Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 14, 2024
Abstract
The
synthesis
of
multicomponent
metal
halide
perovskites
(MHPs)
by
cationic
and/or
alloying
allows
band
gap
tuning,
optimizing
performance
and
improving
stability.
However,
these
materials
often
suffer
from
compositional,
structural,
property
inhomogeneities,
leading
to
uneven
carrier
transport
significant
non‐radiative
recombination
losses
in
lead
perovskites.
While
many
researchers
have
focused
on
the
aggregation
perovskite
ions,
impact
surface
potential
has
received
relatively
less
attention.
In
this
study,
multifunctional
ionic
liquid
1‐allyl‐3‐methylimidazole
dicyanamide
(AMI)
is
introduced
into
precursor
effectively
regulate
layer.
This
approach
inhibits
recombination,
enhances
injection,
improves
device
performance.
Surface
homogenization
within
layer
leads
simultaneous
improvements
both
efficiency
stability
solar
cells.
For
wide‐bandgap
(1.81
eV),
optimal
power
conversion
(PCE)
reaches
20.44%,
with
an
open‐circuit
voltage
(
V
oc
)
1.339
V,
a
short‐circuit
current
density
J
sc
17.92
mA
cm
−2
,
high
fill
factor
(FF)
85%.
strategy
also
proved
effective
for
conventional
bandgap
cells
(PSCs)
(1.53
increase
performance,
PCE
increasing
23.22%
25.41%.
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.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 3, 2025
Abstract
The
inverted
perovskite
solar
cells
based
on
hole‐selective
self‐assembled
molecules
(SAMs)
have
been
setting
new
efficiency
benchmarks.
However,
the
agglomeration
of
SAM
and
lack
defect
passivation
ability
are
two
critical
issues
that
need
to
be
addressed.
It
is
demonstrated
by
blending
co‐adsorbent
4‐phosphoricbutyl
ammonium
iodide
(4PBAI)
with
4‐(7H‐dibenzo[c,g]carbazole‐7‐yl)
phosphonic
acid
(4PADCB),
enhanced
homogeneity,
conductivity,
better
energy
levels
can
realized
for
co‐SAM
contact.
functional
group
4PBAI
also
effectively
passivate
defects
at
buried
interface
template
high‐quality
growth.
Assisted
synergistic
top
modification,
power
conversion
optimized
device
reaches
24.96%,
which
retain
95%
initial
after
1200
h
in
ambient
unencapsulated
device.
findings
suggest
a
well‐designed
address
limitations
further
enhance
performance
cutting‐edge
SAMs.
Advanced Optical Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 5, 2025
Abstract
Controlling
the
formation
of
hybrid
perovskite
thin
films
is
crucial
in
obtaining
high‐performance
optoelectronic
devices,
since
factors
like
morphology
and
film
thickness
have
a
profound
impact
on
film's
functionality.
For
light‐emitting
applications
grain
sizes
sub‐micrometer‐range
previously
shown
enhanced
brightness.
It
therefore
to
develop
simple,
yet
reliable
methods
produce
such
films.
Here,
solution‐based
synthesis
protocol
for
on‐substrate
MAPbBr
3
(MA
=
methylammonium)
nanostructures
by
adding
bifunctional
rac
‐3‐aminobutyric
acid
precursor
solution
reported.
This
route
improves
key
optical
properties
as
photoluminescence
quantum
yields
life
times
excited
states
inducing
controlled
slow‐down
suppressing
agglomeration
effects.
In
situ
spectroscopy
reveals
delayed
slowed
down
crystallization
process,
which
achieves
structures
with
much
reduced
defect
densities.
Further,
aggregation
can
be
amount
amino
added
adjusting
allows
cubic
crystallites
targeted
size
from
nanometer
micrometer
scales.
The
nanocrystalline
samples
show
amplified
spontaneous
emission
(ASE)
intensities,
ASE
thresholds
purer
signals,
compared
pristine
films,
even
under
intense
driving,
making
them
promising
lasing
applications.
Nano-Micro Letters,
Journal Year:
2025,
Volume and Issue:
17(1)
Published: Feb. 11, 2025
Abstract
Despite
significant
advancements
in
the
power
conversion
efficiency
(PCE)
of
perovskite/silicon
tandem
solar
cells,
improving
carrier
management
top
cells
remains
challenging
due
to
defective
dual
interfaces
wide-bandgap
perovskite,
particularly
on
textured
silicon
surfaces.
Herein,
a
series
halide
ions
(Cl
−
,
Br
I
)
substituted
piperazinium
salts
are
designed
and
synthesized
as
post-treatment
modifiers
for
perovskite
Notably,
chloride
induces
an
asymmetric
bidirectional
distribution
from
bottom
surface,
with
large
cations
concentrating
at
surface
small
anions
migrating
downward
accumulate
buried
interface.
