Chinese Journal of Chemistry,
Journal Year:
2022,
Volume and Issue:
41(2), P. 159 - 166
Published: Oct. 4, 2022
Comprehensive
Summary
With
the
emergence
of
Y‐series
small
molecule
acceptors,
polymerizing
acceptors
with
aromatic
linker
units
has
attracted
significant
research
attention,
which
greatly
advanced
photovoltaic
performance
all‐polymer
solar
cells.
Despite
rapid
increase
in
efficiency,
unique
characteristics
(
e.
g
.,
mechanical
stretchability
and
flexibility)
systems
were
still
not
thoroughly
explored.
In
this
work,
we
demonstrate
an
effective
approach
to
simultaneously
improve
device
performance,
stability,
robustness
cells
by
properly
suppressing
aggregation
crystallization
behaviors
polymerized
acceptors.
Strikingly,
when
introducing
50
wt%
PYF‐IT
(a
fluorinated
version
PY‐IT)
into
well‐known
PM6:PY‐IT
system,
devices
delivered
impressive
efficiency
16.6%,
significantly
higher
than
that
control
binary
cell
(15.0%).
Compared
two
systems,
optimal
ternary
blend
exhibits
more
efficient
charge
separation
balanced
transport
accompanying
less
recombination.
Moreover,
a
high‐performance
1.0
cm
2
large‐area
15%
was
demonstrated
for
optimized
blend,
offered
desirable
PCE
14.5%
on
flexible
substrates
improved
flexibility
after
bending
1000
cycles.
Notably,
these
are
among
best
results
OPVs
thus
far.
This
work
also
heralds
bright
future
wearable
energy‐harvesting
applications.
Advanced Materials,
Journal Year:
2022,
Volume and Issue:
35(6)
Published: Nov. 22, 2022
The
morphology
plays
a
key
role
in
determining
the
charge
generation
and
collection
process,
thus
impacting
performances
of
organic
solar
cells
(OSCs).
limited
selection
pool
additives
to
optimize
OSCs,
especially
for
emerging
layer-by-layer
(LbL)
impeding
improvements
photovoltaic
performances.
Herein,
new
method
using
conjugated
polymers
as
improving
LbL-OSCs
is
reported.
Four
PH,
PS,
PF,
PCl
are
developed
with
different
side
chains.
These
exhibit
poor
donor
materials
BHJ
devices,
due
unsuitable
energy
level
alignment
unfavorable
molecular
interactions.
By
contrast,
they
can
be
served
efficient
PM6
fibril
matrix
facilitating
penetration
BTP-eC9
forming
an
intertwined
D/A
bicontinuous
network
vertical
segregation.
Such
optimized
by
chain
engineering,
which
enables
progressive
improvement
separation
collection.
As
result,
adding
small
amount
additive,
contributes
champion
PCE
19.10%
high
FF
80.5%.
Advanced Materials,
Journal Year:
2023,
Volume and Issue:
35(12)
Published: Jan. 18, 2023
Constructing
tandem
and
multi-blend
organic
solar
cells
(OSCs)
is
an
effective
way
to
overcome
the
absorption
limitations
of
conventional
single-junction
devices.
However,
these
methods
inevitably
require
tedious
multilayer
deposition
or
complicated
morphology-optimization
procedures.
Herein,
sequential
utilized
as
simple
method
fabricate
multicomponent
OSCs
with
a
double-bulk
heterojunction
(BHJ)
structure
active
layer
further
improve
photovoltaic
performance.
Two
efficient
donor-acceptor
pairs,
D18-Cl:BTP-eC9
PM6:L8-BO,
are
sequentially
deposited
form
D18-Cl:BTP-eC9/PM6:L8-BO
double-BHJ
layer.
In
OSCs,
light
significantly
improved,
optimal
morphology
also
retained
without
requiring
more
optimization
involved
in
quaternary
blends.
Compared
blend
devices,
energy
loss
(Eloss
)
reduced
by
rationally
matching
each
donor
appropriate
acceptor.
Consequently,
power
conversion
efficiency
(PCE)
improved
from
18.25%
for
18.69%
PM6:L8-BO
based
binary
19.61%
OSCs.
contrast,
D18-Cl:PM6:L8-BO:BTP-eC9
exhibited
dramatically
PCE
15.83%.
