Preparation of Dual-Asymmetric Acceptors via Selenium Substitution Combined with Terminal Group Optimization Strategy for High Efficiency Organic Solar Cells
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 25, 2025
Improving
both
the
open-circuit
voltage
(VOC)
and
short-circuit
current
density
(JSC)
through
development
of
photovoltaic
materials
to
achieve
high
power
conversion
efficiency
(PCE)
is
critical
a
significant
challenge
for
organic
solar
cells
(OSCs).
Here,
we
designed
novel
dual-asymmetric
acceptors
A-SSe-TCF
A-SSe-LSF
by
simultaneously
asymmetrically
regulating
backbone
terminal
groups
investigated
their
synergistic
effects
on
performance
in
comparison
with
monoasymmetric
acceptor
A-SSe-4F.
The
exhibit
broader
spectral
absorption
larger
half-molecule
dipole
moment
differences,
which
favored
enhancement
JSC
reduction
energy
loss
(Eloss).
Among
binary
blends,
PM6:A-SSe-TCF
exhibits
superior
phase
separation,
vertical
distribution
morphology,
more
ordered
π-π
stacking
compared
PM6:A-SSe-LSF
PM6:A-SSe-4F.
As
result,
OSCs
based
achieved
higher
PCE
18.53%
VOC
due
suppressed
nonradiative
recombination
enhanced
charge
extraction
capabilities.
Furthermore,
incorporating
as
third
component,
PM6:L8-BO:A-SSe-TCF-based
device
achieves
champion
19.73%
without
account
decrement
Eloss.
strategy
provides
new
insights
into
molecular
design
improvement
OSCs.
Language: Английский
Volatile Imide Additives with Large Dipole and Special Film Formation Kinetics Enable High‐Performance Organic Solar Cells
Shuangshuang Xia,
No information about this author
Jie Xu,
No information about this author
Zongtao Wang
No information about this author
et al.
Angewandte Chemie International Edition,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 6, 2025
Large
dipole
moment
additives
have
strong
interactions
with
the
host
materials,
which
can
optimize
morphology
and
improve
photovoltaic
performance
of
organic
solar
cells
(OSCs).
However,
these
are
difficult
to
remove
due
their
intermolecular
interactions,
may
impair
stability.
Developing
volatile
large
moments
is
challenging.
Herein,
we
first
report
imide
that
could
effectively
OSCs
through
modification.
Three
N-(o-chlorophenyl)phthalimide
(oClPA),
N-(m-chlorophenyl)phthalimide
(mClPA),
N-(p-chlorophenyl)phthalimide
(pClPA)
were
screened
investigate
effort
positional
isomerization
on
molecular
configuration
interaction.
These
(ClPAs)
larger
(2.0664
Debye
for
oClPA,
4.2361
mClPA,
4.7896
pClPA)
compared
reported
solid
additives.
In
contrast
traditional
simultaneous
nucleation
crystal
growth,
ClPAs
induce
acceptor
nucleate
then
grow,
contributes
forming
high-quality
domains
better
crystallinity.
To
our
knowledge,
this
unique
film
formation
kinetics
was
first.
The
power
conversion
efficiency
(PCE)
based
PM6:BTP-eC9
treated
pClPA
improved
from
16.13
%
18.58
%.
Additive
also
performed
well
in
PM6:L8-BO,
PM6:Y6,
D18:L8-BO
systems,
a
high
PCE
19.04
achieved.
Our
results
indicate
using
unit
construct
simple
effective
strategy,
halogen
atom
has
effect
performance.
Language: Английский
Volatile Imide Additives with Large Dipole and Special Film Formation Kinetics Enable High‐Performance Organic Solar Cells
Shuangshuang Xia,
No information about this author
Jie Xu,
No information about this author
Zongtao Wang
No information about this author
et al.
Angewandte Chemie,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 6, 2025
Abstract
Large
dipole
moment
additives
have
strong
interactions
with
the
host
materials,
which
can
optimize
morphology
and
improve
photovoltaic
performance
of
organic
solar
cells
(OSCs).
However,
these
are
difficult
to
remove
due
their
intermolecular
interactions,
may
impair
stability.
Developing
volatile
large
moments
is
challenging.
Herein,
we
first
report
imide
that
could
effectively
OSCs
through
modification.
Three
N
‐(
o
‐chlorophenyl)phthalimide
(
ClPA),
m
p
ClPA)
were
screened
investigate
effort
positional
isomerization
on
molecular
configuration
interaction.
These
(ClPAs)
larger
(2.0664
Debye
for
ClPA,
4.2361
4.7896
compared
reported
solid
additives.
