Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 5, 2025
Abstract
Photoactivated
circularly
polarized
afterglow
(CPA)
exhibits
broad
application
prospects
in
various
optoelectronic
areas
due
to
its
multidimensional
emission
characteristics,
including
wavelengths,
lifetimes,
and
chirality.
Achieving
photoactivated
CPA
with
extremely
high
dissymmetry
factor
(
g
lum
)
values
is
highly
desired
but
considerably
challenging.
This
work
reports
a
bilayer
assembly
(R/S‐CLC‐TPB)
integrating
TPB@PMMA
thin
film
the
selective
reflection
of
cholesteric
liquid
crystals.
Initially,
R/S‐CLC‐TPB
no
emission,
while
following
1
min
UV
irradiation,
it
achieves
an
noticeable
long
lifetime
125
ms
value
up
1.6.
enhancement
can
be
attributed
oxygen
consumption
properties
under
subsequently
minimizing
loss
triplet
exciton.
Furthermore,
by
employing
triplet‐singlet
Förster
resonance
energy
transfer
(TS‐FRET)
strategy
from
organic
persistent
room‐temperature
phosphorescence
donor
fluorescent
dye
acceptor,
color
successfully
modulated
green
orange.
Ultimately,
these
materials
demonstrate
promising
capabilities
for
advanced
multi‐level
information
encryption
utilizing
their
tunable
color,
create
multiple
layers
that
selectively
accessed
decoded
based
on
photoactivation
chiroptical
properties.
ACS Sustainable Chemistry & Engineering,
Journal Year:
2024,
Volume and Issue:
12(2), P. 916 - 924
Published: Jan. 4, 2024
Room-temperature
phosphorescence
(RTP)
materials
with
high
mechanical
strength
are
attractive
and
important
but
rarely
reported.
In
this
study,
konjac
glucomannan
(KGM),
a
polysaccharide
derived
from
natural
taro,
was
observed
to
emit
long-lived
RTP
via
clusterization-triggered
emission
(CTE).
The
CTE
behavior
of
KGM
fully
investigated
in
solution
the
solid
state.
distinct
concentration-enhanced
for
aqueous
solutions,
combined
its
low
toxicity
biocompatibility,
renders
highly
promising
bioimaging.
foams
were
fixation
multiple
hydrogen
bonds
clusters
oxygen-containing
groups.
lifetime
foam
could
reach
351.2
ms,
lightweight
withstand
compressive
stress
5.73
MPa.
exhibit
typical
excitation
wavelength
(λex)-dependent
color-tunable
RTP,
afterglows
changing
blue-green
grass-green
as
λex
is
increased
310
365
nm.
results
indicate
that
suitable
development
eco-friendly
strength.
ACS Applied Bio Materials,
Journal Year:
2023,
Volume and Issue:
6(11), P. 4572 - 4585
Published: Oct. 26, 2023
This
minireview
focuses
on
recent
advancements
in
organic
molecular-to-supramolecular
self-assembled
room-temperature
phosphorescent
(RTP)
materials
and
their
prospective
biomedical
applications.
RTP
materials,
having
unique
capacity
to
emit
long-lasting
phosphorescence
at
ambient
temperature,
have
piqued
researchers'
interest
various
biological
applications,
including
biosensing,
bioimaging,
drug
delivery,
photodynamic
therapy
(PDT).
These
several
benefits,
high
sensitivity,
remarkable
photostability,
low
cytotoxicity.
materials'
self-assembly
into
supramolecular
structures
improves
performance
broadens
uses.
Researchers
built
systems
with
by
leveraging
weak
noncovalent
interactions
aquatic
conditions.
demonstrated
incredible
promise
as
biosensors
that
enable
sensitive
analyte
detection
photosensitizers
PDT
target
sensitize
specific
cell
types.
The
review
also
outlines
future
directions
challenges
developing
utilizing
pure
for
imaging
purposes,
providing
valuable
guidelines
design
application.
Chemistry - An Asian Journal,
Journal Year:
2024,
Volume and Issue:
19(5)
Published: Feb. 7, 2024
Materials
exhibiting
room
temperature
phosphorescence
(RTP)
have
recently
emerged
as
a
subject
of
significant
interest.