These
results
demonstrate
that
strategy,
relatively
processing
procedure,
can
potentially
enhance
device
performance
lead
widespread
use.
Advanced Materials,
Journal Year:
2022,
Volume and Issue:
35(9)
Published: Dec. 20, 2022
All-polymer
organic
photovoltaic
(OPV)
cells
possessing
high
performance
and
mechanical
robustness
are
promising
candidates
for
flexible
wearable
devices.
However,
developing
photoactive
materials
with
good
properties
so
far
remains
challenging.
In
this
work,
a
polymer
donor
PBDB-TF
weight-average
molecular
weight
(Mw
)
is
introduced
to
enable
highly
efficient
all-polymer
OPV
featuring
excellent
reliability.
By
incorporating
the
high-Mw
as
third
component
into
PBQx-TF:PY-IT
blend,
bulk
heterojunction
morphology
finely
tuned
more
compact
π-π
stacking
distance,
affording
pathways
charge
transport
well
stress
dissipation.
Hence,
based
on
ternary
blend
film
demonstrate
maximum
power
conversion
efficiency
(PCE)
of
18.2%
an
outstanding
fill
factor
0.796.
The
cell
delivers
decent
PCE
16.5%
stability.
These
results
present
strategy
address
boost
cells.
Advanced Functional Materials,
Journal Year:
2023,
Volume and Issue:
33(28)
Published: March 27, 2023
Abstract
Layer‐by‐layer
all‐polymer
solar
cells
(LbL
all‐PSCs)
are
prepared
with
PM6
and
PY‐IT
by
using
sequential
spin
coating
method.
The
exciton
dissociation
efficiency
in
acceptor
layer
near
electrode
is
rather
low
due
to
the
limited
diffuse
distance
impossible
energy
transfer
from
narrow
bandgap
wide
donor.
In
this
study,
less
incorporated
into
enhance
electrode.
A
power
conversion
(PCE)
of
17.45%
achieved
LbL
all‐PSCs
incorporating
10
wt%
layer,
which
much
larger
than
16.04%
PCE
PM6/PY‐IT‐based
all‐PSCs.
Over
8%
enhancement
can
be
realized
attributed
enhanced
utilization
layers
confirmed
quenched
photoluminescence
(PL)
emission
PY‐IT:PM6
films.
Meanwhile,
charge
transport
optimized
PM6,
as
molecular
arrangement.
This
study
indicates
that
strategy
donor
has
great
potential
fabricating
efficient
improving
Advanced Materials,
Journal Year:
2022,
Volume and Issue:
35(8)
Published: Dec. 3, 2022
Although
all-polymer
solar
cells
(all-PSCs)
show
great
commercialization
prospects,
their
power
conversion
efficiencies
(PCEs)
still
fall
behind
small
molecule
acceptor-based
counterparts.
In
blends,
the
optimized
morphology
and
high
molecular
ordering
are
difficult
to
achieve
since
there
is
troublesome
competition
between
crystallinity
of
polymer
donor
acceptor
during
film-formation
process.
Therefore,
it
challenging
improve
performance
all-PSCs.
Herein,
a
ternary
strategy
adopted
modulate
an
blend,
in
which
PM6:PY-82
selected
as
host
blend
PY-DT
employed
guest
component.
Benefiting
from
favorable
miscibility
two
acceptors
higher
regularity
PY-DT,
matrix
features
well-defined
fibrillar
improved
ordering.
Consequently,
champion
PM6:PY-82:PY-DT
device
produces
record-high
PCE
18.03%,
with
simultaneously
open-circuit
voltage,
short-circuit
current
fill
factor
comparison
binary
devices.
High-performance
large-area
(1
cm2
)
thick-film
(300
nm)
all-PSCs
also
successfully
fabricated
PCEs
16.35%
15.70%,
respectively.Moreover,
16.5
organic
module
affords
encouraging
13.84%
when
using
non-halogenated
solvent
,
showing
potential
"Lab-to-Fab"
transition
Advanced Materials,
Journal Year:
2022,
Volume and Issue:
35(7)
Published: Nov. 22, 2022
Abstract
Achieving
a
finely
tuned
active
layer
morphology
with
suitable
vertical
phase
to
facilitate
both
charge
generation
and
transport
has
long
been
the
main
goal
for
pursuing
highly
efficient
bulk
heterojunction
all‐polymer
solar
cells
(all‐PSCs).