In
contrast
traditional
simultaneous
nucleation
crystal
growth,
ClPAs
induce
acceptor
nucleate
then
grow,
contributes
forming
high‐quality
domains
better
crystallinity.
To
our
knowledge,
this
unique
film
formation
kinetics
was
first.
The
power
conversion
efficiency
(PCE)
based
PM6:BTP‐eC9
treated
ClPA
improved
from
16.13
%
18.58
%.
Additive
also
performed
well
in
PM6:L8‐BO,
PM6:Y6,
D18:L8‐BO
systems,
a
high
PCE
19.04
achieved.
Our
results
indicate
using
unit
construct
simple
effective
strategy,
halogen
atom
has
effect
performance.
Language: Английский
High-performance and scalable large-area organic solar cells enabled by alloy-like composite-induced optimized morphology processed from non-halogenated solvent in air
Muhammad Jahankhan,
No information about this author
Du Hyeon Ryu,
No information about this author
Dongchan Lee
No information about this author
et al.
Chemical Engineering Journal,
Journal Year:
2025,
Volume and Issue:
unknown, P. 161811 - 161811
Published: March 1, 2025
Language: Английский
Ternary Blend Organic Photovoltaics with High Efficiency and Stability Through Energy Transfer and Molecular Packing Induced by an A‐D‐A Small Molecule
Bin Chang,
No information about this author
Chung‐Hao Chen,
No information about this author
Atsushi Yabushita
No information about this author
et al.
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 21, 2025
Abstract
A
novel
A‐D‐A
type
small
molecule
(DTP‐2EH‐IO2Cl)
incorporating
dithiophenepyrrole
(DTP)
core
with
indene‐dione
(IO2Cl)
side
chain
an
intermediate
band
gap
and
rigid
structure
is
incorporated
into
polymer
donor
PM6
one
of
the
three
A−DA′D−A
acceptor—L8‐BO,
BTP‐eC9
or
Y6—for
ternary‐blend
organic
photovoltaics
(OPVs).
The
third
component
DTP‐2EH‐IO2Cl
induces
not
only
energy
transfer
but
also
stronger
molecular
packing
acceptors,
resulting
in
a
larger
coherence
length
enhanced
absorption
that
enhances
devices’
power
conversion
efficiencies
(PCE)
thermal
stability.
PCE
values
champion
devices
PM6:L8‐BO,
PM6:BTP‐eC9,
PM6:Y6
are
19.2,
18.3,
17.6%,
respectively,
versus
16.5,
15.8,
15.4%
for
their
corresponding
binary
blend
devices,
displaying
relative
increases
from
14
to
16%.
stability
(T
80
)
PM6:L8‐BO:
ternary
device
dramatically
568
h
57
PM6:L8‐BO
device.
These
enhancements
can
be
attributed
effectiveness
as
increasing
light
through
inducing
intermolecular
providing
effective
way
tune
morphology
boost
both
OPVs.
Language: Английский
Benzo[b]thiophene-Series Solid Additives for Improving the Morphology and Photovoltaic Performance of Organic Solar Cells
ACS Applied Polymer Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 20, 2025
Language: Английский
Crystallization-driven effect enables organic solar cells with efficiency exceeding 19.4 %
Tengfei Han,
No information about this author
Jie Chi,
No information about this author
Ran Dong
No information about this author
et al.
Chemical Engineering Journal,
Journal Year:
2025,
Volume and Issue:
unknown, P. 164137 - 164137
Published: May 1, 2025
Language: Английский
Modulating Aggregation Behavior by Ternary Strategies for Efficient and Stable Thick‐Film Organic Solar Cells
Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 12, 2024
Abstract
Functional
third
components
targeted
to
improve
a
specific
property
of
organic
solar
cells
is
an
effective
strategy.
However,
introducing
component
simultaneously
efficiency
and
stability
achieve
good
performance
in
thick‐film
devices
has
rarely
been
reported.
Herein,
low
diffusion
IDCN
ID2CN
are
reported
power
conversion
(PCE)
18.08%
high
short‐circuit
current
(
J
SC
)
27.82
mA
cm
−2
,
one
the
highest
values
based
on
PM6:Y6.
They
increase
light
harvesting
range
400–500
nm
while
enhancing
energy
transfer
via
Förster
resonance
(FRET).
A
tightly
ordered
molecular
arrangement
achieved
by
modulating
preaggregation
film
formation
kinetics
Y6,
which
enhance
exciton
dissociation
charge
transport.
Moreover,
low‐diffusion
can
effectively
restrict
Y6
morphology
stability,
T
90
lifetime
increased
from
689
1545
h.
In
300
devices,
PM6:ID2CN:Y6
achieves
PCE
15.01%,
much
higher
than
PM6:Y6's
12.83%,
demonstrating
great
potential
devices.
Language: Английский