Buried Interface Modulation Using Self‐Assembled Monolayer and Ionic Liquid Hybrids for High‐Performance Perovskite and Perovskite/CuInGaSe2 Tandem Photovoltaics
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 6, 2025
Effective
modifications
for
the
buried
interface
between
self-assembled
monolayers
(SAMs)
and
perovskites
are
vital
development
of
efficient,
stable
inverted
perovskite
solar
cells
(PSCs)
their
tandem
photovoltaics.
Herein,
an
ionic-liquid-SAM
hybrid
strategy
is
developed
to
synergistically
optimize
uniformity
SAMs
crystallization
above.
Specifically,
ionic
liquid
1-butyl-3-methyl-1H-imidazol-3-iumbis((trifluoromethyl)sulfonyl)amide
(BMIMTFSI)
incorporated
into
SAM
solution,
enabling
reduced
surface
roughness,
improved
wettability,
a
more
evenly
distributed
potential
film.
Leveraging
this
optimized
substrate,
favorable
growth
high-quality
crystals
achieved.
Furthermore,
introduced
functional
ions
readily
bond
with
perovskites,
effectively
passivating
undesirable
cation
or
halide
vacancies
near
interface.
Remarkably,
high
power
conversion
efficiencies
(PCEs)
25.68%
22.53%
obtained
normal-bandgap
(≈1.55
eV)
wide-bandgap
(WBG)
(≈1.66
PSCs
along
operational
stability.
Additionally,
champion
PCE
19.50%
achieved
semitransparent
WBG
PSCs,
further
delivering
impressive
28.34%
integrated
four-terminal
photovoltaics
when
combined
CuInGaSe2
cells.
Language: Английский
Perfluorinated Anionic Surfactant Assisted Homogeneous Crystallization for Efficient and Stable Formamidinium‐Based Sn‐Pb Perovskite Solar Cells
Tengfei Kong,
No information about this author
Yinjiang Liu,
No information about this author
Zihan Zhao
No information about this author
et al.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 15, 2025
Abstract
Formamidinium
(FA)‐based
Sn‐Pb
perovskite
demonstrates
superior
thermal
stability,
making
it
well‐suited
for
all‐perovskite
tandem
solar
cells.
However,
the
uncontrolled
crystallization
process
remains
a
significant
challenge.
In
this
study,
an
effective
strategy
is
presented
to
regulate
of
FA‐based
by
incorporating
perfluoroanionic
surfactant
(perfluorohexanesulfonic
acid
potassium
salt,
F
13
C
6
SO
3
K)
into
precursor.
The
multifunctional
sites
K,
including
atoms
and
−
groups,
interact
with
components
stabilize
colloidal
distribution
precursor
modulate
kinetics.
This
results
in
high‐quality
films
fewer
defects.
Consequently,
cell
(PSC)
achieves
champion
efficiency
24.33%,
open‐circuit
voltage
0.895
V
fill
factor
83.2%.
After
continuous
heating
at
65
°C
1008
h,
still
maintain
91%
its
initial
efficiency,
which
shows
enhanced
stability.
When
coupled
wide‐bandgap
subcell,
reaches
power
conversion
(PCE)
27.57%.
Language: Английский
Stabilizing Precursor Solutions by Proton‐Rich Additive for High‐Performance Air‐Processed Solar Cells
Kongxiang Wang,
No information about this author
Zhongtao Duan,
No information about this author
Hong Liu
No information about this author
et al.
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 10, 2025
Storing
perovskite
precursor
solutions
under
ambient
conditions
poses
a
significant
challenge
to
commercialization,
as
humidity
and
oxidation
accelerate
ageing
introduce
defects
in
devices.
A
major
contributor
solution
impurity
phases
is
the
deprotonation
of
hybrid
organic
cations,
specifically
methylammonium
(MA+)
formamidinium
(FA+).
In
this
work,
proton-rich
additive,
4-(aminomethyl)pyridine
2-iodide,
used
inhibit
MA+
by
generating
free
H+,
thereby
mitigating
degradation
cations
oxygen
stress.
The
treated
stored
for
several
days
exhibits
no
condensation
reaction
products.
Due
synergistic
effect
H+
I-,
films
exhibit
pure
phase
formation
abnormal
"aggregate"
crystals.
Therefore,
additive
reacts
with
FA+
form
new
complexes,
termed
N-(4-methylpyridine)formamidinium),
which
efficiently
passivate
nonradiative
defects.
