Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 10, 2024
Abstract
Unlocking
the
afterglow
properties
of
fluorescence
molecules
at
room
temperature
is
an
urgent
challenge.
Herein,
inks
prepared
with
dimethyl
terephthalate
(DTT)
and
carbazole
(Cz)
analogs
heteroatom
(C,
S,
O)
substituents
on
N
as
host
guest
can
be
directly
sprayed
onto
different
substrates
to
unlock
excitation‐wavelength
dependent
(Ex‐De)
characteristics
compound.
Additionally,
increase
in
number
lone
pair
electrons,
spin‐orbit
coupling
(SOC)
increases,
resulting
a
longer
duration
lasting
up
4.5
s
Φ
p
>27%.
Theory
calculations
experiments
indicate
that
originated
from
interactions
between
restricting
non‐radiative
transition
triplet
excitons.
Different
Ex
(with
watershed
310
nm)
lead
variation
conformation
S
0
DTT
1
,
which
turn
affects
strength
host‐guest
contributes
Ex‐De
characteristics.
Benefiting
facile
preparation,
substrate‐independent
applicability,
characteristics,
samples
are
demonstrated
for
applications
multilevel
information
security
fields.
This
work
proposes
general
strategy
unlocking
emission
traditional
molecules,
valuable
discovery
high‐performance
materials
future.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(45)
Published: July 26, 2024
Organic
ultralong
room
temperature
phosphorescence
(OURTP)
materials
capable
of
combining
various
emission
behaviors
for
diversified
optoelectronic
properties
and
applications
have
recently
gained
a
vigorous
development,
but
it
remains
forbidden
challenge
in
designing
OURTP
molecules
with
hybrid
local
charge-transfer
(HLCT)
feature,
possibly
due
to
the
elevated
difficulties
simultaneously
meeting
stringent
requirements
both
HLCT
emitters.
Here,
through
introducing
multiple
heteroatoms
into
one-dimensional
fused
ring
coumarin
moderate
charge
transfer
perturbation
donor-π-acceptor
architecture,
we
demonstrate
HLCT-featured
molecule
showing
promoted
fluorescence
quantum
yield
77
%
solution
long-lived
lifetime
251
ms
conventional
host
material
used
electroluminescent
device.
Thus,
efficient
organic
light-emitting
diodes
(OLEDs)
were
fabricated,
exhibiting
bright
electroluminescence
an
exciton
utilization
efficiency
85
yellow
lasting
over
2
s
afterglow.
Impressively,
OURTP-OLEDs
can
be
further
optimized
reach
unprecedented
total
external
(EQE)
~12
EQE
up
3.11
%,
representing
highest
performance
among
reported
OURTP-OLEDs.
These
impressive
results
highlight
significance
fuse
together
enriching
improving
afterglow
OLED
performances.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(46)
Published: July 9, 2024
Abstract
In
recent
years,
there
is
a
growing
interest
in
developing
ultralong
organic
room‐temperature
phosphorescence
(ORTP)
with
lifetimes
the
range
of
seconds.
As
one
important
three
primary
colors,
blue
ORTP
an
indispensable
core
component
RTP
regulation
and
application,
however,
large
Stokes
shift
characteristics
pose
certain
challenges
ORTP.
Here,
new
family
phosphors
are
synthesized
realized
through
crystal
assembly
water
phase.
Remarkably,
compared
to
materials
obtained
phases,
enabled
long‐lived
up
2.3
s
quantum
yield
reached
as
high
29.27%.
addition
efficient
green
form,
such
dark
possessed
thermal
stability
flexible
tunability.
Moreover,
superiority
selected
components
demonstrated
by
comparing
them
polymer
proposed
show
great
potential
programmable
information
encryption/anti‐counterfeiting.
Nano Letters,
Journal Year:
2024,
Volume and Issue:
24(42), P. 13307 - 13314
Published: Oct. 10, 2024
Long-wavelength
afterglow
emitters
are
crucial
for
optoelectronics
and
information
security;
however,
it
remains
a
challenge
in
achieving
high
luminescence
efficiency
due
to
the
lack
of
effective
modulation
electronic
coupling
nonradiative
transitions
singlet/triplet
excitons.
Here,
we
demonstrate
an
organic-carbon-dot
(CD)
hybrid
system
that
operates
via
space-confined
energy
transfer
strategy
obtain
bright
emission
centered
at
600
nm
with
near-unity
efficiency.
Photophysical
characterization
theoretical
calculation
confirm
efficient
can
be
assigned
synergistic
effect
intermolecular
from
triplet
excitons
CDs
singlets
subluminophores
intense
restraint
decay
losses
singlet/triplet-state
rationally
rigidification
amination
modification.
By
utilizing
precursor
engineering,
yellow
near-infrared
575
680
efficiencies
94.4%
45.9%
has
been
obtained.
Lastly,
these
highly
emissive
powders
enable
superior
performance
lighting
security.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 18, 2024
Organic
room-temperature
phosphorescent
(RTP)
materials,
especially
with
narrowband
emission
properties,
exhibit
great
potential
for
applications
in
display
and
sensing,
but
have
been
seldom
reported.
