Chinese Journal of Chemistry,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 26, 2024
Comprehensive
Summary
The
power
conversion
efficiencies
(PCEs)
of
non‐fullerene
acceptor
(NFA)‐based
organic
solar
cells
(OSCs)
have
undergone
an
exciting
development
in
recent
years,
but
the
poor
intrinsic
stability
exocyclic
ethylene
bridges
NFAs
poses
a
significant
challenge
to
their
commercialization.
In
this
work,
we
propose
new
pyran‐locking
strategy
that
can
stabilize
bridge
connecting
strong
electron‐deficient
2‐(3‐oxo‐2,3‐dihydroinden‐1‐ylidene)malononitrile
end
group,
based
on
which
two
dimerized
(ITBIC‐F
and
TBTBIC‐F)
with
A‐D‐π‐A‐π‐D‐A
structure
been
successfully
synthesized
significantly
improved
chemical
photochemical
stabilities
comparison
traditional
without
ring‐locked
structure.
ITBIC‐F
TBTBIC‐F
‐based
OSCs
not
only
achieve
promising
PCEs
13.03%
10.01%,
respectively,
also
show
good
device
stability;
ITBIC‐F‐based
unencapsulated
devices
retain
75%
62%
initial
PCEs,
under
continuous
heat
(85
°C)
light
irradiation
(LED,
100
mW·cm
–2
)
nitrogen
atmosphere.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 28, 2025
Abstract
Simultaneously
mitigating
both
photovoltage
and
photocurrent
losses
is
crucial
for
organic
solar
cells
(OSCs)
to
approach
the
Shockley–Queisser
limit
of
ideal
efficiency.
Incorporating
a
narrower
bandgap
nonfullerene
acceptor
(NFA)
as
guest
component
into
host
donor:NFA
system
broadens
absorption
spectrum.
However,
this
can
also
increase
nonradiative
decay
rate
according
energy‐gap
law.
In
work,
ternary
OSCs
are
constructed
by
combining
narrow
AQx‐2F
(as
NFA)
with
lower
eC9
NFA),
significantly
enhancing
generation
without
compromising
photovoltage.
The
addition
acts
crystallization
inducer,
extending
period
increasing
ordered
packing
distance.
This
leads
suppressed
trap
states,
elevated
dielectric
constant,
prolonged
exciton
lifetime,
balanced
hole/electron
transport,
reduced
recombination
loss.
Consequently,
optimized
D18:AQx‐2F:eC9
achieve
champion
power
conversion
efficiency
(PCE)
20.6%
high
open‐circuit
voltage
0.937
V,
short‐circuit
current
density
27.2
mA
cm
−2
fill
factor
80.8%,
validated
an
independently
certified
PCE
20.0%,
establishing
new
benchmark
bulk
heterojunction
OSCs.
work
demonstrates
effective
method
simultaneously
mitigate
losses,
paving
way
high‐performance
Advanced Energy Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 3, 2025
Abstract
Volatile
solid
additives
(VSAs)
have
emerged
as
one
of
the
most
effective
strategies
for
optimizing
active
layer
morphology
organic
solar
cells
(OSCs).
In
this
study,
two
VSAs,
HBT‐1
and
HBT‐2,
are
designed
synthesized
to
investigate
effect
VASs’
conformation
on
photovoltaic
performances.
Compared
HBT‐1,
HBT‐2
incorporates
internal
noncovalent
conformational
locks
(NoCLs),
resulting
in
reduced
disorder,
improved
molecular
planarity,
enhanced
crystallinity.
These
features
significantly
influence
intermolecular
packing
both
donor
acceptor
materials
layer,
which
can
facilitate
charge
transport
reduce
recombination.
Consequently,
D18:L8‐BO:PY‐C11
OSCs
utilizing
additive
achieved
an
impressive
efficiency
20.01%,
markedly
higher
than
devices
fabricated
without
(17.83%)
those
processed
with
(18.76%).
Furthermore,
demonstrated
excellent
compatibility
across
multiple
systems.
This
work
underscores
NoCL
strategy
a
straightforward
approach
designing
VSAs
high
performance
OSCs.
The
rapid
development
of
organic
solar
cells
(OSCs)
has
been
particularly
remarkable
following
the
introduction
high-performance
small
molecule
electron
acceptor
Y6
and
its
derivatives.
Despite
advances
in
state-of-the-art
OSCs,
challenges
remain,
notably
relatively
low
open
circuit
voltage
(VOC)
charge
mobility
imbalance,
which
continue
to
hinder
further
improvements
OSCs'
performance.
To
address
these
issues,
this
work,
we
synthesized
a
main-chain
twisted
wide
bandgap
i-IEDTB,
not
only
possesses
superior
hole
over
but
also
higher
lowest
unoccupied
molecular
orbital
(LUMO)
energy
levels,
adopted
it
as
bifunctional
third
compound
couple
with
terpolymer
Z10
based
OSC
system.
integration
i-IEDTB
Z10:Y6
blend,
either
an
or
donor,
significantly
reduces
excessive
aggregation
facilitates
harmonized
distribution
mobilities
by
modulating
crystallization
properties
materials.
