Advanced Functional Materials,
Journal Year:
2022,
Volume and Issue:
32(29)
Published: April 24, 2022
Abstract
Mixed‐halide
perovskite
has
an
irreplaceable
role
as
wide‐bandgap
absorber
in
multi‐junction
tandem
solar
cells.
However,
large
open‐circuit
voltage
(
V
oc
)
loss
due
to
non‐uniform
halide
distribution
and
compromised
device
stability
photo‐induced
segregation
significantly
limited
the
applications.
Here,
it
is
introduced
4‐(2‐aminoethyl)‐benzenesulfonyl
fluoride
hydrochloride
(ABF)
with
multifunctional
groups
(sulfonyl,
ammonium,
fluoride)
mixed‐halide
precursor
demonstrate
a
downward
homogenized
crystallization
strategy
for
suppressing
initial
vertical
phase
separation
during
reducing
loss.
Furthermore,
strong
electronegativity
effectively
fixes
anions
cations,
while
sulfonyl
ammonium
are
used
passivate
positive
charged
(halide
vacancies)
negative
(FA/MA
defects,
respectively,
thereby
generation
of
ion
vacancies
that
lead
subsequent
segregation.
As
result,
1.63
1.68
eV
cells
inverted
structures
exhibit
champion
power
conversion
efficiency
(PCE)
21.76%
20.11%
1.18
1.21
V,
respectively.
Most
importantly,
optimized
devices
without
encapsulation
preserve
86%
after
240
h
continuous
illumination
under
AM
1.5G,
showing
excellent
light
stability.
Thus,
provides
highly
efficient
performance
future
cell
eScience,
Journal Year:
2022,
Volume and Issue:
2(3), P. 339 - 346
Published: April 19, 2022
Potentially
temperature-resistant
inorganic
perovskite/silicon
tandem
solar
cells
(TSCs)
are
promising
devices
for
boosting
efficiency
past
the
single-junction
silicon
limit.
However,
undesirable
non-radiative
recombination
generally
leads
to
a
significant
voltage
deficit.
Here,
we
introduce
an
effective
strategy
using
nickel
iodide,
halide
salt,
passivate
iodine
vacancies
and
suppress
recombination.
NiI2-treated
CsPbI3-xBrx
perovskite
with
1.80
eV
bandgap
exhibited
of
19.53%
1.36
V,
corresponding
deficit
0.44
V.
Importantly,
treated
device
demonstrated
excellent
operational
stability,
maintaining
95.7%
its
initial
after
maximum
power
point
tracking
300
h
under
continuous
illumination
in
N2
atmosphere.
By
combining
this
top
cell
narrower
bottom
cell,
first
time
achieved
monolithic
TSCs,
which
22.95%
open-circuit
2.04
This
work
provides
passivation
materials
achieve
efficient
stable
cells.
ACS Energy Letters,
Journal Year:
2021,
Volume and Issue:
6(2), P. 827 - 836
Published: Feb. 3, 2021
Vacuum
deposition
methods
are
increasingly
applied
to
the
preparation
of
perovskite
films
and
devices,
in
view
possibility
prepare
multilayer
structures
at
low
temperature.
Vacuum-deposited,
wide-bandgap
solar
cells
based
on
mixed-cation
mixed-anion
perovskites
have
been
scarcely
reported,
due
challenges
associated
with
multiple-source
processing
thin
films.
In
this
work,
we
describe
a
four-source
vacuum
process
type
FA1–nCsnPb(I1–xBrx)3
tunable
bandgap
controlled
morphology,
using
FAI,
CsI,
PbI2,
PbBr2
as
precursors.
The
simultaneous
sublimation
PbI2
allows
relative
Br/Cs
content
be
decoupled
controlled,
resulting
homogeneous
1.7–1.8
eV
range
no
detectable
halide
segregation.
Solar
1.75
show
efficiency
up
16.8%
promising
stability,
maintaining
90%
initial
after
2
weeks
operation.
Advanced Energy Materials,
Journal Year:
2021,
Volume and Issue:
12(4)
Published: May 14, 2021
Abstract
In
recent
years,
perovskite/silicon
tandem
solar
cells
(PK/c‐Si
tandem)
have
demonstrated
high
power
conversion
efficiency
(PCE)
and
great
application
potential
in
photovoltaic
(PV)
systems.
