ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(32), P. 42794 - 42801
Published: Aug. 1, 2024
The
development
of
pure
organic
room-temperature
phosphorescent
(RTP)
materials
greatly
facilitates
the
integrated
application
luminescent
materials.
Herein,
a
type
photoactivated
red
RTP
material
was
constructed
by
simply
doping
4-(benzo[c][1,2,5]thiadiazol-5-ylthio)benzonitrile
(p-NNS)
into
poly(methyl
methacrylate)
(PMMA)
matrix.
obtained
film
realized
controllable
photoactivation
process
regulation
diverse
solvent
levels,
demonstrating
potential
advantages
in
optical
anti-counterfeiting
applications.
Furthermore,
properties
doped
were
utilized
to
detect
oxygen
content
from
2.00%
4.90%,
which
revealed
exact
consumption
ambient
under
UV
light.
Every
CIE
point
luminescence
corresponds
certain
content,
illustrating
visualization
content.
remarkable
effect
and
this
work
will
provide
competitive
for
further
Accounts of Materials Research,
Journal Year:
2023,
Volume and Issue:
4(10), P. 827 - 838
Published: Aug. 26, 2023
ConspectusThe
phosphorescence
is
produced
by
the
radiative
transition
of
excited
triplet
state
which
generated
intersystem
crossing
(ISC)
from
singlet
state.
Compared
with
fluorescence,
it
has
a
longer
luminescence
lifetime
and
larger
Stokes
shift,
so
phosphorescent
materials
have
great
application
value
in
fields
such
as
displays,
anticounterfeiting,
imaging.
But
due
to
low
ISC
rate
organic
molecules,
slow
state,
large
nonradiative
energy
loss
caused
molecular
vibration,
pure
room
temperature
(RTP)
usually
difficult
obtain.
Among
most
widely
used
strategies
including
crystal
assembly,
polymerization,
host–guest
encapsulation,
polymerization
strategy
based
on
rigid
polymers
achieved
success
widespread
attention
their
easy
processing
excellent
performance.The
main
function
fix
luminophore
into
matrix
suppress
transitions
oxygen
quenching.
That
is,
provide
microenvironment
necessary
for
RTP,
although
some
are
flexible
stretchable.
Conventional
limited
interaction
luminophores
do
not
promoting
states.
Therefore,
high
RTP
quantum
yield
depends
more
structural
design
luminophores.
By
modification
structure,
functionalized
can
be
endowed
ability
regulate
levels
luminophores,
enhance
ISC,
increase
RTP.
The
selection
also
enriches
diverse
properties
materials.This
Account
summarizes
latest
research
progress
field
polymer-based
enhancement
polymers.
Luminophores
construct
systems
doping,
covalent
linking,
or
supramolecular
interactions
PAA,
PMMA,
PVA,
PAM.
To
further
strengthen
polymer
rigidity,
secondary
been
successfully
employed
synergistically
nonradioactivation
performance,
hydrogen
bonding
bridges,
cross-linking.
no
suppressing
but
includes
enhancing
states
generating
special
phenomena.
A
few
specially
designed
utilize
external
heavy
atom
effects,
dipole–dipole
interactions,
electrostatic
diffusion
promote
rate.
Due
diversification
functionalization
polymers,
were
developed
various
phenomena
photoactivation,
excitation
wavelength
dependence,
photochromism,
circularly
polarized
stimulus-response.
We
hope
summarized
functions
development
trends
helpful
guidance
designing
high-performance
materials.
Journal of the American Chemical Society,
Journal Year:
2023,
Volume and Issue:
145(30), P. 16748 - 16759
Published: July 20, 2023
Understanding
the
changes
of
molecular
conformations
is
crucial
for
realizing
multiple
emissive
triplet
states
in
room-temperature
phosphorescence
(RTP)
materials.
In
this
work,
we
report
two
molecules,
4,4'-dimethylbenzil
(DMBZ)
and
4,4'-di-tert-butylbenzil
(DBBZ)
with
conformation-dependent
luminescence,
demonstrate
that
stimulus-responsive
wide-tuning
RTP
emissions
can
be
realized
via
synergetic
conformational
regulations
ground
excited
states.
Due
to
changes,
DMBZ
DBBZ
show
abundant
variations
upon
external
stimuli,
including
light,
force,
heat,
fumigation.
Notably,
exhibits
both
states,
which
endow
unique
behaviors.
presents
phase
transitions
between
supercooled
liquid
state
different
solid
accompanied
by
transitions,
excited-state
are
effectively
regulated.
Moreover,
wide-range
(between
cyan,
green,
yellow)
single
component
host-guest
systems
DBBZ,
showing
potential
applications
temperature
sensing,
multicolor
dynamic
displays,
information
encryption.
