ACS Materials Au,
Год журнала:
2024,
Номер
5(1), С. 57 - 71
Опубликована: Ноя. 8, 2024
The
integration
of
fluorinated
benzothiadiazole
(FBT)
into
donor–acceptor
(D–A)
copolymers
represents
a
major
advancement
in
the
field
organic
solar
cells
(OSCs).
fluorination
process
effectively
fine-tunes
energy
levels,
reduces
highest
occupied
molecular
orbital
and
enhances
open-circuit
voltages
polymers.
Furthermore,
improves
packing
crystallinity,
which
significantly
boosts
charge
transport
overall
device
performance.
This
review
provides
detailed
analysis
progress
made
with
FBT-based
polymers
OSCs,
classifying
these
materials
according
to
their
copolymerization
units.
It
discusses
design
strategies
structure–property
relationships
that
have
emerged
as
well
current
challenges
future
directions
for
optimizing
By
offering
comprehensive
overview
existing
research,
this
aims
facilitate
development
high-performance
photovoltaic
materials,
ultimately
contributing
sustainable
solutions.
Advanced Functional Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 9, 2024
Abstract
The
ternary
strategy
has
proven
effective
in
enhancing
the
performance
of
organic
solar
cells
(OSCs),
yet
identifying
optimal
third
component
remains
a
challenge
due
to
lack
theoretical
frameworks
for
predicting
its
impact
based
on
molecular
structure.
This
study
addresses
this
by
proposing
quantitative
parameters
derived
from
surface
electrostatic
potential
(ESP)
as
criteria
selecting
components.
asymmetric
acceptor
BTP‐OS,
which
exhibits
lower
total
average
ESP
and
larger
polarization
index
relative
host
acceptor,
is
introduced
into
PM6:L8‐BO
system.
incorporation
led
weakened
ESP‐induced
intermolecular
interactions
reduce
miscibility
with
donor
polymer,
resulting
an
optimized
multi‐scale
morphology
blend.
Consequently,
device
achieved
efficiency
19.72%,
one
highest
values
PM6:L8‐BO‐based
devices,
enhanced
exciton
dissociation
charge
collection,
energy
disorder,
minimized
non‐radiative
losses.
Comparable
improvements
are
also
verified
PM6:BTP‐eC9
D18:N3
systems,
demonstrating
broad
applicability
proposed
approach.
not
only
provides
practical
principle
components
but
establishes
broader
framework
optimizing
OSCs,
potentially
advancing
development
more
efficient
OSCs
across
diverse
material
systems.
Abstract
A
series
of
layered
all‐polymer
solar
cells
(LA‐PSCs)
with
the
normal
or
inverted
structure
are
prepared
by
employing
a
sequential
spin‐coating
method
PBQx‐TCl,
PM1
as
polymer
donor,
and
PY‐DT
acceptor.
The
power
conversion
efficiency
(PCE)
LA‐PSCs
can
be
improved
from
17.20%
to
18.34%
incorporating
30
wt.%
into
PBQx‐TCl
layer,
resulting
simultaneously
increased
J
SC
25.35
mA
cm
−2
,
V
OC
0.971
FF
74.49%.
PCE
improvement
also
achieved
PBQx‐TCl:PM1
donor
layers.
mixed
prefer
form
alloyed
states
in
LA‐PSCs,
which
confirmed
gradually
s
more
content
Meanwhile,
photogenerated
excitons
layers
dissociated
at
interface
between
PM1,
especially
for
located
near
ITO
electrode.
exciton
dissociation
provide
an
additional
channel
improving
utilization
efficiency,
positive
external
quantum
spectral
difference
(∆EQE)
values
Over
6.6%
realized
using
layer.
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 20, 2025
Abstract
Recently,
through
in‐depth
investigations
of
ternary
organic
solar
cells
(OSCs),
scientists
have
discovered
that
small
molecules
(SMs)
with
edge‐on
orientation
serving
as
the
third
component
can
boost
transverse
charge
transport
and
consequently
enhance
device
performance.
