Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 30, 2024
Abstract
The
solid
additive
strategy
represents
a
simple
yet
effective
approach
to
achieving
high‐efficiency
organic
solar
cells
(OSCs)
by
enhancing
the
morphology
of
active
layer.
In
this
study,
highly
volatile
additive,
2,4,6‐trichloro‐1,3,5‐triazine
(TCT),
is
employed
modulate
morphology.
Unlike
other
additives
previously
reported,
TCT
exhibits
remarkable
intermolecular
interactions
with
both
polymer
donor
and
acceptor,
offering
two
distinct
advantages.
Firstly,
notably
enhances
crystallinity
molecular
order
blend
film,
subtly
optimizing
fiber
network
structure
within,
thereby
facilitating
carrier
transport
significantly
improving
mobility
film.
Secondly,
stabilizes
bi‐continuous
fibrous
mitigating
morphological
evolution
layer
device
stability.
Consequently,
D18:L8‐BO:TCT
higher
power
conversion
efficiency
19.50%
compared
D18:L8‐BO
(18.13%).
Furthermore,
after
960
h
storage,
OSC
treated
retains
90%
its
initial
PCE,
outperforming
(73%).
This
study
presents
promising
avenue
for
high‐performance
OSCs
through
manipulating
additives.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(34)
Published: June 5, 2024
The
structure
of
molecular
aggregates
is
crucial
for
charge
transport
and
photovoltaic
performance
in
organic
solar
cells
(OSCs).
Herein,
the
intermolecular
interactions
aggregated
structures
nonfused-ring
electron
acceptors
(NFREAs)
are
precisely
regulated
through
a
halogen
transposition
strategy,
resulting
noteworthy
transformation
from
2D-layered
to
3D-interconnected
packing
network.
Based
on
3D
pathway,
binary
ternary
devices
deliver
outstanding
power
conversion
efficiencies
(PCEs)
17.46
%
18.24
%,
respectively,
marking
highest
value
NFREA-based
OSCs.
Nature Communications,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Jan. 17, 2025
Developing
active-layer
systems
with
both
high
performance
and
mechanical
robustness
is
a
crucial
step
towards
achieving
future
commercialization
of
flexible
stretchable
organic
solar
cells
(OSCs).
Herein,
we
design
synthesize
series
acceptors
BTA-C6,
BTA-E3,
BTA-E6,
BTA-E9,
featuring
the
side
chains
hexyl,
3,
6,
9
carbon-chain
ethyl
ester
end
groups
respectively.
Benefiting
from
suitable
phase
separation
vertical
distribution,
PM6:BTA-E3-based
OSCs
processed
by
o-xylene
exhibit
lower
energy
loss
improved
charge
transport
characteristic
achieve
power
conversion
efficiency
19.92%
(certified
19.57%),
which
stands
as
highest
recorded
value
in
binary
green
solvents.
Moreover,
due
to
additional
hydrogen-bonding
provided
chain,
enhanced
stretchability
thermal
stability.
Our
work
reveals
significance
dynamic
improving
photovoltaic
performance,
robustness,
morphological
stability
OSCs.
Journal of Materials Chemistry A,
Journal Year:
2024,
Volume and Issue:
12(29), P. 17973 - 17991
Published: Jan. 1, 2024
This
review
comprehensively
summarizes
the
development
history
of
CPDT-based
organic
photovoltaic
materials,
which
contributes
to
a
deeper
understanding
revival
CPDT
driven
by
low-cost
acceptors.
Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 6, 2024
Abstract
High‐performance
perovskite
solar
cells
(PSCs)
fabricated
in
ambient
air
are
considered
inevitable
for
low‐cost
commercial
manufacturing.
However,
passivating
film
defects
and
controlling
the
crystallization
process
critical
achieving
high
performance
PSCs.
This
study
proposes
using
novel
2D
material
MBene
green
antisolvent
to
simultaneously
modulate
passivation
of
perovskites.
facilitates
uncoordinated
Pb
2+
ions,
thereby
enhancing
formation
energy
vacancies
within
adjusting
level
structure.
Moreover,
increases
nucleation
sites
perovskite,
significantly
extending
crystal
growth
improving
crystallinity,
reducing
non‐radiative
recombination.
Consequently,
champion
devices
treated
with
achieve
a
power
conversion
efficiency
(PCE)
24.22%
when
air,
exhibit
superior
humidity
long‐term
stability.
Furthermore,
PSCs
added
significant
stability
under
various
environmental
conditions,
including
heat.