Consequently,
strategy
enables
solar
cells
achieve
power
conversion
efficiency
(PCE)
25.25%,
demonstrating
enhanced
long-term
stability
both
light
thermal
Notably,
optimized
device
retains
95.5%
its
initial
PCE
after
1200
h
continuous
illumination
91.61%
600
at
85
°C
85%
relative
humidity.
Language: Английский
In Situ Construction of Multi‐Functional Polymer Network Toward Durable Perovskite Solar Cells
Advanced Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 30, 2025
Enhancing
the
crystalline
quality
of
perovskite
thin
films
and
stabilizing
their
internal
grain
boundaries
are
essential
in
guaranteeing
extended
longevity
solar
cells.
Herein,
an
situ
polymerization
strategy
is
presented
to
produce
weak
chemical
bond
networks
films.
The
introduction
acrylamide
monomer
into
precursor
solution
facilitates
rearrangement
[PbI6]4-
octahedra,
resulting
a
significant
enhancement
crystal
With
presence
C═C
bonds,
at
can
form
polymer
networks,
which
efficiently
passivate
detrimental
defects
associated
with
boundaries.
cells
impressive
power
conversion
efficiency
(PCE)
26.05%
(certified
25.06%)
achieved,
combined
highly
improved
operational
stability
T98
=
2034
h.
As
expected,
large-area
module
based
on
this
achieved
PCE
23.02%
active
area
14
cm2.
Language: Английский
Surface Passivation to Improve the Performance of Perovskite Solar Cells
H. J. Lee,
No information about this author
Dawen Li
No information about this author
Energies,
Journal Year:
2024,
Volume and Issue:
17(21), P. 5282 - 5282
Published: Oct. 24, 2024
Perovskite
solar
cells
(PSCs)
suffer
from
a
quick
efficiency
drop
after
fabrication,
partly
due
to
surface
defects,
and
can
be
further
enhanced
with
the
passivation
of
defects.
Herein,
is
reviewed
as
method
improve
both
stability
PSCs,
an
emphasis
on
chemical
mechanism
passivation.
Various
molecules
are
utilized
passivants,
such
halides,
Lewis
acids
bases,
amines
(some
result
in
low-dimensional
perovskite),
polymers.
Multifunctional
promising
group
they
capable
passivating
multiple
defects
various
functional
groups.
This
review
categorizes
these
addition
considering
potential
limitations
each
type
passivant.
Additionally,
passivants
for
Sn-based
PSCs
discussed
since
this
has
poor
photovoltaic
performance
compared
their
lead-based
counterpart
severe
Lastly,
future
perspectives
usage
addressed
provide
direction
upcoming
research
practical
applications.
Language: Английский
Visible Light‐Triggered Self‐Welding Perovskite Solar Cells and Modules
Xiongjie Li,
No information about this author
Bin Ding,
No information about this author
Junyi Huang
No information about this author
et al.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 20, 2024
Abstract
Flexible
perovskite
solar
cells
(F‐PSCs)
are
highly
promising
for
both
stationary
and
mobile
applications
because
of
their
advantageous
features,
including
mechanical
flexibility,
lightweight
thin
nature,
cost‐effectiveness.
However,
a
number
drawbacks,
such
as
instability,
make
practical
application
difficult.
Here,
self‐welding
dynamic
diselenide
that
is
triggered
by
visible
light
into
the
structure
F‐PSCs
to
improve
long‐term
stability
repairing
cracks
defects
in
absorber
layer
incorporated.
The
confers
flexibility
properties
Cs
0.05
MA
FA
0.9
PbI
3
layer,
enabling
optimized
F‐PSC
devices
achieve
power
conversion
efficiency
24.85%
while
retaining
ca.
92%
initial
after
undergoing
15
000
bending
cycles
at
curvature
radius
mm.
corresponding
flexible
large‐scale
module
with
an
active
area
15.82
cm
2
achieved
record
PCE
21.65%.
Language: Английский
Buried interface engineering with amphoteric ion for inverted perovskite solar cells
Applied Physics A,
Journal Year:
2025,
Volume and Issue:
131(4)
Published: April 1, 2025
Language: Английский
Energy Level Alignment Regulation and Carrier Management in Perovskite Solar Cells with Various Bandgaps Using Tailored Metal‐Organic Frameworks
Bo Xiao,
No information about this author
Wenguang Zhang,
No information about this author
Yuchen Xiong
No information about this author
et al.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 21, 2024
Abstract
The
interface
energy
level
alignment
modulation
and
charge
carrier
transportation
play
an
important
role
in
the
device
performance
of
perovskite
solar
cells
(PSCs).
