Abstract
Narrow‐band
cyan‐emitting
materials
for
white
light‐emitting
diode
(wLED)
application
have
shown
great
potential
in
increasing
the
maximum
accessible
display
gamut
and
improving
color
rendering
of
full‐spectrum
healthy
lighting.
However,
discovery
novel
narrow‐band
cyan
emitters
with
excellent
luminescence
performances
remains
challenging.
Here,
an
ultra‐narrow‐band
Na
5
K
3
(Li
SiO
4
)
8
:Eu
2+
(N
phosphor
(λ
em
=
483
nm)
full
width
at
half
(FWHM)
only
18
nm
is
developed
from
some
typical
UCr
C
frameworks
phosphors
by
slightly
modifying
crystal
structure
symmetry.
Through
controllable
regulation
ratio
6
2
to
N
,
lattice
sites
forming
shoulder
peaks
are
further
squeezed
generate
narrowest
emission.
Moreover,
exhibits
low
photoluminescence
thermal
quenching
(90%@150
°C)
high
internal
quantum
efficiency
(IQE)
50%.
The
index
wLED
health
lighting
enhanced
92
94.
Using
this
short‐wavelength
emission
instead
a
part
blue
chip
can
effectively
prevent
“blue
hazard”.
This
work
provides
basic
principles
design
phosphors,
thus
achieving
their
applications
fields
eye‐friendly
display.
Inorganic Chemistry Frontiers,
Journal Year:
2024,
Volume and Issue:
11(12), P. 3607 - 3617
Published: Jan. 1, 2024
Sb
3+
/Sm
co-doping
can
effectively
modulate
the
luminescence
by
adjusting
energy
transfer
in
Cs
2
NaYCl
6
double
perovskites.
Two
minima
excited
state
of
3
P
1
enable
self-trapped
exciton
emission
at
low
temperatures.
Inorganic Chemistry,
Journal Year:
2024,
Volume and Issue:
63(4), P. 2241 - 2246
Published: Jan. 12, 2024
Four
silver-lanthanide
double
perovskite
nanocrystals,
namely,
Cs2AgSmCl6,
Cs2AgEuCl6,
Cs2AgGdCl6,
and
Cs2AgErCl6,
were
synthesized
for
the
first
time.
These
four
perovskites
have
yet
to
be
reported
in
any
form
are
found
metastable
bulk
phase.
By
using
colloidal
hot-injection
synthesis
method,
phase
can
arrested
kinetically.
lead-free
nanocrystals
show
a
broadband
emission
owing
self-trapped
exciton
recombination,
with
Cs2AgEuCl6
exhibiting
characteristic
f–f
from
Eu3+.
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(32)
Published: June 26, 2024
Abstract
Lanthanide‐based
NIR‐II‐emitting
materials
(1000–1700
nm)
show
promise
for
optoelectronic
devices,
phototherapy,
and
bioimaging.
However,
one
major
bottleneck
to
prevent
their
widespread
use
lies
in
low
quantum
efficiencies,
which
are
significantly
constrained
by
various
quenching
effects.
Here,
a
highly
oriented
(222)
facet
is
achieved
via
engineering
Cs
2
NaErCl
6
double
perovskites,
enabling
near‐complete
suppression
of
NIR‐II
luminescence
quenching.
The
optimally
(222)‐oriented
Ag
0.10
Na
0.90
ErCl
microcrystals
emit
Er
3+
1540
nm
light
with
unprecedented
high
efficiencies
90
±
6%
under
379
UV
excitation
(ultralarge
Stokes
shift
>1000
nm),
record
near‐unity
yield
98.6%
also
obtained
(222)‐based
NaYb
0.40
0.60
Cl
microcrystallites
980
excitation.
With
combined
experimental
theoretical
studies,
the
underlying
mechanism
facet‐dependent
emissions
revealed,
can
contribute
surface
asymmetry‐induced
breakdown
parity‐forbidden
transition
undesired
non‐radiative
processes.
Further,
role
reexamined
molecular
dynamics
based
on
two
facets,
highlighting
drastic
two‐phonon
coupling
effect
hydroxyl
group
4
I
13/2
level
.
Surface‐functionalized
facets
will
provide
new
insights
tunable
open
up
avenue
developing
efficient
emitters
toward
broad
applications.
Advanced Optical Materials,
Journal Year:
2024,
Volume and Issue:
12(30)
Published: Aug. 13, 2024
Abstract
Recently,
all‐inorganic
halide
double
perovskites
(DPs)
with
a
chemical
formula
of
Cs
2
B
I
III
X
6
have
been
emerging
as
shinning
star
to
be
used
in
modern
optoelectronic
devices,
due
their
unique
advantages
such
environmentally
friendly,
high
absorption
coefficient,
low
trap
densities,
tunable
bandgap,
variable
constituent
elements
and
valences
states
through
or
sites
engineering.
