ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(29), P. 38124 - 38133
Published: July 11, 2024
In
perovskite
solar
cells
(PSCs),
the
electron
transfer
layer
(ETL)
characteristics
have
significant
effects
on
photoelectric
conversion
efficiency
(PCE)
of
devices.
Herein,
a
natural
chelating
agent
polymer
polyaspartic
acid
(PASP)
is
doped
into
SnO
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(16)
Published: Jan. 11, 2024
Abstract
[4‐(3,6‐dimethyl‐9H‐carbazol‐9yl)butyl]phosphonic
acid
(Me‐4PACz)
self‐assembled
molecules
(SAM)
are
an
effective
method
to
solve
the
problem
of
buried
interface
NiO
x
in
inverted
perovskite
solar
cells
(PSCs).
However,
Me‐4PACz
end
group
(carbazole
core)
cannot
forcefully
passivate
defects
at
bottom
film.
Here,
a
Co‐SAM
strategy
is
employed
modify
PSCs.
doped
with
phosphorylcholine
chloride
(PC)
form
improve
monolayer
coverage
and
reduce
leakage
current.
The
phosphate
ions
(Cl
−
)
PC
can
inhibit
surface
defects.
Meantime,
quaternary
ammonium
Cl
fill
organic
cations
halogen
vacancies
film
enable
passivation.
Moreover,
promote
growth
crystals,
collaboratively
defects,
suppress
nonradiative
recombination,
accelerate
carrier
transmission,
relieve
residual
stress
Consequently,
modified
devices
show
power
conversion
efficiencies
as
high
25.09%
well
excellent
device
stability
93%
initial
efficiency
after
1000
h
operation
under
one‐sun
illumination.
This
work
demonstrates
novel
approach
for
enhancing
performance
PSCs
by
modifying
on
.
Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 18, 2024
Abstract
Inverted
perovskite
solar
cells
(PSCs)
comprising
formamidinium‐cesium
(FA‐Cs)
lead
triiodide
have
garnered
considerable
attention
due
to
their
impressive
efficiency
and
remarkable
stability.
Nevertheless,
synthesizing
high‐quality
FA‐Cs
alloyed
films
presents
challenges,
primarily
attributable
the
intricate
interphase
process
involved
absence
of
methylammonium
(MA
+
)
mixed
halogens.
Here,
additive
3‐phosphonopropanoic
acid
(3‐PPA)
is
introduced,
with
bifunctional
phosphonic
groups,
into
precursor
modulate
crystal
growth
provide
passivation
at
grain
boundaries.
In
situ
characterization
reveals
that
3‐PPA
can
form
a
“rapid
nucleation,
slow
growth”
mechanism,
resulting
in
enlarged
grains
enhanced
crystallinity.
addition,
serves
passivate
boundary
defects
release
residual
strain
by
forming
molecular
bridging,
leading
passivated
achieving
fluorescence
lifetime
5.79
microseconds
favorable
n‐type
contact
interface.
As
result,
devices
incorporating
achieve
champion
power
conversion
(PCE)
24.05%
an
ultra‐high
fill
factor
(FF)
84.22%.
More
importantly,
optimized
exhibit
satisfactory
stability
under
various
testing
conditions.
The
findings
underscore
pivotal
role
multifunctional
additives
crystallization
control
defect
for
high‐performance
MA‐free
pure
iodine
PSCs.
Advanced Energy Materials,
Journal Year:
2024,
Volume and Issue:
14(8)
Published: Jan. 9, 2024
Abstract
Numerous
deep/shallow
level
defects
generated
at
the
surface/grain
boundaries
of
perovskite
during
uncontrollable
crystallization
pose
a
formidable
challenge
to
photovoltaic
performance
solar
cells
(PSCs).
Herein,
an
organometallic
cobaltocenium
salt
additive,
1‐propanol‐2‐(1,2,3‐triazol‐4‐yl)
hexafluorophosphate
(PTCoPF
6
),
is
incorporated
into
precursor
solution
regulate
and
minimize
holistic
for
high‐performance
inverted
PSCs.
