Solar RRL,
Journal Year:
2024,
Volume and Issue:
8(8)
Published: March 13, 2024
In
the
rapidly
developing
field
of
photovoltaics,
organic–inorganic
metal
halide
perovskites
are
outstanding
for
their
exceptional
power
conversion
efficiencies
(PCE),
exceeding
26%.
However,
full
potential
these
materials
is
often
undermined
by
prevalence
defects
within
structure
and
at
grain
surfaces,
leading
to
significant
nonradiative
recombination
losses.
To
meet
this
critical
challenge,
study
introduces
a
novel
strategy
involving
pyrrolidinium
derivative
tetrafluoroborate
ionic
liquid,
specifically
2‐pyrrolidin‐1‐ium‐1‐ethylammonium
(PyE(BF
4
)
2
),
as
an
additive
in
perovskite
precursor.
This
approach
aims
meticulously
control
crystallization
processes
effectively
passivate
on
surface
boundaries
perovskite.
The
formation
N─H…I
−
hydrogen
bonds
strong
interactions,
PyE(BF
not
only
stabilizes
[PbI
6
]
4−
framework
but
also
optimizes
valence
band
alignment
with
hole
transport
layer.
Empirical
results
demonstrate
that
solar
cells
modified
have
achieved
notable
PCE
23.80%
remarkable
stability
1300
h
under
standard
testing
protocols
(ISOS‐V‐1).
findings
emphasize
transformative
multifunctional
liquids
enhancing
performance
durability
perovskite‐based
photovoltaic
devices,
marking
step
forward
pursuing
sustainable
efficient
energy
solutions.
Nature Communications,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Jan. 11, 2025
Suppressing
deep-level
defects
at
the
perovskite
bulk
and
surface
is
indispensable
for
reducing
non-radiative
recombination
losses
improving
efficiency
stability
of
solar
cells
(PSCs).
In
this
study,
two
Lewis
bases
based
on
chalcogen-thiophene
(n-Bu4S)
selenophene
(n-Bu4Se)
having
tetra-pyridine
as
bridge
are
developed
to
passivate
in
film.
The
uncoordinated
Pb2+
iodine
vacancy
can
interact
with
chalcogen-concave
group
pyridine
through
formation
acid-base
adduct,
particularly
both
be
surrounded
by
concave
molecules,
resulting
effective
suppression
charge
recombination.
This
approach
enables
a
power
conversion
(PCE)
high
25.37%
(25.18%
certified)
n-i-p
PSCs
stable
operation
65
°C
1-sun
illumination
1300
hours
N2
(ISOS-L-2
protocol),
retaining
94%
initial
efficiency.
Our
work
provides
insight
into
bowl-shaped
base
passivation
coordinated
strategy
high-performance
photovoltaic
devices.
Nature Communications,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Jan. 17, 2025
Interfacial
trap-assisted
nonradiative
recombination
hampers
the
development
of
metal
halide
perovskite
solar
cells
(PSCs).
Herein,
we
report
a
rationally
designed
universal
passivator
to
realize
highly
efficient
and
stable
single
junction
tandem
PSCs.
Multiple
defects
are
simultaneously
passivated
by
synergistic
effect
anion
cation.
Moreover,
defect
healing
is
precisely
modulated
carefully
controlling
number
hydrogen
atoms
on
cations
steric
hindrance.
Due
minimized
interfacial
energy
loss,
L-valine
benzyl
ester
p-toluenesulfonate
(VBETS)
modified
inverted
PSCs
deliver
power
conversion
efficiency
(PCE)
26.28%
using
vacuum
flash
processing
technology.
suppressing
carrier
recombination,
large-area
modules
with
an
aperture
area
32.144
cm2
perovskite/Si
coupled
VBETS
passivation
PCE
21.00%
30.98%,
respectively.
This
work
highlights
critical
role
hindrance
in
designing
molecular
modulators
advance
stability
Energy & Environmental Science,
Journal Year:
2024,
Volume and Issue:
17(13), P. 4670 - 4680
Published: Jan. 1, 2024
The
tricyclic
alkaloid
colchicine
is
applied
to
catalyzed
crystallization
(CC)
of
high-quality
α-FAPbI
3
perovskite
film
in
the
one-step
antisolvent-free
process
for
high
performance
solar
cells.
Communications Materials,
Journal Year:
2024,
Volume and Issue:
5(1)
Published: July 23, 2024
Abstract
In
the
last
decade,
laboratory-scale
single-junction
perovskite
solar
cells
have
achieved
a
remarkable
power
conversion
efficiency
exceeding
26.1%.
