–1
s–1
transporting.
Interdisciplinary materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 17, 2024
Abstract
Stretchable
conjugated
polymer
films
are
pivotal
in
flexible
and
wearable
electronics.
Despite
significant
advancements
film
stretchability
through
molecular
engineering
multicomponent
blending,
these
often
exhibit
limited
elastic
ranges
reduced
carrier
mobilities
under
large
strain
or
after
cyclic
stretching.
These
limitations
hinder
their
application
Therefore,
it
is
imperative
to
reveal
the
mechanical
fatigue
mechanisms
incorporate
multiple
energy
dissipation
strategies
enhance
deformation
electrical
performance
of
stretched
films.
In
this
review,
we
begin
by
introducing
typical
behaviors
Subsequently,
discuss
multiscale
structural
evolution
various
stretching
conditions
based
on
both
in‐situ
ex‐situ
characterizations.
This
analysis
further
related
diverse
mechanisms.
We
next
establish
correlation
between
strain‐induced
microstructure
After
that,
propose
develop
highly
constructing
stable
crosslinks
promoting
dynamics
low‐crystalline
Finally,
highlight
future
opportunities
for
high‐performance
mechanically
devices
stretchable