Advanced Functional Materials,
Год журнала:
2022,
Номер
32(34)
Опубликована: Июнь 15, 2022
Abstract
Three
terpolymer
donors
(PL1,
PL2,
and
PL3)
employing
repeating
units
of
two
popular
photovoltaic
polymers
PM6
D18
are
synthesized
by
random
copolymerization.
The
terpolymers
can
reduce
the
regio‐regularity
polymer
backbones
endow
them
with
much‐enhanced
solubility
in
nonhalogenated
solvents
such
as
o
‐xylene.
Furthermore,
along
appearance
temperature‐dependent
aggregation
behavior,
indicating
adaptability
for
fabricating
organic
solar
cells
(OSCs)
eco‐friendly
solvent
processing.
Among
them,
PL1‐based
OSCs
display
higher
more
balanced
hole
electron
mobilities,
longer
charge
separation
exciton
lifetime,
better
dissociation
collection
capabilities
than
parent
(PM6
D18)
based
ones.
A
power
conversion
efficiency
18.14%
a
very
low
energy
loss
is
achieved
on
PL1,
which
much
that
(15.16%)
(16.18%).
result
provides
an
effective
way
to
realize
high‐performance
processing
donor
materials.
Angewandte Chemie International Edition,
Год журнала:
2023,
Номер
62(10)
Опубликована: Янв. 2, 2023
Side-chain
tailoring
is
a
promising
method
to
optimize
the
performance
of
organic
solar
cells
(OSCs).
However,
asymmetric
alkyl
chain-based
small
molecular
acceptors
(SMAs)
are
still
difficult
afford.
Herein,
we
adopted
novel
n-nonyl/undecyl
substitution
strategy
and
synthesized
two
A-D1
A'D2
-A
double
isomeric
SMAs
with
selenophene-based
central
core
for
OSCs.
Crystallographic
analysis
indicates
that
AYT9Se11-Cl
forms
more
compact
order
intermolecular
packing
compared
AYT11Se9-Cl,
which
contributed
higher
electron
mobility
in
neat
film.
Moreover,
PM6
:
blend
film
shows
better
morphology
appropriate
phase
separation
distinct
face-on
orientation
than
AYT11Se9-Cl.
The
OSCs
obtain
superior
PCE
18.12
%
AYT11Se9-Cl
(17.52
%),
best
efficiency
selenium-incorporated
binary
BHJ
Our
findings
elucidate
chains
precisely
modulates
crystal
enhances
photovoltaic
selenophene-incorporated
SMAs.
Ternary
strategy
has
attracted
extensive
attention
for
bulk
heterojunction
organic
solar
cells
(BHJ
OSCs)
owing
to
their
potentially
improved
light
harvesting,
cascaded
energy
levels,
and
optimized
film
morphology
of
binary
BHJs.
Herein,
three
novel
star‐shaped
unfused
ring
electron
acceptors
(SSUFREAs),
i.e.,
H
1–3,
with
without
fluorine‐substituent
in
phenyl
core
or
peripheral
group
are
designed
synthesized
as
third
components
via
direct
C–H
arylation
incorporate
into
PM6:Y6
BHJ
films.
The
structure–property–performance
dependence
study
reveals
that
the
isotropic
charge
transfer,
complementary
star‐shape
structure
absorption,
energy‐level
cascades
1–3
PM6
Y6
allow
ternary
BHJs
have
higher
power
conversion
efficiency
(PCE)
compared
BHJ.
Among
them,
involving
fluorine‐free
1,
1:PM6:Y6,
possesses
highest
PCE
(16.57%)
high‐lying
frontier
molecular
orbital
enlarged
torsion
angle,
which
enhances
open‐circuit
voltage,
inhibits
excessive
crystallization
Y6,
facilitates
exciton
dissociation
well
collection.
findings
indicate
SSUFREAs
great
potential
serve
optimize
improve
voltage
OSCs.
Energy & Environmental Science,
Год журнала:
2023,
Номер
16(7), С. 2732 - 2758
Опубликована: Янв. 1, 2023
This
review
summarizes
the
side-chain
engineering
of
nonfullerene
small-molecule
acceptors
(SMAs)
in
field
organic
solar
cells,
discusses
key
structure–property
relationships
depth
and
future
directions
engineering.
Advanced Functional Materials,
Год журнала:
2022,
Номер
32(34)
Опубликована: Июнь 15, 2022
Abstract
Three
terpolymer
donors
(PL1,
PL2,
and
PL3)
employing
repeating
units
of
two
popular
photovoltaic
polymers
PM6
D18
are
synthesized
by
random
copolymerization.
The
terpolymers
can
reduce
the
regio‐regularity
polymer
backbones
endow
them
with
much‐enhanced
solubility
in
nonhalogenated
solvents
such
as
o
‐xylene.
Furthermore,
along
appearance
temperature‐dependent
aggregation
behavior,
indicating
adaptability
for
fabricating
organic
solar
cells
(OSCs)
eco‐friendly
solvent
processing.
Among
them,
PL1‐based
OSCs
display
higher
more
balanced
hole
electron
mobilities,
longer
charge
separation
exciton
lifetime,
better
dissociation
collection
capabilities
than
parent
(PM6
D18)
based
ones.
A
power
conversion
efficiency
18.14%
a
very
low
energy
loss
is
achieved
on
PL1,
which
much
that
(15.16%)
(16.18%).
result
provides
an
effective
way
to
realize
high‐performance
processing
donor
materials.