The
cations
PF
−
in
PTCoPF
stabilize
Pb‐I
framework
repair
shallow‐level
positively
negatively
charged
vacancies
perovskite.
N═N
triazole
ring
can
passivate
deep‐level
uncoordinated
lead.
interaction
between
materials
delays
nucleation
crystal
growth,
ensuring
high‐quality
with
large
grains,
suppressing
non‐radiative
recombination
ion
migration.
Therefore,
‐incorporated
PSC
achieves
impressive
power
conversion
efficiency
25.03%
outstanding
long‐term
stability.
Unencapsulated
encapsulated
PSCs
maintain
93%
95%
their
initial
efficiencies
under
85
°C
storage
nitrogen
atmosphere
1000
h
maximum
point
tracking
nearly
h,
respectively.
Synergistic
kinetic
modulation
defect
passivation
ionized
metal‐organic
complex
additives
will
become
prevalent
methods
improve
stability
Carbon Energy,
Journal Year:
2024,
Volume and Issue:
6(9)
Published: April 12, 2024
Abstract
The
buried
interface
in
the
perovskite
solar
cell
(PSC)
has
been
regarded
as
a
breakthrough
to
boost
power
conversion
efficiency
and
stability.
However,
comprehensive
manipulation
of
terms
transport
layer,
interlayer,
layer
largely
overlooked.
Herein,
we
propose
use
volatile
heterocyclic
compound
called
2‐thiopheneacetic
acid
(TPA)
pre‐buried
additive
achieve
cross‐layer
all‐interface
defect
passivation
through
an
situ
bottom‐up
infiltration
diffusion
strategy.
TPA
not
only
suppresses
serious
interfacial
nonradiative
recombination
losses
by
precisely
healing
underlying
defects
but
also
effectively
enhances
quality
film
releases
residual
strain
film.
Owing
this
versatility,
TPA‐tailored
CsPbBr
3
PSCs
deliver
record
11.23%
with
enhanced
long‐term
This
manipulating
using
opens
new
avenues
for
further
improving
performance
reliability
PSC.
Energy & Environmental Science,
Journal Year:
2023,
Volume and Issue:
16(10), P. 4251 - 4279
Published: Jan. 1, 2023
This
paper
reviews
the
performance
modulation
of
perovskite
solar
cells
by
cross-linking
polymerization
with
different
molecular
structures
from
points
grain
boundaries,
lattice
interior,
and
charge
transport
layers.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(21)
Published: March 26, 2024
Abstract
Despite
the
remarkable
progress
of
perovskite
solar
cells
(PSCs),
challenges
remain
in
terms
finding
effective
and
viable
strategies
to
enhance
their
long‐term
stability
while
maintaining
high
efficiency.
In
this
study,
a
new
insulating
hydrophobic
fluorinated
polyimide
(FPI:
6FDA‐6FAPB)
was
used
as
interface
layer
between
hole
transport
(HTL)
PSCs.
The
functional
groups
FPI
play
pivotal
role
passivating
defects
within
device.
Due
its
work
function,
demonstrates
field‐effect
passivation
(FEP)
capabilities
an
layer,
effectively
mitigating
non‐radiative
recombination
at
interface.
Notably,
does
not
impede
carrier
transmission
interface,
which
is
attributed
presence
tunneling
effects.
optimized
PSCs
achieve
outstanding
power
conversion
efficiency
(PCE)
24.61
%
demonstrate
excellent
stability,
showcasing
efficacy
enhancing
device
performance
reliability.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(52)
Published: Aug. 28, 2024
Abstract
[4‐(3,6‐dimethyl‐9H‐carbazol‐9yl)butyl]phosphonic
acid
(Me‐4PACz)
self‐assembly
material
has
been
recognized
as
a
highly
effective
approach
for
mitigating
nickel
oxide
(NiO
x
)
surface‐related
challenges
in
inverted
perovskite
solar
cells
(IPSCs).
However,
its
uneven
film
generation
and
failure
to
effectively
passivate
the
buried
interface
defects
limit
device‘s
performance
improvement
potential.