These
results
may
provide
new
visions
understanding
complicated
aggregated
state,
as
well
insights
into
relationship
conformations,
emissions,
stimulus
responsiveness.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(27)
Published: April 23, 2024
Abstract
The
development
of
single‐system
materials
that
exhibit
both
multicolor
room‐temperature
phosphorescence
(RTP)
and
thermally
activated
delayed
fluorescence
(TADF)
with
tunable
after
glow
colors
channels
is
challenging.
In
this
study,
four
metal‐free
carbon
dots
(CDs)
are
developed
through
structural
tailoring,
panchromatic
high‐brightness
RTP
achieved
via
strong
chemical
encapsulation
in
urea.
maximum
lifetime
quantum
yield
reaches
2141
ms
56.55%,
respectively.
Moreover,
CDs‐IV@urea,
prepared
coreshell
interaction
engineering,
exhibits
a
dual
afterglow
red
green
TADF.
degree
conjugation
functional
groups
precursors
affects
the
binding
interactions
nitrogen
cladding
on
CDs,
which
turn
stabilizes
triplet
energy
levels
gap
between
S
1
T
(Δ
E
ST
)
to
induce
RTP.
enhanced
wrapping
lowers
Δ
,
promoting
reverse
intersystem
crossing,
leads
This
fully
state,
thus
stabilizing
material
water,
even
extreme
environments
such
as
acids
oxidants.
These
tested
multicolor,
time,
temperature
multiencryption
well
vivo
bioimaging.
Hence,
these
have
promising
practical
applications
information
security
biomedical
diagnosis
treatment.
Angewandte Chemie International Edition,
Journal Year:
2023,
Volume and Issue:
62(44)
Published: Aug. 19, 2023
Abstract
The
stimulus‐responsive
room
temperature
phosphorescent
(RTP)
materials
have
endowed
wide
potential
applications.
In
this
work,
by
introducing
naphthalene
and
spiropyran
(SP)
into
polyacrylamide
as
the
energy
donor
acceptor
respectively,
a
new
kind
of
brilliant
dynamic
color‐tunable
amorphous
copolymers
were
prepared
with
good
stability
processibility,
afterglow
emissions
from
green
to
orange
in
response
stimulus
photo
or
acid,
thanks
multi‐responsibility
SP
transfer
between
SP.
addition
deeply
exploring
inherent
mechanism,
these
been
successfully
applied
dynamically
controllable
applications
information
protection
delivery.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: March 15, 2024
Abstract
There
is
interest
in
developing
sustainable
materials
displaying
circularly
polarized
room-temperature
phosphorescence,
which
have
been
scarcely
reported.
Here,
we
introduce
biobased
thin
films
exhibiting
luminescence
with
simultaneous
phosphorescence.
For
this
purpose,
phosphorescence-active
lignosulfonate
biomolecules
are
co-assembled
cellulose
nanocrystals
a
chiral
construct.
The
shown
to
capture
the
chirality
generated
by
within
films,
emitting
phosphorescence
0.21
dissymmetry
factor
and
103
ms
lifetime.
By
contrast
most
organic
materials,
chiral-phosphorescent
system
possesses
stability,
no
significant
recession
under
extreme
chemical
environments.
Meanwhile,
luminescent
resist
water
humid
environments
but
fully
biodegradable
(16
days)
soil
conditions.
introduced
bio-based,
environmentally-friendly
expected
open
many
opportunities,
as
demonstrated
here
for
information
processing
anti-counterfeiting.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(22)
Published: March 26, 2024
Abstract
Tunable‐lifetime
room‐temperature
phosphorescence
(RTP)
materials
have
been
widely
studied
due
to
their
broad
applications.
However,
only
few
reports
achieved
wide‐range
lifetime
modulation.
In
this
work,
ultra‐wide
range
tunable‐lifetime
efficient
dark
blue
RTP
were
realized
by
doping
methyl
benzoate
derivatives
into
polyvinyl
alcohol
(PVA)
matrix.
The
lifetimes
of
the
doped
films
can
be
increased
from
32.8
ms
1925.8
ms.
Such
wide
modulation
is
extremely
rare
in
current
reports.
Moreover,
emission
4‐hydroxybenzoate‐doped
film
located
region
and
quantum
yield
reaches
as
high
15.4
%,
which
broadens
applications
organic
optoelectronic
information.
Further
studies
demonstrated
that
reason
for
tunable
was
magnitude
electron‐donating
ability
substituent
group
modulates
HOMO–LUMO
singlet‐triplet
energy
gap
derivatives,
well
non‐covalent
interactions
with
PVA.
potential
luminescent
displays
optical
anti‐counterfeiting
these
high‐performance
conducted.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(4), P. 2484 - 2493
Published: Jan. 17, 2024
Organic
cocrystals
obtained
from
multicomponent
self-assembly
have
garnered
considerable
attention
due
to
their
distinct
phosphorescence
properties
and
broad
applications.
