Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 15, 2025
Abstract
Developing
high‐performance
all‐polymer
solar
cells
(all‐PSCs)
remains
a
challenge
due
to
the
difficulty
in
controlling
morphology
of
polymer
blends.
In
this
study,
benzo[1,2‐d:4,5‐d′]bisthiazole
(BBTz)
is
incorporated
into
PM6
main
chain
create
series
terpolymer
donors,
leveraging
entropy
increase
and
superior
miscibility
with
acceptors
modulate
blend
morphology.
The
introduction
BBTz
broadened
absorption
range,
enhanced
film
crystallinity,
significantly
improved
donor‐acceptor
through
its
low
dipole
moment
high
electrostatic
potential.
This
facilitated
formation
nanofiber
structures
active
layer,
thus
optimizing
As
result,
PBZ‐10:PY‐IT‐based
device
achieved
an
impressive
power
conversion
efficiency
(PCE)
19.06%.
Incorporation
PBQx‐TF
binary
can
further
improve
morphology,
charge
transport,
exciton
lifetime,
dissociation,
collection,
as
well
suppressed
recombination,
finally
leading
record‐breaking
PCE
20.04%
for
all‐PSCs
date.
findings
demonstrate
effectiveness
strategy
enhancing
all‐PSC
performance.
By
molecular
design
component
selection,
approach
provides
viable
pathway
achieving
higher
supports
advancement
renewable
energy
technologies.
Advanced Materials,
Год журнала:
2024,
Номер
36(16)
Опубликована: Янв. 12, 2024
Abstract
All‐polymer
solar
cells
have
garnered
particular
attention
thanks
to
their
superior
thermal,
photo,
and
mechanical
stabilities
for
large‐scale
manufacturing,
yet
the
performance
enhancement
remains
largely
restrained
by
inherent
morphological
challenges
of
bulk‐heterojunction
active
layer.
Herein,
a
3D
Y‐branched
polymerized
small‐molecule
acceptor
named
PYBF
,
characteristic
high
molecular
weight
glass
transition
temperature,
is
designed
synthesized
precisely
linking
C
3h
‐symmetric
benzotrifuran
with
Y6
acceptors.
In
comparison
benchmark
thiophene‐bridged
linear
PYIT
acceptor,
an
optical
blue‐shift
absorption
observed
slightly
higher
power
conversion
efficiency
(PCE)
15.7%
(vs
15.14%)
obtained
when
paired
polymer
donor
PM6,
which
benefit
from
more
crystalline
face‐on‐oriented
domains.
However,
star‐like
bulky
structure
results
in
nucleation‐growth
dominant
phase‐separation
polymeric
blends,
generates
stumpy
droplet‐like
fibrils
impairs
continuity
phases.
This
issue
however
surprisingly
resolved
incorporating
small
amount
PYIT,
leads
formation
interconnective
neuron‐like
dual‐acceptor
domains
long‐chain
entanglements
acceptors
alleviates
bimolecular
recombination.
Thus,
champion
device
realizes
respectable
PCE
up
≈17%
importantly
exhibits
thermal
storage
counterpart.
National Science Review,
Год журнала:
2024,
Номер
11(12)
Опубликована: Ноя. 4, 2024
ABSTRACT
Solid
additive
engineering
has
been
intensively
explored
on
morphology
tuning
for
highly
efficient
all-polymer
solar
cells
(all-PSCs),
a
promising
photovoltaic
technology
towards
multi-scenario
application.
Although
the
nano-fibrillar
network
of
active
layer
induced
by
treatment
is
confirmed
as
key
factor
power
conversion
efficiency
(PCE)
all-PSCs,
its
formation
mechanism
not
clearly
revealed,
lack
precise
and
convincing
real-time
observation
crystallization
phase
separation
during
liquid-to-solid
transition
process
spin-coating.
Herein
we
report
an
in-situ
grazing
incidence
wide-angle/small-angle
X-ray
scattering
(GIWAXS/GISAXS)
screening
that
reveals
fact
naphthalene
derived
solid
additives
can
suppress
aggregation
polymer
acceptor
(PY-IT)
at
beginning
stage
spin
coating,
which
provides
sufficient
time
space
donor
(PM6)
to
form
fibril
structure.
Moreover,
guided
this
knowledge,
ternary
system
proposed,
achieves
cutting-edge
level
PCEs
both
small-area
(0.04
cm2)
(also
decent
operational
stability)
large-area
(1
devices.
Advanced Energy Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 2, 2025
Abstract
In
recent
years,
polymer
solar
cells
(PSCs)
have
achieved
rapid
progress,
with
power
conversion
efficiencies
(PCEs)
reaching
up
to
20.25%,
driven
by
significant
advancements
in
device
fabrication
and
active‐layer
materials.
The
ternary
polymerization
strategy
has
proven
be
a
straightforward
effective
approach
for
developing
high‐performance
photoelectric
polymers
incorporating
third
monomer
into
the
backbone.
This
incorporation
effectively
optimizes
intrinsic
properties,
including
UV–vis
absorption,
energy
levels,
solubility,
crystallinity,
morphology,
charge
transfer,
mechanical
robustness,
batch‐to‐batch
reproducibility,
stability.
review
highlights
latest
designing
photoactive
copolymers
(both
donors
acceptors),
particular
focus
on
stability,
potential
applications
commercial
development.
aim
is
provide
valuable
guidance
development
of
materials
using
strategy.
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 15, 2025
Abstract
Developing
high‐performance
all‐polymer
solar
cells
(all‐PSCs)
remains
a
challenge
due
to
the
difficulty
in
controlling
morphology
of
polymer
blends.
In
this
study,
benzo[1,2‐d:4,5‐d′]bisthiazole
(BBTz)
is
incorporated
into
PM6
main
chain
create
series
terpolymer
donors,
leveraging
entropy
increase
and
superior
miscibility
with
acceptors
modulate
blend
morphology.
The
introduction
BBTz
broadened
absorption
range,
enhanced
film
crystallinity,
significantly
improved
donor‐acceptor
through
its
low
dipole
moment
high
electrostatic
potential.
This
facilitated
formation
nanofiber
structures
active
layer,
thus
optimizing
As
result,
PBZ‐10:PY‐IT‐based
device
achieved
an
impressive
power
conversion
efficiency
(PCE)
19.06%.
Incorporation
PBQx‐TF
binary
can
further
improve
morphology,
charge
transport,
exciton
lifetime,
dissociation,
collection,
as
well
suppressed
recombination,
finally
leading
record‐breaking
PCE
20.04%
for
all‐PSCs
date.
findings
demonstrate
effectiveness
strategy
enhancing
all‐PSC
performance.
By
molecular
design
component
selection,
approach
provides
viable
pathway
achieving
higher
supports
advancement
renewable
energy
technologies.