In
this
study,
we
successfully
created
inclusion
crystals
by
introducing
halobenzenes
guests
into
host
molecule
combining
benzophenone
with
naphthalene
diimide.
This
approach
led
to
the
creation
fascinating
fluorescence
and
RTP
properties
dependent
on
guest
molecules.
Notably,
containing
chlorobenzene
showed
cyan
fluorescence,
while
those
iodobenzene
displayed
red
RTP.
difference
highlights
impact
luminescent
properties,
external
heavy-atom
effect
playing
key
role
in
promoting
efficient
intersystem
crossing
between
excited
singlet
triplet
states.
Crystals
bromobenzene
exhibited
unique
blend
RTP,
both
from
diimide,
highlighting
moderate
effect.
These
findings
reveal
composite
materials
remarkably
diverse
interesting
optical
characteristics.
The Journal of Physical Chemistry Letters,
Journal Year:
2023,
Volume and Issue:
14(28), P. 6451 - 6458
Published: July 12, 2023
Pure
organic
persistent
room-temperature
phosphorescence
(p-RTP)
is
in
urgent
demand
for
advanced
optoelectronic
and
bioelectronic
applications.
However,
it
remains
an
enormous
challenge
to
modulate
the
emission
colors
while
simultaneously
boosting
lifetimes
efficiencies.
Herein,
we
report
co-crystallization
between
melamine
cyclic
imide-based
non-conventional
luminophores,
which
affords
co-crystals
owning
multiple
hydrogen
bonds
effective
clustering
of
electron-rich
units,
thus
resulting
diverse
emissive
species
with
highly
rigidified
conformations
promoted
spin–orbit
coupling.
Consequently,
p-RTP
enhanced
efficiencies
up
12.0%
898
ms,
alongside
remarkably
improved
color
tunability,
are
obtained.
These
results
may
spur
future
rational
design
high-performance
materials
advance
mechanism
understanding
origin
color-tunable
phosphorescence.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 26, 2024
Abstract
Phosphorescent
supramolecular
hydrogels
are
currently
a
prevalent
topic
for
their
great
promise
in
various
photonic
applications.
Herein,
an
efficient
near‐infrared
(NIR)
phosphorescence
hydrogel
is
reported
via
the
hierarchical
assembly
strategy
aqueous
solution,
which
fabricated
from
amphiphilic
bromonaphthalimide
pyridinium
derivative
(G),
exfoliated
Laponite
(LP)
nanosheets,
and
polymeric
polyacrylamide
(PAAm).
Initially,
G
spontaneously
self‐aggregates
into
spherical
nanoparticles
covered
with
positively
charged
units
emits
single
fluorescence
at
410
nm.
Driven
by
electrostatic
interactions
negatively
subsequently
function
as
cross‐linked
binders
coassemble
LP
engendered
red
room‐temperature
(RTP)
up
to
620
Benefiting
hydrogen‐bonding
interactions‐mediated
physical
cross‐linkage,
further
introduction
of
PAAm
not
only
significantly
elevates
mechanical
strength
showing
fast
self‐healing
capability,
but
also
increases
lifetime
2.49
4.20
ms,
especially
generating
even
higher
temperature
(
τ
363
K
=
2.46
ms).
Additionally,
RTP
energy
transfer
occurs
after
doping
small
amount
organic
dye
heptamethine
cyanine
(IR780)
acceptor
hydrogels,
resulting
long‐lived
NIR
emission
823
nm
high
donor/acceptor
ratio,
successfully
applied
cell
labeling
window.
Smart Molecules,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 4, 2025
Abstract
Stimulus‐responsive
organic
room
temperature
phosphorescent
(RTP)
materials
have
received
significant
attention
in
bioimaging,
sensing,
and
data
storage
because
of
their
controllable
dynamic
variability
rapid
response.
Organic
co‐crystals,
with
tailor‐designed
optical
properties
through
manipulation
aggregate
structures,
proven
to
be
very
effective
elucidating
the
structure‐property
relationship
RTP
at
molecular
level.
Therefore,
enhancing
rigid
frameworks
that
promote
intersystem
crossing
is
a
valid
approach.
Notably,
realization
co‐crystal
performance
by
altering
components
or
adjusting
crystal
lattices
highly
appealing;
however,
this
has
not
been
fully
addressed.
