Journal of Materials Chemistry C,
Journal Year:
2024,
Volume and Issue:
12(38), P. 15644 - 15653
Published: Jan. 1, 2024
Strategically
designed
self-assembled
molecules
(SAMs)
of
C-2PACz
and
S-2PACz
are
developed
as
hole-selective
layers
for
efficient
inverted
perovskite
solar
cells.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 3, 2025
Abstract
The
inverted
perovskite
solar
cells
based
on
hole‐selective
self‐assembled
molecules
(SAMs)
have
been
setting
new
efficiency
benchmarks.
However,
the
agglomeration
of
SAM
and
lack
defect
passivation
ability
are
two
critical
issues
that
need
to
be
addressed.
It
is
demonstrated
by
blending
co‐adsorbent
4‐phosphoricbutyl
ammonium
iodide
(4PBAI)
with
4‐(7H‐dibenzo[c,g]carbazole‐7‐yl)
phosphonic
acid
(4PADCB),
enhanced
homogeneity,
conductivity,
better
energy
levels
can
realized
for
co‐SAM
contact.
functional
group
4PBAI
also
effectively
passivate
defects
at
buried
interface
template
high‐quality
growth.
Assisted
synergistic
top
modification,
power
conversion
optimized
device
reaches
24.96%,
which
retain
95%
initial
after
1200
h
in
ambient
unencapsulated
device.
findings
suggest
a
well‐designed
address
limitations
further
enhance
performance
cutting‐edge
SAMs.
Energy & Environmental Science,
Journal Year:
2024,
Volume and Issue:
17(19), P. 6974 - 7016
Published: Jan. 1, 2024
This
review
overviews
the
challenges
at
buried
interface
of
PSCs,
defect
passivation
capabilities
SAMs,
and
its
effectiveness
compared
to
other
passivating
agents.
Angewandte Chemie International Edition,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 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.
Journal of Materials Chemistry A,
Journal Year:
2024,
Volume and Issue:
12(22), P. 12983 - 13058
Published: Jan. 1, 2024
This
review
focuses
on
deciphering
the
structural
divergence
of
organic
molecular
hole
selective
materials
in
determining
photovoltaic
performance
and
stability
p-i-n
type
perovskite
solar
cell
devices.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(46)
Published: Aug. 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
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(24), P. 31114 - 31125
Published: June 10, 2024
Albeit
the
undesirable
attributes
of
NiOx,
such
as
low
conductivity,
unmanageable
defects,
and
redox
reactions
occurring
at
perovskite/NiOx
interface,
which
impede
progress
in
inverted
perovskite
solar
cells
(i-PSCs),
it
is
most
favorable
choice
technology
for
industrialization
PSCs.
In
this
study,
we
propose
a
novel
Ni
vacancy
defect
modulate
approach
to
leverage
conformal
growth
surface
self-limiting
reaction
characteristics
atomic
layer
deposition
(ALD)-fabricated
NiOx
by
varying
O2
plasma
injection
time
(tOE)
induce
self-doping.
Consequently,
thin
films
with
enhanced
an
appropriate
Ni3+/Ni2+
ratio,
stable
states,
ultrathinness
are
realized
hole-transporting
layers
(HTLs)
p-i-n
As
result
these
improvements,
ALD-NiOx-based
devices
exhibit
highest
power
conversion
efficiency
(PCE)
19.86%
fill
factor
(FF)
81.86%.
Notably,
optimal
interfacial
defects
effectively
suppressed
severe
between
NiOx.
This
suppression
evidenced
lowest
decay
rate
observed
harsh
environment,
lasting
500
consecutive
hours.
The
proposed
introduces
possibility
hierarchical
distribution
offers
feasibility
fabrication
large-area,
uniform,
high-quality
films.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 28, 2024
Abstract
The
non‐wetting
issue
of
the
self‐assembled
monolayer
(SAM)
layer
can
complicate
subsequent
perovskite
deposition
and
impact
device
efficiency.
This
study
addresses
this
challenge
using
a
dual
approach
involving
co‐self‐assembly
buffer
to
enhance
wettability
interfacial
contact
buried
film.
A
weakly
acidic
boronic
acid
derivative,
4‐N,
N‐dimethylbenzeneboronic
hydrochloride
(4NPBA),
is
used
co‐self‐assemble
with
regular
SAM
molecule
on
ITO
FAI
further
increased
film
coverage
89%.
interface
strategy—SAM‐4NPBA/FAI—results
in
flat
dense
interface.
optimized
demonstrates
high
fill
factor
88.35%,
power
conversion
efficiency
25.29%,
retains
over
99%
its
initial
after
500
h
maximum
point
testing.