ACS Applied Materials & Interfaces,
Journal Year:
2023,
Volume and Issue:
15(33), P. 39896 - 39904
Published: Aug. 9, 2023
Developing
polymer-based
organic
afterglow
materials
with
switchable
ultralong
phosphorescence
(UOP)
that
are
insensitive
to
moisture
remains
challenging.
Herein,
two
luminogens,
BBCC
and
BBCS,
were
synthesized
by
attaching
7H-benzo[c]carbazole
(BBC)
benzophenone
diphenyl
sulfone.
These
emitters
employed
as
guest
molecules
doped
into
epoxy
polymers
(EPs),
which
constructed
in
situ
polymerization
achieve
polymer
BBCC-EP
BBCS-EP.
It
was
found
BBCS-EP
films
exhibited
significant
photoactivated
UOP
properties.
After
light
irradiation,
they
could
produce
a
conspicuous
quantum
yields
lifetimes
up
5.35%
1.91
s,
respectively.
Meanwhile,
also
presented
photochromic
characteristics.
Upon
thermal
annealing,
the
be
turned
off,
recovered
their
pristine
state,
showing
afterglow.
In
addition,
displayed
excellent
water
resistance
still
produced
obvious
after
soaking
for
4
weeks.
Inspired
unique
properties,
BBCS
mixtures
of
diglycidyl
ether
bisphenol
A
(DGEBA)
1,3-propanediamine
security
inks
light-controlled
multilevel
anticounterfeiting.
This
work
may
provide
helpful
guidance
developing
photostimuli-responsive
materials,
especially
those
stable
under
ambient
conditions.
Angewandte Chemie International Edition,
Journal Year:
2023,
Volume and Issue:
62(39)
Published: Aug. 14, 2023
Harnessing
the
potential
of
thermally
activated
delayed
fluorescence
(TADF)
and
room
temperature
phosphorescence
(RTP)
is
crucial
for
developing
light-emitting
diodes
(LEDs),
lasers,
sensors,
many
others.
However,
effective
strategies
in
this
domain
are
still
relatively
scarce.
This
study
presents
a
new
approach
to
achieving
highly
efficient
deep-blue
TADF
(with
PLQY
25
%)
low-energy
orange
RTP
90
through
fabrication
lead-free
hybrid
halides.
class
monomeric
dimeric
0D
antimony
halides
can
be
facilely
synthesized
using
bottom-up
solution
process,
requiring
only
few
seconds
minutes,
which
offer
exceptional
stability
nontoxicity.
By
leveraging
adaptable
molecular
arrangement
crystal
packing
modes,
demonstrate
ability
self-assemble
into
regular
1D
microrod
2D
microplate
morphologies.
self-assembly
facilitated
by
multiple
non-covalent
interactions
between
inorganic
cores
organic
shells.
Notably,
these
microstructures
exhibit
outstanding
polarized
luminescence
function
as
low-dimensional
optical
waveguides
with
remarkably
low
optical-loss
coefficients.
Therefore,
work
not
pioneering
demonstration
halides,
but
also
introduces
micro/nanostructures
that
hold
promising
applications
white
LEDs
photonic
systems.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: June 29, 2024
Dynamically
responsive
materials,
capable
of
reversible
changes
in
color
appearance
and/or
photoemission
upon
external
stimuli,
have
attracted
substantial
attention
across
various
fields.
This
study
presents
an
effective
approach
wherein
switchable
modulation
photochromism
and
ultralong
phosphorescence
can
be
achieved
simultaneously
a
zero-dimensional
organic-inorganic
halide
hybrid
glass
doped
with
4,4´-bipyridine.
The
facile
fabrication
large-scale
glasses
is
accomplished
through
combined
grinding-melting-quenching
process.
persistent
luminescence
regulated
the
photochromic
switch
induced
by
photo-generated
radicals.
Furthermore,
incorporation
aggregation-induced
chirality
effect
generates
intriguing
circularly
polarized
luminescence,
optical
dissymmetry
factor
(g
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(18)
Published: Jan. 25, 2024
Abstract
Long‐lived
and
highly
efficient
room
temperature
phosphorescence
(RTP)
materials
are
in
high
demand
for
practical
applications
lighting
display,
security
signboards,
anti‐counterfeiting.
Achieving
RTP
aqueous
solutions,
near‐infrared
(NIR)
emission,
NIR‐excited
crucial
bio‐imaging,
but
these
goals
pose
significant
challenges.
Supramolecular
self‐assembly
provides
an
effective
strategy
to
address
the
above
problems.
This
review
focuses
on
recent
advances
enhancement
of
via
supramolecular
self‐assembly,
covering
four
key
aspects:
small
molecular
cocrystals,
macrocyclic
hosts
guests,
multi‐stage
self‐assembly.
not
only
highlights
progress
areas
also
underscores
prominent
challenges
associated
with
developing
materials.