In
study,
an
co‐crystal,
4,4′‐bipyridine
(44BD),
was
employed
as
host,
1,4‐diiodotetrafluorobenzene
(DITF)
4‐bromo‐2,3,5,6‐tetrafluorobenzoic
acid
(TFBA)
were
guests.
The
44BD‐DITF
exhibited
orange
RTP,
whereas
44BD‐TFBA
displayed
bright
yellow
RTP.
Crystal
analysis
theoretical
calculations
revealed
dense
packing
abundant
intermolecular
interactions
within
these
co‐crystals
are
crucial
for
emergence
both
show
reversible
acid/base
stimulus
response,
is,
exposure
hydrochloric
(HCl)
fumes
results
quenching
which
can
subsequently
restored
triethylamine
(TEA)
fumigation.
This
study
presents
approach
towards
switching
thus
offering
opportunities
development
stimulus‐responsive
next‐generation
applications.
Journal of Materials Chemistry C,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Balancing
the
donor–acceptor
(D–A)
systems
and
spatial
configurations
to
precisely
modulate
dual-state
emission
(DSE)
properties
in
imidazo[1,2-
a
]pyridine-derived
luminogens
for
applications
cell
imaging
hydrazine
sensing.
Currently,
numerous
afterglow
materials
often
suffer
from
low
phosphorescence
quantum
yields
(ΦPh)
and
are
confined
to
a
singular
luminescent
color.
In
this
study,
we
devised
an
approach
by
incorporating
four
distinct
carbazole
derivative
guest
molecules,
featuring
varying
degrees
of
halogen
substitution
naphthalene
group
sites,
into
β-estradiol
host
molecules
through
high-temperature
melt
doping
create
exceptional
organic
composites.
Remarkably,
all
exhibit
characteristics,
including
prolonged
lifetimes
ultrahigh
yields,
with
the
pinnacle
lifetime
soaring
904.76
ms
peak
yield
achieving
remarkable
40.0%.
Notably,
even
without
heavy
atom
incorporation,
phosphors
managed
attain
ΦPh
18.0%,
underscoring
their
unique
properties.
Furthermore,
our
experiments
unveiled
intriguing
phenomenon:
rather
than
single
fluorescence
or
emission,
these
dual-emission
encompassing
both
phosphorescence.
The
versatility
in
luminescence
color
manipulation
was
further
demonstrated
adjusting
temperature
excitation
wavelength,
offering
unparalleled
flexibility.
Moreover,
hues
could
be
finely
tuned
number
atoms,
adding
another
layer
tunability.
Theoretical
calculations
provided
valuable
insights,
showing
that
changes
bromine
substitutions
positions
significantly
affect
molecule's
spin–orbit
coupling
constants
nature
its
excited
states.
This
understanding
not
only
highlights
molecular
mechanisms
behind
observed
properties
but
also
provides
roadmap
for
future
design
optimization
such
advanced
materials.
Advanced Optical Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 14, 2025
Abstract
Organic
room‐temperature
phosphorescence
(RTP)
with
rich
photophysical
properties
has
attracted
great
interest,
but
it
remains
a
big
challenge
to
realize
pure
RTP
without
fluorescence
in
steady‐state
photoluminescence
(SSPL)
and
blue‐shifted
that
intrinsically
restricted
by
the
spin‐forbidden
intersystem
crossing
(ISC)
radiative
decay
of
low‐lying
triplet
excited
state.
Herein,
two
fluorescence‐free
molecules
based
on
β‐diketone‐bridged
phenoselenazine/phenothiazine
are
developed,
which
contain
either
Se
or
S
heteroatom
phosphor
significantly
promote
ISC;
and,
both
isolated
J‐aggregated
phosphors
formed
crystal,
where
J‐aggregation
can
not
only
facilitate
ISC
for
also
strength
emission
high
phosphorescent
quantum
yield
22.3%,
while
affords
longer
lifetime
up
131
ms.
Excitingly,
(35
nm
compare
SSPL)
from
yellow‐green
(525
nm)
cyan
(490
dynamically
depending
time
temperature
is
observed
first
time.
Experimental
theoretical
results
indicate
regulation
time/temperature‐dependent
attributed
different
lifetimes
aggregated
owing
dynamic
competition
between
accumulation
modes
crystal
aided
interrupted
conjugation
sp
3
C
β‐diketone.