This
results
effective
dual-interface
defect
passivation
energy
band
modulation,
enabling
(1.68
eV)
achieve
PCE
22.3%
record
product
open-circuit
voltage
×
fill
factor
(84.4%
relative
Shockley–Queisser
limit).
Furthermore,
device
retains
91.3%
its
initial
after
1200
h
maximum
point
tracking
without
encapsulation.
When
integrated
double-textured
heterojunction
remarkable
31.5%
is
achieved
1.04
cm
2
monolithic
cell,
exhibiting
excellent
long-term
operational
stability
(
T
80
=
755
h)
encapsulation
ambient
air.
work
provides
convenient
strategy
engineering
making
high-efficiency
stable
platforms.
Advanced Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 20, 2025
Abstract
PTAA
as
a
widely
studied
polymeric
hole
transporting
material,
has
garnered
significant
attention
due
to
its
outstanding
thermal
and
chemical
stability.
However,
the
performance
of
PTAA‐based
p‐i‐n
devices
is
shown
lag
behind
counterpart
utilizing
oxides
or
SAMs.
In
this
study,
ionic
liquid,
1‐ethyl‐3‐methylimidazolium
formate
(EMIMCOOH),
innovatively
introduced
into
lead
iodide
(PbI
2
)
precursor
solution,
resulting
in
more
pronounced
mesoporous
PbI
film
with
expended
pore‐size
denser
pores.
This
enhancement
attributed
coordination
bond
between
─C═O
group
EMIMCOOH
Pb
2+
.
intensified
morphology
not
only
facilities
reaction
organic
layer,
but
also
promotes
conversion
perovskite
material.
Importantly,
incorporation
slows
down
process,
increasing
domain
size
suppressed
0
trap
density,
uniform
layer
enhanced
charge
transport
properties,
evidenced
by
conducting
atomic
force
microscope
(c‐AFM)
results.
As
result,
yields
power
efficiency
(PCE)
24.10%
high
fill
factor
exceeding
85%.
Notably,
PCE
EMIMCOOH‐modified
device
can
still
maintain
86%
initial
value
after
1500
h
at
25
°C
an
N
atmosphere.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 12, 2025
Abstract
The
operational
stability
issues
of
perovskite
devices
under
illumination
pose
significant
challenges
for
practical
applications,
attributed
to
substantial
alterations
in
lattice
distortion,
defect
enrichment,
and
stress
distribution
the
excited
state.
However,
most
existing
modification
strategies
predominantly
focus
on
elimination
chemical
transformations
at
ground
state
level,
which
may
not
yield
desired
outcomes
To
address
this
challenge,
study
introduces
a
dynamic
management
strategy
utilizing
4‐aminoazobenzene
hydrochloride,
exhibits
photoinduced
cis‐trans
isomerism,
buried
interface
within
devices.
Experimental
results
demonstrate
that
isomerized
molecules
anchored
effectively
inhibit
formation
defects
mitigate
interfacial
accumulation.
A
comprehensive
mechanism
through
isomerism
transformation
has
been
proposed
elucidate
process.
Consequently,
device
efficiency
have
markedly
enhanced,
achieving
peak
25.65%
retaining
over
92%
its
initial
after
1200
h
continuous
International
Summit
Organic
Photovoltaic
Stability
protocol
(ISOS
).
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 20, 2025
Abstract
Diammonium
derivatives
with
electron‐withdrawing
cores
of
cyclohexyl
or
phenyl
have
demonstrated
enormous
potential
in
achieving
high‐performance
perovskite
solar
cells.
Nevertheless,
the
critical
role
these
diammonium
passivation
on
device
performance
is
yet
to
be
elucidated.
Herein,
two
kinds
ligands
1,
4‐cyclohexyldimethylammonium
diiodide
(CyDMADI)
and
4‐phenyldimethylammonium
(PhDMADI)
are
introduced
into
precursor
for
bulk
passivation.
The
PhDMADI
system
exhibits
a
stronger
unit
comparison
CyDMADI
core,
thus
resulting
enhanced
electrostatic
interaction
between
uncoordinated
Pb
2+
groups
hydrogen
bonds
I─Pb
skeleton.
Such
strengthened
interactions
effectively
inhibit
generation
trap
states
therefore
significantly
decrease
non‐radiative
recombination.
PhDMADI‐passivated
film
demonstrates
mitigated
microstrain
decreased
grain
boundary
grooves
(GBGs)
compared
CyDMADI‐based
counterpart.
Simultaneously,
treatment
can
efficiently
slow
down
hot‐carriers
cooling
dynamics
process,
benefiting
transfer
hot‐carriers.
Consequently,
achieves
an
impressive
efficiency
26.04%,
along
excellent
operating
stability
which
retains
90%
its
initial
after
1100
h
tracking
at
maximum
power
point
under
continuous
one
sun
illumination.