Progress in Photovoltaics Research and Applications,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 6, 2025
ABSTRACT
This
study
initially
employs
Cs₀.₀₅FA₀.₈₁MA₀.₁₄PbI₂.₈₆Cl₀.₁₄
as
the
active
layer
for
perovskite
solar
cells
and
explores
impact
of
using
different
concentrations
natural
Centella
asiatica
(CICA)
extracts
mixed
with
chlorobenzene
(CB)
anti‐solvent
in
one‐step
method
film
preparation.
is
rich
antioxidants
asiatic
acid.
It
contains
many
hydroxyl
ions,
which
are
capable
capturing
uncoordinated
heavy
metal
Pb
atoms.
We
found
that
devices
made
15%
extract
CB
achieved
highest
power
conversion
efficiency
(PCE),
increasing
from
14.3%
to
18.5%.
Moreover,
maintained
85%
their
initial
after
being
stored
a
glove
box
25
days.
Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 10, 2024
Abstract
Molecular
self‐assembled
monolayers
(SAMs),
anchored
on
a
transparent
conductive
oxide,
serve
as
class
of
effective
hole‐selective
contacts
in
high‐performance
lab‐scale
perovskite
solar
cells
(PSCs).
However,
scaling
these
SAM‐based
PSCs
to
large‐area
modules
introduces
challenges,
such
the
de‐wetting
ink
glass
around
P1
scribe
zones—a
part
module
design
–
which
compromises
film
uniformity
and
reproducibility.
To
overcome
coverage
anomalies,
study
incorporates
1,3‐dimethyl‐3,4,5,6‐tetrahydro‐2(1H)‐pyrimidinone
(DMPU)
into
SAM
solution,
enhancing
interaction
between
improving
wettability.
The
approach
leads
fabrication
wide‐bandgap
(1.67
eV)
with
power
conversion
efficiencies
(PCEs)
up
22.4%
for
small‐area
devices
(0.057
cm
2
)
20%
mini‐modules
(9.8
high
Additionally,
target
demonstrate
enhanced
photostability,
maintaining
80%
their
initial
PCE
after
490
hours
maximum
point
tracking
under
continuous
1‐sun
illumination.
This
identifies
key
challenges
presents
promising
strategy
fabricating
scalable
modules.
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(43), P. 59477 - 59487
Published: Oct. 18, 2024
Self-assembled
monolayers
(SAMs)
deposited
on
the
hole-collecting
electrodes
of
p-i-n
perovskite
solar
cells
effectively
replace
bulky
hole
transporting
layers.
However,
mechanism
by
which
control
electronic
processes
and
how
they
depend
properties
monolayer
molecules
remain
poorly
understood.
In
this
study,
we
developed
a
simplified
cell
imitator
with
blocked
electron
extraction
to
investigate
photocurrent
dynamics
between
ITO
electrode.
We
investigated
photoluminescence
photovoltage
under
short
laser
pulse
excitation
addressed
influence
monomolecular
transport
Our
findings
reveal
that
is
significantly
affected
layers,
in
turn
methods
sample
preparation
exploration.
Photocurrent
determined
several
processes,
including
charge
carrier
displacement
local
electric
field,
ITO,
trapping
holes
interface
trap
states,
electron-hole
recombination
at
interface.
propose
model
takes
into
account
molecular
dipole
moments
their
ionization
potentials
partially
explain
different
influences
interfacial
rates.
Additionally,
also
strongly
depends
illumination
shows
memory
effects
persist
over
minutes
hours
are
attributed
redistribution
ions.
Small,
Journal Year:
2025,
Volume and Issue:
21(11)
Published: Feb. 2, 2025
Abstract
The
self‐assembling
molecule
2PACz
tends
to
aggregate
in
thin
films,
which
negatively
impacts
the
performance
of
organic
solar
cells
(OSCs)
when
used
as
a
hole‐transporting
layer
(HTL),
particularly
large‐area
devices.
To
overcome
this,
binary
conjugated
molecular
system
incorporating
carbazole
(Cz),
shares
similar
backbone
with
2PACz,
is
introduced.
Despite
strong
aggregation
tendencies
and
Cz
individually,
their
blend
forms
homogeneous
films
due
hydrogen
bonding
interactions
between
two
molecules.
These
suppress
aggregation,
resulting
smooth
well‐ordered
films.
Devices
modified
HTL
show
significantly
enhanced
charge
transfer,
achieving
power
conversion
efficiency
(PCE)
20.10%,
fill
factor
80.3%,
short‐circuit
current
28.98
mA
cm
−
2
,
outperforming
those
unmodified
2PACz.
Large‐area
devices
(1.0
)
achieve
record‐high
PCE
18.56%
retention
rate
92.7%,
compared
43%
for
findings
highlight
potential
carbazole‐modified
improve
both
stability
OSCs,
offering
promising
strategy
high‐performance
development.
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 4, 2025
Abstract
Six
novel
organic
small
molecules,
TPA‐Sp‐PA
(
1
),
TPA‐Sp‐PE
1E
TPA‐T‐PA
2
TPA‐T‐PE
2E
TPA‐P‐PA
3
)
and
TPA‐P‐PE
3E
are
developed
applied
to
NiOx
films
as
self‐assembled
monolayers
(SAMs)
for
tin
perovskite
solar
cells
(TPSCs).
The
linker
between
acceptor
(phosphonic
acid
(PA)
or
phosphonic
ester
(PE))
donor
(triphenylamine
(TPA))
plays
an
important
role
in
facilitating
the
growth
of
high‐quality
using
a
two‐step
method.