Herein,
p‐xylylenediphosphonic
(p‐XPA)
containing
bilateral
phosphate
groups
(−PO
3
H
2
is
introduced
an
layer
between
NiO
/Me‐4PACz
layer.
P‐XPA
can
flatten
surface
of
hole
transport
optimize
contact.
Meanwhile,
p‐XPA
achieves
better
energy
level
alignment
promotes
interfacial
transport.
In
addition,
−PO
chelate
with
Pb
2+
form
hydrogen
bond
FA
+
(formamidinium
cation),
thereby
suppressing
non‐radiative
recombination
loss.
Consequently,
IPSC
modification
champion
power
conversion
efficiency
25.87
%
(certified
at
25.45
%)
laboratory
scale
(0.0448
cm
).
The
encapsulated
target
device
exhibits
operational
stability.
Even
after
1100
hours
maximum
point
tracking
50
°C,
remains
impressive
82.7
initial
efficiency.
Molecules
featuring
passivation
contact
inhibit
recombination,
providing
enhancing
stability
devices.
Interdisciplinary materials,
Journal Year:
2024,
Volume and Issue:
3(2), P. 316 - 325
Published: Feb. 20, 2024
Abstract
In
the
realm
of
photovoltaics,
organometallic
hybridized
perovskite
solar
cells
(PSCs)
stand
out
as
promising
contenders
for
achieving
high‐efficiency
photoelectric
conversion,
owing
to
their
remarkable
performance
attributes.
Nevertheless,
defects
within
layer,
especially
at
grain
boundaries
and
surface,
have
a
substantial
impact
on
both
overall
long‐term
operational
stability
PSCs.
To
mitigate
this
challenge,
we
propose
method
water‐induced
condensation
polymerization
small
molecules
involving
incorporation
1,3‐phenylene
diisocyanate
(1,3‐PDI)
into
film
using
an
antisolvent
technique.
Subsequent
step,
introduction
water
triggers
[P(1,3‐PDI)],
thereby
facilitating
in
situ
passivation
uncoordinated
lead
inherent
film.
This
process
demonstrates
notable
enhancement
efficiency
approach
has
led
attainment
noteworthy
power
conversion
(PCE)
24.66%
inverted
Furthermore,
based
P(1,3‐PDI)
modification,
these
devices
maintain
90.15%
initial
after
5000
h
storage
under
ambient
conditions
25°C
50
±
5%
relative
humidity.
Additionally,
even
maximum
point
tracking
1000
h,
PSCs
modified
with
sustain
82.05%
PCE.
Small
can
rationally
manipulate
turn
harm
benefit,
providing
new
directions
methods
improving
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 10, 2024
Abstract
The
presence
of
various
defects
within
the
electron
transport
layer
(ETL),
perovskite
(PVK)
layer,
and
their
interfaces
significantly
affects
efficiency,
hysteresis,
stability
solar
cells
(PSCs)
in
n–i–p
structure.
Herein,
a
defect
passivation
strategy
employing
potassium
4‐methoxysalicylate
(MSAK)
is
utilized
to
efficiently
modulate
ETL,
PVK,
ETL/PVK
interface.
functional
groups
−COO−
−OH
MSAK
molecules,
along
with
K
+
cations,
effectively
reduce
tin
oxide
(SnO
2
)
improve
properties.
Importantly,
MSAK‐SnO
provides
favorable
substrate
for
growth
highly
crystallization
dense
layers.
molecules
also
passivate
bottom
interface
PVK
by
coordinating
under‐coordinated
Pb
2+
ions.
Furthermore,
cations
can
migrate
into
further
enhancing
improving
photovoltaic
performance
PSC
devices.
PSCs
fabricated
using
based
on
achieve
remarkable
power
conversion
efficiency
(PCE)
25.47%,
alongside
reduced
hysteresis
enhanced
stability.
After
being
stored
under
ambient
conditions
60
days,
device
maintains
nearly
90%
its
initial
PCE,
whereas
PCE
pristine
decreases
69.7%
after
aging.