This
strategic
intervention
leads
marked
improvement
VOC
fill
factor
(FF).
Consequently,
power
conversion
efficiency
(PCE)
optimized
Z10:(Y6:i-IEDTB)
ternary
device
is
elevated
impressive
17.70%,
surpassing
16.50%
binary
OSC.
Besides,
after
doping
5%
weight
replaced
that
Z10,
device's
VOC,
FF
were
increased
0.846
V
78.08%
respectively,
resulting
enhanced
PCE
17.47%.
Further
investigation
demonstrates
universality
PM6:BTP-eC9-based
PM6:L8-BO-based
achieving
champion
efficiencies
18.14
18.08%,
respectively.
work
highlights
key
role
complementary
component
crystallographic
order
carrier
balance
within
Y-type
acceptor-based
OSCs.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 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.
Journal of Materials Chemistry C,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Optimization
of
small
molecule
donor
morphology
in
OSCs:
allyl
group-driven
enhancements
H35
for
superior
PCEs
15.21%
(ASM)
and
10.78%
(SMD:PA)
via
improved
miscibility,
domain
structure,
charge
transfer.
Advanced Energy Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 2, 2025
Abstract
In
recent
years,
polymer
solar
cells
(PSCs)
have
achieved
rapid
progress,
with
power
conversion
efficiencies
(PCEs)
reaching
up
to
20.25%,
driven
by
significant
advancements
in
device
fabrication
and
active‐layer
materials.
The
ternary
polymerization
strategy
has
proven
be
a
straightforward
effective
approach
for
developing
high‐performance
photoelectric
polymers
incorporating
third
monomer
into
the
backbone.
This
incorporation
effectively
optimizes
intrinsic
properties,
including
UV–vis
absorption,
energy
levels,
solubility,
crystallinity,
morphology,
charge
transfer,
mechanical
robustness,
batch‐to‐batch
reproducibility,
stability.
review
highlights
latest
designing
photoactive
copolymers
(both
donors
acceptors),
particular
focus
on
stability,
potential
applications
commercial
development.
aim
is
provide
valuable
guidance
development
of
materials
using
strategy.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 11, 2025
Abstract
Connecting
small
molecule
acceptors
through
conjugated
or
nonconjugated
linker
to
form
giant
molecular
(GMAs)
represents
a
strategic
approach
enhancing
the
morphological
stability
of
organic
solar
cells
(OSCs).
In
this
study,
we
employed
benzothiadiazole
(BT)
as
typical
n
‐type
design
and
synthesize
two
GMAs
linking‐site
isomerization:
i‐BT‐DY
o‐BT‐DY.
Compared
i‐BT‐DY,
o‐BT‐DY
exhibits
enhanced
crystallinity
more
favorable
face‐on
orientation
but
lower
electron
mobility.
This
can
be
well
explained
by
theoretical
calculations,
demonstrates
delocalized
LUMO
distribution
significantly
stronger
intramolecular
super‐exchange
coupling
(43.7
meV
versus
22.2
for
o‐BT‐DY).
Additionally,
also
red‐shifted
absorption.
Combining
these
attributes,
PM6:
blend
achieved
an
impressive
power
conversion
efficiency
(PCE)
18.86%.
The
PCE
further
increased
19.49%
in
ternary
blend.
As
expected,
OSCs
based
on
both
exhibit
exceptional
long‐term
photostability
(T85%
>1000
hours).
work
deepens
our
understanding
how
linkers
at
different
linking
sites
influence
performance
GMAs,
concluding
that
interaction,
rather
than
intermolecular,
are
primary
factor
affecting
charge
transport
acceptors.
it
highlights
potential
components
OSCs.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 15, 2025
Abstract
Developing
high‐performance
all‐polymer
solar
cells
(all‐PSCs)
remains
a
challenge
due
to
the
difficulty
in
controlling
morphology
of
polymer
blends.
In
this
study,
benzo[1,2‐d:4,5‐d′]bisthiazole
(BBTz)
is
incorporated
into
PM6
main
chain
create
series
terpolymer
donors,
leveraging
entropy
increase
and
superior
miscibility
with
acceptors
modulate
blend
morphology.
The
introduction
BBTz
broadened
absorption
range,
enhanced
film
crystallinity,
significantly
improved
donor‐acceptor
through
its
low
dipole
moment
high
electrostatic
potential.
This
facilitated
formation
nanofiber
structures
active
layer,
thus
optimizing
As
result,
PBZ‐10:PY‐IT‐based
device
achieved
an
impressive
power
conversion
efficiency
(PCE)
19.06%.
Incorporation
PBQx‐TF
binary
can
further
improve
morphology,
charge
transport,
exciton
lifetime,
dissociation,
collection,
as
well
suppressed
recombination,
finally
leading
record‐breaking
PCE
20.04%
for
all‐PSCs
date.
findings
demonstrate
effectiveness
strategy
enhancing
all‐PSC
performance.
By
molecular
design
component
selection,
approach
provides
viable
pathway
achieving
higher
supports
advancement
renewable
energy
technologies.