Abstract
Understanding
and
management
of
triplet
excitons
transition
in
the
same
molecule
remain
a
great
challenge.
Hence,
for
first
time,
by
host
engineering,
manageable
transitions
naphthalimide
derivative
NDOH
were
achieved,
monitored
through
intensity
ratio
(I
TADF
/I
RTP
)
between
thermally
activated
delayed
fluorescence
(TADF)
room-temperature
phosphorescence
(RTP).
Energy
differences
lowest
excited
states
guest
changed
from
0.03
to
0.17
eV,
I
decreased
200
times,
thus
red
shifting
afterglow
color.
It
was
proposed
that
shorter
conjugation
length
led
larger
band
gaps
materials,
contributing
efficient
Dexter
inefficient
Förster
energy
transfer.
Interestingly,
no
singlet
state
only
strongest
with
quantum
yield
13.9%
could
be
observed,
when
PBNC
loosest
stacking
largest
gap
acted
as
host.
This
work
provides
novel
insight
prediction
exciton
development
smart
materials.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: April 5, 2024
Abstract
Intrinsic
polymer
room-temperature
phosphorescence
(IPRTP)
materials
have
attracted
considerable
attention
for
application
in
flexible
electronics,
information
encryption,
lighting
displays,
and
other
fields
due
to
their
excellent
processabilities
luminescence
properties.
However,
achieving
multicolor
long-lived
luminescence,
particularly
white
afterglow,
undoped
polymers
is
challenging.
Herein,
we
propose
a
strategy
of
covalently
coupling
different
conjugated
chromophores
with
poly(acrylic
acid
(AA)-AA-N-succinimide
ester)
(PAA-NHS)
by
simple
rapid
one-pot
reaction
obtain
pure
RTPs
various
colors.
Among
these
polymers,
the
highest
quantum
yield
PAPHE
reaches
14.7%.
Furthermore,
afterglow
colors
can
be
modulated
from
blue
red
introducing
three
into
them.
Importantly,
acquired
TPAP-514
exhibits
at
room
temperature
chromaticity
coordinates
(0.33,
0.33)
when
ratio
suitable
value
owing
three-primary-color
mechanism.
Systematic
studies
prove
that
emission
comes
superposition
triplet
excited
states
components.
Moreover,
potential
applications
obtained
light-emitting
diodes
dynamic
anti-counterfeiting
are
explored.
The
proposed
provides
new
idea
constructing
intrinsic
diverse
white-light
RTPs.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: April 27, 2024
Abstract
Organic
room
temperature
phosphorescence
(RTP)
has
significant
potential
in
various
applications
of
information
storage,
anti-counterfeiting,
and
bio-imaging.
However,
achieving
robust
organic
RTP
emission
the
single-component
system
is
challenging
to
overcome
restriction
crystalline
state
or
other
rigid
environments
with
cautious
treatment.
Herein,
we
report
a
persistent
aggregated
forms,
such
as
crystal,
fine
powder,
even
amorphous
states.
Our
experimental
data
reveal
that
vigorous
emissions
rely
on
their
tight
dimers
based
strong
large-overlap
π
-
interactions
between
polycyclic
aromatic
hydrocarbon
(PAH)
groups.
The
dimer
structure
can
offer
not
only
excitons
low
energy
levels
for
visible-light
excited
red
long-lived
but
also
suppression
nonradiative
decays
an
good
resistance
heat
(up
70
°C)
water.
Furthermore,
demonstrate
water-dispersible
nanoparticle
over
600
nm
lifetime
0.22
s
cellular
in-vivo
imaging,
prepared
through
common
microemulsion
approach
without
overcaution
nanocrystal
formation.
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.
Abstract
Understanding
and
management
of
triplet
excitons
transition
in
the
same
molecule
remain
a
great
challenge.
Hence,
for
first
time,
by
host
engineering,
manageable
transitions
naphthalimide
derivative
NDOH
were
achieved,
monitored
through
intensity
ratio
(I
TADF
/I
RTP
)
between
thermally
activated
delayed
fluorescence
(TADF)
room-temperature
phosphorescence
(RTP).
Energy
differences
lowest
excited
states
guest
changed
from
0.03
to
0.17
eV,
I
decreased
200
times,
thus
red
shifting
afterglow
color.
It
was
proposed
that
shorter
conjugation
length
led
larger
band
gaps
materials,
contributing
efficient
Dexter
inefficient
Förster
energy
transfer.
Interestingly,
no
singlet
state
only
strongest
with
quantum
yield
13.9%
could
be
observed,
when
PBNC
loosest
stacking
largest
gap
acted
as
host.
This
work
provides
novel
insight
prediction
exciton
development
smart
materials.