Macromolecular Rapid Communications,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 18, 2024
In
order
to
realize
high-performance
bulk-heterojunction
(BHJ)
all-polymer
solar
cells,
achieving
appropriate
aggregation
and
moderate
miscibility
of
the
polymer
blends
is
one
critical
factor.
Herein,
this
study
designs
synthesizes
two
new
acceptors
(P
Chemical Society Reviews,
Journal Year:
2024,
Volume and Issue:
53(9), P. 4674 - 4706
Published: Jan. 1, 2024
This
review
summarizes
the
recent
progress,
key
design
principles
and
prospects
of
dimer
multimer
acceptors
for
developing
polymer
solar
cells
(PSCs)
with
high
efficiency
long-term
stability.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(32)
Published: May 28, 2024
Abstract
Indoor
photovoltaics
(IPVs)
are
garnering
increasing
attention
from
both
the
academic
and
industrial
communities
due
to
pressing
demand
of
ecosystem
Internet‐of‐Things.
All‐polymer
solar
cells
(all‐PSCs),
emerging
as
a
sub‐type
organic
photovoltaics,
with
merits
great
film‐forming
properties,
remarkable
morphological
light
stability,
hold
promise
simultaneously
achieve
high
efficiency
long‐term
operation
in
IPV's
application.
However,
dearth
polymer
acceptors
medium‐bandgap
has
impeded
rapid
development
indoor
all‐PSCs.
Herein,
highly
efficient
acceptor
(PYFO‐V)
is
reported
through
synergistic
effects
side
chain
engineering
linkage
modulation
applied
for
all‐PSCs
operation.
As
result,
PM6:PYFO‐V‐based
all‐PSC
yields
highest
27.1%
under
LED
condition,
marking
value
binary
date.
More
importantly,
blade‐coated
devices
using
non‐halogenated
solvent
(
o
‐xylene)
maintain
an
over
23%,
demonstrating
potential
industry‐scale
fabrication.
This
work
not
only
highlights
importance
fine‐tuning
intramolecular
charge
transfer
effect
intrachain
coplanarity
developing
high‐performance
but
also
provides
strategy
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.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 27, 2024
Abstract
High
power
conversion
efficiency
(PCE)
and
long‐term
stability
are
prerequisites
for
commercialization
of
organic
solar
cells
(OSCs).
Herein,
two
dimer
acceptors
(DYTVT
DYTCVT)
developed
with
different
properties
through
linker
engineering,
study
their
effects
as
alloy‐like
on
the
photovoltaic
performance
photostability
OSCs.
These
ternary
OSCs
effectively
combine
advantages
both
acceptors.
DYTVT,
characterized
by
its
high
backbone
planarity,
ensures
elevated
electron
mobility
glass‐transition
temperature
(
T
g
),
leading
to
efficient
charge
transport
enhanced
Conversely,
DYTCVT,
significant
dipole
moment
electrostatic
potential,
enhances
compatibility
alloy
donors
refines
blend
morphology,
facilitating
generation
in
Consequently,
D18:DYTVT:DYTCVT
exhibit
higher
PCE
(18.4%)
compared
D18:MYT
(monomer
acceptor,
=
16.5%),
D18:DYTVT
(PCE
17.4%),
D18:DYTCVT
17.0%)
Furthermore,
owing
(133
°C)
than
MYT
80
DYTCVT
120
°C),
have
significantly
t
80%
lifetime
4250
h
under
1‐sun
illumination)
40
h)
2910
h).
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(41)
Published: July 3, 2024
Abstract
The
dimerization
of
small
molecule
acceptors
(SMAs)
is
a
promising
strategy
for
enhancing
the
long‐term
stability
and
power
conversion
efficiency
(PCE)
organic
solar
cells
(OSCs).
However,
reported
DSMAs
are
primarily
limited
to
end‐linked
molecular
configurations,
highlighting
need
further
exploration
various
dimer
architectures.
Herein,
development
two
distinct
core‐linked
dimerized
SMAs
(DYF‐V
DYF‐E)
with
tailored
linker
structures
(vinylene
ethynyl,
respectively),
achieving
high‐performance
OSCs
(PCE
=
18.53%).
Interestingly,
subtle
change
in
results
markedly
different
properties
photovoltaic
performances
acceptors.
DYF‐E
an
ethynyl
exhibits
more
twisted
backbone
conformation
mitigated
aggregation
property
compared
DYF‐V,
inducing
desirable
blend
morphologies
polymer
donor
including
high
crystallinity,
face‐on
oriented
packing
structures,
well‐intermixed
domains.
Thus,
DYF‐E‐based
exhibit
PCE
(17.02%),
which
significantly
outperforms
DYF‐V‐based
9.98%).
Furthermore,
ternary
based
on
achieve
higher
18.53%.
this
study
highlights
significance
selecting
appropriate
producing
OSCs.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 15, 2024
Abstract
All‐polymer
solar
cells
(all‐PSCs)
present
compelling
advantages
for
commercial
applications,
including
mechanical
durability
and
optical
thermal
stability.
However,
progress
in
developing
high‐performance
polymer
donors
has
trailed
behind
the
emergence
of
excellent
acceptors.
In
this
study,
we
report
a
new
electron‐deficient
arene,
fluorinated
bithiophene
imide
(F‐BTI)
its
donor
SA1,
which
two
fluorine
atoms
are
introduced
at
outer
β
‐positions
thiophene
rings
BTI
to
fine‐tune
energy
levels
aggregation
resulting
polymers.
SA1
exhibits
deep
HOMO
level
−5.51
eV,
wide
bandgap
1.81
eV
suitable
miscibility
with
acceptor.
Polymer
chains
incorporating
F‐BTI
result
highly
ordered
π–π
stacking
favorable
phase‐separated
morphology
within
all‐polymer
active
layer.