Three
different
types
linkers,
phenyl
ring
(P),
thiophene
(T),
selenophene
(Sp),
studied,
which
Sp‐based
SAMs
provide
best
device
performance
with
achieving
PCE
8.7%,
its
acidic
analog,
reaching
maximum
8.3%.
Single
crystal
structures
successfully
obtained,
expectation
that
uniform
SAM
would
form
on
NiOx/ITO
substrate.
research
introduces
approach
enhance
TPSC
by
integrating
HTMs,
offering
promising
avenue
future
progress
technology
through
fabrication
technique.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 25, 2025
Abstract
Perovskite
films
have
long
been
plagued
by
defects,
mainly
located
at
grain
boundaries,
leading
to
device
degradation,
especially
the
effects
of
residual
PbI
2
.
As
effective
boundary
passivators,
organic
ammonium
salts
are
thus
extensively
investigated.
Here,
study
introduces
a
nitrogen
heterocyclic
molecule,
1,3‐diphenyl‐benzimidazole
iodide
(DBI),
for
post‐treatment
perovskite
film
construct
robust
one‐dimensional
(1D)/three‐dimensional
(3D)
structure.
The
1D
structure
DBPbI
3
formed
from
interaction
between
and
DBI
enables
repair
local
defects
enhancement
stability.
Concurrently,
double
conjugated
benzene
imidazole
rings
synergistically
facilitate
charge
transfer
promote
optimization
energy
levels,
thereby
boosting
extraction.
corresponding
1D/3D
solar
cells
(PSCs)
yielded
high
efficiency
25.04%
with
excellent
photo/thermal
stabilities.
module
exhibited
an
21.04%
total
area
36
cm
long‐term
Advanced Energy Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 24, 2025
Abstract
The
widespread
application
of
self‐assembled
monolayer
(SAM)
hole
transport
materials
has
driven
rapid
advancements
in
the
performance
inverted
perovskite
solar
cells
(PSCs).
However,
difficulty
achieving
a
highly
ordered
SAM
for
and
weak
binding
strength
between
layer
not
only
leads
to
defective
bottom
interface
but
also
reduces
compatibility
with
large‐area
device
fabrication.
In
this
work,
co‐assembled
molecule
functionalized
diamide
terminal
group
is
demonstrated
that
able
form
supramolecular
interaction
popular
carbazole‐based
SAMs
regulating
their
structural
ordering,
improve
chemical
bonding
Pb‐I
frameworks
synergistically,
which
enables
efficient
long‐term
stable
PSCs.
As
result,
target
contributes
champion
small‐area
power
conversion
efficiency
(PCE)
25.3%
(certified
25.0%),
demonstrates
good
fabrication
by
reproducible
performances
1.02
cm
2
devices.
encapsulated
devices
exhibit
stability
92.8%
91.2%
initial
PCE
after
1500
hours
aging
under
85
°C
maximum
point
(MPP)
tracking
at
65
hours,
respectively.
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.
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 7, 2025
The
power
conversion
efficiency
(PCE)
of
inverted
lead-halide
perovskite
solar
cells
(PSCs)
via
vapor
deposition
has
undergone
significant
enhancement
through
the
incorporation
a
self-assembled
monolayer
(SAM)
serving
as
hole
transport
layer.
To
achieve
high-performance
PSCs,
SAM
layer
needs
to
maintain
dense
and
high-coverage
configuration
during
fabrication
process.
Our
investigation
revealed
that
solid-vapor
reaction,
conditions
high
temperature
low
pressure
can
potentially
lead
migration
molecules,
particularly
those
adsorbed
on
surface
but
have
not
yet
formed
covalent
bonds.
In
this
study,
overcome
limitation,
we
developed
an
impregnation
process
for
mixed
molecules
with
(4-(7H-dibenzo[c,g]carbazol-7-yl)butyl)phosphonic
acid
(4PADCB)
glycine
hydrochloride
(GH),
which
reduces
agglomeration
enhances
their
strong
anchoring
ability
substrate,
thereby
maintaining
extremely
coverage
rate
even
in
high-temperature
low-pressure
environment
reactions.
Consequently,
champion
efficiencies
22.15%
(0.16
cm2)
19.18%
(5
cm
×
5
module)
are
achieved,
is
highest
record
PSCs
based
deposition.
Moreover,
advantages
reusability,
good
uniformity,
cost,
very
broad
commercial
prospects.
Solar RRL,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 7, 2025
For
self‐assembled
molecule
(SAM)‐based
inverted
perovskite
solar
cell,
the
buried
interface
(SAM/perovskite
interface)
significantly
determines
overall
efficiency
and
stability
of
device,
which
requires
meticulous
modulation.
In
this
work,
a
series
phthalimide
derivatives
(namely
4‐(1,3‐dioxoisoindolin‐2‐yl)butan‐1‐ammonium
iodide
[DBAI],
2‐(1,3‐dioxoisoindolin‐2‐yl)ethan‐1‐ammonium
[DEAI],
6‐(1,3‐dioxoisoindolin‐2‐yl)hexan‐1‐ammonium
[DHAI])
are
developed
as
interfacial
modification
materials
to
improve
surface
homogeneity,
optimize
morphology,
passivate
defect
sites.
Among
them,
DHAI
with
longest
alkyl
chain
outperforms
others,
is
attributed
steric
electronic
effect
molecular
structure.
Intriguingly,
these
can
introduce
‘island‐like’
morphology
on
hole‐selective
layer,
boosts
transmittance
absorption,
resulting
in
substantially
enhanced
short‐circuit
density
power
conversion
24.71%.
These
findings
reveal
structure–property–performance
relationship
propose
novel
strategy
for
light
management
at
interface.