Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 17, 2024
A
stable
and
compact
fullerene
electron
transport
layer
(ETL)
is
crucial
for
high-performance
inverted
perovskite
solar
cells
(PSCs).
However,
traditional
fullerene-based
ETLs
like
C
Advanced Energy Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 31, 2024
Abstract
The
uncontrolled
crystallization
of
perovskite
generates
a
significant
number
internal
and
interfacial
defects,
posing
major
challenge
to
the
performance
solar
cells
(PSCs).
In
this
paper,
novel
bi‐interfacial
modification
strategy
utilizing
5‐fluoropyridinic
acid
(FPA)
is
proposed
modulate
crystal
growth
provide
defect
passivation.
It
demonstrated
that
FPA
self‐deposited
at
both
top
bottom
interfaces
films
during
thermal
annealing.
CO
N
functional
groups
in
serve
as
chelating
agents,
binding
closely
uncoordinated
Pb
2+
/Pb
clusters,
thereby
passivating
defects
reducing
charge
recombination
interfaces.
strong
chemical
interactions
between
further
stabilize
Pb‐I
framework,
promoting
formation
high‐quality
films,
confirmed
by
situ
photoluminescence
measurements.
Consequently,
modified
inverted
PSCs
achieved
an
exceptional
power
conversion
efficiency
(PCE)
25.37%.
Moreover,
devices
retained
over
93.17%
initial
after
3000
h
continuous
illumination
under
one‐sun
equivalent
conditions
nitrogen
atmosphere.
This
paper
presents
promising
pathway
for
enhancing
stability
through
self‐induced
approach.
Nature Communications,
Год журнала:
2025,
Номер
16(1)
Опубликована: Янв. 30, 2025
All-perovskite
tandem
solar
cells
(APTSCs)
offer
the
potential
to
surpass
Shockley-Queisser
limit
of
single-junction
at
low
cost.
However,
high-performance
APTSCs
contain
unstable
methylammonium
(MA)
cation
in
tin-lead
(Sn-Pb)
narrow
bandgap
subcells.
Currently,
MA-free
Sn-Pb
perovskite
(PSCs)
show
lower
performance
compared
with
their
MA-containing
counterparts.
This
is
due
high
trap
density
associated
Sn2+
oxidation,
which
exacerbated
by
rapid
crystallization
Sn-containing
perovskite.
Here,
a
multifunctional
additive
rubidium
acetate
(RbAC)
proposed
passivate
We
find
that
RbAC
can
suppress
alleviate
microstrain,
and
improve
crystallinity
Consequently,
resultant
PSCs
achieve
power
conversion
efficiency
(PCE)
23.02%,
an
open
circuit
voltage
(Voc)
0.897
V,
filling
factor
(FF)
80.64%,
more
importantly
stability
device
significantly
improved.
When
further
integrated
1.79-electron
volt
wide-bandgap
PSC,
29.33%
(certified
28.11%)
efficient
Voc
2.22
volts
achieved.
The
tin
(II)
oxidation
impacts
cation-free
cells.
authors
employ
for
defect
passivation
stable
all-perovskite
Advanced Energy Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 23, 2025
Abstract
The
rapid
crystallization
process
of
perovskite
produces
a
large
number
defects
that
remain
critical
factor
disturbs
the
performance
solar
cells
(PSCs).
In
this
research,
these
challenges
are
mitigated
by
introducing
multifunctional
2,6‐pyridinedicarboxylic
acid
chloride
(PAC)
as
an
additive
into
perovskite.
During
thermal
annealing
process,
predominant
accumulation
PAC
occurs
at
upper
and
buried
interfaces
film.
possesses
multiple
passivating
sites
facilitate
anchoring
lead
iodine
defects,
thereby
enhancing
quality
material
across
both
its
dual
grain
boundaries.
With
unique
property,
combined
with
advantages
enhanced
crystallization,
reduced
non‐radiative
recombination,
boosted
charge
carrier
mobility,
optimal
energy
level
alignment,
PSC
achieved
power
conversion
efficiency
(PCE)
25.60%
maintained
more
than
90%
after
3000
h
under
one
equivalent
light
1400
dark
high
temperature
(85
°C).
interface
passivation
strategy
provides
sustainable
solution
to
stability
environmental
for
commercialization
cells.
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.
