Harnessing Pb–S Interactions for Long‐Term Water Stability in Cesium Lead Halide Perovskite Nanocrystals
Small,
Год журнала:
2024,
Номер
20(35)
Опубликована: Апрель 16, 2024
Lead
halide
perovskite
nanocrystals
(LHP
NCs)
have
garnered
attention
as
promising
light-harvesting
materials
for
optoelectronics
and
photovoltaic
devices,
attributed
to
their
impressive
optoelectronic
properties.
However,
susceptibility
moisture-induced
degradation
has
hindered
practical
applications.
Despite
various
encapsulation
strategies,
challenges
persist
in
maintaining
stability
performance
simultaneously.
Here,
a
ligand
exchange
approach
is
proposed
using
(11-mercaptoundecyl)-N,N,N-trimethylammonium
bromide
(MUTAB)
enhance
the
dispersibility
of
CsPbBr
Язык: Английский
Perovskite–Molecular Photocatalyst Synergy and Surface Engineering for Superior Photocatalytic Performance
ACS Applied Materials & Interfaces,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 15, 2025
Metal
halide
perovskite
nanocrystals
(NCs),
known
for
their
strong
visible-light
absorption
and
tunable
optoelectronic
properties,
show
significant
promise
photocatalytic
applications.
However,
efficiency
is
often
hindered
by
rapid
charge
recombination
insufficient
exciton
dissociation,
limiting
effective
catalysis.
Excited-state
interactions
at
the
NC
interface
are
critical
in
determining
performance,
underscoring
need
strategies
that
enhance
separation
minimize
recombination.
To
address
these
challenges,
we
developed
a
composite
material
combining
cesium
lead
bromide
(CsPbBr3)
with
ferrocene
carboxylic
acid
(FcA),
hole-extracting
moiety.
This
integration
enhances
dissociation
through
energy
level
alignment
suppression,
resulting
3-fold
increase
oxidation
yield
of
benzylamine
to
N-benzylidenebenzylamine
(35
±
5%
versus
12
2%
pristine
CsPbBr3).
Additionally,
thionyl
(SOBr2)
surface
modification
strips
off
ligands
introduces
ions
onto
CsPbBr3
NCs,
further
improving
transfer
substrate
accessibility,
27
within
3
h.
While
SOBr2
treatment
initial
catalytic
its
acidic
nature
may
reversible
reactions
side
products
over
extended
reaction
times.
study
highlights
impact
molecular
engineering
on
optimizing
interfacial
dynamics,
providing
pathway
toward
robust,
high-efficiency
photocatalysts
sustainable
chemical
transformations.
Язык: Английский
Metal Halide Perovskite Nanocrystals for C–X Activation: Role of Halide Vacancies
ACS Applied Nano Materials,
Год журнала:
2024,
Номер
7(14), С. 16913 - 16921
Опубликована: Июль 16, 2024
Metal
halide
perovskite
nanocrystals
(NCs)
possess
immense
potential
in
photocatalysis.
However,
deciphering
the
intricate
surface
chemistry
that
governs
these
catalytic
processes
remains
a
challenge.
This
study
investigates
C–X
bond
activation
with
CsPbBr3
NCs,
focusing
on
elucidating
role
of
dynamic
molecular
domains
dictating
activity.
By
manipulating
interactions
through
ligand
dynamics,
we
identify
vacancies
as
critical
sites
for
activation.
A
systematic
exploration
different
types
reveals
varying
kinetics
exchange,
oleyl
amine-capped
NCs
demonstrating
highest
reactivity.
Temperature-dependent
photoluminescence
measurements
corroborate
findings,
highlighting
influence
dynamics
interactions.
Additionally,
postsynthetic
treatments,
such
lead
oleate
modification,
which
leads
to
an
increase
density
active
(halide
vacancies),
significantly
enhance
performance.
Conversely,
SOBr2
treatment,
repairs
bromide
vacancies,
results
almost
completely
suppressed
So,
by
engineering
environments,
demonstrate
significant
improvement
performance
metal
offering
valuable
insights
future
development.