Herein,
tailored
hydrophobic
metal‐organic
frameworks
(MOFs)
are
employed
as
interfacial
layers
between
absorbers
hole
transport
(HTLs).
MOFs
feature
abundant
carboxylic
acid
groups
capable
bonding
with
Pb
2+
organic
cations,
which
can
effectively
passivate
defects
suppress
non‐radiative
recombination.
Meanwhile,
MOF
optimized
HTL,
further
facilitating
transportation.
Specifically,
CsFAMA‐based
PSCs
a
bandgap
1.63
eV
attained
power
conversion
efficiency
(PCE)
23.06%
upon
modification
MOFs.
Additionally,
MOFs‐treated
FA‐based
1.55
achieved
remarkable
PCE
24.81%,
accompanied
by
outstanding
fill
factor
84.3%
minimal
open‐circuit
voltage
loss
merely
0.386
V.
Furthermore,
integration
layer
substantially
improved
moisture
stability
PSCs.
unencapsulated
CsFAMA
modified
retained
91.2%
their
initial
after
2500
h
aging
under
ambient
conditions
40%
relative
humidity
(RH).
This
work
underpins
commercialization
diverse
bandgaps.
Language: Английский
Boosting Stability of Cesium/Formamidinium Based Perovskite Solar Cells via Eliminating Intermediate Phase Transition and X-Anion Vacancy
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
17(1), P. 991 - 1000
Published: Dec. 23, 2024
Boosting
the
stability
of
cesium/formamidinium
(Cs/FA)
based
perovskite
solar
cells
(PSCs)
has
received
tremendous
attention.
However,
crystallization
perovskites
usually
undergoes
complex
intermediate
phase
transitions
and
ion
loss
processes,
which
seriously
degrade
efficiency
PSCs.
Herein,
iodine
monobromide
(IBr,
an
interhalogen)
is
incorporated
into
precursor
solution
to
regulate
process.
IBr
can
directly
induce
formation
crystal
nuclei
in
film,
avoiding
a
transformation
(2H-4H-3C).
This
leads
reduction
impurity
phase,
increase
grain
size,
improvement
quality.
Furthermore,
effectively
compensate
X-anion
vacancy,
thereby
reducing
defect
density
nonradiative
recombination,
enhances
device
performance.
Thus,
optimal
24.82%.
Simultaneously,
demonstrated
excellent
stability.
After
400
h
continuous
operation,
value
unencapsulated
PSCs
still
retains
89%
its
initial
value.
study
provides
effective
strategy
for
manufacturing
with
Language: Английский
Multistage Regulation Strategy via Fluorine‐Rich Small Molecules for Realizing High‐Performance Perovskite Solar Cells
Xiong Chang,
No information about this author
Kunpeng Li,
No information about this author
Yong Han
No information about this author
et al.
Advanced Science,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 12, 2024
Abstract
Perovskite
solar
cells
(PSCs)
are
an
ideal
candidate
for
next‐generation
photovoltaic
applications
but
face
many
challenges
their
wider
application,
including
uncontrolled
fast
crystallization,
trap‐assisted
nonradiative
recombination,
and
inefficient
charge
transport.
Herein,
a
multistage
regulation
(MSR)
strategy
addressing
these
is
proposed
via
the
introduction
of
fluorine‐rich
small
molecules
with
multiple
active
points
(i.e.,
1‐[Bis(trifluoromethanesulfonyl)methyl]‐
2,3,4,5,6‐pentafluorobenzene
(TFSP))
into
precursor
solution
perovskite
film.
The
addition
TFSP
effectively
delays
regulates
crystallization
growth
process
film
larger
grains
fewer
defects,
it
improves
coverage
self‐assembled
efficient
induce
strong
binding
affinity
uncoordinated
defects
in
Moreover,
high
fluorine
content
induces
electronegativity
to
establish
strength
between
electron
transport
layer.
Finally,
PSCs
prepared
by
MSR
demonstrated
optimal
power
conversion
efficiency
(PCE)
25.46%
maintained
91.16%
initial
PCE
under
nonpackaged
air
conditions
at
relative
humidity
45%
after
3000
h.
Language: Английский