Advanced Functional Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 12, 2024
Abstract
Currently,
all‐perovskite
tandem
solar
cells
have
achieved
power
conversion
efficiencies
exceeding
29%.
The
further
improvement
is
limited
by
mixed
Sn–Pb
narrow‐bandgap
perovskite
subcells.
facile
oxidation
of
Sn
2+
to
4+
poses
an
inherent
challenge
that
limits
the
efficiency
and
stability
cells.
In
this
study,
a
multi‐dentate
chelating
additive,
3‐amino‐2‐chloroisonicotinamide
(ACPC),
developed.
Its
amino
group
could
anchor
I
−
lattice
hydrogen
bonds,
thereby
preventing
migration
oxidation.
On
other
hand,
carbonyl
ACPC
as
Lewis
base
coordinate
with
,
effectively
protecting
from
Ultimately,
effect
helps
suppress
its
related
nonradiative
recombination.
resulting
obtain
top
power‐conversion
(PCE)
23.09%
high
open‐circuit
voltage
(
V
OC
)
0.902
while
control
values
only
reach
19.11%
0.825
V.
As
result
improved
performance
cells,
corresponding
achieve
PCE
27.60%,
retaining
85.7%
initial
after
500
h
continuous
1
sun
illumination.
Abstract
Tin‐lead
(Sn‐Pb)
mixed
perovskite
with
a
narrow
bandgap
is
an
ideal
candidate
for
single‐junction
solar
cells
approaching
the
Shockley‐Queisser
limit.
However,
due
to
easy
oxidation
of
Sn
2+
,
efficiency
and
stability
Sn‐Pb
(PSCs)
still
lag
far
behind
that
Pb‐based
cells.
Herein,
highly
efficient
stable
FA
0.5
MA
Pb
I
0.47
Br
0.03
compositional
PSCs
are
achieved
by
introducing
appropriate
amount
multifunctional
Tin
(II)
oxalate
(SnC
2
O
4
).
SnC
compensative
reductive
group
C
2−
effectively
passivates
cation
anion
defects
simultaneously,
thereby
leading
more
n‐type
films.
Benefitting
from
energy
level
alignment
suppression
bulk
nonradiative
recombination,
cell
treated
achieves
power
conversion
21.43%.
More
importantly,
chemically
suppresses
notorious
significant
enhancement
in
stability.
Particularly,
it
dramatically
improves
light
Nature Communications,
Год журнала:
2025,
Номер
16(1)
Опубликована: Апрель 11, 2025
Low-bandgap
(LBG)
mixed
tin-lead
(Sn-Pb)
perovskite
solar
cells
(PSCs)
suffer
from
inferior
performance
due
to
their
high
defect
density.
Conventionally,
ethylenediammonium
diiodide
(EDADI)
is
used
as
a
surface
passivator
reduce
defects
and
improve
device
photovoltaic
performance,
but
it
introduces
severe
hysteresis
caused
by
excessive
mobilized
ions
at
the
top
interface.
Here,
we
report
mobile
ion
suppressing
strategy
of
using
hydrazine
monohydrochloride
(HM)
bulk
anchor
free
in
LBG
perovskites.
The
protonated
(N2H5+)
HM
formed
hydrogen
bonds
with
iodine
(I-)
ions,
while
chloride
(Cl-)
occupied
I-
vacancies,
collectively
impeding
migration
thus
mitigating
movement-induced
that
arose
EDADI
usage.
synergistic
doping
post-treatment
significantly
suppresses
oxidation
Sn2+,
decreases
trap
density,
inhibits
rapid
crystallization
perovskite.
Consequently,
achieved
champion
efficiency
23.21%
for
PSCs.
Integrating
these
wide-bandgap
PSCs
into
all-perovskite
tandem
yields
28.55%
(certified
28.31%)
negligible
hysteresis.
Advanced Functional Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Июль 16, 2024
Abstract
Mixed
tin–lead
(Sn–Pb)
perovskites
often
face
a
daunting
challenge:
rapid
and
uncontrollable
crystallization,
leading
to
plethora
of
defects
significant
stress.
This
issue
is
particularly
exacerbated
during
the
blade‐coating
preparation
scalable
Sn–Pb
perovskite
films.
In
this
study,
facile
strategy
involving
addition
ammonium
citrate
(AC)
narrow‐bandgap
mixed
precursors
introduced.