Thus,
:
PY‐IT‐based
all‐PSCs
exhibit
an
efficiency
16.31
%
stability,
is
further
enhanced
record
value
19.33
(certified:
19.17
%)
by
constructing
ternary
device.
This
work
demonstrates
that
offers
effective
route
materials
improved
optoelectronic
properties,
will
change
scenario
terms
stable
all‐PSCs.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 10, 2024
Concurrently
achieving
high
efficiency,
mechanical
robustness
and
thermal
stability
is
critical
for
the
commercialization
of
all-polymer
solar
cells
(APSCs).
However,
APSCs
usually
demonstrate
complicated
morphology,
primarily
attributed
to
polymer
chain
entanglement
which
has
a
detrimental
effect
on
their
fill
factors
(FF)
morphology
stability.
To
address
these
concerns,
an
end-group
extended
acceptor,
PY-NFT,
was
synthesized
studied.
The
analysis
showed
tightly
ordered
molecular
packing
mode
favorable
phase
separation
formed.
PM6
:
PY-NFT-based
device
achieved
exceptional
PCE
19.12
%
(certified
as
18.45
%),
outperforming
control
PY-FT
devices
(17.14
%).
This
significant
improvement
highlights
record-high
binary
APSCs.
aging
study
revealed
that
PY-NFT
blend
exhibited
excellent
morphological
stability,
thereby
superior
retaining
90
initial
efficiency
after
enduring
stress
(65
°C)
1500
hours.
More
importantly,
film
outstanding
ductility
with
crack
onset
strain
24.1
%.
Overall,
rational
chemical
structure
innovation,
especially
conjugation
extension
strategy
trigger
appropriate
stable
key
improved
robust
ChemSusChem,
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 18, 2024
Abstract
With
the
rapid
development
of
non‐fullerene
acceptors
(NFAs),
power
conversion
efficiency
(PCE)
organic
solar
cells
(OSCs)
is
increasing.
According
to
their
different
chemical
structures,
NFAs
can
initially
be
divided
into
two
categories:
small
molecule
(SMAs)
and
polymerized
(PSMAs).
Due
strong
absorption
capacity
controllable
energy
levels,
PCE
devices
based
on
SMAs
has
approached
20
%.
Compared
with
SMAs,
PSMAs
have
advantages
in
stability
flexibility,
PSMA‐based
exceeded
18
However,
higher
synthesis
cost
lower
batch
repeatability
hinder
its
further
development.
Recently,
concept
giant
(GMAs)
been
proposed.
These
materials
a
clear
molecular
structure
are
considered
novel
acceptor
that
combine
PSMAs.
Currently,
GMAs
19
In
this
review,
we
will
introduce
latest
developments
PSMAs,
GMAs.
Then,
relationship
between
performance
analyzed.
end,
perspectives
opportunities
challenges
these
provided,
which
could
inspire
for
advanced
OSCs.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 1, 2024
Abstract
Discrete
dimer
or
multimer
acceptors
have
enhanced
the
stability
of
organic
solar
cells
(OSCs)
due
to
their
slow
diffusion
kinetics
resulting
from
large
molecular
sizes.
However,
development
with
chain
length
longer
than
trimers
has
been
challenging,
which
often
require
multistep
reactions
low
synthetic
yield.
In
this
study,
a
new
discrete
tetramer
acceptor
(TetA)
using
one‐pot
reaction
and
subsequent
purification
processes
is
developed.
During
purification,
(DA)
trimer
(TA)
are
also
obtained.
The
OSCs
for
TetA
demonstrate
higher
power
conversion
efficiency
(PCE)
16.14%
those
shorter
lengths,
such
as
monomer
(MA,
12.85%),
DA
(14.31%),
TA
(15.10%).
Additionally,
despite
having
similar
number‐average
weight,
TetA‐based
exhibit
significantly
PCE
(16.14%)
compared
based
on
mixture
(MixA)
dispersity
(10.72%).
Furthermore,
highest
photostability
mechanical
robustness
among
series.
For
example,
superior
(
t
70%
lifetime
=
2180
h
under
1‐sun
illumination)
(crack‐onset
strain
(COS)
8%)
MA
220
h,
COS
2%),
MixA
745
6%).
ACS Applied Materials & Interfaces,
Journal Year:
2025,
Volume and Issue:
17(9), P. 14329 - 14341
Published: Feb. 25, 2025
As
all-polymer
solar
cells
(all-PSCs)
have
achieved
impressive
power
conversion
efficiencies
(PCEs),
extending
their
lifetime
under
long-term
operation
is
also
increasingly
important.
To
address
this
issue,
in
study,
a
new
pseudo-quaternary
blend
composed
of
conjugated
block
copolymer
donors
and
acceptors,
PM6-b-TT:b-PYT,
introduced
as
the
active
layer
for
all-PSCs.
Compared
to
all-PSC
based
on
traditional
binary
blend,
PM6:BTTP-T,
those
exhibited
significantly
improved
thermal
stability
after
annealing
harsh
conditions
150
°C
an
ambient
atmosphere.
More
importantly,
elucidate
morphological
layer,
visible
evidence
thin
film's
surface
internal
structure
carefully
investigated
by
multiple
advanced
techniques.
After
extended
stress
at
°C,
bulk
heterojunction
(BHJ)
films
exhibit
excessive
polymer
chain
aggregation,
phase
separation
polymers,
increased
roughness,
forming
charge
traps
increasing
exciton
recombination.
Meanwhile,
BHJ
maintain
crystallinity
nanostructure
improving
Overall,
study
provides
detailed
understanding
high-efficiency
all-PSCs,
offering
key
insights
into
section
proposing
promising
structures