Herein,
solution
address
above
challenge
via
synergistically
combining
ternary
blend
strategy
layer‐by‐layer
(LbL)
procedure
is
proposed.
By
introducing
synthesized
polymer
acceptor
(
P
A
),
PY‐Cl,
higher
crystallinity
into
designed
host
PY‐SSe‐V,
distribution
molecular
ordering
of
LbL‐type
all‐PSCs
can
be
improved
in
comparison
PM6/PY‐SSe‐V
binary
all‐PSCs.
The
formation
superior
microstructure
not
only
promote
extraction
properties
but
also
reduce
energetic
disorder
non‐radiative
recombination
loss,
thus
improving
all
three
photovoltaic
parameters
simultaneously.
Consequently,
PM6/(PY‐SSe‐V:PY‐Cl)
show
best
efficiency
18.14%,
which
among
highest
values
reported
date
This
work
provides
facile
effective
obtaining
high‐efficiency
Advanced Materials,
Journal Year:
2023,
Volume and Issue:
35(32)
Published: May 11, 2023
Abstract
Sequentially
deposited
organic
solar
cells
(SD‐OSCs)
have
attracted
great
attention
owing
to
their
ability
in
achieving
a
more
favorable,
vertically
phase‐separated
morphology
avoid
the
accumulation
of
counter
charges
at
absorber/transporting
layer
interfaces.
However,
processing
SD‐OSCs
is
still
quite
challenging
preventing
penetration
small‐molecule
acceptors
into
polymer
donor
via
erosion
or
swelling.
Herein,
solid
additives
(SAs)
with
varied
electrostatic
potential
distributions
and
steric
hinderance
are
introduced
investigate
effect
evaporation
dynamics
selective
interaction
on
vertical
component
distribution.
Multiple
modelings
indicate
that
π
–
dominates
interactions
between
aromatic
SAs
active
components.
Among
them,
p
‐dibromobenzene
shows
stronger
while
2‐chloronaphthalene
(2‐CN)
interacts
preferably
acceptor.
Combining
depth‐dependent
morphological
study
aided
by
multiple
X‐ray
scattering
methods,
it
concluded
can
drive
stronger‐interaction
upward
surface,
having
minor
impact
overall
molecular
packing.
Ultimately,
2‐CN‐treated
devices
reduced
acceptor
concentration
bottom
surface
deliver
high
power
conversion
efficiency
19.2%,
demonstrating
effectiveness
applying
improve
OSCs
using
proper
structure.
Advanced Materials,
Journal Year:
2023,
Volume and Issue:
36(3)
Published: Aug. 9, 2023
Abstract
Most
top‐rank
organic
solar
cells
(OSCs)
are
manufactured
by
the
halogenated
solvent
chloroform,
which
possesses
a
narrow
processing
window
due
to
its
low‐boiling
point.
Herein,
based
on
two
high‐boiling
solvents,
chlorobenzene
(CB)
and
non‐halogenated
green
ortho‐xylene
(OX),
preparing
active
layers
with
hot
solution
is
put
forward
enhance
performance
of
OSCs.
In
situ
test
morphological
characterization
clarify
that
hot‐casting
strategy
assists
in
fast
synchronous
molecular
assembly
both
donor
acceptor
layer,
contributing
preferable
donor/acceptor
ratio,
vertical
phase
separation,
stacking,
beneficial
charge
generation
extraction.
Based
PM6:BO‐4Cl,
OSCs
wide
achieve
efficiencies
18.03%
CB
18.12%
OX,
much
higher
than
devices
processed
room
temperature
solution.
Moreover,
PM6:BTP‐eC9
deliver
remarkable
fill
factor
80.31%
efficiency
18.52%
representing
record
value
among
binary
solvent.
This
work
demonstrates
facile
manipulate
distribution
arrangement
for
boosting
solvents.