Incorporation of Self‐Assembled Monolayer with Polyaniline Backbone as Hole‐Transporting Layer for Organic Solar Cells
Macromolecular Rapid Communications,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 3, 2025
Abstract
In
addition
to
the
heterojunction
layer,
interfacial
layers
also
determine
performance
of
organic
solar
cells
(OSCs)
owing
their
great
role
in
promoting
charge
extraction.
Herein,
study
explores
use
rarely
reported
polyaniline
(PANI)‐derived
polymers
as
self‐assembled
hole‐transporting
layer
(HTL)
OSCs.
It
is
observed
that
tailoring
either
spacer
groups
or
polymerization
sites
can
greatly
affect
material
aggregation
and
thus
OSC
performance.
Specifically,
polymer
with
phenyl
(36‐Ph‐PANI)
largely
outperforms
alkyl
linkers,
which
ascribed
enhanced
aspect
ratio
dipole
moment
former
molecule
contributes
substrate
coverage
hole
Moreover,
linking
PANI
carbazole
at
2,7‐sites
much
inferior
than
3,6‐positions,
attributing
higher
mobility
latter
induced
by
formation
radical
cation.
The
combined
merits
36‐Ph‐PANI,
including
high
transmittance,
appropriate
doping,
efficient
extraction,
enable
a
decent
efficiency
15.08%
This
work
provides
subtle
strategy
for
developing
self‐assemble
into
monolayers,
paving
way
more
stable
Language: Английский
Vacuum Processability of Self-Assembled Monolayers and Their Chemical Interaction with Perovskite Interfaces
Energies,
Journal Year:
2025,
Volume and Issue:
18(7), P. 1782 - 1782
Published: April 2, 2025
Self-assembled
monolayers
(SAMs)
have
gained
significant
attention
as
an
interfacial
engineering
strategy
for
perovskite
solar
cells
(PSCs)
due
to
their
efficient
charge
transport
ability
and
work
function
tunability.
While
solution-based
methods
such
dip-coating
spin-coating
are
widely
used
SAM
deposition,
challenges
non-uniform
coverage,
solvent
contamination,
limited
control
over
molecular
orientation
hinder
scalability
reproducibility.
In
contrast,
vacuum
deposition
techniques,
including
thermal
evaporation,
overcome
these
limitations
by
enabling
the
formation
of
highly
uniform
materials
with
precise
thickness
arrangement.
Importantly,
chemical
interactions
between
layers,
coordination
bonding
Pb2+
ions,
play
important
role
in
passivating
surface
defects,
modulating
energy
levels,
promoting
crystallization.
These
not
only
enhance
wettability
but
also
improve
overall
quality
stability
films.
This
review
highlights
advantages
vacuum-deposited
SAMs,
strong
layers
improving
properties
critical
scalable
applications.
Language: Английский
Optimized Self‐Assembled Monolayer Coverage using Molybdenum Trioxide‐Modified Indium Tin Oxide for High‐Performance Organic Solar Cells
Xiong Xiao-ying,
No information about this author
Bin Hu,
No information about this author
Shuya Tai
No information about this author
et al.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 4, 2025
Abstract
Self‐assembled
monolayers
(SAMs)
have
recently
emerged
as
promising
candidates
for
interfacial
materials
in
organic
photovoltaics
(OPVs).
However,
the
quality
and
integrity
of
SAM
growth
are
significantly
influenced
by
surface
morphology
indium
tin
oxide
(ITO)
substrates,
which
can
compromise
performance
reproducibility
OPVs.
To
achieve
controlled
high‐quality
SAMs
assembly,
this
study
presents
an
effective
strategy
to
eliminate
sensitivity
polycrystalline
ITO
depositing
amorphous
molybdenum
trioxide
(MoO
3
)
thin
layer
on
top.
The
application
MoO
homogenize
roughness
circumvent
issues
related
preferential
grain
orientation
distinct
boundaries
associated
with
ITO.
This
results
a
more
uniform
denser
coverage
compared
direct
bare
Consequently,
resulting
OPVs
based
PM6/BTP‐eC9
system
exhibit
outstanding
power
conversion
efficiency
19.9%
(certified
at
19.3%),
primarily
due
reduced
defects
optimized
active
morphology.
More
importantly,
introduction
between
enhances
long‐term
stability
devices
those
solely
SAMs.
progress
highlights
importance
refining
microstructure
facilitate
favorable
formation
subsequently
construct
high‐performance
Language: Английский
Decoding the Role of Molecular Orientation in Conjugated Self‐Assembled Monolayers for High‐Performance Binary Organic Photovoltaics Approaching 20% Efficiency
Yibo Kong,
No information about this author
Wanhai Wang,
No information about this author
Xiangwei Guo
No information about this author
et al.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 10, 2025
Abstract
Molecular
orientation
stands
as
the
quintessential
hallmark
of
conjugated
self‐assembled
monolayers
(SAMs),
which
have
recently
catalyzed
noteworthy
advancements
in
organic
photovoltaics
(OPVs).
Nevertheless,
an
unambiguous
understanding
these
directional
arrangements
and
their
impact
on
optoelectronic
properties
remains
elusive.
To
address
this
issue,
herein
three
SAMs
with
representative
orientations,
i.e.,
edge‐on
(BCZ‐1),
tilt‐on
(4PACz)
face‐on
(BCZ‐2)
are
meticulously
designed.
These
orientations
been
rigorously
validated
by
sum
frequency
generation
vibrational
spectroscopy
first‐principles
calculations.
Remarkably,
unequivocal
correlation
between
molecular
device
performance
is
discerned.
Particularly,
oriented
BCZ‐1
exhibits
largest
dipole
moment
normal
to
electrode,
accompanied
a
dense
uniform
coverage.
features
collectively
contribute
its
strongest
work
function
increment
for
ultra‐fast
hole
extraction
minimum
interfacial
carrier
recombination.
As
result,
champion
power
conversion
efficiency
19.93%
achieved
devices
based
D18:L8‐BO
active
layer,
representing
one
highest
values
reported
binary
bulk
heterojunction
OPVs.
Besides,
shows
great
potential
practical
applications
due
superior
up‐scalability
enhanced
shelf‐stability.
Overall,
offers
in‐depth
insights
into
behaviors
SAMs,
opening
new
avenues
unlock
Language: Английский