Nevertheless,
little
research
has
been
conducted
on
determining
how
to
select
an
appropriate
improve
3D
transport.
Herein,
four
SMs
are
designed
by
gradually
increasing
quantity
alkyl
thiophene
π‐bridge
adjust
their
crystallinity
orientation.
The
resulting
show
similar
but
different
crystalline
degrees,
due
complex
effects
molecular
steric
hindrance
extended
conjugation.
After
introduction
SMs,
most
devices
exhibited
a
pronounced
improvement
in
power
conversion
efficiencies
(PCEs)
than
control
binary
counterparts.
An
elegant
PCE
19.02%
fill
factor
approaching
80%
collected
OSCs.
A
balanced
bimodal
mechanism
is
proposed
effectively
elucidated
blend
film,
enabling
charges
bypass
interfering
domains
thereby
This
provides
guidance
for
development
SM
components
form
percolation
paths
facilitate
subsequently
performance
devices.
Advanced Science,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 22, 2025
Abstract
The
conductivity
of
AgNWs
electrodes
can
be
enhanced
by
incorporating
Ag
grids,
thereby
facilitating
the
development
large‐area
flexible
organic
solar
cells
(FOSCs).
grids
from
vacuum
evaporation
offer
advantages
simple
film
formation,
adjustable
thickness,
and
unique
structure.
However,
complex
3D
multi‐component
structure
will
exacerbate
aggregation
large
particles,
causing
device
short
circuits.
To
address
this
issue,
relationship
between
surface
energy
modification
layers
morphology
ultrathin
on
is
studied.
amorphous
ZnO
(α‐ZnO)
layer
promotes
growth
Volmer–Weber
(VW)
to
Frank–Van
der
Merwe
(FM),
reducing
particle
aggregation.
1
µm
thick
PET/AgNWs/Ag
grid
electrode
with
α‐ZnO
exhibited
low
contact
resistance
high
conductivity.
As
a
result,
cm
2
FOSCs
achieve
power
conversion
efficiency
(PCE)
16.01%.
area
increased
4
9
,
performance
monolithic
14.70%
12.69%,
showing
less
loss
during
upscaling.
8
16
modules
constructed
series
parallel
connection
devices
yield
PCEs
14.47%
12.92%,
respectively.
This
study
offers
valuable
insights
into
constructing
for
highly
efficient
FOSCs.
Perovskite-based
tandem
solar
cells
(PTSCs)
are
promising
for
achieving
higher
efficiency
limits,
making
them
candidates
energy
supply.
However,
the
commercialization
in
complex
scenarios
necessitate
extreme
stability
and
reliability
of
devices,
particularly
ambient
conditions.
Herein,
use
a
high-efficiency
air-stable
quaternary
all-polymer
bulk
heterojunction
(BHJ)
is
pioneered
to
optimize
spectral
absorption,
facilitate
charge
transport,
suppress
exciton
recombination,
resulting
18.0%
power
conversion
(PCE)
organic
subcell.
The
resultant
monolithic
perovskite/organic
cell
(POTSC)
delivers
an
impressive
PCE
24.8%,
with
minimal
distribution
negligible
hysteresis.
Ambient
tests
on
devices
reveal
outstanding
stability,
which
attributed
reduced
increase
recombination.
Remarkably,
unencapsulated
device
maintained
88%
its
initial
after
exposure
air
500
h.
superior
owing
enhanced
resistance
hydrophobic
BHJ
water
oxygen,
thereby
protecting
perovskite
active
layer.
This
work
provides
novel
approach
from
perspective
POTSC
holds
promise
future
real-world
applications
field
cells.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
64(3)
Опубликована: Сен. 9, 2024
Abstract
This
study
puts
forth
a
novel
terminal
group
design
to
develop
medium‐band
gap
Y‐series
acceptors
beyond
conventional
side‐chain
engineering.