Herein,
a
rare
example
of
the
intrinsic
blue
RTP
material
is
fabricated
A
series
indolo[3,2,1-kl]phenothiazine
derivatives,
named
Cphpz,
1O-Cphpz,
2O-Cphpz,
are
designed
synthesized.
Due
to
their
relatively
rigid
structures,
these
three
compounds
showed
deep
emissions
ranging
from
396
434
nm
full
width
at
half
maximum
(FWHM)
31,
26,
31
nm,
respectively.
To
delight,
compound
2O-Cphpz
displayed
448
FWHM
36
long-lived
lifetime
1.08
s
hydroxyethyl
acrylate
acrylic
acid
matrix.
Photophysical
studies,
single
crystal
analyses,
TD-DFT
calculations
performed
elucidate
further
relationships
between
molecular
structures
properties.
Meanwhile,
because
highly
sensitive
humidity,
visualizing
droplet
path
optical
microfluidic
chip
efficiently
through
digital
light
processing
3D
printing.This
work
provides
reliable
strategy
realize
expand
self-monitoring
printed
structures.
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.
Phosphorescent
materials
have
potential
applications
in
anticounterfeiting
and
optoelectronics,
but
their
luminescence
is
generally
quenched
at
elevated
temperatures.
Herein,
a
synergistic
locking
strategy
has
been
developed
to
achieve
high-temperature
phosphorescence
(HTP)
of
carbon
dot
(CD)
composites.
Impressively,
the
CD
composites
retain
over
90%
75%
intensity
temperatures
up
110
170
°C,
respectively.
Even
higher
than
persists
for
5
s,
demonstrating
remarkable
stabilization
triplet
excitons.
Experimental
theoretical
results
revealed
that
this
outstanding
thermal
resistance
stems
from
effect
interlayer
covalent
bridges
multiple
hydrogen
bonding
interface.
Furthermore,
by
adjusting
degree
graphitization,
multicolor
HTP
ranging
blue
red
achieved
This
work
not
only
provides
facile
versatile
way
construct
CD-based
also
expands
heat-resistant
display
environments.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 6, 2025
Abstract
Organic
phosphorescence
holds
significant
potential
for
its
important
applications
in
sensors,
optoelectronics,
and
security
technologies.
However,
achieving
long‐lived
blue
phosphorescence,
particularly
at
high
temperatures,
remains
a
challenge.
In
this
work,
an
unusual
thermally
enhanced
is
investigated
observed
readily
synthesized
polymer
(P1),
which
created
by
copolymerizing
acrylamide
with
phenyl
terpyridine‐containing
monomer
(M1).
Remarkably,
P1
exhibits
ultra‐long
cyan
493
nm
lifetime
of
1.04
s
room
temperature
450
when
exposed
to
150
°C.
Experimental
simulation
results
suggest
that
the
high‐temperature
originates
from
activated
rotation
terpyridine
group,
triggering
conformational
transition
low‐energy
Iso2
high‐energy
Iso3
state.
Furthermore,
heat‐resistant
phosphorescent
can
be
easily
fabricated
into
optical
waveguide
low
loss
coefficient,
making
it
suitable
high‐performance
switches.
This
work
provides
novel
strategy
designing
high‐temperature‐resistant
materials,
promising
advanced
photonic
optoelectronic
devices.
Pure
organic
persistent
room
temperature
phosphorescence
(RTP)
has
shown
great
potential
in
numerous
applications,
ranging
from
information
encryption
and
display
technologies
to
bio-applications
beyond.
In
this
work,
a
suite
of
multi-color
long-lived
RTP
materials
featuring
distinct
afterglow
emissions
was
constructed
using
an
ion-radical
mediated
approach.
b[c]p/MeBPO
emitted
vivid
yellow
centered
at
560
nm
with
impressively
long
lifetime
860.01
ms.
While
compound
b[a]a
exhibited
near-infrared
(NIR)
(τ
=
215.96
ms)
after
doping
into
the
matrix.
The
transient
absorption
spectroscopy
investigations
disclosed
that
observed
phenomenon
fundamentally
tied
generation
radical
ions
rather
than
exciplex.
These
resulted
reduction
quenching
process
triplet
excited
state
BPO
by
ground
agent.
A
novel
evaluation
methodology
devised,
rooted
Marcus
theory,
gauge
specific
dopant-matrix
combination
towards
generating
pronounced
afterglow.
According
framework,
enhancement
is
directly
proportional
decrease
activation
energy
(ΔG≠)
associated
electron
transfer
reaction
occurring
between
dopant
Notably,
when
ΔG≠
surpasses
30
kcal/mol,
no
observable
occurs,
as
higher
values
significantly
impede
two
components.
Furthermore,
system
exhibits
exceptional
sensitivity,
low
0.02‰
molar
ratio
host
material.
This
remarkable
dependence
intensity
on
concentration
renders
bi-component
highly
promising
for
applications
requiring
ultra-high
sensitivity
broad-spectrum
detection
capabilities.