Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 18, 2024
Abstract
High
efficiency,
stability,
and
flexibility
are
key
prerequisites
for
the
commercial
applications
of
organic
solar
cells
(OSCs).
Herein,
three
back‐to‐back
connected
dimers
(2Qx‐TT,
2Qx‐C3,
2Qx‐C6)
developed
as
guest
acceptors
OSCs
with
improved
comprehensive
performance.
By
regulating
linkage
from
rigid
bithiophene
to
flexible
alkyl
chain,
display
quite
different
molecular
geometry
intermolecular
interactions,
consequently
influencing
their
packing
arrangement,
film‐forming
process,
carrier
mobilities,
device
flexibility.
introducing
these
dimer
into
active
layer,
form
alloy
phases
host
acceptor,
promoting
process
charge
dynamics.
All
ternary
devices
exhibit
PCEs
over
18%
than
control
binary
device.
Among
them,
2Qx‐C3‐based
obtains
best
efficiency
high
19.03%.
Moreover,
thanks
stronger
entanglement
favored
by
linkage,
PM6:BTP‐eC9:2Qx‐C3‐based
shows
outstanding
stability
The
displays
an
PCE
16.09%
a
crack‐onset
strain
15.0%,
showing
excellent
mechanical
robustness
close
all‐polymer
devices.
This
work
demonstrates
potential
highly
efficient,
stable
OSCs.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(34)
Published: March 29, 2024
Abstract
Solvent
additives
are
pivotal
for
enhancing
the
morphology,
efficiency,
and
stability
of
organic
solar
cells
(OSCs).
However,
widely
used
additive,
1,8‐diiodooctane
(DIO),
has
drawbacks
like
harmful
halogen
content
potential
OSC
degradation.
To
address
these
issues,
novel
non‐halogenated,
thienyl‐alkyl‐thienyl
structural
solvent
additives—DTP,
DTH,
DTN—featuring
varying
alkyl
linker
lengths
(CH
2
)
3
,
6
9
respectively
introduced.
Additives
with
longer
linkers,
DTH
DTN,
effectively
dissolve
strongly
interact
both
donor
polymer
PM6
acceptor
L8‐BO.
This
dual
interaction
enables
precise
tuning
their
microstructures,
resulting
in
enhanced
crystallinity.
Upon
incorporating
as
an
additive
OSCs
(PM6:L8‐BO),
a
minimal
voltage
loss
is
observed,
leading
to
impressive
efficiency
18.51%,
surpassing
17.90%
achieved
DIO.
Furthermore,
DTH‐based
devices
demonstrated
superior
photostability.
In
ternary
blend
system
(PM6:D18‐Cl:L8‐BO),
19.07%
attained,
outperforming
previous
non‐halogenated
additive‐based
OSCs.
employing
processing
combination
toluene
carbon
disulfide,
high
PCE
18.82%
achieved.
These
results
underscore
efficacy
designing
aromatic
units,
enabling
tailored
interactions
acceptor,
thereby
presenting
robust
strategy
optimizing
performance
stability.
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(31)
Published: June 17, 2024
Abstract
Halogenation
of
Y‐series
small‐molecule
acceptors
(Y‐SMAs)
is
identified
as
an
effective
strategy
to
optimize
photoelectric
properties
for
achieving
improved
power‐conversion‐efficiencies
(PCEs)
in
binary
organic
solar
cells
(OSCs).
However,
the
effect
different
halogenation
2D‐structured
large
π‐fused
core
guest
Y‐SMAs
on
ternary
OSCs
has
not
yet
been
systematically
studied.
Herein,
four
2D‐conjugated
(X‐QTP‐4F,
including
halogen‐free
H‐QTP‐4F,
chlorinated
Cl‐QTP‐4F,
brominated
Br‐QTP‐4F,
and
iodinated
I‐QTP‐4F)
by
attaching
halogens
into
2D‐conjugation
extended
dibenzo[
f
,
h
]quinoxaline
are
developed.