However,
transition
to
industrial-scale
production
has
unveiled
significant
gap.
The
central
challenge
lies
in
difficulty
of
achieving
uniform,
high-quality
films
on
large
scale.
To
tackle
this
issue,
various
innovative
strategies
for
manipulating
crystallization
emerged
recent
years.
Based
an
in-depth
fundamental
understanding
nucleation
and
growth
mechanisms
large-area
prepared
through
blade/slot-die
coating
methods,
review
offers
critical
examination
manipulation
modules.
Lastly,
we
explore
future
avenues
aimed
at
enhancing
stability
PSMs,
thereby
steering
field
toward
commercially
viable
applications.
Exploration,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 6, 2025
ABSTRACT
Perovskite
solar
cells
(PSCs)
have
attracted
considerable
attention
due
to
their
potential
for
high‐efficiency
conversion
and
cost‐effective
fabrication.
Although
the
fabrication
of
perovskite
films
in
ambient
air
offers
environmental
cost
advantages,
presence
water
vapor
oxygen
may
induce
instability
these
films,
thereby
affecting
device
performance.
This
review
aims
comprehensively
explore
recent
advancements
PSCs
air,
while
investigating
various
factors
contributing
degradation.
Addressing
challenges,
diverse
strategies
are
outlined,
encompassing
compositional,
additive,
solvent,
interface
engineering
enhance
performance
stability
fabricated
under
air.
To
facilitate
commercialization
PSCs,
this
paper
summarizes
several
widely
employed
methods
large‐scale
manufacturing
PSCs.
Through
review,
we
aim
offer
some
invaluable
insights
guidance
trajectory
as
well
pros
cons
widespread
applications
field
renewable
energy.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 16, 2024
Abstract
Formamidinium‐cesium
lead
triiodide
(FA
1‐x
Cs
x
PbI
3
)
perovskite
holds
great
promise
for
solar
cells
(PSCs)
with
both
high
efficiency
and
stability.
However,
the
defective
surfaces
induced
by
defects
residual
tensile
strain
largely
limit
photovoltaic
performance
of
corresponding
devices.
Here,
passivation
capability
alkylamine‐modified
pyridine
derivatives
surface
FA
is
systematically
studied.
Among
studied
passivators,
3‐(2‐aminoethyl)pyridine
(3‐PyEA)
suitable
size
demonstrated
to
be
most
effective
in
reducing
iodine
impurities
(V
I
2
through
its
strong
coordination
N
.
Additionally,
tail
amino
group
(─NH
from
3‐PyEA
can
react
+
cations
reduce
roughness
films,
reaction
products
also
passivate
vacancies
),
further
strengthen
their
binding
interaction
surfaces.
These
merits
suppressed
nonradiative
recombination
loss,
release
stress
a
favorable
energy‐level
alignment
at
perovskite/[6,6]‐phenyl‐C
61
‐butyric
acid
methyl
ester
interface.
Consequently,
resulting
inverted
PSCs
obtain
an
impressive
power
conversion
(PCE)
25.65%
(certified
25.45%,
certified
steady‐state
25.06%),
along
retaining
96.5%
initial
PCE
after
1800
h
1‐sun
operation
55
°C
air.
Small,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 12, 2024
Abstract
Pb‐related
imperfections
(surface
or
halide
vacancy
induced
uncoordinated
Pb
2+
,
Pb‐I
antisite,
and
defects)
of
the
ionic
crystal
perovskite
film
seriously
restrict
photovoltaic
performance
solar
cells
(PSCs).
Here,
an
aniline
derivative
N‐(4‐cyanophenyl)acetamide
(CAL)
is
rationally
designed,
incorporating
bilateral
functional
sites
cyano
acetyl
groups,
acting
as
Lewis
base
molecule
for
managing
in
surface
through
post‐treatment.
Theoretical
calculation
experimental
verification
together
proved
reduced
defect
density,
improved
crystallinity,
inhibited
ion
migration
CAL‐modified
perovskite.
Precisely,
a
side
group
another
can
both
coordinate
with
its
low
electrostatic
potential
energy.
Further,
core
π‐π
conjugate
structure
benzene
ring
ligand
tend
to
form
dimer
improve
mobility
carrier
transportation
collection.
The
strategy
demonstrates
champion
PCE
24.35%
air‐processed
PSCs
over
1200
hours
maximum
power
point
tracking
(MPPT)
stability.
This
study
presents
comprehensive
approach
overcoming
current
limitations
PSCs,
paving
way
their
integration
into
mainstream
technologies.