New Journal of Chemistry,
Journal Year:
2024,
Volume and Issue:
48(36), P. 16119 - 16126
Published: Jan. 1, 2024
Two
new
multi-resonance
(MR)
blue
emitters
with
benzothiophene
within
B/N
skeletons
exhibit
emissions
narrow
FWHMs,
achieving
high
PLQYs
and
long
device
lifetimes.
Chemical Reviews,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 12, 2024
Since
the
seminal
report
by
Adachi
and
co-workers
in
2012,
there
has
been
a
veritable
explosion
of
interest
design
thermally
activated
delayed
fluorescence
(TADF)
compounds,
particularly
as
emitters
for
organic
light-emitting
diodes
(OLEDs).
With
rapid
advancements
innovation
materials
design,
efficiencies
TADF
OLEDs
each
primary
color
points
well
white
devices
now
rival
those
state-of-the-art
phosphorescent
emitters.
Beyond
electroluminescent
devices,
compounds
have
also
found
increasing
utility
applications
numerous
related
fields,
from
photocatalysis,
to
sensing,
imaging
beyond.
Following
our
previous
review
2017
(
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 21, 2024
Abstract
In
the
development
of
organic
light‐emitting
diodes
(OLEDs)
with
high
efficiency
and
minimal
roll‐off,
fast
reverse
intersystem
crossing
(RISC)
in
multi‐resonance
thermally
activated
delayed
fluorescence
(MR‐TADF)
materials
is
critical.
The
RISC
process
typically
hindered
by
insufficient
spin‐orbital
coupling
(SOC).
Incorporating
heavy
atom
selenium
into
MR‐TADF
structure
has
potential
to
enhance
SOC
through
effect.
However,
specific
placement
within
molecule
results
different
enhancements
SOC,
detailed
interplay
between
these
factors
yet
be
elucidated.
introduction
a
selenium‐containing
moiety,
phenoxaselenine,
at
substituted
positions
undertaken,
revealing
that
3‐substituted
phenoxaselenine
exhibits
faster
transition
significant
increase
higher
triplet
excited
states
S
1
state,
compared
2‐substituted
phenoxaselenine.
Significantly
reduced
roll‐off
achieved
for
narrow‐band
emission
OLEDs
based
on
owing
enhanced
effect,
giving
an
impressive
external
quantum
above
20%
even
under
10
000
cd
m
−2
corresponding
OLED
device.
These
underscore
strategic
effect
manipulation
efficient
spin‐flipping.
Advanced Optical Materials,
Journal Year:
2024,
Volume and Issue:
12(21)
Published: April 9, 2024
Abstract
While
the
development
of
solution‐processed
organic
light‐emitting
diodes
(sOLEDs)
utilizing
multiple
resonance‐induced
thermally
activated
delayed
fluorescence
(MR‐TADF)
is
highly
significant,
it
restricted
by
limited
solubility
and
film‐forming
property
resulting
from
rigid
conjugate
planarity
MR‐TADF
materials.
Herein,
an
effective
strategy
presented
to
obtain
narrowband
emitters
introducing
inert
steric
bulky
hindrance
group
into
resonance
skeleton,
thereby
mitigating
issues
arising
intermolecular
packing‐induced
poor
solution
processing
ability
quenching
effects.
The
target
emitter,
designed
as
3CzSF‐BN,
exhibits
pure‐green
emission
with
a
peak
at
520
nm
small
full
width
half
maximum
(FWHM)
30
(0.14)
eV.
Remarkably,
achieves
exceptional
photoluminescence
quantum
yield
(PLQY)
100%
notable
advancements
in
attributes.
optimized
bottom‐emitting
sOLED
(BE‐sOLED)
device
external
efficiency
(EQE)
over
20%
Commission
Internationale
de
I’Éclairage
(CIE)
coordinates
(0.214,
0.716).
Notably,
top‐emitting
(TE‐sOLED)
ultra‐pure
green
color
FWHM
22
CIE
(0.138,
0.771),
highlighting
effectiveness
this
designing
high‐performance
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(31)
Published: May 23, 2024
Luminescent
materials
with
narrowband
emission
have
extraordinary
significance
for
developing
ultrahigh-definition
display.
B-N-containing
multiple
resonance
thermally
activated
delayed
fluorescence
(MR-TADF)
are
strong
contenders.
