Modulation of Near‐Infrared Afterglow Luminescence in Inorganic Nanomaterials for Biological Applications
Linshuo Gao,
No information about this author
Yawei Liu,
No information about this author
Juanjuan Su
No information about this author
et al.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 10, 2025
Near-infrared
afterglow
luminescent
inorganic
nanomaterials
(NIR-ALINs)
possess
the
unique
property
of
continuing
to
emit
near-infrared
(NIR)
luminescence
after
excitation
ceases.
They
demonstrate
excellent
photostability,
deep
tissue
penetration,
and
high
imaging
signal-to-noise
ratio
(SNR).
Additionally,
NIR-ALINs
can
be
re-excited
in
vivo
using
visible
(Vis),
NIR
light
or
X-rays,
which
avoids
need
for
continuous
situ
excitation,
thus
eliminating
autofluorescence
biological
tissues
reducing
tediousness
multiple
injections.
These
features
make
particularly
attractive
applications.
In
recent
years,
a
series
with
prolonged
time
enhanced
intensity
have
been
discovered.
However,
development
still
faces
significant
challenges,
as
their
performance
is
usually
insufficient
satisfy
practical
There
lack
systematic
analysis
strategies
regulation
nanomaterials.
This
review
highlights
rational
design
modulation
NIR-ALINs,
focusing
on
host
substrate
selection,
trap
engineering
surface
modification.
Moreover,
applications
bioimaging,
bio-detection
disease
therapy
are
summarized.
Finally,
present
challenges
perspectives
applications,
such
properties
unclear
biosafety,
also
discussed.
Language: Английский
Organic Ionic Host–Guest Phosphor with Dual-Confined Nonradiation for Constructing Ultrahigh-Temperature X-ray Scintillator
Ying Wang,
No information about this author
Jiahong Yu,
No information about this author
Zixing Zhou
No information about this author
et al.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 20, 2025
Scintillators
with
X-ray-excitable
luminescence
have
attracted
great
attention
in
the
fields
of
medical
radiography,
nondestructive
inspection,
and
high-energy
physics.
However,
thermal
quenching
significantly
reduces
radioluminescence
efficiency,
particularly
for
those
phosphorescent
scintillators
promising
radiation-induced
triplet
exciton
utilization,
ultimately
limiting
their
applications
high-temperature
scenarios.
Herein,
we
develop
ultrahigh-temperature
based
on
organic
ionic
host–guest
phosphorescence
systems
unprecedented
thermal-stable
emissions
up
to
673
K.
The
guest
phosphor
features
spin-vibronic
coupling-assisted
intersystem
crossing,
effectively
transforming
thermally
activated
delayed
fluorescence
overcoming
inactivation
excitons.
Meanwhile,
rigid
host
robust
electrostatic
interactions
minimize
both
intrinsic
extrinsic
nonradiations
excitons,
so-called
dual-confined
nonradiation.
These
two
mechanisms
work
synergistically,
contributing
highly
efficient
exciton-based
a
room-temperature
efficiency
38.7%
ultrahigh-temperature-resistant
dual
emissions.
Such
an
innovative
scintillator
achieves
impressively
low
X-ray
detection
limit
71.5
nGy
s–1
remarkably
bright
photoluminescence
(efficiency
80.4%
at
483
K),
enabling
imaging.
Language: Английский
Enabling Multicolor Circularly Polarized Organic Long Persistent Luminescence through Chiral Exciplex
Hui Li,
No information about this author
Xin Zhang,
No information about this author
Cheng Tan
No information about this author
et al.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 1, 2025
Abstract
Circularly
polarized
organic
long
persistent
luminescence
(CP‐OLPL)
has
garnered
significant
attention
due
to
its
distinctive
properties.
However,
achieving
CP‐OLPL
materials
with
ultralong
durations
remains
a
formidable
challenge.
Herein,
an
effective
strategy
is
proposed
obtain
long‐lived
by
constructing
self‐designed
chiral
donor
for
developing
host–guest
exciplex
system.
The
gradual
recombination
of
charge‐separated
states
enables
green
emission
persist
over
1.5
hours
asymmetry
factor
(|
g
lum
|)
4.5
×
10
−3
.
More
intriguingly,
doping
rubrene
fluorophore
yields
orange‐red
system,
exhibiting
duration
1
hour
and
|
2.3
through
synergistic
singlet‐singlet
chirality
energy
transfer.
These
properties
render
the
development
afterglow
display,
multi‐level
information
encryption,
lighting.
This
work
not
only
represents
advancement
in
design
donors
system
but
also
provides
valuable
insights
into
exciton
dynamics.
Language: Английский
Day‐Long Organic Persistent Luminescence in Flexible Polymeric Materials
Longming Jin,
No information about this author
Wanqi Mo,
No information about this author
Ziyi Wang
No information about this author
et al.
Angewandte Chemie,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 26, 2025
Abstract
The
progress
in
organic
afterglow
materials
has
drawn
significant
attention
due
to
their
extensive
applications
fields
such
as
optoelectronics,
anti‐counterfeiting,
and
bioimaging.
Nonetheless,
a
general
limitation
of
is
short
emission
lifetimes,
typically
spanning
from
milliseconds
seconds,
which
creates
substantial
challenge
developing
day‐long
(DOA).
In
this
study,
DOA
system
demonstrated
through
the
incorporation
electron
donor/acceptor
exciplexes.
