Bulk Passivation of Perovskite Films With Phthalocyanine Derivative for Enhanced Perovskite Solar Cells Efficiency and Stability
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 10, 2025
Abstract
Perovskite
solar
cells
(PSCs)
have
emerged
as
a
promising
candidate
for
low‐cost
and
high‐efficiency
photovoltaic
solutions,
poised
to
rival
conventional
technologies.
Despite
their
potential,
the
path
commercialization
is
impeded
by
significant
defect
state
density
present
within
films.
In
this
work,
phthalocyanine
derivative,
tetra‐2‐(benzyloxy)ethoxy
substituted
Zn(II)
(BE‐ZnPc),
characterized
multiple
binding
sites,
introduced
into
perovskite
precursor
solution.
This
innovative
approach
designed
modulate
crystallization
process
of
passivate
defects
through
strategic
doping
mechanism.
The
BE‐ZnPc
molecule,
with
its
planar
macrocyclic
structure
electron‐donating
attributes,
engages
effectively
undercoordinated
Pb
2+
ions,
thereby
diminishing
enhancing
overall
film
quality.
resultant
PSCs,
optimized
BE‐ZnPc,
achieved
power
conversion
efficiencies
(PCE)
high
26%
(with
certified
PCE
26.05%),
marking
milestone
in
PSC
performance.
Moreover,
these
devices
maintain
an
impressive
92%
initial
following
550
h
operation
at
maximum
point.
study
delineates
novel
strategy
bolstering
both
efficiency
durability
PSCs
utilization
functional
phthalocyanines,
charting
new
course
advancement
technology.
Language: Английский
Achieving 32% Efficiency in Perovskite/Silicon Tandem Solar Cells with Bidentate‐Anchored Superwetting Self‐Assembled Molecular Layers
Chi Li,
No information about this author
Yong Chen,
No information about this author
Yuheng Li
No information about this author
et al.
Angewandte Chemie International Edition,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 2, 2025
The
inhomogeneity
of
hole-selective
self-assembled
molecular
layers
(SAMLs)
often
arises
from
the
insufficient
bonding
between
anchors
and
metal
oxide,
particularly
on
textured
silicon
surfaces
when
fabricating
monolithic
perovskite/silicon
tandem
solar
cells
(P/S-TSCs)
hydrophobic
carbazole
complicates
fabrication
high-quality
perovskite
films.
To
address
this,
we
developed
a
novel
bidentate-anchored
superwetting
aromatic
SAM
based
an
upside-down
core
as
layer
(HSL),
denoted
((9H-carbazole-3,6-diyl)bis(4,1-phenylene))bis(phosphonic
acid)
(2PhPA-CzH).
bisphosphonate-anchored
exhibited
enhanced
adsorption
capabilities
efficient
hole
extraction/transport,
reversely
substituted
ring
contributed
friendly
super
wetting
underlayer
that
enabled
films
with
minimized
energetic
mismatches,
which
2PhPA-CzH
played
pivotal
role
in
dual
interfacial
energy
regulation.
Through
these
advancements,
optimized
wide-bandgap
(1.68
eV)
PSCs
demonstrated
improved
PCE
22.83%
excellent
stability
T90
exceeding
1000
h
under
damp-heat
conditions
(ISOS-D-3,
85%
RH,
85
°C),
representing
one
best
performances
for
SAMs
HSL-based
PSCs.
Notably,
2PhPA-CzH-functionalized
recombination
extended
to
submicron-pyramid
texture
SHJ
fabricate
P/S-TSCs,
achieving
impressive
efficiency
32.19%
at
active
area
1
cm2
(certified
31.54%)
while
maintaining
photostability.
This
work
offers
guidance
designing
multidentate-anchored
realize
record
P/S-TSCs.
Language: Английский
Achieving 32% Efficiency in Perovskite/Silicon Tandem Solar Cells with Bidentate‐Anchored Superwetting Self‐Assembled Molecular Layers
Chi Li,
No information about this author
Yong Chen,
No information about this author
Yuheng Li
No information about this author
et al.
Angewandte Chemie,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 2, 2025
Abstract
The
inhomogeneity
of
hole‐selective
self‐assembled
molecular
layers
(SAMLs)
often
arises
from
the
insufficient
bonding
between
anchors
and
metal
oxide,
particularly
on
textured
silicon
surfaces
when
fabricating
monolithic
perovskite/silicon
tandem
solar
cells
(P/S‐TSCs)
hydrophobic
carbazole
complicates
fabrication
high‐quality
perovskite
films.