However,
their
device
performances
pervasively
encounter
detrimental
aggregation-caused
quenching
effect
that
is
highly
vulnerable
to
doping
concentration,
complicating
fabrication.
Therefore,
constructing
efficient
and
concentration-independent
MR-TADF
emitters
of
pragmatic
importance
improving
controllability
reproducibility,
simplifying
manufacturing
procedures,
conserving
production
costs.
Here,
by
systematic
arrangement
donor
triphenylamine
fluorophore
BNCz
on
distinct
bridges,
a
spatial
confinement
strategy
has
been
developed
donor-bridge-fluorophore
architecture.
Structurally
fine
modulation
progressive
evolution
construct
molecular
entities
congested
steric
hindrance
can
suppress
intermolecular
interactions
without
substantially
affecting
the
luminescence
tone
BNCz,
resulting
in
emitters;
through
isomer
engineering,
two
isomers
BN-PCz-TPA
TPA-PCz-BN
different
crystal
stacking
patterns
synthesized
altering
connection
mode
between
BNCz.
As
result,
BN-PCz-TPA-based
showcases
maximum
external
quantum
efficiency
(EQE)
36.3%
narrow
full-width
at
half-maximum
27
nm
10
wt%
concentration.
Even
20
EQE
remains
32.5%
spectrum
almost
unchanged.
Chemical Communications,
Journal Year:
2024,
Volume and Issue:
60(53), P. 6728 - 6740
Published: Jan. 1, 2024
This
review
overviews
recent
research
on
circularly
polarized
luminescence
from
planar
chiral
organic
compounds,
focusing
their
synthetic
strategies,
properties
and
applications.
Advanced Optical Materials,
Journal Year:
2024,
Volume and Issue:
12(20)
Published: March 27, 2024
Abstract
The
development
of
efficient,
bright,
and
stable
narrowband
light‐emitting
electrochemical
cells
(LECs)
has
remained
a
challenge.
Here,
intrinsically
ionic
multi‐resonance
thermally
activated
delayed
fluorescence
(MR‐TADF)
emitters
are
reported
as
guest
for
LECs,
which
developed
by
attaching
an
imidazolium
cation
onto
typical
MR‐TADF
emitter.
In
solution,
the
show
green–blue
emission
peaked
at
486−497
nm
with
small
full
widths
half‐maximum
(FWHMs)
24−26
nm.
doped
films,
they
high
luminescent
efficiencies
≈90%.
LECs
using
exciplex
host
494−503
FWHMs
31−34
nm,
afford
external
quantum
(EQEs)
up
to
10%
under
constant‐voltage
driving.
With
TADF
small‐molecule
hosts,
EQEs
13.0%
driving,
is
highest
among
all
peak
brightness/EQE/half
lifetime
780
cd
m
−2
/5.6%/62.2
h
constant‐current
A
long
half‐lifetime
≈630
further
been
achieved
136
.
work
demonstrates
great
potential
use
hosts
develop
LECs.
Journal of Semiconductors,
Journal Year:
2024,
Volume and Issue:
45(8), P. 082402 - 082402
Published: Aug. 1, 2024
Abstract
Boron−nitrogen
doped
multiple
resonance
(BN-MR)
emitters,
characterized
by
B−N
covalent
bonds,
offer
distinctive
advantages
as
pivotal
building
blocks
for
facile
access
to
novel
MR
emitters
featuring
narrowband
spectra
and
high
efficiency.
However,
there
remains
a
scarcity
of
exploration
concerning
synthetic
methods
structural
derivations
expand
the
library
BN-MR
emitters.
Herein,
we
present
synthesis
emitter,
t
Cz[B−N]N,
through
one-pot
borylation
reaction
directed
amine
group,
achieving
an
impressive
yield
94%.
The
emitter
is
decorated
incorporating
two
3,6-di-t-butylcarbazole
(
Cz)
units
into
bond
parent
molecule
via
para
-C−π−D
-N−π−D
conjugations.
This
peripheral
decoration
strategy
enhances
reverse
intersystem
crossing
process
shifts
emission
band
towards
pure
green
region,
peaking
at
526
nm
with
full-width
half
maximum
(FWHM)
41
nm.
Consequently,
organic
light
emitting
diodes
(OLEDs)
employing
this
achieved
external
quantum
efficiency
(EQE
max
)
value
27.7%,
minimal
roll-off.
Even
practical
luminance
1000
cd∙m
−2
,
device
maintains
EQE
24.6%.