Advanced Energy Materials,
Journal Year:
2023,
Volume and Issue:
14(3)
Published: Nov. 21, 2023
Abstract
Achieving
high‐performance
in
all‐small‐molecule
organic
solar
cells
(ASM‐OSCs)
significantly
relies
on
precise
nanoscale
phase
separation
through
domain
size
manipulation
the
active
layer.
Nonetheless,
for
ASM‐OSC
systems,
forging
a
clear
connection
between
tuning
of
and
intricacies
proves
to
be
formidable
challenge.
This
study
investigates
intricate
interplay
adjustment
creation
optimal
morphology,
crucial
ASM‐OSCs’
performance.
It
is
demonstrated
that
exceptional
layer
achieved
by
meticulously
controlling
continuity
uniformity
domains
via
re‐packing
process.
A
series
halogen‐substituted
solvents
(Fluorobenzene,
Chlorobenzene,
Bromobenzene,
Iodobenzene)
adopted
tune
kinetics,
ASM‐OSCs
treated
with
CB
exhibited
an
impressive
16.2%
power
conversion
efficiency
(PCE).
The
PCE
enhancement
can
attributed
gradual
crystallization
process,
promoting
smoothly
interconnected
uniformly
distributed
size.
This,
turn,
leads
favorable
enhanced
charge
transfer,
extended
carrier
lifetime,
consequently,
reduced
recombination
free
charges.
findings
emphasize
pivotal
role
kinetics
achieving
ASM‐OSCs,
offering
valuable
insights
designing
fabrication
strategies.
Advanced Materials,
Journal Year:
2023,
Volume and Issue:
36(9)
Published: Sept. 13, 2023
Abstract
Organic
solar
cells
(OSCs)
exhibit
complex
charge
dynamics,
which
are
closely
correlated
with
the
dielectric
constant
(ɛ
r
)
of
photovoltaic
materials.
In
this
work,
a
series
novel
conjugated
copolymers
based
on
benzo[1,2‐b:4,5‐b′]difuran
(BDF)
and
benzotriazole
(BTz)
is
designed
synthesized,
differ
by
nature
π‐bridge
from
one
another.
The
PBDF‐TF‐BTz
asymmetric
furan
thiophene
demonstrates
larger
ɛ
4.22
than
PBDF‐dT‐BTz
symmetric
(3.15)
PBDF‐dF‐BTz
(3.90).
also
offers
more
favorable
molecular
packing
appropriate
miscibility
non‐fullerene
acceptor
Y6
its
counterparts.
corresponding
PBDF‐TF‐BTz:Y6
OSCs
display
efficient
exciton
dissociation,
fast
transport
collection,
reduced
recombination,
eventually
leading
to
power
conversion
efficiency
17.01%.
When
introducing
fullerene
derivative
(PCBO‐12)
as
third
component,
PBDF‐TF‐BTz:Y6:PCBO‐12
yield
remarkable
FF
80.11%
high
18.10%,
highest
value
among
all
reported
BDF‐polymer‐based
OSCs.
This
work
provides
an
effective
approach
developing
high‐permittivity
materials,
showcasing
promising
polymer
donor
for
constructing
high‐performance
Advanced Functional Materials,
Journal Year:
2023,
Volume and Issue:
34(13)
Published: Dec. 15, 2023
Abstract
Controlled
sequential
crystallization
of
donors
and
acceptors
is
a
critical
factor
for
achieving
enhanced
phase
separation
efficient
charge
transfer
performance
in
polymer
solar
cells
(PSCs).
In
this
study,
comprehensive
investigation
structurally
simple
solvent
additive,
1‐fluoro‐2‐iodobenzene
(OFIB)
conducted,
which
efficiently
controls
the
morphology
active
layer,
resulting
fibrous
assembly
significantly
enhancing
power
conversion
efficiency
from
16.34%
to
18.38%
based
on
PM6:L8‐BO
system.
Density
functional
theory,
molecular
dynamics
simulations,
grazing
incidence
small‐
wide‐angle
X‐ray
scattering
techniques
reveal
that
addition
OFIB
processed
blend
aligns
orientation
acceptor
molecules,
thereby
overall
π–π
stacking
layer.
establishes
nearly
equal‐strength
interactions
with
conjugated
frameworks
both
donor
materials,
benefiting
multiple
electron
conjugation
between
its
iodine
atom
framework
Femtosecond‐timescale
photophysical
studies
demonstrate
OFIB‐optimized
layer
shows
reduced
exciton
losses
at
donor–acceptor
interface.