The
resulting
strategies
development
high‐performance
discussed,
aiming
satisfy
biomedical
science.
Small,
Journal Year:
2023,
Volume and Issue:
20(1)
Published: Aug. 30, 2023
Abstract
Room
temperature
phosphorescence
(RTP)
has
emerged
as
an
interesting
but
rare
phenomenon
with
multiple
potential
applications
in
anti‐counterfeiting,
optoelectronic
devices,
and
biosensing.
Nevertheless,
the
pursuit
of
ultralong
lifetimes
RTP
under
visible
light
excitation
presents
a
significant
challenge.
Here,
new
phosphorescent
materials
that
can
be
excited
by
record‐long
are
demonstrated,
realized
through
embedding
nitrogen
doped
carbon
dots
(N‐CDs)
into
poly(vinyl
alcohol)
(PVA)
film.
The
lifetime
N‐CDs@PVA
film
is
remarkably
extended
to
2.1
s
420
nm,
representing
highest
recorded
value
for
light‐excited
materials.
Theoretical
experimental
studies
reveal
robust
hydrogen
bonding
interactions
effectively
reduce
non‐radiative
decay
rate
radiative
transition
triplet
excitons,
thus
dramatically
prolong
lifetime.
Notably,
emission
also
activated
easily
accessible
low‐power
white‐light‐emitting
diode.
More
significantly,
practical
state‐of‐the‐art
anti‐counterfeiting
security
optical
information
storage
domains
further
demonstrated.
This
research
offers
exciting
opportunities
utilizing
light‐activated
ultralong‐lived
systems
wide
range
promising
applications.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: May 8, 2024
Abstract
Room
temperature
phosphorescence
materials
have
garnered
significant
attention
due
to
their
unique
optical
properties
and
promising
applications.
However,
it
remains
a
great
challenge
finely
manipulate
phosphorescent
achieve
desirable
performance
on
demand.
Here,
we
show
feasible
strategy
organic
by
introducing
dynamic
lanthanide
coordination.
The
phosphors
of
terpyridine
phenylboronic
acids
possessing
excellent
coordination
ability
are
covalently
embedded
into
polyvinyl
alcohol
matrix,
leading
ultralong
room
with
lifetime
up
0.629
s.
Notably,
such
performance,
including
intensity
lifetime,
can
be
well
controlled
varying
the
dopant.
Relying
modulable
these
lanthanide-manipulated
films,
multi-level
information
encryption
attacker-misleading
spatial-time-resolved
applications
is
successfully
demonstrated
greatly
improved
security
level.
This
work
opens
an
avenue
for
manipulating
meet
versatile
uses
in
Science Advances,
Journal Year:
2024,
Volume and Issue:
10(10)
Published: March 8, 2024
Developing
stable
room-temperature
phosphorescence
(RTP)
emission
without
being
affected
by
moisture
and
mechanical
force
remains
a
great
challenge
for
purely
organic
systems,
due
to
their
triplet
states
sensitive
the
infinitesimal
motion
of
phosphors
oxygen
quencher.
We
report
kind
highly
robust
phosphorescent
doping
rigid
phosphor
into
copolymer
(polyvinyl
butyral
resin)
matrix
with
balance
mutually
exclusive
features,
including
rigidly
hydrophilic
hydrogen
bond
network
elastically
hydrophobic
constituent.
Impressively,
these
RTP
polymeric
films
have
superior
adhesive
ability
on
various
surfaces
showed
reversible
photoactivated
lifetimes
up
5.82
seconds,
which
can
be
used
as
in
situ
modulated
anticounterfeit
labels.
They
maintain
bright
afterglow
over
25.0
seconds
under
practical
conditions,
such
storage
refrigerators,
soaking
natural
water
month,
or
even
subjected
strong
collisions
impacts.
These
findings
provide
deep
insights
developing
ultralong
materials
desirable
comprehensive
performance.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: April 9, 2024
Abstract
Creating
circularly
polarized
organic
afterglow
system
with
elevated
triplet
energy
levels,
suppressed
non-radiative
transitions,
and
effective
chirality,
which
are
three
critical
prerequisites
for
achieving
blue
afterglow,
has
posed
a
formidable
challenge.
Herein,
straightforward
approach
is
unveiled
to
attain
materials
by
covalently
self-confining
isolated
chiral
chromophore
within
polymer
matrix.
The
formation
of
robust
hydrogen
bonds
the
matrix
confers
distinctly
stabilized
molecular
state
chromophores,
endowing
emission
band
at
414
nm,
lifetime
3.0
s,
luminescent
dissymmetry
factor
~
10
−2
.
Utilizing
synergistic
chirality
transfer,
full-color
systems
endowed
doping
colorful
fluorescent
molecules
into
designed
polymers,
empowering
versatile
applications.
This
work
paves
way
streamlined
design
materials,
expanding
horizons
various
domains.