Advanced Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 1, 2025
Abstract
Interfacial
localized
charges
and
interfacial
losses
from
incompatible
underlayers
are
critical
factors
limiting
the
efficiency
improvement
market‐integration
of
perovskite
solar
cells
(PSCs).
Herein,
a
novel
chemical
tuning
strategy
is
proposed
involving
proton
transfer
between
amine
head
pyridoxamine
(PM)
phosphonic
acid
anchoring
group
[4‐(3,6‐dimethyl‐9H‐carbazol‐9‐yl)butyl]phosphonic
(Me‐4PACz),
with
simultaneous
enhancement
charge
delocalization
through
electrostatic
attraction
opposite
charged
molecules.
The
Me‐4PACz‐PM
polarization
interface
modulates
nickel
oxide
(NiO
x
)
states
coordination
environment
at
buried
interfaces,
consequently
enhancing
p‐type
conductivity
obtaining
more
compatible
band
arrangement.
high‐coverage
wettability
NiO
/Me‐4PACz‐PM
underlayer
also
facilitate
deposition
high‐quality
films,
releasing
lattice
strain
mitigating
trap‐assisted
non‐radiative
recombination.
Attributing
to
implementation
tunable
small‐area
devices
modules
an
aperture
area
69
cm
2
achieved
impressive
power
conversion
efficiencies
(PCEs)
26.34%
(certified
25.48%)
21.94%
20.50%),
respectively,
unencapsulated
maintained
their
initial
PCEs
≈90%
after
aging
for
2000
h
(ISOS‐L‐1)
1500
(ISOS‐D‐1).
broad
applicability
interfaces
successful
scaling
large‐area
provide
reference
expanding
PSCs
applications.
Energy & Environmental Science,
Год журнала:
2024,
Номер
17(17), С. 6157 - 6203
Опубликована: Янв. 1, 2024
HSSAMs
with
diverse
structures,
encompassing
various
anchoring
and
functional
groups,
were
systematically
categorized
their
multifaceted
roles
in
inverted
PSCs
TSCs
correlation
device
performance
investigated.
Angewandte Chemie International Edition,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 9, 2025
Abstract
Currently,
the
development
of
polymeric
hole‐transporting
materials
(HTMs)
lags
behind
that
small‐molecule
HTMs
in
inverted
perovskite
solar
cells
(PSCs).
A
critical
challenge
is
conventional
are
incapable
forming
ultra‐thin
and
conformal
coatings
like
self‐assembly
monolayers
(SAMs),
especially
for
substrates
with
rough
surface
morphology.
Herein,
we
address
this
by
designing
anchorable
(CP1
to
CP5).
Specifically,
coordinative
pyridyl
groups
introduced
as
side‐chains
on
poly‐triarylamine
(PTAA)
backbone
varied
contents
copolymerization
method,
resulting
chemical
interactions
between
substrates.
The
strong
interaction
allows
them
be
processed
into
ultra‐thin,
uniform,
robust
layers
through
employing
low‐concentration
solutions
(0.1
mg
mL
−1
,
vs.
2.0–5.0
PTAA),
greatly
decreasing
charge
transport
losses.
Moreover,
upon
systematically
tuning
substitution
ratio,
energy
levels,
wetting,
solution
processability,
defect
passivation
capability
such
simultaneously
optimized.
Based
optimal
CP4,
achieved
highly
efficient
PSCs
power
conversion
efficiencies
(PCEs)
up
26.21
%,
which
par
state‐of‐the‐art
SAM‐based
PSCs.
Furthermore,
these
devices
exhibit
enhanced
stabilities
under
repeated
current–voltage
scans
reverse
bias
ageing
compared
devices.
Abstract
[4‐(3,6‐dimethyl‐9H‐carbazol‐9‐yl)butyl]phosphonic
acid
(Me‐4PACz)
consistently
exhibits
inhomogeneous
distribution
on
the
substrate,
which
makes
it
a
challenge
for
growth
of
high‐quality
perovskite
film,
resulting
in
undesired
interfacial
losses
at
buried
interfaces.
