Advanced Functional Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 11, 2024
Abstract
All‐perovskite
tandem
solar
cells
(TSCs)
hold
a
great
promise
to
break
the
Shockley‐Queisser
(S‐Q)
efficiency
limit
of
single‐junction
cells.
However,
inferior
performance
tin‐lead
(Sn–Pb)
mixed
perovskites
based
narrow‐bandgap
bottom
subcells
largely
limits
development
all‐perovskite
TSCs
due
serious
defects
assisted
non‐radiative
charge
recombination
loss,
especially
at
perovskite/electron
transport
layer
(ETL)
interface.
Herein,
dual‐source
defect
managing
strategy
is
demonstrated
modify
top
surface
Sn–Pb
perovskites.
Specifically,
ethylenediammonium
diiodide
(EDAI
2
)
and
(3‐mercaptopropyl)
trimethoxysilane
(MPTS)
are
simultaneously
introduced
passivate
organic
cations
metal
related
defects,
respectively.
The
strong
interactions
between
passivators
perovskite
result
in
effectively
reduced
carrier
recombination,
obviously
suppressed
Sn
2+
oxidation
accelerated
transportation
perovskite/ETL
Ultimately,
champion
22.7%
for
an
impressive
28.26%
achieved
on
strategy.
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. 2, 2025
Self-assembled
monolayers
(SAMs)
have
displayed
unpredictable
potential
in
efficient
perovskite
solar
cells
(PSCs).
Yet
most
of
SAMs
are
largely
suitable
for
pure
Pb-based
devices,
precisely
developing
promising
hole-selective
contacts
(HSCs)
Sn-based
PSCs
and
exploring
the
underlying
general
mechanism
fundamentally
desired.
Here,
based
on
prototypical
donor-acceptor
SAM
MPA-BT-BA
(BT),
oligoether
side
chains
with
different
length
(i.e.,
methoxy,
2-methoxyethoxy,
2-(2-methoxyethoxy)ethoxy
group)
were
custom-introduced
benzothiadiazole
unit
to
produce
target
acronyms
MPA-MBT-BA
(MBT),
MPA-EBT-BA
(EBT),
MPA-MEBT-BA
(MEBT),
respectively,
acting
as
HSCs
Sn-Pb
all-perovskite
tandems.
The
introduction
enables
effectively
accelerate
hole
extraction,
regulate
crystal
growth
passivate
surface
defects
perovskites.
In
particular,
benefiting
from
enhanced
film
quality
suppressed
interfacial
non-radiative
recombination
losses,
EBT-tailored
LBG
devices
yield
a
champion
efficiency
23.54%,
enabling
28.61%
monolithic
tandems
an
impressive
VOC
2.155
V
excellent
operational
stability
well
28.22%-efficiency
4-T
development
is
highly
desirable.
authors
report
self-assembled
achieve
operationally
stable
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 7, 2025
Abstract
Defective
perovskite
surfaces
severely
limit
the
development
of
inverted
solar
cells
(PSCs).
Here,
impacts
surface
treatment
are
systematically
investigated
with
organic
ammonium
salts,
namely
piperidinium
iodide
(PpI)
and
piperazinedihydroiodide
(PDI),
on
performance
formamidinium‐cesium
(FACs)‐based
PSCs.
These
results
indicate
that
PpI,
its
high
dipole
moment,
tends
to
form
1D
structures
surface,
which
hinders
electron
transport.
By
contrast,
PDI
post‐treatment
does
not
lead
formation
such
structures;
instead,
it
forms
a
thin
passivation
layer
homogenizes
electric
potential
across
surface.
This
merit
in
favorable
alignment
energy
levels
significant
reduction
non‐radiative
recombination
at
perovskite/electron
transport
interface.
As
result,
module
(PSM)
achieved
power
conversion
efficiency
(PCE)
22.08%
an
aperture
area
11.1
cm
2
(certified
21.58%),
showing
low‐efficiency
discrepancy
versus
small‐area
counterpart
25.09%.
Notably,
PSM
can
maintain
92.5%
initial
PCE
after
continuous
1000
h
1‐sun
operation
65
°C
ambient
air.