This
study
offers
new
perspective
mechanism
underlying
function
additives
presents
research
methodology
will
guide
development
next‐generation
non‐fullerene
PSCs.
Aggregate,
Journal Year:
2023,
Volume and Issue:
5(2)
Published: Nov. 6, 2023
Abstract
Organic
solar
cells
(OSCs)
have
demonstrated
over
19%
power
conversion
efficiency
(PCE)
with
the
help
of
material
innovation
and
device
optimization.
Co‐working
newly
designed
materials,
traditional
solvent
additives,
1‐chloronaphthalene
(CN),
1,8‐diodooctane
(DIO)
are
still
powerful
in
morphology
modulation
towards
satisfying
efficiencies.
Here,
we
chose
recently
reported
high‐performance
polymer
donors
(PM6
&
D18‐Fu)
small
molecular
acceptors
(Y6
L8‐BO)
as
active
layer
materials
processed
them
by
different
conditions
(CN
or
DIO
none).
Based
on
corresponding
12
groups
results,
their
film
characterizations
(both
ex‐situ
in‐situ
ones),
property‐performance
relationships
revealed
case
case.
It
is
thereby
supposed
to
be
taken
a
successful
attempt
demonstrate
importance
complexity
donor‐acceptor‐additive
interaction,
since
performance
physics
analyses
also
tightly
combined
variation.
Furthermore,
ternary
blend
construction
for
PCE
improvement
provides
an
approaching
level
showcases
potential
understanding‐guided‐optimization
(UGO)
future
OSCs.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: March 24, 2024
Abstract
The
critical
step
in
commercializing
organic
solar
cells
(OSCs)
involves
achieving
high‐performance
modules
through
environmentally
friendly
solvents.
incorporation
of
solid
additives,
recognized
as
an
effective
method
for
modulating
the
morphology
active
layers
layer‐by‐layer
(LBL)
deposition,
plays
a
significant
role.
Here,
novel
volatile
additive
is
introduced
individually
into
non‐halogenated
solution
donor
PM6
morphology‐modulating
agent.
induces
conformational
and
crystalline
orientation
change
PM6,
resulting
enhanced
balanced
charge
transport
layer.
With
focus
on
exciton
dynamics,
optimized
layer
inhibits
formation
low‐energy
triplet
states.
It
facilitates
strong
reverse
hole
transfer
processes,
leading
to
more
efficient
dissociation.
final
small‐area
LBL
blade‐coated
OSCs
fabricated
under
ambient
conditions
achieve
power
conversion
efficiency
(PCE)
18.42%.
Furthermore,
large‐area
module
with
area
28.82
cm
2
manufactured,
PCE
16.04%
high
geometric
fill
factor
93.8%.
This
highlights
modulation
use
additives
provides
successful
strategy
fabricating
OSC
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
64(1)
Published: Aug. 24, 2024
Disordered
polymer
chain
entanglements
within
all-polymer
blends
limit
the
formation
of
optimal
donor-acceptor
phase
separation.
Therefore,
developing
effective
methods
to
regulate
morphology
evolution
is
crucial
for
achieving
morphological
features
in
organic
solar
cells
(APSCs).
In
this
study,
two
isomers,
4,5-difluorobenzo-c-1,2,5-thiadiazole
(SF-1)
and
5,6-difluorobenzo-c-1,2,5-thiadiazole
(SF-2),
were
designed
as
solid
additives
based
on
widely-used
electron-deficient
benzothiadiazole
unit
nonfullerene
acceptors.
The
incorporation
SF-1
or
SF-2
into
PM6
:
PY-DT
blend
induces
stronger
molecular
packing
via
interaction,
leading
continuous
interpenetrated
networks
with
suitable
phase-separation
vertical
distribution.
Furthermore,
after
treatment
SF-2,
exciton
diffusion
lengths
films
are
extended
over
40
nm,
favoring
charge
transport.
asymmetrical
characterized
by
an
enhanced
dipole
moment,
increases
power
conversion
efficiency
(PCE)
PY-DT-based
device
18.83
%
due
electrostatic
interactions.
Moreover,
a
ternary
strategy
boosts
PCE
SF-2-treated
APSC
19
%.