To
address
this,
we
developed
a
novel
bidentate‐anchored
superwetting
aromatic
SAM
based
an
upside‐down
core
as
layer
(HSL),
denoted
((9H‐carbazole‐3,6‐diyl)bis(4,1‐phenylene))bis(phosphonic
acid)
(2PhPA‐CzH).
bisphosphonate‐anchored
exhibited
enhanced
adsorption
capabilities
efficient
hole
extraction/transport,
reversely
substituted
ring
contributed
friendly
super
wetting
underlayer
that
enabled
films
with
minimized
energetic
mismatches,
which
2PhPA‐CzH
played
pivotal
role
in
dual
interfacial
energy
regulation.
Through
these
advancements,
optimized
wide‐bandgap
(1.68
eV)
PSCs
demonstrated
improved
PCE
22.83%
excellent
stability
T
90
exceeding
1000
h
under
damp‐heat
conditions
(ISOS‐D‐3,
85%
RH,
85
°C),
representing
one
best
performances
for
SAMs
HSL‐based
PSCs.
Notably,
2PhPA‐CzH‐functionalized
recombination
extended
to
submicron‐pyramid
texture
SHJ
fabricate
P/S‐TSCs,
achieving
impressive
efficiency
32.19%
at
active
area
1
cm
2
(certified
31.54%)
while
maintaining
photostability.
This
work
offers
guidance
designing
multidentate‐anchored
realize
record
P/S‐TSCs.
Language: Английский
Improving the Stability of Wide Bandgap Perovskites: Mechanisms, Strategies, and Applications in Tandem Solar Cells
Wenye Jiang,
No information about this author
Yuemin Zhu,
No information about this author
Jin Liu
No information about this author
et al.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 7, 2025
Abstract
Tandem
solar
cells
(TSCs)
based
on
wide
bandgap
(WBG)
perovskites
have
gained
significant
attention
for
their
higher
power
conversion
efficiency
(PCE)
compared
to
single‐junction
cells.
The
role
of
WBG
perovskite
(PSCs)
as
the
sub‐cell
in
tandem
consists
absorbing
high‐energy
photons
and
producing
open‐circuit
voltages
(
V
OC
).
However,
PSCs
face
serious
phase
separation
issues,
resulting
poor
long‐term
stability
substantial
loss
TSCs.
In
response,
researchers
developed
a
range
strategies
mitigate
these
challenges,
showing
promising
progress,
comprehensive
review
is
expected.
this
review,
we
discuss
mechanism
organic–inorganic
hybrids
all‐inorganic
perovskites.
Additionally,
conduct
an
in‐depth
investigation
various
enhance
stability,
including
component
engineering,
additive
interface
dimension
control,
solvent
encapsulation.
Furthermore,
application
TSCs
summarized
detail.
Finally,
perspectives
are
provided
offer
guidance
development
efficient
stable
field
Language: Английский
Heterogeneous Amine with Polycyclic‐Aromatics‐Modified Hole Transport Material for Efficient and Operationally Durable Perovskite Solar Cells
Yang Luo,
No information about this author
Tianyu Li,
No information about this author
Lifei He
No information about this author
et al.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 10, 2024
Abstract
Achieving
efficient
perovskite
solar
cells
(PSCs)
with
high
operational
durability
is
a
challenging
task.
Here,
by
exploiting
the
heterogeneous
amine
strategy
at
molecular
level,
novel
spirobifluorene
derivative
bearing
methoxynaphthalene
and
9,9‐dimethylfluorene
peripheral
groups
(
N
2
,
2′
7
7′
‐tetrakis(9,9‐dimethyl‐9
H
‐fluoren‐2‐yl)‐
‐tetrakis(6‐methoxynaphthalen‐2‐yl)‐9,9′‐spirobi[fluorene]‐2,2′,7,7′‐tetraamine,
denoted
as
Spiro‐NADF)
hole
transport
material
(HTM)
developed
to
address
efficiency
issues
of
PSCs.
Compared
2,2′,7,7′‐tetrakis(
‐di‐
p
‐methoxyphenyl)‐amine‐9,9′‐spirobifluorene,
Spiro‐NADF
exhibits
not
only
favorable
energy
level
alignment
but
also
higher
glass
transition
temperature
strong
adhesion
perovskite.
Moreover,
Spiro‐NADF‐based
layer
shows
excellent
morphological
stability
in
devices
against
damp
heat
stress.
These
advantages
reduce
voltage
loss
suppress
decomposition
ion
migration.
Consequently,
PSCs
based
on
exhibit
champion
24.66%
an
open‐circuit
1.19
V.
The
corresponding
show
greatly
enhanced
harsh
environments,
retaining
over
92%
initial
efficiencies
for
500
h
aging
under
test
(85
°C
70–90%
relative
humidity)
illumination
maximum
power
point
tracking,
respectively.
This
work
demonstrates
that
engineering
HTMs
using
amines
polycyclic
aromatics
leaves
considerable
room
developing
stable
Language: Английский