The
suboptimal
interfacial
quality
between
the
perovskite
absorption
layer
and
electron‐transport
constrains
performance
of
solar
cells.
Introducing
an
interface
passivation
is
generally
recognized
as
effective
method
for
addressing
this
issue.
A
uniform
film
with
a
large
area
can
be
prepared
using
evaporation
technique.
In
study,
we
designed
fabricated
inorganic
CsPbCl
3
by
coevaporation
PbCl
2
CsCl.
evaporated
passivator
exhibited
excellent
effects
relatively
low
thickness
sensitivity
to
device
performance.
As
result,
open‐circuit
voltage
cells
1.68
eV
absorber
was
improved
nearly
100
mV,
efficiency
achieved
21.84%,
ranking
highest
based
on
hybrid
evaporation‐solution
method.
proposed
approach
has
potential
applications
in
large‐area
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Сен. 1, 2024
Self-assembled
monolayers
(SAMs)
have
become
pivotal
in
achieving
high-performance
perovskite
solar
cells
(PSCs)
and
organic
(OSCs)
by
significantly
minimizing
interfacial
energy
losses.
In
this
study,
we
propose
a
co-adsorb
(CA)
strategy
employing
novel
small
molecule,
2-chloro-5-(trifluoromethyl)isonicotinic
acid
(PyCA-3F),
introducing
at
the
buried
interface
between
2PACz
perovskite/organic
layers.
This
approach
effectively
diminishes
2PACz's
aggregation,
enhancing
surface
smoothness
increasing
work
function
for
modified
SAM
layer,
thereby
providing
flattened
with
favorable
heterointerface
perovskite.
The
resultant
improvements
crystallinity,
minimized
trap
states,
augmented
hole
extraction
transfer
capabilities
propelled
power
conversion
efficiencies
(PCEs)
beyond
25%
PSCs
p-i-n
structure
(certified
24.68%).
OSCs
CA
achieve
remarkable
PCEs
of
19.51%
based
on
PM1:PTQ10:m-BTP-PhC6
photoactive
system.
Notably,
universal
also
been
achieved
other
two
popular
OSC
systems.
After
1000-hour
maximal
point
tracking,
encapsulated
retain
approximately
90%
80%
their
initial
PCEs,
respectively.
introduces
facile,
rational,
effective
method
to
enhance
performance
SAMs,
realizing
efficiency
breakthroughs
both
device
structure,
along
improved
operational
stability.
are
essential
high
Here,
authors
develop
molecule
provide
heterointerface,
devices.
Energy & Environmental Science,
Год журнала:
2024,
Номер
17(17), С. 6157 - 6203
Опубликована: Янв. 1, 2024
HSSAMs
with
diverse
structures,
encompassing
various
anchoring
and
functional
groups,
were
systematically
categorized
their
multifaceted
roles
in
inverted
PSCs
TSCs
correlation
device
performance
investigated.
Nature Communications,
Год журнала:
2025,
Номер
16(1)
Опубликована: Фев. 1, 2025
Carrier
transport
and
recombination
at
the
buried
interface
of
perovskite
have
seriously
restricted
further
development
inverted
solar
cells
(PSCs).
Herein,
an
interfacial
dipolar
chemical
bridge
strategy
to
address
this
issue
is
presented.
2-(Diphenylphosphino)
acetic
acid
(2DPAA)
selected
as
linker
reconstruct
dipole,
which
effectively
enlarges
dipole
moment
5.10
D
optimizes
a
positive
orientation,
thereby
accelerating
vertical
hole
transport,
suppressing
nonradiative
promoting
crystallization.
The
champion
device
yields
high
power
conversion
efficiency
(PCE)
26.53%
(certified
26.02%).
Moreover,
extended
wide-bandgap
large-area
devices,
delivers
PCEs
22.02%
24.11%,
respectively.
optimized
devices
without
encapsulation
also
demonstrate
great
long-term
shelf
operational
stability.
Our
work
highlights
importance
orientation
realize
efficient
stable
PSCs.
hindered
cells.
Here,
authors
employ
achieving
maximum
24.11%
for
small-
Advanced Energy Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 5, 2025
Abstract
The
interfaces
of
each
layer
in
perovskite
solar
cells
(PSCs)
have
a
significant
impact
on
the
charge
transfer
and
recombination.
Especially,
interface
between
hole
transport
(HTL)
p‐i‐n
type
PSCs
significantly
affects
contact
characteristics
HTL
perovskite,
hindering
further
improvements
performance
stability.
Herein,
small
molecule
9‐Fluorenylmethoxycarbonyl
chloride
(9‐YT)
is
introduced
as
bridge
for
PSCs,
which
enhances
interaction
self‐assembly
molecules
(SAMs)
perovskite.
conjugated
backbone
9‐YT
can
interact
with
SAM
(MeO‐2PACz)
by
π–π
stacking
reaction.
Moreover,
also
improves
interfacial
through
strong
interactions
where
carbonyl
groups
Cl
atoms
uncoordinated
Pb
2+
layer.
incorporation
demonstrated
to
markedly
enhance
extraction
at
perovskite/hole
interface,
optimize
energy
level
alignment,
mitigate
recombination,
passivate
defects
Finally,
device
treated
achieves
power
conversion
efficiency
(PCE)
24.82%.