However,
the
PCE
of
PK/c‐Si
devices
is
still
below
theoretical
limit.
From
a
broader
perspective,
their
poor
stability
difficulty
large‐area
realization
are
crucial
barriers
for
commercial
viability.
this
report,
detailed
constraints
facing
corresponding
solutions
discussed.
The
authors
propose
that
main
obstacle
comes
from
limitation
perovskite
top
cell.
careful
understanding
optical
electrical
properties
each
functional
layer
expected
to
be
core
process
further
promote
efficiency.
Regarding
environmental
intrinsic
instability
issues,
encapsulation
considered
most
effective
method
address
instability.
Preventing
ion
migration
one
fundamental
methods
eliminate
It
believed
low
dimensional
materials
will
become
competitive
solution
simultaneously
solve
these
two
instabilities.
Finally,
some
suggestions
reducing
costs
preparation
on
large‐scale
also
discussed
which
provides
guidance
boosting
development
tandem.
Chemical Reviews,
Journal Year:
2023,
Volume and Issue:
123(15), P. 9565 - 9652
Published: July 10, 2023
Three-dimensional
(3D)
organic-inorganic
lead
halide
perovskites
have
emerged
in
the
past
few
years
as
a
promising
material
for
low-cost,
high-efficiency
optoelectronic
devices.
Spurred
by
this
recent
interest,
several
subclasses
of
such
two-dimensional
(2D)
begun
to
play
significant
role
advancing
fundamental
understanding
structural,
chemical,
and
physical
properties
perovskites,
which
are
technologically
relevant.
While
chemistry
these
2D
materials
is
similar
that
3D
their
layered
structure
with
hybrid
interface
induces
new
emergent
can
significantly
or
sometimes
subtly
be
important.
Synergistic
realized
systems
combine
different
exhibiting
dimensionalities
exploiting
intrinsic
compatibility.
In
many
cases,
weaknesses
each
alleviated
heteroarchitectures.
For
example,
3D-2D
demonstrate
novel
behavior
neither
would
capable
separately.
This
review
describes
how
structural
differences
between
give
rise
disparate
properties,
discusses
strategies
realizing
mixed-dimensional
various
architectures
through
solution-processing
techniques,
presents
comprehensive
outlook
use
solar
cells.
Finally,
we
investigate
applications
beyond
photovoltaics
offer
our
perspective
on
perovskite
semiconductor
unrivaled
tunability,
efficiency,
relevant
durability.
Advanced Functional Materials,
Journal Year:
2022,
Volume and Issue:
32(29)
Published: April 24, 2022
Abstract
Mixed‐halide
perovskite
has
an
irreplaceable
role
as
wide‐bandgap
absorber
in
multi‐junction
tandem
solar
cells.
However,
large
open‐circuit
voltage
(
V
oc
)
loss
due
to
non‐uniform
halide
distribution
and
compromised
device
stability
photo‐induced
segregation
significantly
limited
the
applications.
Here,
it
is
introduced
4‐(2‐aminoethyl)‐benzenesulfonyl
fluoride
hydrochloride
(ABF)
with
multifunctional
groups
(sulfonyl,
ammonium,
fluoride)
mixed‐halide
precursor
demonstrate
a
downward
homogenized
crystallization
strategy
for
suppressing
initial
vertical
phase
separation
during
reducing
loss.
Furthermore,
strong
electronegativity
effectively
fixes
anions
cations,
while
sulfonyl
ammonium
are
used
passivate
positive
charged
(halide
vacancies)
negative
(FA/MA
defects,
respectively,
thereby
generation
of
ion
vacancies
that
lead
subsequent
segregation.
As
result,
1.63
1.68
eV
cells
inverted
structures
exhibit
champion
power
conversion
efficiency
(PCE)
21.76%
20.11%
1.18
1.21
V,
respectively.
Most
importantly,
optimized
devices
without
encapsulation
preserve
86%
after
240
h
continuous
illumination
under
AM
1.5G,
showing
excellent
light
stability.
Thus,
provides
highly
efficient
performance
future
cell