Molecular Design of Hole-Collecting Materials for Co-Deposition Processed Perovskite Solar Cells: A Tripodal Triazatruxene Derivative with Carboxylic Acid Groups
Journal of the American Chemical Society,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 10, 2025
High-performance
and
cost-effective
hole-collecting
materials
(HCMs)
are
indispensable
for
commercially
viable
perovskite
solar
cells
(PSCs).
Here,
we
report
an
anchorable
HCM
composed
of
a
triazatruxene
core
connected
with
three
alkyl
carboxylic
acid
groups
(3CATAT-C3).
In
contrast
to
the
phosphonic
acid-containing
tripodal
analog
(3PATAT-C3),
3CATAT-C3
molecules
can
form
hydrophilic
monolayer
on
transparent
conducting
oxide
surface,
which
is
beneficial
subsequent
film
deposition
in
traditional
layer-by-layer
fabrication
process.
More
importantly,
larger
diffusion
coefficient
higher
surface
energy
make
suitable
simplified,
one-step
co-deposition
process
was
directly
added
as
part
precursor
solution.
predominantly
located
at
bottom
after
spin-coating
mixed
solution,
facilitating
charge
extraction.
Devices
fabricated
by
this
method
exhibit
superior
performance
champion
power
conversion
efficiency
over
23%.
The
unencapsulated
devices
showed
good
operational
stability
(retaining
90%
initial
output
100
h),
thermal
durability
95%
value
heating
105
°C
under
air),
excellent
storage
(showing
no
drop
8000
h).
Based
results
time-of-flight
secondary-ion
mass
spectroscopy
(ToF-SIMS)
order
nuclear
magnetic
resonance
(DOSY),
elucidated
effect
anchoring
HCMs
PSCs
well
mechanism
Our
findings
provide
valuable
insights
molecular
design
multifunctional
materials,
further
advancing
cells.
Язык: Английский
Tailoring Buried Interface and Minimizing Energy Loss Enable Efficient Narrow and Wide Bandgap Inverted Perovskite Solar Cells by Aluminum Glycinate Based Organometallic Molecule
Advanced Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 3, 2025
Abstract
Rational
regulation
of
Me‐4PACz/perovskite
interface
has
emerged
as
a
significant
challenge
in
the
pursuit
highly
efficient
and
stable
perovskite
solar
cells
(PSCs).
Herein,
an
organometallic
molecule
aluminum
glycinate
(AG)
that
contained
amine
(‐NH
2
)
hydroxyl
(Al‐OH)
groups
is
developed
to
tailor
buried
minimize
interface‐driven
energy
losses.
The
Al‐OH
selectively
bonded
with
unanchored
O═P‐OH
bare
NiO‐OH
optimize
surface
morphology
levels,
while
‐NH
group
interacted
specifically
Pb
2+
retard
crystallization,
passivate
Pb‐related
defects,
release
residual
stress.
These
interactions
facilitate
carrier
extraction
reduce
losses,
thereby
realizing
balanced
charge
transport.
Consequently,
AG‐modified
narrow
bandgap
(1.55
eV)
PSC
demonstrates
efficiency
26.74%
(certified
26.21%)
fill
factor
86.65%;
wide
(1.785
realizes
20.71%
champion
excellent
repeatability.
PSCs
maintain
91.37%,
91.92%,
92.00%
their
initial
after
aging
air
atmosphere,
nitrogen‐filled
atmosphere
at
85
°C,
continuously
tracking
maximum
power‐point
under
one‐sun
illumination
(100
mW
cm
−2
for
1200
h,
respectively.
Язык: Английский
Squaric Acid-Containing Hole-Collecting Monolayer Materials for p–i–n Perovskite Solar Cells
ACS Applied Materials & Interfaces,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 23, 2025
The
development
of
hole-collecting
materials
is
indispensable
to
improving
the
performance
perovskite
solar
cells
(PSCs).
To
date,
several
anchorable
molecules
have
been
reported
as
effective
monolayer
(HCM)
for
p–i–n
PSCs.
However,
their
structures
are
limited
well-known
electron-donating
skeletons,
such
carbazole,
triarylamine,
etc.