AC,
armed
with
its
arsenal
multiple
carboxyl
amino
groups,
acts
as
virtuoso
conductor,
orchestrating
controlled
crystal
growth
by
harmonizing
Pb
2+
Sn
ions.
significantly
boosts
crystallinity
films,
alleviates
interface
stress,
inhibits
oxidation,
mitigates
interfacial
defects.
Consequently,
The
blade‐coated
AC‐incorporated
solar
cells
achieve
high
photovoltaic
conversion
efficiency
nearly
21%.
Furthermore,
extending
two‐terminal
all‐perovskite
tandem
yielded
remarkable
maximum
27.20%.
work
presents
an
effective
for
producing
efficient
cells,
heralding
pathway
toward
fabrication
cells.
Catalysts,
Год журнала:
2025,
Номер
15(3), С. 214 - 214
Опубликована: Фев. 24, 2025
In
this
study,
a
TiO2/(MA)2SnCl4
nanocomposite
film
was
synthesized
using
sustainable,
sunlight-driven
approach,
demonstrating
enhanced
photocatalytic
performance
for
environmental
remediation.
TiO2
nanoparticles
(TiO2-NPs)
were
dispersed
in
ethanol
and
mixed
with
methylammonium
(MA)
SnCl2
precursor
solution,
followed
by
drop-casting
onto
glass
substrate
exposure
to
direct
sunlight
2
h.
Sunlight
served
as
an
energy
source,
facilitating
situ
structural
modifications
leading
the
formation
of
well-integrated
hybrid
structure,
where
effectively
encapsulated.
Characterization
revealed
band
gap
reduction
from
3.1
eV
2.6
nanocomposite,
extending
light
absorption
into
visible
range.
The
Sn–O–Ti
interactions
charge
separation,
minimized
electron–hole
recombination,
improved
carrier
dynamics.
Photocatalytic
degradation
tests
methylene
blue
(MB)
under
showed
that
achieved
90%
MB
within
60
min,
outperforming
TiO2-NPs,
which
only
75%
degradation.
presence
oxygen
vacancies
(OVs)
generated
during
further
efficiency
acting
traps
reaction
sites.
This
study
introduces
green
synthesis
strategy
leveraging
renewable
marking
first
integration
(MA)2SnCl4
TiO2-NPs
photocatalysis.
synergistic
effects
extended
visible-light
absorption,
defect
engineering,
efficient
separation
make
films
scalable,
cost-effective
solution
water
purification
applications,
offering
promising
solar-driven
approach
addressing
global
contamination
challenges.
Advanced Energy Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 26, 2025
Abstract
Tin
perovskite
solar
cells
(PSCs)
have
garnered
considerable
attention
as
promising
alternatives
to
lead
PSCs
due
their
lower
toxicity
and
outstanding
optoelectronic
properties.
However,
efficiency
stability,
particularly
in
2D/3D
tin
PSCs,
are
usually
hindered
by
high
defect
densities
inefficient
carrier
transport.
In
this
study,
a
small‐molecule
Lewis
base
with
multiple
functional
groups‐cyanoacetohydrazide
(CAH)
is
employed
mitigate
defects
enhance
charge
transport
PSCs.
It
revealed
that
the
carbonyl,
amine,
cyano
groups
CAH
form
strong
chemical
bonds
Sn
2+
ions,
resulting
synergetic
coordination
effects.
Moreover,
interaction
between
effectively
regulates
crystallization
process
of
film,
high‐quality
film
enhanced
crystallinity,
reduced
density,
modulated
phase
distribution.
As
result,
optimized
achieve
remarkable
power
conversion
15.06%,
marking
one
highest
values
for
Furthermore,
devices
exhibit
retaining
95%
initial
performance
after
2000
h
storage
nitrogen
atmosphere.
Energies,
Год журнала:
2024,
Номер
17(11), С. 2671 - 2671
Опубликована: Май 31, 2024
In
recent
years,
all-inorganic
perovskite
solar
cells
have
become
a
research
hotspot
in
the
field
of
photovoltaics
due
to
their
excellent
stability
and
optoelectronic
performance,
power
conversion
efficiency
has
increased
from
initial
2.9%
over
20%.
This
article
briefly
introduces
development
cesium
lead-based
(CsPbX3-IPSC),
including
characteristics
CsPbX3
materials,
preparation
methods,
structure
working
principle
IPSCs.
Different
optimization
strategies
for
preparing
high
performance
high-stability
IPSCs,
such
as
element
doping
interface
modification,
are
discussed.