Moreover,
flexible
alkyl
chains
Me‐4PACz
are
not
conducive
to
intermolecular
interactions
and
hinder
charge
flow.
Here,
novel
molecule
with
4‐Methoxy‐N‐(4‐methoxyphenyl)‐N‐phenylaniline
(TPA)
carbazole
backbone,
named
CzTPA
is
designed,
constituted
Co‐SAM
Me‐4PACz.
The
two
carboxyls
end
will
act
as
an
anchoring
group
cover
inadequate
coverage
NiO
x
.
methoxy
TPA
can
passivation
uncoordinated
Pb
2+
interface
by
interaction
Pb─O.
Additionally,
be
restrained
self‐aggregation
interacting
CzTPA.
cooperation
realizes
more
homogeneous
,
efficient
transport,
minimize
defects.
Accordingly,
modification
significantly
enhance
efficiency
1.54‐eV
PSCs
from
23.53%
25.66%
sustain
91.4%
its
original
after
1992
h
under
continuous
illumination
65
°C.
More
importantly,
1.68
eV
wide‐bandgap
PSC
achieved
PCE
22.75%
good
photostability.
The
power
conversion
efficiency
(PCE)
of
inverted
lead-halide
perovskite
solar
cells
(PSCs)
via
vapor
deposition
has
undergone
significant
enhancement
through
the
incorporation
a
self-assembled
monolayer
(SAM)
serving
as
hole
transport
layer.
To
achieve
high-performance
PSCs,
SAM
layer
needs
to
maintain
dense
and
high-coverage
configuration
during
fabrication
process.
Our
investigation
revealed
that
solid-vapor
reaction,
conditions
high
temperature
low
pressure
can
potentially
lead
migration
molecules,
particularly
those
adsorbed
on
surface
but
have
not
yet
formed
covalent
bonds.
In
this
study,
overcome
limitation,
we
developed
an
impregnation
process
for
mixed
molecules
with
(4-(7H-dibenzo[c,g]carbazol-7-yl)butyl)phosphonic
acid
(4PADCB)
glycine
hydrochloride
(GH),
which
reduces
agglomeration
enhances
their
strong
anchoring
ability
substrate,
thereby
maintaining
extremely
coverage
rate
even
in
high-temperature
low-pressure
environment
reactions.
Consequently,
champion
efficiencies
22.15%
(0.16
cm2)
19.18%
(5
cm
×
5
module)
are
achieved,
is
highest
record
PSCs
based
deposition.
Moreover,
advantages
reusability,
good
uniformity,
cost,
very
broad
commercial
prospects.
Advanced Functional Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Июнь 10, 2024
Abstract
In
the
rapidly
advancing
realm
of
perovskite
solar
cells,
rectification
defects
has
surfaced
as
a
crucial
scientific
challenge.
The
control
over
defect
states,
especially
in
printable
mesoscopic
cells
(p‐MPSCs),
is
hindered
by
complexities
screen‐printing
technology.
Here
novel
“two‐in‐one”
passivation
strategy
presented,
through
doping
TiO
2
paste
with
cesium
halide
salts
(CsX,
where
X
=
F,
Cl,
Br,
I)
to
integrate
all‐inorganic
Cs
halides,
particularly
CsF,
into
electron
transport
layer
p‐MPSCs.
Owing
robust
interaction
between
F
−
ions
and
compared
+
ions,
inability
infiltrate
lattice,
play
distinct
roles
starting
from
buried
interface
Specifically,
can
rectify
oxygen
vacancies
on
surface,
thus
alleviating
residual
stress
at
perovskite's
interface.
Simultaneously,
diffuses
top
mends
methylamine
vacancies.
As
result,
PCE
optimal
device,
based
F‐doped
,
witnesses
significant
improvement
16.18%
(control)
18.24%.
two‐in‐one
utilizing
CsX
well
realize
rectification,
thereby
offering
promising
prospect
for
enhancement
p‐MPSC
performance.