We
focused
on
the
strategical
integration
of
an
electron‐donating
methoxy
and
electron‐withdrawing
halogen
atom
at
benzene‐fused
groups.
combination
precisely
modulated
dipole
moment
electron
density
groups,
effectively
attenuating
intramolecular
charge
transfer
effect,
widening
band
acceptors.
The
incorporation
these
groups
yielded
two
asymmetric
acceptors,
named
BTP‐2FClO
BTP‐2FBrO,
both
which
exhibited
open‐circuit
voltage
(
V
oc
)
as
high
0.96
in
binary
devices,
representing
highest
OC
s
among
small
molecule
More
importantly,
BTP‐2FBrO
exhibit
modest
aggregation
behaviors
molecular
crystallinity,
making
them
suitable
third
component
mitigate
excess
PM6
:
BTP‐eC9
blend
optimize
devices’
morphology.
As
result,
optimized
BTP‐2FClO‐based
ternary
organic
solar
cells
(OSCs)
achieved
remarkable
power
conversion
efficiency
(PCE)
19.34
%,
positioning
it
highest‐performing
OSCs.
Our
highlights
importance
manipulating
moments
developing
offers
highly
efficient
for
high‐performance
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
64(1)
Опубликована: Сен. 12, 2024
The
difluorobenzothiadizole
(ffBT)
unit
is
one
of
the
most
classic
electron-accepting
building
blocks
used
to
construct
D-A
copolymers
for
applications
in
organic
solar
cells
(OSCs).
Historically,
ffBT-based
polymers
have
achieved
record
power
conversion
efficiencies
(PCEs)
fullerene-based
OSCs
owing
their
strong
temperature-dependent
aggregation
(TDA)
characteristics.
However,
excessive
miscibility
and
rapid
kinetics
during
film
formation
hindered
performance
with
state-of-the-art
non-fullerene
acceptors
(NFAs).
Herein,
we
synthesized
two
copolymers,
PffBT-2T
PffBT-4T,
incorporating
different
π-bridges
modulate
intermolecular
interactions
tendencies.
Experimental
theoretical
studies
revealed
that
PffBT-4T
exhibits
reduced
electrostatic
potential
differences
L8-BO
compared
PffBT-2T.
This
facilitates
improved
phase
separation
active
layer,
leading
enhanced
molecular
packing
optimized
morphology.
Moreover,
demonstrated
a
prolonged
nucleation
crystal
growth
process,
Consequently,
PffBT-4T-based
devices
remarkable
PCE
17.5
%,
setting
new
photovoltaic
polymers.
Our
findings
underscore
importance
conjugate
backbone
modulation
controlling
behavior
kinetics,
providing
valuable
insights
design
high-performance
polymer
donors
photovoltaics.
ACS Nano,
Год журнала:
2024,
Номер
18(41), С. 28178 - 28188
Опубликована: Окт. 3, 2024
Conjugated
polymers
are
becoming
popular
near-infrared
II
(NIR-II)
phototheranostic
agents
(PTAs)
due
to
their
numerous
advantages,
such
as
high
photostability,
large
molar
extinction
coefficients,
and
excellent
photothermal
properties.
However,
the
strong
π-π
interactions
between
chains
of
conjugated
resulted
in
generally
low
NIR-II
emission
quantum
yields
(QY).
Therefore,
synthesis
with
QY
is
an
interesting
but
challenging
task.
Herein,
we
proposed
a
spacer
twisting
strategy
realize
ultrabright
polymer
nanoparticles
for
fluorescence
imaging-guided
tumor
phototheranostics.
Theoretical
calculations
indicated
that
PY-IT
has
largest
dihedral
angle
largely
π-conjugated
skeleton
spacer,
which
can
effectively
inhibit
intermolecular
stacking,
resulting
improved
16.5%
nanoparticles.
In
addition,
NPs
perform
imaging
treatment
tumors.
The
work
presents
some
valuable
guides
achieving
polymeric
PTAs
QY.