Язык: Английский
Ligand modulation of active center to promote lead-free Cs2AgInCl6 photocatalytic CO2 reduction
Journal of Energy Chemistry,
Год журнала:
2024,
Номер
95, С. 660 - 669
Опубликована: Апрель 24, 2024
Язык: Английский
Insights into interfacial mechanisms: CsPbBr3 nanocrystals as sustainable photocatalysts for primary amine oxidation
Chemical Communications,
Год журнала:
2024,
Номер
60(17), С. 2365 - 2368
Опубликована: Янв. 1, 2024
This
study
highlights
CsPbBr
3
nanocrystals
as
a
potent
photocatalyst
for
oxidative
coupling
of
primary
amines
to
imines,
where
interfacial
interactions
markedly
impact
the
reaction
yield.
Язык: Английский
Long‐Lived Charge Separation Enabled by Molecular Engineering of Phenazine‐Based Hole Transport Materials
Small,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 18, 2025
Abstract
Achieving
long‐lived
charge‐separated
states
is
paramount
for
advancing
perovskite
solar
cells
technology,
enhancing
efficiency,
and
enabling
kinetically
slow
processes
like
photocatalysis.
While
hole
transport
materials
(HTMs)
are
essential
efficient
charge
extraction,
conventional
suffer
from
high
defect
densities
at
the
perovskite/HTM
interface,
leading
to
severe
nonradiative
recombination
losses.
Previous
strategies
surface
passivation
often
rely
on
external
treatments,
which
pose
scalability
challenges.
This
work
overcomes
these
limitations
by
integrating
functionality
directly
into
HTMs
through
targeted
molecular
engineering
of
phenazine
derivatives.
By
leveraging
anchoring
capability
1,10‐phenanthroline
(Phen)
skeleton
strategically
incorporating
electron‐donating
(─NH
2
,
─OCH
3
)
electron‐withdrawing
(─NO
─Br)
groups,
electron
density
systematically
modulated
control
transfer
dynamics.
Electron‐donating
groups
(EDGs)
increase
core,
suppressing
trap‐assisted
stabilizing
states.
In
contrast,
(EWGs)
promote
dipole
formation
sites,
prolonged
separation,
as
confirmed
observed
sustained
bleaching
in
transient
absorption
spectroscopy.
study
reveals
profound
impact
substituent
electronic
effects
interfacial
interactions,
offering
a
design
strategy
optimizing
mitigation
optoelectronics.
These
findings
provide
scalable
approach
perovskite‐based
photovoltaics
photocatalytic
applications.
Язык: Английский
Semiconductor Photocatalysts in Photopolymerization Processes: Mechanistic Insights, Recent Advances, and Future Prospects
Progress in Polymer Science,
Год журнала:
2024,
Номер
unknown, С. 101891 - 101891
Опубликована: Сен. 1, 2024
Язык: Английский
Leveraging Phenazine‐Based Ligands for Optimized Perovskite Optoelectronic Performance Through Chelation and Redox Engineering
Advanced Optical Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 29, 2024
Abstract
Perovskite
nanocrystals
(PNCs)
hold
immense
potential
for
optoelectronic
and
photovoltaic
applications.
However,
their
performance
is
hindered
by
surface
defects
that
promote
non‐radiative
recombination
reduce
stability.
Surface
engineering,
particularly
through
defect
passivation,
crucial
achieving
high‐performing
perovskite
solar
cells.
Chelation
has
been
shown
to
significantly
improve
the
efficiency
stability
of
In
this
study,
a
novel
chelation
strategy
using
1,10‐Phenanthroline
(Phen)
presented
as
bidentate
chelating
ligand
effectively
target
passivate
these
detrimental
defects.
By
strategically
designing
Phenanthroline
derivative,
dipyrido[3,2‐a:2′,3′‐c]phenazin‐11‐amine
(Phen‐derivative)
with
optimized
redox
potentials,
dual
functionality:
efficient
passivation
hole
transport
achieved.
X‐ray
photoelectron
spectroscopy
(XPS)
confirms
superior
binding
capability
Phen‐derivative
due
chelation.
This
strong
interaction
facilitates
ultrafast
charge
transfer
from
PNCs
formation
long‐lived
charge‐separated
state,
evidenced
sustained
bleaching
in
transient
absorption
spectra.
A
metal‐dipyrido[3,2‐a:2′,3′‐c]phenazin‐11‐amine
complex
(Ir‐complex)
derived
dipyrido[3,2‐a:2′,3′‐c]phenazin‐11‐amine,
but
lacking
site,
hinders
desired
despite
similar
energetics.
work
emphasizes
critical
role
chelation‐mediated
interfacial
interactions
energy
alignment
effective
shuttle
molecules
unlocking
lead‐chelating
transporters
next‐generation
light‐harvesting
technologies.
Язык: Английский