At
same
time,
still
maintain
92.6%
original
PCE
after
long‐term
stability
test
1200
h.
Journal of the American Chemical Society,
Год журнала:
2025,
Номер
147(9), С. 8004 - 8011
Опубликована: Фев. 18, 2025
Self-assembled
monolayer
molecules
have
been
widely
employed
as
interfacial
transport
materials
in
inverted
perovskite
solar
cells
(PSCs),
demonstrating
high
efficiency
and
improved
device
stability.
However,
self-assembling
(SAM)
often
suffer
from
aggregation
weak
interactions
with
the
layer,
resulting
inefficient
charge
transfer
significant
energy
losses,
ultimately
limiting
power
conversion
long-term
stability
of
cells.
In
this
work,
we
developed
a
series
novel
skeleton-matching
carbazole
isomer
SAMs
based
on
following
key
design
principles:
(1)
introducing
benzene
ring
structure
to
distort
molecular
skeleton
SAM,
thereby
preventing
achieving
uniform
distribution
fluorine-doped
tin
oxide
(FTO)
substrates;
(2)
strategically
incorporating
methoxy
groups
onto
at
different
positions
(ortho,
meta,
para).
These
functional
not
only
increase
anchoring
points
layer
but
also
fine-tune
dipole
moment.
Among
SAMs,
m-PhPACz
exhibits
most
favorable
properties,
maximum
moment
2.4
D
an
O-O
distance
that
aligns
excellently
diagonal
lead
ions
adjacent
lattice,
enhancing
SAM-perovskite
interactions,
facilitating
efficient
extraction,
improving
As
result,
new
SAM-based
PSCs
achieved
impressive
26.2%,
12.9%
improvement.
Moreover,
devices
demonstrated
outstanding
photothermal
stability,
retaining
96%
their
initial
PCE
after
1000
h
85
°C
maintaining
90%
300
UV-light
exposure.
Energy & Environmental Science,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 30, 2024
Through
a
bimolecular
energy-level-tunable
design,
an
ET-HTL
reaches
optimal
energy
level
alignment
with
three
different
perovskite
compositions,
providing
balanced
interface
defect
passivation,
charge
extraction,
and
transition
loss
suppression.
ACS Energy Letters,
Год журнала:
2024,
Номер
9(9), С. 4209 - 4217
Опубликована: Авг. 1, 2024
Improving
the
uniformity
and
density
of
self-assembled
monolayers
(SAMs)
is
crucial
to
elevate
photovoltaic
performance
organic
solar
cells
(OSCs).
Herein,
we
introduced
small
molecules
1-hydroxybenzotriazole
(HOBT)
modulate
distribution
electrical
properties
(4-(7H-dibenzo[c,g]carbazol-7-yl)butyl)phosphonic
acid
(4PADCB)
on
indium
tin
oxide
(ITO)
transparent
electrodes
in
an
innovative
manner.
The
hydroxyl
group
HOBT
interacts
with
phosphate
SAMs,
while
steric
repulsion
exerted
by
backbone
efficiently
regulates
SAMs.
This
led
a
more
uniform
dense
SAMs
ITO.
Furthermore,
HOBT-modified
have
improved
crystallization
vertical
phase
separation
upper
active
layer.
Consequently,
PM6:BTP-eC9
binary
OSCs
based
exhibit
impressive
PCE
19.66%.
Our
work
presents
effective
strategy
for
regulating
SAM
morphology
offers
promising
approach
advancing
OSCs.
Energy & Environmental Science,
Год журнала:
2024,
Номер
17(19), С. 6974 - 7016
Опубликована: Янв. 1, 2024
This
review
overviews
the
challenges
at
buried
interface
of
PSCs,
defect
passivation
capabilities
SAMs,
and
its
effectiveness
compared
to
other
passivating
agents.
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 16, 2025
Abstract
Self‐assembled
monolayers
(SAMs),
particularly
those
molecules
composed
of
carbazole
and
phosphonic
acid,
are
widely
employed
as
effective
hole‐selective
layer
(HSL)
in
inverted
perovskite
solar
cells
(PSCs).
However,
the
insufficient
chemical
bond
formation
with
metal
oxides
(ITO)
self‐aggregation
solvents
acid
SAM
led
to
non‐uniform
HSL,
which
turn
affect
power
conversion
efficiency
(PCE)
stability
PSCs.
Herein,
a
series
benzoic
materials
(BAs),
including
p‐fluorobenzoic
(FBA)
p‐methylbenzoic
(MBA),
used
post‐assembly
effectively
fill
voids
between
[4‐(3,6‐dimethyl‐9H‐carbazole‐9‐yl)butyl]phosphonic
(Me‐4PACz)
form
denser
facilitates
passivation
buried
interface.
In
addition,
post‐assembled
BAs
different
dipole
moments
can
adjust
work
function
Me‐4PACz
facilitating
transport
extraction
charge
carriers.
Consequently,
PSCs
based
on
Me‐4PACz/FBA
HSL
realize
champion
PCE
25.58%.
Moreover,
unencapsulated
devices
maintain
82%
94%
after
800
h
outdoor
storage
(RH≈60%)
2000
glove
box,
respectively.
This
technique
enhances
both
device,
blazing
simple
pathway
for
further
development