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 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%.
Nature Communications,
Год журнала:
2025,
Номер
16(1)
Опубликована: Март 28, 2025
The
employment
of
self-assembled
molecular
hybrid
could
improve
buried
interface
in
perovskite
solar
cells
(PSCs).
However,
the
interplay
among
monolayers
(SAMs)
during
deposition
process
has
not
been
well-studied.
Herein,
we
study
interaction
between
co-adsorbents
and
commonly
used
SAM
material,
[4-(3,6-dimethyl-9H-carbazol-9-yl)butyl]phosphonic
acid
(Me-4PACz)
for
wide-bandgap
(WBG)
PSCs.
It
is
found
that
co-adsorbent,
6-aminohexane-1-sulfonic
(SA)
tends
to
fill
uncovered
sites
without
interference
with
Me-4PACz,
ensuring
formation
a
dense
hole
selective
layer.
Moreover,
use
SA/Me-4PACz
mixed
SAMs
effectively
reduce
interfacial
non-radiative
recombination
loss,
optimize
energy
alignment
at
regulate
crystallization
WBG
perovskite.
As
result,
1.77
eV
PSCs
deliver
power
conversion
efficiency
(PCE)
20.67%
(20.21%
certified)
an
impressive
open-circuit
voltage
(VOC)
1.332
V
(1.313
certified).
By
combining
1.26
narrow-bandgap
(NBG)
PSC,
further
fabricate
2-terminal
all-perovskite
tandem
(TSCs)
PCE
28.94%
(28.78%
0.087
cm2
23.92%
mini-module
aperture
area
11.3
cm2.
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.
ACS Photonics,
Год журнала:
2024,
Номер
11(11), С. 4916 - 4922
Опубликована: Окт. 25, 2024
The
buried
interface
is
pivotal
for
enhancing
both
the
efficiency
and
stability
of
p-i-n
perovskite
solar
cells
(PSCs).
This
because
carrier
extraction
recombination
processes
can
be
significantly
affected
by
defects
that
tend
to
form
on
bottom
side.
Herein,
a
dual-reaction
site
molecule
homopiperazine-1,4-bis
(2-ethanesulfonic
acid)
(HEA)
employed
as
an
effective
multifunctional
passivator
self-assembled
monolayer
(SAM)/perovskite
inverted
PSCs.
HEA
has
two
sulfonic
acid
groups
with
double
action
sites,
which
effectively
fill
ITO
vacancies
unanchored
SAM
simultaneously
passivate
uncoordinated
Pb2+
molecular
bridge,
achieving
full
coverage
substrate
orderly
crystallization
perovskites.
resultant
device
presented
satisfactory
efficiencies
25.71%
(0.0982
cm2)
24.26%
(1
cm2).
Our
retained
91.8%
its
initial
power
conversion
(PCE)
after
1000
h
operation
under
1-sun
illumination
in
nitrogen
atmosphere.
research
offers
important
insights
into
further
refinement
enhancement
interfaces
Abstract
To
approach
the
Shockley‐Queisser
(S‐Q)
limit
in
perovskite
solar
cells
(PSCs),
enhancing
fill
factor
(FF),
a
crucial
parameter
associated
with
carrier
transport
and
nonradiative
recombination,
is
of
paramount
importance.
In
this
paper,
rare
earths
(RE),
neodymium
salt
used
as
dopant
4‐(3‐,6‐dimethoxy‐9h‐carbazol‐9‐butyl)
phosphonic
acid
(MeO‐4PACz)
to
obtain
MeO‐4PACz:Nd
3+
,
Nd
migration
induced
during
annealing.
It
worth
noting
that
uniform
diffusion
layer
significantly
increases
defect‐formation
energy
perovskite,
thus
reducing
density
defect
states,
greatly
improving
rate
inhibited
non‐radiative
recombination.
The
experimental
results
show
wide‐band
gap
(WBG)
PSCs
based
on
has
an
excellent
power
conversion
efficiency
(PCE)
22.82%
FF
86.35%.
proposed
method
provides
direct
for
RE
promote
perovskites.