In
this
review,
first,
the
impact
cation
doping
on
electronic
structure
optical
properties
DPs
are
systematically
overviewed,
which
cover
several
key
issues
including
interconversion
between
direct
indirect
band
gaps,
enhancement
light
absorption,
promotion
exciton
localization,
elucidation
energy
transfer
mechanisms,
regulation
defect
density
improvement
both
stability
luminescence
efficiency.
Subsequently,
state‐of‐the‐art
research
activities
regarding
interesting
device
applications
discussed,
light‐emitting
diodes,
anticounterfeiting
encryption,
X‐ray
scintillators,
thermometry.
Finally,
existing
difficulties,
prospects,
directions
field
proposed.
Abstract
Driven
by
the
escalating
demand
for
cutting‐edge
materials
in
interactive
encryption
and
customized
display,
optimization
of
excitonic
coupling
mechanisms
perovskite‐based
luminescent
systems
has
emerged
as
a
pivotal
focus
advanced
research.
Inspired
synergistic
doping
(SD),
photoswitchable
energy
transfer
channel
is
realized
utilizing
UV‐responsive
Cs
2
NaInCl
6
:
Sb
3+
‐Ho
(CNIC:
Sb‐Ho)
phosphor.
Benefiting
from
self‐trapped
exciton
,
visible
blue
luminescence
Ho
achieves
excitation
reconstruction
through
SD,
with
sensitization
coefficient
to
CNIC
reaching
two
orders
magnitude.
Notably,
CNIC:
Sb‐Ho
quantum
dot
embedded
into
polyacrylonitrile
(PAN)
polymethyl
methacrylate
(PMMA)
fibers,
respectively,
distinct
color
coordinate
channels
are
created
altering
concentration
fiber
matrix,
thereby
enabling
personalization
customization
desired
colors
enhanced
precision.
Furthermore,
excellent
read‐in
performance
under
UV
irradiation
achieved
screen‐printing
microcrystal
on
nanofibers
combining
it
ACSII
code,
which
endows
UV‐induced
controllable
shape
programming
behavior
multidimensional
information
encryption.
This
work
establishes
an
visual
interaction
framework
effectively
integrating
perovskite
fluorescence
tunability
nanofiber
adaptive
structures,
thus
opening
new
possibilities
smart
application
next‐generation
optical
technology.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 2, 2025
Abstract
The
toxicity
and
the
poor
thermal
stability
of
all‐inorganic
lead
perovskite
nanocrystals
(NCs)
have
been
major
limitation
for
their
scale‐up
purpose.
In
this
study,
a
novel
lead‐free
KEu
4
F
13
NCs
are
synthesized
first
time
using
facile
eco‐friendly
hydrothermal
strategy.
High‐resolution
synchrotron
X‐ray
diffraction
study
indicates
that
adopt
cubic
fluorite
structure
with
excess
fluorine
intercalated
into
spare
rooms
lattice.
obtained
characteristic
emission
peaks
Eu
3+
ions
excited
by
wavelength
394
nm.
More
importantly,
show
excellent
due
to
small
radius
−
its
high
lattice
energy.
relative
photoluminescence
(PL)
intensity
at
594
nm
retains
≈72%
initial
value
20
°C
when
heated
200
°C.
Furthermore,
PL
shows
negligible
degradation
after
undergoing
three
consecutive
cycles
between
(XRD)
remain
identical
those
cycled
samples
(after
1st/3rd
cycles),
confirming
structural
robustness
under
stress.
lifetimes
measured
180
calculated
be
2.10
2.04
ms,
respectively.
red‐emitting
encapsulated
on
an
ultraviolet
(UV)‐emitting
chip
fabricate
red
light‐emitting
diodes
(LED).
Abstract
Co‐doping
of
rare
earth
(RE)
and
ns
2
metal
ions
with
in
double
perovskites
shows
great
promise
for
applications
anti‐counterfeiting,
display,
radiation
detection.
However,
the
intrinsic
physical
nature
enhanced
photoluminescence
remains
unclear.
Herein,
we
use
gadolinium‐based
perovskite
as
model
propose
an
effective
strategy
co‐doping
RE3+
Sb3+
(5s
)
to
modulate
energy
transfer.
The
incorporation
Sb
3+
increases
absorption
cross
section,
thereby
overcoming
limitation
4f–4f
narrowband
transitions.
Furthermore,
acts
a
bridge
transfer,
significantly
facilitating
this
process.
Density
functional
theory
calculations
reveal
that
introduction
disrupts
symmetry
[RECl
6
]
3–
octahedra,
leading
increased
distortion.
Additionally,
electrons
octahedra
exhibit
stronger
localization
/RE
co‐doped
system,
which
enhances
Cl
–
–RE
charge
transfer
process,
increasing
radiative
transition
rates
resulting
high
quantum
yield.
Our
research
elucidates
essence
luminescence
RE‐based
from
both
experimental
theoretical
perspectives,
providing
valuable
insights
into
modulation
luminescent
properties
understanding
underlying
mechanisms
RE
doped
materials.