The
application
prospects
IPSCs
also
summarized.
Flexible
tin-lead
(Sn-Pb)
mixed
perovskite
solar
cells
(PSCs)
are
among
the
promising
flexible
photovoltaics,
owing
to
narrow
bandgap
(NBG)
of
Sn-Pb
perovskites,
and
wearable
features,
their
role
as
a
critical
component
in
all-perovskite
tandem
photovoltaics.
However,
PSCs
suffer
from
low
power
conversion
efficiency,
no
higher
than
18.5%,
along
with
limited
stability.
Herein,
we
reported
an
efficient
stable
NBG
PSC
via
Tin‐lead
(Sn‐Pb)
perovskites
with
narrow
bandgaps
can
be
used
as
bottom
cells
for
tandem
to
boost
the
efficiency
of
perovskite
solar
(PSCs).
However,
uncontrollable
crystallization
Sn–Pb
and
straightforward
oxidation
Sn
2+
4+
are
two
key
factors
that
restrict
their
stability.
Compared
anti‐solvent
method,
vacuum
flash
assisted
solution
processing
(VASP)
offers
advantages
environmental
protection
excellent
controllability.
In
this
study,
we
combined
VASP
post‐processing
sodium
triacetoxyboro‐hydride
(STAB)
a
reducing
agent
passivator.
The
experimental
theoretical
results
demonstrat
interactions
occurred
between
specific
functional
groups
(−CH
3
,
B–H,
CO)
perovskite.
Therefore,
was
successfully
inhibited
film
quality
improved.
optimized
PSCs
STAB
increased
from
18.2%
21.64%,
which
is
highest
power
conversion
among
fabricated
using
method.
addition,
device
retained
81%
its
initial
after
being
stored
in
N
2
under
−0.1
MPa
1400
h.
Angewandte Chemie,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 12, 2025
Abstract
The
integration
of
organic
dyes
in
perovskite
solar
cells
(PSCs)
to
utilize
near‐infrared
(NIR)
photons
remains
a
challenge.
In
this
study,
selenium‐incorporated
ortho‐benzodipyrrole‐based
NIR
dye
CB‐2Se
was
developed.
CB‐2Se,
featuring
lower
bandgap
1.35
eV,
blended
with
PCBM
form
bulk‐heterojunction
layer
PSCs
for
electron
extraction
and
transport.
Compared
Y6‐16
acceptor,
the
removal
Tz
unit
suppresses
self‐aggregation,
improving
its
compatibility
PCBM.
A
CB‐2Se:PCBM‐incorporated
PSC
achieved
remarkable
power
conversion
efficiency
(PCE)
25.18%
V
OC
1.164
V,
J
SC
25.71
mA/cm
2
,
Fill
Factor
84.15%,
outperforming
that
PCBM‐only
reference
device
(24.35%)
PCBM:Y6‐16‐based
(24.49%).
PCBM:CB‐2Se
enhanced
long‐term
stability
PSCs,
retaining
88%
initial
after
1000
h
under
ambient
air
thermal
conditions.
photophysical
interactions
between
have
been
comprehensively
investigated
by
using
femtosecond
transient
absorption
spectroscopy.
Ultrafast
exciton
separation
into
free
charges
occurs
within
200
femtoseconds
at
interfaces
CB‐2Se.
For
first
time,
transfer
holes
from
back
detected,
providing
valuable
insights
charge
dynamics
utilizing
dyes.
Sn─Pb
hybrid
perovskite
has
attracted
more
attention
due
to
its
ideal
bandgap
and
excellent
photoelectric
properties.
However,
easy
oxidation
poor
crystallinity
caused
by
the
introduction
of
Sn2+
have
become
two
major
problems.
In
this
study,
is
doped
in
Pb-based
prepare
high
crystalline
mixed
with
larger
grain
size
using
solvent
engineering
technique
cooperation
optimization
HCOOH.
The
reducibility
HCOOH
inhibition
deprotonation
significantly
prevent
decomposition
A-site
cations.
experimental
theoretical
results
show
that
interactions
between
Pb2+,
which
reduce
defect
density
improve
stability
film
addition,
compact
SnO2
prepared
atomic
layer
deposition
as
electronic
transformation
further
devices.
conversion
efficiency
solar
cells
(PSCs)
dopant
growth
method
can
reach
21.53%
better
than
PSCs
traditional
method.