Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate)
(PEDOT:PSS)
has
been
widely
used
as
a
hole
transporting
layer
(HTL)
in
two-dimensional
(2D)
Ruddlesden-Popper
perovskite
(RPP)-based
solar
cells
(2D-PSCs)
due
to
its
simple
preparation
process
and
low
cost.
However,
the
devices
based
on
PEDOT:PSS
exhibit
efficiency
poor
stability
number
of
buried
interfacial
defects,
energy
level
mismatching,
corrosivity
HTL.
In
this
study,
guanidinium
iodide
(GAI)-modified
HTL
was
adopted
tune
crystallization
2D
RPPs,
leading
formation
films
with
preferential
crystal
orientation,
improved
crystallinity,
suppressed
defect
density.
The
addition
GAI
not
only
enhances
conductivity
intrinsic
layers
but
also
improves
their
matching
those
films.
Upon
doping
into
PEDOT:PSS,
power
conversion
2D-PSCs
increased
from
13.11%
16.04%
maintained
80%
initial
value
under
65%
relative
humidity
condition
for
60
days.
This
work
demonstrates
novel
synergetic
modification
strategy
gives
new
insight
underlying
mechanism,
which
should
lead
further
improvements
performance
other
optoelectronic
RPPs.
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
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 Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 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.
ACS Applied Electronic Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 17, 2025
Tin–lead
(Sn–Pb)
mixed
perovskites
have
emerged
as
promising
light-absorbing
materials
for
single-junction
and
all-perovskite
tandem
solar
cells
due
to
their
favorable
narrow
bandgaps
high
theoretical
power
conversion
efficiencies.
However,
the
easy
oxidation
of
Sn2+
Sn4+
results
in
formation
rampant
defects
during
fast
crystallization
Sn–Pb
perovskite
thin
films
remarkable
photovoltaic
performance
decay
under
operation,
impeding
practical
applications.
Herein,
this
spotlight
presents
intrinsic
origins
instability
summarizes
recent
advances
antioxidation
strategies
regarding
raw
material
purification,
additive
engineering,
composition
interfacial
engineering.
Then,
remaining
challenges
future
directions
are
discussed
inspire
more
rational
design
toward
efficient
durable
cells.
Advanced Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 16, 2024
Abstract
Hybrid
tin‐lead
(Sn‐Pb)
perovskites
have
garnered
increasing
attention
due
to
their
crucial
role
in
all‐perovskite
tandem
cells
for
surpassing
the
efficiency
limit
of
single‐junction
solar
cells.
However,
easy
oxidation
Sn
2+
and
fast
crystallization
Sn‐based
perovskite
present
significant
challenges
achieving
high‐quality
hybrid
Sn‐Pb
films,
thereby
limiting
device's
performance
stability.
Herein,
an
all‐in‐one
additive,
2‐amino‐3‐mercaptopropanoic
acid
hydrochloride
(AMPH)
is
proposed,
which
can
function
as
a
reducing
agent
suppress
formation
4+
throughout
film
preparation.
Furthermore,
strong
binding
between
AMPH
precursor
significantly
slows
down
process,
resulting
with
enhanced
crystallinity.
The
remaining
its
products
within
contribute
improves
resistance
substantial
reduction
defect
density,
specifically
vacancies.
Benefiting
from
multifunctionalities
AMPH,
power
conversion
(PCE)
23.07%
achieved
narrow‐bandgap
best‐performing
monolithic
cell
also
exhibits
PCE
28.73%
(certified
27.83%),
among
highest
reported
yet.
devices
retain
over
85%
initial
efficiencies
after
500
hours
continuous
operation
at
maximum
point
under
one‐sun
illumination.
Applied Physics Letters,
Год журнала:
2025,
Номер
126(10)
Опубликована: Март 1, 2025
Organic–inorganic
hybrid
perovskite
solar
cells
(PSCs)
have
shown
tremendous
promise
due
to
their
excellent
optoelectronic
properties
and
cost-efficient
fabrication.
However,
the
efficiency
of
traditional
lead
halide
PSCs
is
approaching
Shockley–Queisser
limit,
prompting
interest
in
tin-lead
(Eg
≈
1.25
eV)
as
a
candidate
for
tandem
configurations
with
potential
surpass
this
limit.
A
key
challenge
lies
optimizing
hole
transport
layer
(HTL),
widely
used
PEDOT:PSS
suffers
from
high
acidity
poor
crystallinity,
hindering
device
performance.
In
work,
we
formic
acid
modification
enhance
its
conductivity,
energy
band
alignment,
crystallinity.
Acid
treatment
promotes
proton
transfer,
reducing
insulating
PSS
chains
improving
phase
separation,
thereby
facilitating
efficient
transport.
Tin–lead
films
fabricated
on
acid-treated
(Fa-PEDOT:PSS)
exhibit
improved
larger
grain
size,
reduced
defect
density.
Devices
incorporating
Fa-PEDOT:PSS
demonstrate
enhanced
photovoltaic
performance,
achieving
power
conversion
(PCE)
21.87%
hysteresis
stability,
retaining
∼90%
initial
after
1600
h
an
inert
atmosphere.
These
findings
highlight
optimized
HTL
tin–lead
PSCs,
paving
way
high-efficiency,
environmentally
friendly
technologies.
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.
Hybrid
organic-inorganic
lead
halide
perovskite
solar
cells
(PSCs)
have
rapidly
emerged
as
a
promising
photovoltaic
technology,
with
record
efficiencies
surpassing
26%,
approaching
the
theoretical
Shockley-Queisser
limit.
The
advent
of
all-perovskite
tandem
(APTSCs),
integrating
Pb-based
wide-bandgap
(WBG)
mixed
Sn-Pb
narrow-bandgap
(NBG)
perovskites,
presents
compelling
pathway
to
surpass
this
Despite
recent
innovations
in
hole
transport
layers
(HTLs)
that
significantly
improved
efficiency
and
stability
lead-based
PSCs,
an
effective
HTL
tailored
for
NBG
PSCs
remains
unmet
need.
This
review
highlights
essential
role
HTLs
enhancing
performance
focusing
on
their
ability
mitigate
non-radiative
recombination
optimize
buried
interface,
thereby
improving
film
quality.
distinct
attributes
such
lower
energy
levels
accelerated
crystallization
rates,
necessitate
specialized
properties.
In
study,
latest
advancements
are
systematically
examined
encompassing
organic,
self-assembled
monolayer
(SAM),
inorganic
materials,
HTL-free
designs.
critically
assesses
inherent
limitations
each
category,
finally
proposes
strategies
surmount
these
obstacles
reach
higher
device
performance.