Polymers,
Journal Year:
2025,
Volume and Issue:
17(3), P. 284 - 284
Published: Jan. 22, 2025
Planar
heterojunction
(PHJ)
is
employed
to
obtain
proper
vertical
phase
separation
for
highly
efficient
polymer
solar
cells
(PSCs).
However,
it
heavily
relies
on
the
choice
of
orthogonal
solvent
in
production
process.
Here,
we
fabricated
a
pseudo-bilayer
bulk
(PBHJ)
PSC
with
cross-distribution
direction
by
preparing
two
layers
PM6
and
BTP-eC9
blends
an
o-XY
solution
different
dilution
ratios
study
morphological
evolution
PBHJ
film.
We
found
that
film
exhibits
more
uniform
suitable
continuous
interpenetrating
network
morphology
formation
p-i-n
structure.
This
provides
effective
channel
exciton
dissociation
charge
transport,
which
confirmed
both
generation
simulations
dynamics
measurements.
The
devices
can
effectively
inhibit
trap
recombination
accelerate
transfer.
Based
good
active
layer
balanced
mobility,
all-green
solvent-processed
PSCs
champion
power
conversion
efficiencies
(PCEs)
18.48%
16.83%
are
obtained
PM6:BTP-eC9
PTQ10:BTP-eC9
systems,
respectively.
work
reveals
potential
mechanism
induced
structure
alternative
approach
developing
processing
PSCs.
Chemical Society Reviews,
Journal Year:
2024,
Volume and Issue:
53(9), P. 4674 - 4706
Published: Jan. 1, 2024
This
review
summarizes
the
recent
progress,
key
design
principles
and
prospects
of
dimer
multimer
acceptors
for
developing
polymer
solar
cells
(PSCs)
with
high
efficiency
long-term
stability.
Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
14(18)
Published: Feb. 9, 2024
Abstract
The
progress
of
stretchable
and
wearable
photovoltaics
relies
heavily
on
intrinsically
active
layer
films.
Nevertheless,
there
is
a
paucity
research
clarifying
the
connections
between
their
microstructure,
performance,
adaptation
to
large
strain
in
polymer
electronic
current
study
utilizes
multiple
synchrotron
X‐ray
scattering
methods
collectively
examine
correlations
morphology
stretchability,
as
well
microstructural
evolution
induced
by
stretching
three
sample
cases
highly
ternary
blend
These
blends
contain
over
30%
weight
elastomer,
such
styrene‐ethylene‐butylene‐styrene
block
copolymer,
integrated
into
high‐performance
polymer:nonfullerene
small
molecule
mixture.
Specifically,
real‐time
changes
these
durable
organic
photovoltaic
films
with
elastomers
are
monitored
when
subjected
tensile
through
situ
scattering.
experiments
demonstrate
that
polymeric
can
effectively
lower
degree
crystallinity
deform
crystallites
semiconductor
molecules.
elastomeric
component
aids
stress
dispersion
during
stretching,
thereby
improving
durability
This
provides
new
recommendations
for
advancing
optoelectronic
devices.
Cyborg and Bionic Systems,
Journal Year:
2024,
Volume and Issue:
5
Published: Jan. 1, 2024
With
the
prevalence
of
cardiovascular
disease,
it
is
imperative
that
medical
monitoring
and
treatment
become
more
instantaneous
comfortable
for
patients.
Recently,
wearable
implantable
optoelectronic
devices
can
be
seamlessly
integrated
into
human
body
to
enable
physiological
in
an
imperceptible
spatiotemporally
unconstrained
manner,
opening
countless
possibilities
intelligent
healthcare
paradigm.
To
achieve
biointegrated
cardiac
healthcare,
researchers
have
focused
on
novel
strategies
construction
flexible/stretchable
systems.
Here,
we
overview
progress
flexible
stretchable
optoelectronics
devices.
Firstly,
device
design
addressed,
including
mechanical
design,
interface
adhesion,
encapsulation
strategies.