In
this
work,
we
developed
a
series
squaraine
derivatives
that
π-conjugated
core
composed
squaric
acid
moiety
connected
an
indoline
moiety.
Thanks
polar
carbonyl
group
acid,
all
were
found
form
hydrophilic
monolayers
after
being
chemisorbed
on
transparent
conducting
oxide
surfaces,
which
beneficial
subsequent
deposition
layer.
effect
substituents
and
anchoring
groups
molecular
electronic
structure
well
cell
device's
was
elucidated.
PSC
devices
fabricated
by
using
these
exhibited
high
power
conversion
efficiencies
up
22.1%,
together
with
good
stability.
This
work
highlights
potential
simple
skeleton
building
block
realize
high-efficiency
cost-effective
Язык: Английский
Nickel Chlorophyll-Derived Hole Transport Materials for Stable and Efficient Inverted Perovskite Solar Cells
Nano Letters,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 4, 2025
Hole-selective
layers
(HSLs)
are
critical
for
efficient
and
stable
perovskite
solar
cells
(PSCs).
Chlorophylls
(Chls)
their
analogs
exhibit
unique
optoelectronic
properties,
making
them
attractive
photovoltaics.
However,
dopant-free
Chl-based
materials
remain
underexplored,
with
reported
power
conversion
efficiencies
(PCEs)
below
19%.
This
study
investigates
three
nickel
chlorins
(NiChls)
as
monomers
functional
materials.
Nickel
methyl
pyropheophorbide-a
(NiChl-Oxo),
derived
from
natural
Chl-a,
was
chemically
modified
at
the
C13-keto-carbonyl
group,
yielding
NiChl-Deoxo
NiChl-CN.
Electrochemical
polymerization
used
to
fabricate
corresponding
polymerized
NiChl
films
HSLs.
Without
dopants,
NiChl-Deoxo-based
PSCs
achieved
a
record
PCE
of
21.8%,
fill
factor
83.8%,
which
is
highest
efficiency
date.
Additionally,
these
devices
exhibited
exceptional
long-term
stability.
highlights
effectiveness
strategic
molecular
modifications
in
advancing
presents
promising
pathway
developing
high-performance,
HSLs
next-generation
PSCs.
Язык: Английский
Self-assembled monolayers for perovskite solar cells
Опубликована: Апрель 1, 2025
Язык: Английский
Optimization of Band Alignment by Organic Molecules for Perovskite Solar Cells
The Journal of Physical Chemistry C,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 28, 2025
Язык: Английский
Multifunctional additives for the enhanced performance of the doctor-blading printed perovskite solar modules
Journal of Energy Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 1, 2025
Язык: Английский
Lattice Matching Anchoring of Hole‐Selective Molecule on Halide Perovskite Surfaces for n‐i‐p Solar Cells
Advanced Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 27, 2024
Abstract
Exploiting
the
self‐assembled
molecules
(SAMs)
as
hole‐selective
contacts
has
been
an
effective
strategy
to
improve
efficiency
and
long‐term
stability
of
perovskite
solar
cells
(PSCs).
Currently,
research
works
are
focusing
on
constructing
SAMs
metal
oxide
surfaces
in
p‐i‐n
PSCs,
but
realizing
a
stable
dense
SAM
contact
halide
n‐i‐p
PSCs
is
still
challenging.
In
this
work,
molecule
for
device
developed
featuring
terephthalic
methylammonium
core
structure
that
possesses
double‐site
anchoring
ability
matching
diameter
(6.36
Å)
with
lattice
constant
formamidinium
lead
iodide
(FAPbI
3
)
(6.33
Å),
which
facilitates
ordered
full‐coverage
atop
FAPbI
perovskite.
Moreover,
theoretical
calculations
experimental
results
indicate
compared
frequently
used
acid
or
ester
groups,
ionic
group
dipolar
charge
distribution
much
larger
adsorption
energy
both
organic
terminated
surfaces,
resulting
synergistic
improvement
carrier
extraction
defect
passivation
ability.
Benefiting
from
these
merits,
increased
21.68%
24.22%.
The
operational
under
white
LED
illumination
(100
mW
cm
−2
at
high
temperature
85
°C
also
improved.
Язык: Английский