Optimizing Buried Interface Quality in Inverted Perovskite Solar Cells by Modulating the Spatial Orientation of Polymer Hole Transport Materials Using Rigid copolymer Units
Dyes and Pigments,
Год журнала:
2025,
Номер
unknown, С. 112676 - 112676
Опубликована: Янв. 1, 2025
Язык: Английский
Organic Molecule Vapor‐Assisted Passivation for Efficient and Stable Perovskite Solar Cells
Advanced Energy Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 26, 2025
Abstract
Effective
suppression
of
non‐radiative
recombination
caused
by
surface
defects
in
perovskite
is
crucial
for
achieving
high‐efficiency
solar
cells
(PSCs).
However,
conventional
passivators
such
as
organic
amine
salts
are
prone
to
deprotonation
amines
and
rapid
reaction
with
formamidine,
leading
device
degradation.
Meanwhile,
the
solvent
processing
can
also
decompose
layer
due
dissolution
salts.
In
this
work,
an
small
molecule,
2‐Thiophenacetamide
(TAM),
features
multiple
active
sites
presented.
TAM
demonstrates
ability
passivate
thin
films
through
sublimation
deposition.
It
demonstrated
that
solvent‐free
method
effect
thiophene
carbonyl
group
efficiently
uncoordinated
Pb
2+
,
while
amino
aids
stabilizing
structures
forming
hydrogen
bonds
iodide
ions.
As
a
result,
vapor
treatment
enhanced
efficiency
25.33%,
operational
stability
maintained
at
95%
original
after
continuous
operation
over
1000
h.
Additionally,
submodules
area
14
cm
2
successfully
assembled
up
22.17%.
Язык: Английский
Nucleation Engineering to Strengthen Interface Contacts in Single‐Crystal Perovskite Photovoltaics
Angewandte Chemie International Edition,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 5, 2025
Perovskite
solar
cells
(PSCs)
based
on
single
crystals
hold
potential
for
higher
efficiency
and
stability,
while
the
incomplete
interface
contact
hinders
hole
carrier
extraction
device
performance.
Herein,
we
report
strengthening
crystal/substrate
by
nucleation
engineering
in
situ
growth
strategy.
Through
modulating
transport
layer
(HTL)
to
induce
process
at
substrate
surface,
residual
solution,
voids,
small-sized
are
eliminated,
thus
ensuring
intimate
physically.
Combining
with
strong
interaction
between
perovskites
HTL,
balanced
electron/hole
suppressed
nonradiative
recombination
achieved.
As
a
result,
an
impressive
power
conversion
(PCE)
of
25.8
%
is
obtained,
setting
new
benchmark
single-crystal
PSCs.
Moreover,
thermal-induced
peeling-off
from
substrates
mitigated,
which
improves
thermal
stability
distinctly.
Язык: Английский
Nucleation Engineering to Strengthen Interface Contacts in Single‐Crystal Perovskite Photovoltaics
Angewandte Chemie,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 5, 2025
Abstract
Perovskite
solar
cells
(PSCs)
based
on
single
crystals
hold
potential
for
higher
efficiency
and
stability,
while
the
incomplete
interface
contact
hinders
hole
carrier
extraction
device
performance.
Herein,
we
report
strengthening
crystal/substrate
by
nucleation
engineering
in
situ
growth
strategy.
Through
modulating
transport
layer
(HTL)
to
induce
process
at
substrate
surface,
residual
solution,
voids,
small‐sized
are
eliminated,
thus
ensuring
intimate
physically.
Combining
with
strong
interaction
between
perovskites
HTL,
balanced
electron/hole
suppressed
nonradiative
recombination
achieved.
As
a
result,
an
impressive
power
conversion
(PCE)
of
25.8
%
is
obtained,
setting
new
benchmark
single‐crystal
PSCs.
Moreover,
thermal‐induced
peeling‐off
from
substrates
mitigated,
which
improves
thermal
stability
distinctly.
Язык: Английский
Minireview and Outlook of Carbazole and Phenothiazine-Modified Triphenylamines as Hole Transporting Materials for Enhancing Perovskite Solar Cells
Rachel Chetri,
T.N. Ahipa
Energy & Fuels,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 13, 2025
Язык: Английский
Halogenated Chiral Organic Spacer Cation Regulation for Efficient and Stable 2D Ruddlesden‐Popper Perovskite Solar Cells
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 20, 2025
Abstract
2D
Ruddlesden‐Popper
(2DRP)
perovskites
have
emerged
as
promising
candidates
for
next‐generation
photovoltaic
devices
owing
to
their
excellent
environmental
stability,
moisture
resistance,
and
photo‐stability.
However,
power
conversion
efficiencies
(PCEs)
still
lag
behind
those
of
3D
counterparts,
primarily
due
the
poor
charge‐carrier
transport
associated
with
insulating
bulky
organic
spacer
cations.
In
this
work,
a
series
halogenated
chiral
spacers–
S
‐
α
‐fluorophenylethylamine
acrylate
(
‐α‐FPEAAA),
‐α‐chlorophenylethylamine
‐α‐ClPEAAA),
S‐α‐bromophenylethylamine
‐α‐BrPEAAA)–are
employed
regulate
charge
within
2DRP
framework.
Incorporating
halogen
atoms
facilitates
halogen–halogen
interactions
between
spacers
PbI
6
4−
octahedral
framework,
thereby
enhancing
structural
ordering
electronic
coupling.
Among
these,
‐α‐BrPEAAA‐based
exhibit
superior
film
morphology,
improved
crystallinity,
an
exceptional
carrier
lifetime
3.353
µs.
Notably,
inverted
perovskite
solar
cell
based
on
‐α‐BrPEAAA
achieves
high
PCE
20.30%,
rivaling
best‐performing
systems
reported
recently.
Moreover,
device
demonstrates
long‐term
retaining
over
95%
initial
efficiency
after
2000
h
storage
under
nitrogen
atmosphere.
These
findings
highlight
potential
in
advancing
high‐performance
stable
photovoltaics.
Язык: Английский