Among
these
X‐QTP‐4F,
Cl‐QTP‐4F
a
higher
absorption
coefficient,
optimized
molecular
crystallinity
packing,
suitable
cascade
energy
levels,
complementary
with
PM6:L8‐BO
host.
Moreover,
among
PM6:L8‐BO:X‐QTP‐4F
blends,
PM6:L8‐BO:Cl‐QTP‐4F
obtains
more
uniform
size‐suitable
fibrillary
network
morphology,
well
vertical
phase
distribution,
thus
boosting
charge
generation,
transport,
extraction,
suppressing
loss
OSCs.
Consequently,
PM6:L8‐BO:Cl‐QTP‐4F‐based
achieve
19.0%
efficiency,
which
state‐of‐the‐art
based
superior
devices
host
(17.70%)
guests
H‐QTP‐4F
(18.23%),
Br‐QTP‐4F
(18.39%),
I‐QTP‐4F
(17.62%).
The
work
indicates
that
promising
gain
efficient
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).
Energy & Environmental Science,
Journal Year:
2024,
Volume and Issue:
17(15), P. 5719 - 5729
Published: Jan. 1, 2024
Efficient
3D
dimeric
acceptors
linking
two
monomers
with
flexible
alkyl
linkers
were
developed.
The
resulting
CH8-6-based
OSCs
achieved
a
high
PCE
of
19.2%
and
also
exhibited
excellent
thermal
stability
mechanical
flexibility.
Small,
Journal Year:
2025,
Volume and Issue:
21(11)
Published: Feb. 7, 2025
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 Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 3, 2025
Abstract
The
development
of
organic
solar
cells
(OSCs)
with
high
efficiency
and
stability
is
highly
desirable
to
facilitate
its
commercial
applications.
Although
dimeric
acceptors
distinctive
advantages
have
been
widely
studied,
high‐performance
binary
OSCs
based
on
such
molecules
rarely
achieved.
In
this
work,
a
new
acceptor
(DY‐FL)
constructed
by
simultaneously
optimizing
the
linking
sites
units,
as
well
building
blocks.
Thanks
effective
molecular
design,
DY‐FL
provides
improved
stacking
for
fibrous
morphology
favorable
exciton/charge
dynamics.
Consequently,
DY‐FL‐based
render
superior
power
conversion
(PCE)
19.78%,
representing
record‐breaking
acceptors.
Importantly,
devices
display
significantly
enhanced
operational
under
external
stimuli
light
heat,
in
comparison
their
small
molecule
(Y‐F)‐based
counterpart.
These
findings
highlight
significance
blocks
modes,
providing
insight
into
design
strategy
state‐of‐the‐art
OSCs.
Chinese Journal of Chemistry,
Journal Year:
2024,
Volume and Issue:
42(11), P. 1307 - 1318
Published: March 13, 2024
Comprehensive
Summary
In
the
last
few
years,
organic
solar
cells
(OSCs)
have
made
significant
progress
in
photovoltaic
performance,
mainly
due
to
innovative
development
of
active
layer
materials,
especially
Y‐series
and
related
derivatives
as
acceptors
which
become
key
factor
that
boosts
power
conversion
efficiency.
Recently,
achieve
high‐performance
OSCs,
an
emerging
molecular
design
strategy
applying
flexible
alkyl
units
linkers
construct
non‐fully
conjugated
has
been
developed
addressed
great
attention.
This
review
highlights
materials
with
backbone
enable
OSCs.
Impressive
OSCs
achieved
by
some
representative
material
systems.
The
strategies
are
discussed
detail.
Finally,
a
brief
summary
future
prospect
provided
advancing
towards
brighter
future.
Key
Scientists
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.
Energy & Environmental Science,
Journal Year:
2024,
Volume and Issue:
17(19), P. 7318 - 7329
Published: Jan. 1, 2024
An
in-situ
cross-linkable
monomer
is
carefully
developed
into
blend
films
to
finely
manipulate
the
molecular
packing,
crystallization
and
nanomorphology
during
film
formation.
As
a
result,
stabilized
PCEs
of
19.84%
for
rigid
device
18.32%
flexible
organic
solar
cells
are
achieved.