Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
137(1)
Published: Aug. 24, 2024
Abstract
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‐
(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.
Energy & Environmental Science,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 15, 2024
Two
volatile
solid
additives
were
developed
to
modulate
the
active-layer
morphology
of
all-polymer
solar
cells
(all-PSCs).
Among
them,
4-BDBTP-treated
all-PSC
achieved
an
outstanding
efficiency
19.30%.
ACS Applied Energy Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 10, 2025
Morphology
optimization
of
blend
films
is
an
essential
strategy
to
enhance
the
photovoltaic
performance
organic
solar
cells
(OSCs).
Additive
engineering
effective
for
fine-tuning
active
layer
morphology.
Given
limited
efforts
and
achievements
in
designing
synthesizing
liquid
additives,
new
solid
additives
manipulate
morphology
layers
have
gained
widespread
attention.
Herein,
1,4-dimethoxynaphthalene
(DMNA),
with
merits
simple
structure,
low
cost,
ecofriendliness,
successfully
incorporated
as
a
novel
additive
optimize
OSCs
based
on
D18-Cl:N3.
The
relationship
between
different
DMNA
contents
device
has
been
investigated.
It
found
that
can
be
effectively
regulated
by
DMNA,
leading
enhanced
molecular
packing
films,
which
favors
exciton
dissociation,
charge
transfer,
suppression
recombination.
As
result,
18.61%
power
conversion
efficiency
(PCE)
obtained
D18-Cl:N3
binary
devices
better
than
17.21%
PCE
control
device.
This
primarily
due
simultaneous
increase
short-circuit
current
density
fill
factor.
Furthermore,
general
applicability
confirmed
other
systems.
These
results
suggest
presents
potential
prospects
regulating
bulk
heterojunction
toward
high-performance
high-stability
OSCs.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 26, 2025
Abstract
Recently,
benzene‐based
solid
additives
(BSAs)
have
emerged
as
pivotal
components
in
modulating
the
morphology
of
blend
film
organic
solar
cells
(OSCs).
However,
since
almost
all
substituents
on
BSAs
are
weak
electron‐withdrawing
groups
and
contain
halogen
atoms,
study
with
non‐halogenated
strong
has
received
little
attention.
Herein,
an
additive
strategy
is
proposed,
involving
incorporation
benzene
ring.
An
effective
BSA,
4‐nitro‐benzonitrile
(NBN),
selected
to
boost
efficiency
devices.
The
results
demonstrate
that
NBN‐treated
device
exhibits
enhanced
light
absorption,
superior
charge
transport
performance,
mitigated
recombination,
more
optimal
compared
additive‐free
OSC.
Consequently,
D18:BTP‐eC9+NBN‐based
binary
D18:L8‐BO:BTP‐eC9+NBN‐based
ternary
OSC
processed
by
solvent
achieved
outstanding
efficiencies
20.22%
20.49%,
respectively.
Furthermore,
universality
NBN
also
confirmed
different
active
layer
systems.
In
conclusion,
this
work
demonstrates
introduction
electron‐absorbing
moieties
ring
a
promising
approach
design
BSAs,
which
can
tune
achieve
highly
efficient
devices,
certain
guiding
significance
for
development
BSAs.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 7, 2025
Abstract
Polymer
solar
cells
(PSCs)
rely
on
blends
of
small‐molecule
acceptors
(SMAs)
and
polymer
donors,
but
the
thermodynamic
relaxation
SMAs
requires
an
oligomeric
approach
to
enhance
operational
stability.
However,
high‐efficiency
devices
often
depend
expensive
synthesis
costly
posing
a
significant
barrier
achieving
sustainable
renewable
energy.
Here,
challenge
is
addressed
through
thermodynamically
derived
compatibility
giant
with
low‐cost
donor
PTQ10.
This
achieved
by
strategically
employing
conjugated
side
chains
modulate
dimerize
acceptors,
thereby
precisely
tuning
their
properties
optimize
compatibility.
Our
synthetic
route
avoids
toxic
reagents,
halogenated
solvents,
harsh
conditions.
The
dimer
(DYBT)
incorporating
n
‐type
linker
enhances
crystallinity,
absorption,
intramolecular
superexchange
coupling
compared
its
p
counterpart,
achieves
device
efficiency
19.53%.
Considering
efficiency,
stability,
material
cost,
potential
cost
per
kilowatt
for
PTQ10:DYBT
0.10
$
kW
−1
,
while
most
systems
exceed
10
.
These
findings
offer
valuable
insights
cost‐effective
well
pair
donors
reduce
overall
photo‐active
layer
durable
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
137(1)
Published: Aug. 24, 2024
Abstract
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‐
(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.