Next,
practical
applications
monitoring,
optogenetics,
nongenetic
stimulation
are
presented.
Finally,
outlook
systems
discussed.
Science,
Journal Year:
2025,
Volume and Issue:
387(6732), P. 381 - 387
Published: Jan. 23, 2025
Emerging
wearable
devices
would
benefit
from
integrating
ductile
photovoltaic
light-harvesting
power
sources.
In
this
work,
we
report
a
small-molecule
acceptor
(SMA),
also
known
as
non–fullerene
(NFA),
designed
for
stretchable
organic
solar
cell
(
s
-OSC)
blends
with
large
mechanical
compliance
and
performance.
Blends
of
the
organosilane-functionalized
SMA
BTP-Si4
polymer
donor
PNTB6-Cl
achieved
conversion
efficiency
(PCE)
>16%
ultimate
strain
(ε
u
)
>95%.
Typical
SMAs
suppress
OSC
blend
ductility,
but
addition
enhances
it.
Although
is
less
crystalline
than
other
SMAs,
it
retains
considerable
electron
mobility
highly
miscible
essential
enhancing
ε
.
Thus,
-OSCs
PCE
>
14%
operating
normally
under
various
deformations
(>80%
retention
an
80%
strain)
were
demonstrated.
Analysis
several
SMA-polymer
revealed
general
molecular
structure–miscibility–stretchability
relationships
designing
blends.
Nature Communications,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Feb. 4, 2025
The
seamless
integration
of
rigid/flexible
electronic
components
into
stretchable
substrates
is
imperative
for
the
realization
reliable
electronics.
However,
transition
from
flexible-to-stretchable
presents
inherent
challenges
in
interfacial
behavior,
predominantly
arising
disparities
elastic
moduli,
thereby
rendering
their
arduous
practical
deployment.
Here,
we
introduce
a
bioinspired
interface-engineered
flexible
island
(BIEFI),
which
effectively
facilitates
creation
highly
electronics
by
optimizing
interface
with
mechanical
interlocking
mechanisms,
resilient
to
physical
deformations.
Various
components,
such
as
light-emitting
diodes
(LEDs)
and
solar
cells,
are
affixed
onto
island,
showcasing
its
versatility
robust
platform
rigid
while
ensuring
entire
substrate
maintains
high
stretchability.
Additionally,
smart
workout
monitoring
system
demonstrated
integrating
resistance
band
platform.
This
approach
seamlessly
integrates
wide
range
rigid,
flexible,
durability
under
diverse
limited
behavior.
authors
present
an
design
deformations
Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
14(26)
Published: May 13, 2024
Abstract
High
power
conversion
efficiency
(PCE)
and
mechanical
robustness
are
prerequisites
for
wearable
applications
of
organic
solar
cells
(OSCs).
However,
stretchability
present
active
systems
(i.e.,
crack‐onset
strain
(COS)
<
30%)
should
be
improved.
While
introducing
elastomers
into
is
considered
a
simple
method
improving
stretchability,
the
inclusion
typically
results
in
decrease
PCE
OSC
with
limited
enhancement
due
to
lack
interconnected
electrical
pathways.
In
this
study,
it
developed
efficient
intrinsically
stretchable
(IS)‐OSCs
exceptional
robustness,
by
constructing
co‐continuous
networks
conjugated
polymers
(D18)
(SEBS)
within
layers.
It
demonstrated
that
blend
film
specific
ratio
(40:60
w/w)
D18:SEBS
crucial
forming
structures,
establishing
well‐connected
channels.
Consequently,
D18
0.4
:SEBS
0.6
/L8‐BO
OSCs
achieve
16‐times
higher
(COS
=
126%)
than
based
on
D18/L8‐BO
8%),
while
achieving
4‐times
(12.13%)
compared
SEBS‐rich
layers
(D18
0.2
0.8
/L8‐BO,
3.15%).