The
results
lay
foundation
development
materials
photovoltaics,
revealing
their
mechanism
as
new
type
perovskites,
providing
insights
industrially
producing
efficient
stable
cells.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 3, 2024
Minimizing
energy
loss
is
crucial
for
breaking
through
the
efficiency
bottleneck
of
organic
solar
cells
(OSCs).
The
main
mechanism
can
be
attributed
to
non-radiative
recombination
(ΔEnr)
that
occurs
due
exciton-vibration
coupling.
To
tackle
this
challenge,
tuning
intramolecular
noncovalent
interactions
strategically
utilized
tailor
novel
fused
ring
electron
acceptors
(FREAs).
Upon
comprehensive
analysis
both
theoretical
and
experimental
results,
approach
effectively
enhance
molecular
rigidity,
suppress
structural
relaxation,
reduce
exciton
reorganization
energy,
weakens
coupling
strength.
Consequently,
binary
OSC
device
based
on
Y-SeSe,
which
features
dual
strong
Se
⋅
O
interactions,
achieves
an
outstanding
power
conversion
(PCE)
19.49
%,
accompanied
by
extremely
small
ΔEnr
0.184
eV,
much
lower
than
those
Y-SS
Y-SSe
devices
with
weaker
interactions.
These
achievements
not
only
set
record
selenium-containing
OSCs,
but
also
mark
lowest
reported
value
among
high-performance
devices.
Furthermore,
ternary
blend
showcases
a
remarkable
PCE
20.51
one
highest
PCEs
single-junction
OSCs.
This
work
demonstrates
effectiveness
in
suppressing
coupling,
thereby
achieving
low-energy-loss
high-efficiency
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 7, 2025
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.
The Journal of Physical Chemistry B,
Journal Year:
2025,
Volume and Issue:
129(11), P. 3109 - 3119
Published: March 6, 2025
The
development
of
nonfused
ring
electron
acceptors
(NFREAs)
has
garnered
significant
attention
due
to
their
simplified
molecular
design
and
cost-effectiveness.
Recent
advancements
have
pushed
the
power
conversion
efficiency
(PCE)
NFREAs
beyond
19%.
Despite
these
advantages,
most
adopt
A-D-A
structures,
where
electron-donating
core
is
typically
a
benzene
substituted
with
fluorine
or
alkoxy
groups.
This
restricts
tunability
energy
levels,
selection
substituents
for
rings
as
central
units
relatively
constrained,
which
hampers
further
optimization
material
properties.
In
this
work,
we
designed
three
A-D-A′-D-A
structured
fully
featuring
distinct
nitrogen
heterocyclic
cores:
linear-shaped
TT,
star-shaped
TYT,
quad-rotor-shaped
TTVP.
nitrogen-containing
aromatic
units,
strong
electron-withdrawing
groups,
enable
precise
tuning
levels.
Moreover,
cores
enhance
rigidity,
facilitating
efficient
π–π
stacking
improving
mobility.
Although
share
identical
π-bridges
terminal
unique
exert
divergent
effects
on
photovoltaic
performance.
Theoretical
calculations
reveal
that
TT
TTVP
exhibit
higher
affinity,
greater
absorption
intensity,
lower
exciton
binding
energy,
mobility
compared
high-performance
reference
NFREA,
TBT-26.
Notably,
TTVP,
an
four
exhibits
exceptional
electronic
It
achieves
highest
narrowest
bandgap
1.76
eV,
predicted
4.43
×
10–4
cm2
V–1
s–1,
surpassing
These
findings
underscore
potential
in
diversifying
NFREA
advancing
next-generation
NFREAs.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 23, 2025
Abstract
Thin
film
organic
photovoltaics
(OPVs)
aim
to
harness
solar
energy
environmentally
friendly,
highly
efficient,
and
cost‐effective
means,
thereby
offering
a
sustainable
solution
for
production
ecological
preservation.
Efforts
are
undertook
optimize
engineering
preparation
technology
OPV
devices
mini‐modules,
through
the
development
of
low‐ecological‐impact
solvent
processing
method.
A
newly
developed
strategy
employing
benign
o
‐xylene
(OXY)
with
synergistic
dual
additives
(DIM
DIB)
achieved
an
optimal
power
conversion
efficiency
(PCE)
20.0%
(
J
SC
26.6
mA
cm
−2
,
V
OC
0.935
V,
FF
80.3%)
alongside
exceptional
stability
metrics
(82%–1500h).
The
mini‐module
processed
optimized
TCE:OXY
(1:3
v/v)
demonstrated
scalable
performance
reaching
17.6%
(18.4
2
),
representing
highest
in
safe
based
OPVs.
Suitable
microscale
patterns
contributed
broader
range
receiving
angles,
enabling
more
flexible
installation
geometries
building‐integrated
applications.