The Journal of Physical Chemistry Letters,
Год журнала:
2025,
Номер
unknown, С. 1261 - 1266
Опубликована: Янв. 26, 2025
Lead-free
tin
halide
perovskite
solar
cells
(TPSCs)
have
recently
made
significant
progress
in
power
conversion
efficiency
(PCE).
However,
the
presence
of
mismatched
energy
levels
and
weak
interlayer
interactions
between
electron
transport
materials
(ETMs)
perovskites
has
limited
achievable
PCE.
Here,
a
new
fluorinated
fullerene
derivative,
C60-FTPA
(F12),
was
designed
synthesized
to
construct
binary
ETM
with
C60-ETPA
(F6)
reported
our
group,
resulting
reduction
defects
improved
molecular
structure
ordering.
Furthermore,
exhibited
stronger
interaction
delivered
PCE
up
11.93%.
Narrow
bandgap
mixed
tin-lead
perovskite
solar
cells
(PSCs)
have
garnered
substantial
research
interest
owing
to
their
remarkable
optoelectronic
properties.
However,
non-radiative
recombination
and
carrier
transport
losses
at
the
interface
between
layer
charge
(C60)
significantly
reduce
overall
efficiency
of
PSCs.
To
address
this
challenge,
9-Fluorenylmethyl
carbazate
(9FC)
is
incorporated
C60.
The
hydrazide
group
present
in
9FC
effectively
mitigates
oxidation
Sn2+.
Furthermore,
can
engage
chemical
bonding
with
perovskite,
while
outward-facing
aromatic
rings
create
effective
π-π
interactions
C60,
thereby
promoting
enhanced
interfacial
transfer.
highest-performing
PSCs
achieve
a
power
conversion
(PCE)
23.97%,
accompanied
by
an
impressive
open-circuit
voltage
0.91
V.
Additionally,
these
facilitate
development
highly
efficient
two-terminal
four-terminal
all-perovskite
tandem
cells,
which
demonstrate
efficiencies
27.01%
28.07%,
respectively.
Although
C
60
is
usually
the
electron
transport
layer
(ETL)
in
inverted
perovskite
solar
cells,
its
molecular
nature
of
leads
to
weak
interfaces
that
lead
non-ideal
interfacial
electronic
and
mechanical
degradation.
Here,
we
synthesized
an
ionic
salt
from
,
4-(1',5′-dihydro-1'-methyl-2'
H
-[5,6]
fullereno-C
-
I
h
-[1,9-c]pyrrol-2'-yl)
phenylmethanaminium
chloride
(CPMAC),
used
it
as
shuttle
PSCs.
The
CH
2
-NH
3
+
head
group
CPMA
cation
improved
ETL
interface
enhanced
packing,
leading
~3-fold
increase
toughness
compared
.
Using
CPMAC,
obtained
~26%
power
conversion
efficiencies
(PCEs)
with
~2%
degradation
after
2,100
hours
1-sun
operation
at
65°C.
For
minimodules
(four
subcells,
6
centimeters
square),
achieved
PCE
~23%
<9%
2,200
55°C.
Angewandte Chemie,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 17, 2024
Abstract
A
stable
and
compact
fullerene
electron
transport
layer
(ETL)
is
crucial
for
high‐performance
inverted
perovskite
solar
cells
(PSCs).
However,
traditional
fullerene‐based
ETLs
like
C
60
PCBM
are
prone
to
aggregate
under
operational
conditions,
a
challenge
recently
recognized
by
academic
industrial
researchers.
Here,
we
designed
synthesized
novel
cross‐linkable
molecule,
bis((3‐methyloxetan‐3‐yl)methyl)
malonate‐C
monoadduct
(BCM),
use
as
an
ETL
in
PSCs.
Upon
low‐temperature
annealing
at
100
°C,
BCM
undergoes
situ
cross‐linking
form
robust
cross‐linked
(CBCM)
film,
which
demonstrates
excellent
mobility
suitable
band
structure
efficient
Our
results
show
that
PSCs
incorporating
CBCM‐based
achieve
impressive
efficiency
of
25.89
%
(certified:
25.36
%),
significantly
surpassing
the
23.25
PCBM‐based
devices.
The
intramolecular
covalent
interactions
within
CBCM
films
effectively
prevent
aggregation
enhance
film
compactness,
creating
internal
encapsulation
mitigates
decomposition
ion
migration
components.
Consequently,
exceptional
stability,
maintaining
97.8
their
initial
after
1000
hours
maximum
power
point
tracking,
compared
only
78.6
retention
devices
less
than
820
hours.