Advanced Science,
Год журнала:
2024,
Номер
unknown
Опубликована: Июль 30, 2024
Lately,
carbazole-based
self-assembled
monolayers
(SAMs)
are
widely
employed
as
effective
hole-selective
layers
(HSLs)
in
inverted
perovskite
solar
cells
(PSCs).
Nevertheless,
these
SAMs
tend
to
aggregate
solvents
due
their
amphiphilic
nature,
hindering
the
formation
of
a
monolayer
on
ITO
substrate
and
impeding
passivation
deep
defects
perovskites.
In
this
study,
series
new
including
DPA-B-PY,
CBZ-B-PY,
POZ-B-PY,
POZ-PY,
POZ-T-PY,
POZ-BT-PY
synthesized,
which
interfacial
repairers
coated
atop
CNph
SAM
form
robust
SAM@pseudo-planar
HSL
efficient
PSCs.
The
strategy
enables
well-aligned
interface
with
perovskites,
synergistically
promoting
crystal
growth,
improving
charge
extraction/transport,
minimizing
nonradiative
recombination
loss.
As
result,
POZ-BT-PY-modified
PSC
realizes
an
impressively
enhanced
efficiency
up
24.45%
together
fill
factor
82.63%.
Furthermore,
wide
bandgap
achieving
over
19%
efficiency.
Upon
treatment
monolayer,
also
demonstrates
non-fullerene
organic
photovoltaics
(OPVs)
based
PM6:BTP-eC9
blend,
achieves
17.07%.
Importantly,
modified
PSCs
OPVs
all
show
remarkably
improved
stability
under
various
testing
conditions
compared
control
counterparts.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
63(46)
Опубликована: Авг. 8, 2024
Abstract
Hole‐collecting
monolayers
have
greatly
advanced
the
development
of
positive‐intrinsic‐negative
perovskite
solar
cells
(p‐i‐n
PSCs).
To
date,
however,
most
anchoring
groups
in
reported
monolayer
materials
are
designed
to
bind
transparent
conductive
oxide
(TCO)
surface,
resulting
less
availability
for
other
functions
such
as
tuning
wettability
surface.
In
this
work,
we
developed
two
anchorable
molecules,
4PATTI‐C3
and
4PATTI‐C4
,
by
employing
a
saddle‐like
indole‐fused
cyclooctatetraene
π‐core
with
four
phosphonic
acid
linked
through
propyl
or
butyl
chains.
Both
molecules
form
on
TCO
substrates.
Thanks
saddle
shape
skeleton,
were
found
point
upward,
hydrophilic
surfaces.
Compared
devices
using
hole‐collecting
monolayer,
‐based
exhibit
faster
hole‐collection
process,
leading
higher
power
conversion
efficiencies
up
21.7
%
21.4
mini‐cell
(0.1
cm
2
)
mini‐module
(1.62
),
respectively,
together
good
operational
stability.
This
work
represents
how
structural
modification
multipodal
could
substantially
modulate
after
being
adsorbed
onto
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 30, 2024
Abstract
Self‐assembled
monolayers
(SAM)
as
hole
transport
layers
have
been
widely
used
in
high‐efficiency
inverted
perovskite
solar
cells
(PSCs)
exceeded
26
%.
However,
the
poor
coverage
and
non‐uniform
distribution
on
substrate
of
SAM
further
restrict
improvement
device
performance.
Herein,
we
utilize
mixed
strategy
via
MeO‐2PACz
along
with
perfluorotripropylamine
(FC‐3283)
to
improve
coverage,
aiming
accelerate
carrier
transport,
promote
growth,
regulate
surface
energy
levels
suppress
nonradiative
recombination.
The
champion
mixed‐SAM
achieves
an
efficiency
25.70
%
(certified
25.6
%)
long‐term
stability
(maintained
initial
90
after
1000
h
180
under
ISOS‐L‐1
ISOS‐L‐2).