Furthermore,
‐based
IS‐OSCs
preserve
86
90%
original
PCEs
at
50%
after
200
stretching/releasing
cycles
15%
strain,
respectively,
demonstrating
highest
among
reported
IS‐OSCs.
Chemical Society Reviews,
Journal Year:
2024,
Volume and Issue:
53(14), P. 7426 - 7454
Published: Jan. 1, 2024
Over
the
past
decades,
field
of
organic
solar
cells
(OSCs)
has
witnessed
a
significant
evolution
in
materials
chemistry,
which
resulted
remarkable
enhancement
device
performance,
achieving
efficiencies
over
19%.
The
photoactive
layer
OSCs
play
crucial
role
light
absorption,
charge
generation,
transport
and
stability.
To
facilitate
scale-up
OSCs,
it
is
imperative
to
address
photostability
these
electron
acceptor
donor
materials,
as
their
photochemical
degradation
process
remains
challenge
during
photo-to-electric
conversion.
In
this
review,
we
present
an
overview
development
emphasizing
aspects
chemical
stability
behavior
that
are
linked
OSCs.
Throughout
each
section,
highlight
pathways
for
link
degradation.
We
also
discuss
existing
interdisciplinary
challenges
obstacles
impede
photostable
materials.
Finally,
offer
insights
into
strategies
aimed
at
enhancing
future
directions
developing
photo-active
layers,
facilitating
commercialization
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(46)
Published: June 26, 2024
Abstract
Mechanical
stretchability
is
a
vital
criterion
for
the
wearable
application
of
organic
solar
cells
(OSCs),
while
excessive
rigidity
fused‐ring
small
molecular
acceptors
make
photovoltaic
film
hard
to
meet
stretchable
requirements.
Herein,
an
effective
strategy
developed
construct
intrinsically
active
layer
by
inserting
copolymer
PM6
‐b‐
PYSe
as
interlayer
between
layer‐by‐layer
processed
D18
and
BTP‐eC9.
The
shunts
penetration
BTP‐eC9
facilitates
appropriate
phase
separation,
favoring
enhanced
crack
onset
strain
17.69%
compared
D18/BTP‐eC9
(9.67%).
Combining
with
optimal
energy
levels,
prolonged
carrier
lifetime,
suppressed
bimolecular
recombination
aroused
incorporation
PM6‐
b
‐PYSe,
D18/PM6‐
‐PYSe/BTP‐eC9‐based
OSC
yields
encouraging
efficiency
17.97%.
In
particular,
device
demonstrates
excellent
mechanical
property,
which
can
retain
over
80%
after
4000
bending
cycles.
This
work
provides
simultaneously
enhance
intrinsic
performance
flexible
OSCs.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 27, 2024
Abstract
High
power
conversion
efficiency
(PCE)
and
long‐term
stability
are
prerequisites
for
commercialization
of
organic
solar
cells
(OSCs).
Herein,
two
dimer
acceptors
(DYTVT
DYTCVT)
developed
with
different
properties
through
linker
engineering,
study
their
effects
as
alloy‐like
on
the
photovoltaic
performance
photostability
OSCs.
These
ternary
OSCs
effectively
combine
advantages
both
acceptors.
DYTVT,
characterized
by
its
high
backbone
planarity,
ensures
elevated
electron
mobility
glass‐transition
temperature
(
T
g
),
leading
to
efficient
charge
transport
enhanced
Conversely,
DYTCVT,
significant
dipole
moment
electrostatic
potential,
enhances
compatibility
alloy
donors
refines
blend
morphology,
facilitating
generation
in
Consequently,
D18:DYTVT:DYTCVT
exhibit
higher
PCE
(18.4%)
compared
D18:MYT
(monomer
acceptor,
=
16.5%),
D18:DYTVT
(PCE
17.4%),
D18:DYTCVT
17.0%)
Furthermore,
owing
(133
°C)
than
MYT
80
DYTCVT
120
°C),
have
significantly
t
80%
lifetime
4250
h
under
1‐sun
illumination)
40
h)
2910
h).