This
work
not
only
demonstrates
one
best
performances
APSCs
but
also
offers
approach
manipulate
using
rational-designed
additives.
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(23)
Published: March 25, 2024
Abstract
Volatile
solid
additives
have
attracted
increasing
attention
in
optimizing
the
morphology
and
improving
performance
of
currently
dominated
non‐fullerene
acceptor‐based
organic
solar
cells
(OSCs).
However,
underlying
principles
governing
rational
design
volatile
remain
elusive.
Herein,
a
series
efficient
are
successfully
developed
by
crossbreeding
effect
chalcogenation
iodination
for
photovoltaic
performances
OSCs.
Five
benzene
derivatives
1,4‐dimethoxybenzene
(DOB),
1‐iodo‐4‐methoxybenzene
(OIB),
1‐iodo‐4‐methylthiobenzene
(SIB),
1,4‐dimethylthiobenzene
(DSB)
1,4‐diiodobenzene
(DIB)
systematically
studied,
where
widely
used
DIB
is
as
reference.
The
on
overall
property
comprehensively
investigated,
which
indicates
that
versatile
functional
groups
provided
various
types
noncovalent
interactions
with
host
materials
modulating
morphology.
Among
them,
SIB
combination
sulphuration
enabled
more
appropriate
blend,
giving
rise
to
highly
ordered
molecular
packing
favorable
As
result,
binary
OSCs
based
PM6:L8‐BO
PBTz‐F:L8‐BO
well
ternary
PBTz‐F:PM6:L8‐BO
achieved
impressive
high
PCEs
18.87%,
18.81%
19.68%,
respectively,
among
highest
values
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(25)
Published: April 18, 2024
Abstract
The
energy
loss
induced
open‐circuit
voltage
(
V
OC
)
deficit
hampers
the
rapid
development
of
state‐of‐the‐art
organic
solar
cells
(OSCs),
therefore,
it
is
extremely
urgent
to
explore
effective
strategies
address
this
issue.
Herein,
a
new
volatile
solid
additive
1,4‐bis(iodomethyl)cyclohexane
(DIMCH)
featured
with
concentrated
electrostatic
potential
distribution
utilized
act
as
morphology‐directing
guest
reduce
in
multiple
state‐of‐art
blend
system,
leading
one
highest
efficiency
(18.8%)
at
forefront
reported
binary
OSCs.
Volatile
DIMCH
decreases
radiative/non‐radiative
recombination
(Δ
E
2
/Δ
3
by
rationally
balancing
crystallinity
donors
and
acceptors
realizing
homogeneous
network
structure
crystal
domain
reduced
D–A
phase
separation
during
film
formation
process
weakens
disorder
trap
density
It
believed
that
study
brings
not
only
profound
understanding
emerging
additives
but
also
hope
further
improve
performance
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 3, 2024
Abstract
By
selectively
interacting
with
acceptor
components,
various
typed
solid
additives
achieve
boosted
power
conversion
efficiency
(PCE)
in
organic
solar
cells
(OSCs).
However,
due
to
the
efficient
active
layer
being
composed
of
donor
and
materials,
it
is
difficult
obtain
desired
morphology
by
manipulating
component
alone,
limiting
further
improvement
PCEs.
Herein,
two
a
same
backbone
thiophene‐benzene‐thiophene
(halogen‐free
D1‐H)
but
different
halogen
substituents
(fluorinated
D1‐F
chlorinated
D1‐Cl)
are
developed
probe
working
mechanism
halogenated
variation
OSCs.
Unlike
D1‐H
continuous
charge
distributions,
D1‐Cl
show
isolated
positive
distribution
benzene‐core
negative
thiophene,
offering
stronger
non‐covalent
interactions
both
(PM6)
(L8‐BO),
especially
D1‐Cl.
Consequently,
D1‐Cl‐treated
obtains
an
optimized
phase
separation
improved
molecular
packing,
boosting
PCE
18.59%
device
stability
OSCs,
17.62%
for
D1‐H‐treated
counterparts.
Moreover,
using
D18:L8‐BO
D18:BTP‐eC9
as
layers,
binary
OSCs
impressive
PCEs
19.29%
19.39%,
respectively.
This
work
indicates
that
halogenation
engineering
can
effectively
regulate
improving
elucidates
underlying
mechanism.