Yet,
there
been
limited
reports
on
cocrystal
systems
that
showcase
efficient
deep-red
near-infrared
(NIR)
charge-transfer
(CT)
phosphorescence.
Furthermore,
effective
strategies
modulate
the
emission
pathways
of
both
fluorescence
remain
underexplored.
In
this
work,
we
dedicated
our
work
four
self-assembled
called
"pyrene
box"
cages
using
1,3,6,8-pyrenetetrasulfonate
anions
(PTS4–),
4-iodoaniline
(1),
guanidinium
(G+),
diaminoguanidinium
(A2G+),
hydrated
K+
countercations.
The
binding
such
cations
PTS4–
platforms
adaptively
modulates
supramolecular
stacking
with
guest
molecules
1,
allowing
steer
pathways.
Notably,
confinement
molecule
1
within
PTSK{1}
PTSG{1}
leads
an
NIR
CT
emission.
addition
fuming
gases
like
triethylamine
HCl
allows
reversible
pH
modulations
binding,
which
in
turn
induce
a
transition
cage
between
states.
This
capability
was
further
illustrated
through
proof-of-concept
demonstration
shrimp
freshness
detection.
Our
findings
not
only
lay
foundation
for
future
designs
leveraging
weak
intermolecular
host–guest
interactions
engineer
excited
states
interacting
chromophores
but
also
broaden
prospective
applications
room-temperature
materials
food
safety
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(18)
Published: March 8, 2024
A
general
approach
to
constructing
room
temperature
phosphorescence
(RTP)
materials
involves
the
incorporation
of
a
phosphorescent
emitter
into
rigid
host
or
polymers
with
high
glass
transition
temperature.
However,
these
often
suffer
from
poor
processability
and
suboptimal
mechanical
properties,
limiting
their
practical
applications.
In
this
work,
we
developed
benzothiadiazole-based
dialkene
(BTD-HEA),
multifunctional
remarkable
yield
intersystem
crossing
(Φ
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 11, 2025
Abstract
The
pursuit
of
sustainable,
high‐performance
organic
ultralong
room
temperature
phosphorescence
(OURTP)
materials
with
stimulus‐responsive
properties
presents
a
significant
and
enticing
yet
formidable
challenge.
Herein,
an
efficient
strategy
to
confining
boric
acid‐based
compounds
into
biomass
macrocycle
γ‐cyclodextrin
through
multiple
interactions
is
developed,
enabling
the
construction
multicolor
OURTP
doped
systems.
synergistic
effects
strong
hydrogen
bonding,
C─O─B
covalent
cross‐linking,
host–guest
encapsulation
significantly
suppress
non‐radiative
transition,
culminating
in
extraordinary
lifetime
excellent
quantum
yield
4.65
s
32.8%,
respectively,
which
are
far
superior
reported
RTP
materials.
Additionally,
merging
phosphors
contributes
stimulus
responses,
overcoming
inherent
limitations
degradation
recycling
compounds,
dynamically
modulating
signals
multiple‐stimulus
achieving
integration
multifunctional
dynamic
data
processing
techniques.
This
work
will
provide
direction
for
new
environmentally
friendly
potentially
commercially
available
Advanced Functional Materials,
Journal Year:
2023,
Volume and Issue:
34(7)
Published: Nov. 3, 2023
Abstract
Organic
room
temperature
phosphorescent
(ORTP)
materials
have
garnered
significant
interest
in
the
fields
of
anti‐counterfeiting,
optical
display,
and
bio‐imaging
owing
to
their
distinctive
properties.
However,
a
major
drawback
most
existing
ORTP
is
short
phosphorescence
lifetime
low
quantum
yields
(QYs),
which
greatly
limit
applicability
across
multiple
fields.
In
this
paper,
covalently
assisted
host‐guest
doping
strategy
that
involves
embedding
three
aminobenzoic
acids
with
different
carboxylate
substitution
positions
into
cyanuric
acid
(CA)
matrix
through
covalent
bonding
using
microwave
heating
proposed.
All
prepared
exhibit
long
exceeding
600
ms
high
(PhQYs)
surpassing
20%.
Among
them,
composite
2‐aminoterephthalic
(2‐A)
anuric
stands
out
its
unique
blue
phosphorescence,
boasting
an
exceptional
absolute
photoluminescence
yield
(PLQY)
98.95%
remarkable
(PhQY)
76.42%,
along
800
ms.
Importantly,
these
high‐performance
been
successfully
utilized
anti‐counterfeiting
display
applications.