Polyethylene
naphthalate
used
for
both
acceptor
charge
storage
units,
coupling
with
spirobifluorene‐carbazole
derivative
donor,
providing
effective
separations
under
UV‐light
sunlight
excitation.
resulting
polymers
demonstrate
an
exceptional
bluish‐green
that
endures
over
28
h
ambient
conditions,
setting
new
record
longest
duration
polymeric
materials.
Moreover,
DOA‐doped
polymers,
films
fibers,
exhibit
outstanding
flexibility
transparency,
making
them
highly
suitable
flexible
technologies
wearable
devices.
Language: Английский
Day‐Long Organic Persistent Luminescence in Flexible Polymeric Materials
Longming Jin,
No information about this author
Wanqi Mo,
No information about this author
Ziyi Wang
No information about this author
et al.
Angewandte Chemie International Edition,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 26, 2025
Abstract
The
progress
in
organic
afterglow
materials
has
drawn
significant
attention
due
to
their
extensive
applications
fields
such
as
optoelectronics,
anti‐counterfeiting,
and
bioimaging.
Nonetheless,
a
general
limitation
of
is
short
emission
lifetimes,
typically
spanning
from
milliseconds
seconds,
which
creates
substantial
challenge
developing
day‐long
(DOA).
In
this
study,
DOA
system
demonstrated
through
the
incorporation
electron
donor/acceptor
exciplexes.
Polyethylene
naphthalate
used
for
both
acceptor
charge
storage
units,
coupling
with
spirobifluorene‐carbazole
derivative
donor,
providing
effective
separations
under
UV‐light
sunlight
excitation.
resulting
polymers
demonstrate
an
exceptional
bluish‐green
that
endures
over
28
h
ambient
conditions,
setting
new
record
longest
duration
polymeric
materials.
Moreover,
DOA‐doped
polymers,
films
fibers,
exhibit
outstanding
flexibility
transparency,
making
them
highly
suitable
flexible
technologies
wearable
devices.
Language: Английский
Through‐space interaction enables simultaneous enhancements of kr and kRISC in highly efficient spiro‐acridine based thermally activated delayed fluorescence emitter with acridone acceptor
Smart Molecules,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 1, 2024
Abstract
Most
of
acridine
based
thermally
activated
delayed
fluorescence
(TADF)
emitters
are
characterized
by
advantageous
reverse
intersystem
crossing
(RISC)
rate
(
k
RISC
s)
due
to
the
perpendicular
orientation
donor
acceptor
moiety,
but
suffer
from
a
poor
radiation
r
)
typically
in
order
10
6
s
−1
.
Herein,
two
sky
blue
TADF
3,6‐DMAC‐AD‐Py
and
3,6‐SFAC‐AD‐Py
were
developed
linking
(DMAC)
spiro‐fluorene‐acridine
(SFAC)
donors
10‐(pyridin‐2‐yl)acridin‐9(10
H
)‐one
(AD‐Py)
acceptor.
Larger
SFAC
electron‐deficient
pyridyl
groups
deliberately
incorporated
since
unique
through‐space
interaction
between
them
is
designed
drive
rotation
inner
ring
for
enhancing
frontier
molecular
orbitals
overlap
while
keeping
decent
behavior.
Thus,
increased
1.5
×
7
Simultaneously,
improve
spin
orbital
coupling
strength
reduce
energy
gaps,
generating
1.8
This
first
emitter
realizing
strategy.
enables
highly
efficient
sky‐blue
organic
light‐emitting
diode
with
maximum
external
quantum
efficiency
(EQE)
34.7%
Commission
International
de
I'Eclairage
coordinates
(0.19,
0.37).
More
importantly,
EQE
still
remained
27.6%
16.9%
at
high
brightness
1000
10,000
cd
m
−2
Language: Английский
Scaffolding and Heavy-Atom Effects of Metal Chains Enhanced Tunable Long Persistent Luminescence in Metal–Organic Frameworks
Xudong Xue,
No information about this author
Zheng Wang
No information about this author
Inorganic Chemistry,
Journal Year:
2024,
Volume and Issue:
64(1), P. 435 - 442
Published: Dec. 28, 2024
Metal–organic
frameworks
(MOFs)
with
long
persistent
luminescence
(LPL)
have
attracted
extensive
research
attention
due
to
their
potential
applications
in
information
encryption,
anticounterfeiting
technology,
and
security
logic.
The
strategic
combinations
of
organic
phosphor
linkers
metal
ions
lead
tremendous
frameworks,
which
could
unveil
many
undiscovered
properties
organics.
Here,
the
synthesis
characterization
a
three-dimensional
MOF
(Cd-MOF)
is
reported,
demonstrates
enhanced
blue
photoluminescence
phosphorescent
lifetime
124
ms
as
compared
pristine
linker
(H2L)
under
ambient
conditions
scaffolding
heavy-atom
effects
chains
framework.
Notably,
Cd-MOF
exhibits
intriguing
excitation-,
time-,
temperature-dependent
LPL,
duration
3
s
at
room
temperature
ability
shift
from
green
yellow
lower
temperatures.
Optical
characterizations
theoretical
calculations
reveal
that
H2L
molecules
are
responsible
for
emissions
Cd-MOF,
while
LPL
molecular
phosphors
can
be
significantly
regulated
through
coordination
interactions
effect
chains.
This
work
highlights
such
materials
promising
candidates
multiple
anticounterfeiting,
displaying,
encryption
applications.
Language: Английский