Advanced Energy Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 29, 2024
Abstract
Regulating
the
morphology
and
molecular
ordering
of
active
layer
is
crucial
for
developing
high‐performance
organic
solar
cells
(OSCs).
However,
enhancing
stacking
challenging
as
non‐fullerene
acceptors
(NFAs)
are
confined
within
polymer
network
owing
to
well
donor/acceptor
miscibility
fast
solvent
evaporation.
Herein,
2,5‐dibromothiazol
(DBrTz)
removable
solid
additive
chosen
optimize
film‐forming
kinetics
aggregation
PM6:L8‐BO
blends.
During
film
formation
process,
chloroform
evaporates
first,
trapping
DBrTz
in
(pseudo‐dry
state).
Thereafter,
will
gradually
volatilize,
persistently
prompting
L8‐BO
stack
aggregate
orderly
until
volatilization
completed.
The
behavior
designated
“enhanced
pseudo‐dry
film,”
an
occurrence
hitherto
unobserved
other
additives.
This
results
more
compact
π
–
long‐range
L8‐BO.
Furthermore,
facilitated
increased
face‐on
orientations
improved
vertical
component
distributions.
optimized
facilitates
charge
generation,
transport,
extraction.
Consequently,
DBrTz‐processed
OSCs
achieved
a
power
conversion
efficiency
(PCE)
19.4%.
work
elucidates
principles
additives
offers
valuable
insights
fostering
development
novel
improve
OSCs.
Advanced Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 12, 2025
Abstract
Volatile
solid
additives
(VSAs)
with
single
or
fused‐ring
structures
have
attracted
much
attention
for
enhancing
power
conversion
efficiencies
(PCEs)
of
organic
solar
cells
(OSCs).
While
the
working
mechanisms
high‐volatility
single‐ring
been
well
studied,
influence
low‐volatility
VSAs
on
molecular
aggregations
and
exciton/carrier
dynamics
remains
still
unclear.
Herein,
3,6‐dibromothieno[3,2‐b]thiophene
(3,6TTBr)
is
selected
as
a
representative
VSA
to
elucidate
its
mechanism.
Via
theoretical
experimental
joint
investigation,
it
found
that
rigid
planar
3,6TTBr
molecules
adsorb
onto
terminal
units
L8‐BO
(acceptor),
inducing
loose
space
adjacent
molecules.
The
thus
favors
center‐terminal
packing
larger
interfragment
distance,
which
relieves
over‐aggregation
induces
ordered
packing.
Consequently,
treatment
reduces
aggregation‐caused
quenching,
photoluminescence
quantum
yield
exciton
lifetime
film.
combination
above
properties
reduced
trap
density
improved
carrier
transport
in
3,6TTBr‐treated
devices
contributed
PCE
20.1%.
To
validate
broad
applicability
findings,
1,5‐dibromonaphthalene
(1,5‐BN),
another
solid,
explored.
1,5‐BN
achieved
an
impressive
20.5%,
verifying
validity
strategy
boosting
OSC
performances.
Angewandte Chemie International Edition,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 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.
Abstract
Morphology
control
plays
a
key
role
for
improving
efficiency
and
stability
of
bulk
heterojunctions
(BHJ)
organic
solar
cells
(OSCs).
Halogenation
methoxylation
are
two
separate
ways
successfully
adopted
in
additives
morphology
optimization.
In
this
work,
these
strategies
combined
together.
A
series
halogenated
methoxylated
thiophenes
is
designed
synthesized
as
volatile
to
the
evolution
BHJ
morphology.
Specifically,
addition
2,5‐diiodo‐3,4‐dimethoxythiophene
(MT‐I)
prominently
improves
performance
photostability
OSCs.
Computational
simulations
reveal
noncovalent
interactions
MT‐I
with
active
layer
materials
that
corresponds
inhibition
excessive
aggregation
behavior
PM6
Y6
during
film‐forming
process,
facilitating
favorable
phase
separation
enhanced
molecular
stacking.
Consequently,
PM6:Y6‐based
binary
OSCs
treatment
achieves
high
PCE
17.93%.
Furthermore,
demonstrates
broad
feasibility
across
diverse
high‐efficiency
OSCs,
leading
superior
photovoltaic
(PCE
over
18%).
This
study
offers
valuable
guidance
design
application
high‐performance
future
endeavors.
Angewandte Chemie,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 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.
Abstract
Achieving
high‐performance
organic
solar
cells
(OSCs)
relies
heavily
on
precise
morphology
optimization,
a
challenging
task
due
to
the
intrinsic
differences
in
crystallization
kinetics
and
interfacial
compatibility
between
polymer
donors
small‐molecule
acceptors.
In
this
work,
2,7‐dibromonaphthalene
(DBN)
is
introduced
as
an
innovative
solid
additive
that
uniquely
regulates
both
donor
acceptor
phases
within
PM6:Y6
system.
Unlike
conventional
liquid
additives,
which
often
induce
excessive
Y6
crystallization,
DBN
achieves
balanced
enhancing
molecular
order
PM6
while
mitigating
over‐aggregation
Y6.
This
dual‐phase
effect
improves
light
absorption,
exciton
generation
dissociation,
charge
transport,
reduces
recombination
losses.
As
result,
OSCs
treated
with
achieved
remarkable
power
conversion
efficiency
(PCE)
of
18.5%,
open‐circuit
voltage
(
V
OC
)
0.848
V,
high
short‐circuit
current
density
J
SC
28.15
mA
cm
−2
,
enhanced
fill
factor
(FF)
77.7%.
Adding
anti‐reflection
MgF
2
layer
further
boosts
19.0%,
setting
new
benchmark
for
binary
devices.
study
establishes
promising
regulator
presents
robust
strategy
control,
advancing
development
photovoltaic
applications.
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 24, 2025
Abstract
In
the
field
of
organic
solar
cells
(OSCs),
bulk
heterojunction
(BHJ)
structure
is
most
widely
used.
On
contrary,
layer‐by‐layer
(LBL)
gives
a
p‐i‐n
separation
where
donor
close
to
transparent
electrode
while
acceptor
reflective
electrode,
which
shows
be
an
ideal
for
OSCs.
this
work,
volatile
solid
additives
2,5‐dibromoprazine
(DBP)
and
2‐bromine‐5‐iodopyrazine
(BIP)
are
introduced
regulate
morphology
LBL
active
layers.
Comprehensive
analysis
reveals
that
DBP
BIP
can
promote
stronger
molecular
packing
crystallinity
BTP‐eC9,
resulting
in
higher
charge
mobility,
more
efficient
separation,
suppressed
bimolecular
recombination
significantly
improve
device
filling
factor
(FF),
especially
devices.
Consequently,
by
combining
engineering
additive
BIP,
outstanding
power
conversion
efficiency
(PCE)
19.63%
based
on
PM1/BTP‐eC9
achieved
further
applied
PM1/BTP‐eC9:eC9‐2Cl
ternary
system,
PCE
exceeded
20%.
The
results
provide
comprehensive
insights
into
synergistic
effect
high‐performance
photovoltaics.
Advanced Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 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.