Angewandte Chemie,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 7, 2024
Abstract
Multi‐resonance
thermally
activated
delayed
fluorescence
(MR‐TADF)
emitters
offer
natural
advantages
for
creating
power‐efficient,
wide‐color‐gamut
OLEDs.
However,
current
green
MR‐TADF
face
challenges
in
simultaneously
achieving
high
color
purity
and
efficient
reverse
inter‐system
crossing
(RISC),
leading
to
suboptimal
device
performance.
In
this
study,
we
propose
a
synergistic
molecular
design
approach
that
combines
π‐extension
peripheral
locking
address
these
challenges.
This
allows
the
construction
of
quadruple
borylated
not
only
deliver
precisely
tuned
pure‐green
emission
with
narrow
full
width
at
half
maximum
(FWHM)
15
nm,
but
also
exhibit
close‐to‐unity
quantum
yield,
rapid
RISC,
optimal
horizontal
dipole
orientation.
The
resulting
sensitizer‐free
OLED
approaches
BT.2020
standard
CIE
coordinates
(0.18,
0.74)
demonstrates
impressive
external
efficiency
(EQE)
36.6
%
31.8
1000
cd
m
−2
.
Additionally,
shows
good
operational
stability,
lifetime
(LT
80
)
485
hours
an
initial
luminance
study
hence
offers
promising
strategy
effectively
enhances
comprehensive
Advanced Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 23, 2025
Abstract
Herein,
a
parallel
“bifunctional
group”
modulation
method
is
proposed
to
achieve
controlled
of
the
emission
wavelength
and
full‐width
at
half‐maximum
(FWHM)
values.
As
result,
three
proof‐of‐concept
emitters,
namely
DBNDS‐TPh,
DBNDS‐DFPh,
DBNDS‐CNPh,
are
designed
synthesized,
with
first
functional
dibenzo[
b,d
]thiophene
unit
concurrently
reducing
bandgap
elevate
their
triplet
state
energy.
A
second
group
1
,
′:
3
′,
″‐
triphenyl
electron
acceptors
1,3‐difluorobenzene
benzonitrile
respectively,
deepen
HOMO
LUMO
levels.
Accordingly,
CIE
coordinates
DBNDS‐CNPh
(0.13,
0.77),
(0.14,
0.76)
in
dilute
toluene
solution.
This
marks
instance
achieving
y
value
0.77
solutions.
Significantly,
non‐sensitized
pure‐green
OLEDs
based
on
DBNDS‐TPh
DBNDS‐DFPh
demonstrate
peak
EQE
35.0%
34.5%,
corresponding
(0.18,
0.75),
(0.17,
doping
concentration
wt.%,
representing
green
OLED
reaching
0.76
bottom‐emitting
device
structure
as
reported
literature.
Advanced Functional Materials,
Год журнала:
2024,
Номер
34(32)
Опубликована: Март 26, 2024
Abstract
Sulfone
group
plays
a
pivotal
role
in
narrowing
emission
spectra,
while,
precise
modification
with
sulfone
for
carbonyl‐based
narrowband
emitters
that
maintain
high
color
purity
remains
challenging.
Herein,
comprehensive
exploration
of
the
function
is
performed
various
sulfur
valences
and
positions
fused
into
traditional
unit
QAO,
namely
SpiroS‐QAO,
SpiroSO
2
‐QAO,
SpiroO‐QAO,
SpiroOSO
‐QAO.
A
rigid
molecular
skeleton
spiro
structure
as
an
intramolecular
lock
enables
four
to
exhibit
emissions.
After
full
oxidization
sulfur,
band
‐QAO
further
narrowed,
width
at
half
maximum
32
nm,
compared
43
nm
sulfane‐decorated
which
attributed
suppressed
C─S
bond‐length
variation
by
introduction
group.
Nearly
identical
spectra
SpiroO‐QAO
suggest
should
be
directly
linked
core
maximize
its
function.
Maximum
external
quantum
efficiencies
30.8%,
30.3%,
29.2%
are
achieved
SpiroS‐QAO‐based
sensitized
organic
light‐emitting
diodes
highly
efficient
thermally
activated
delayed
fluorescence
assistant
host.
These
results
offer
understanding
embedded
respect
band.
Chemical Reviews,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 9, 2025
Fluorescence
emitters
with
a
multiple-resonant
(MR)
effect
have
become
research
hotspot.
These
MR
mainly
consist
of
polycyclic
aromatic
hydrocarbons
boron/nitrogen,
nitrogen/carbonyl,
and
indolocarbazole
frameworks.
The
staggered
arrangement
the
highest
occupied
molecular
orbital
lowest
unoccupied
facilitates
MR,
resulting
in
smaller
internal
reorganization
energy
narrower
emission
bandwidth.
Optimal
charge
separation
suppresses
gap
between
singlet
triplet
excited
states,
favoring
thermally
activated
delayed
fluorescence
(TADF).
MR-TADF
materials,
due
to
color
purity
high
efficiency,
are
excellent
candidates
for
organic
light-emitting
diodes.
Nevertheless,
significant
challenges
remain;
particular,
limitation
imposed
by
alternated
core
configuration
hinders
their
diversity
versatility.
Most
existing
materials
concentrated
blue-green
range,
only
few
red
near-infrared
spectra.
This
review
provides
timely
comprehensive
screening
from
pioneering
work
present.
Our
goal
is
gain
understandings
structure-performance
relationship
both
basic
advanced
perspectives.
Special
emphasis
placed
on
exploring
correlations
chemical
structure,
photophysical
properties
electroluminescent
performance
depth
breadth
an
aim
promote
future
development
emitters.
The Journal of Physical Chemistry C,
Год журнала:
2024,
Номер
128(33), С. 13756 - 13762
Опубликована: Авг. 14, 2024
Organic
light-emitting
diodes
(OLEDs)
based
on
multiresonance-induced
thermally
activated
delayed
fluorescent
(MR-TADF)
materials
are
revolutionizing
the
field
of
organic
electroluminescence
and
expected
to
be
next-generation
ultrahigh
definition
display
technology.
The
rapid
reverse
intersystem
crossing
(RISC)
process
TADF
emitter
is
crucial
for
achieving
high-performance
OLEDs
with
low-efficiency
roll-off.
Here,
we
present
a
novel
B–N
framework-based
MR-TADF
emitter,
Cz-2PTz-BN,
which
exhibits
narrow
full
width
at
half
maxima
37
nm
in
toluene
high
photoluminescence
quantum
yield
(PLQY)
93%
doped
film.
introduced
sulfur
atoms
Cz-2PTz-BN
enhance
its
spin–orbital
couplings
(SOC)
accelerate
RISC
process.
corresponding
OLED
demonstrates
maximum
external
efficiency
(EQEmax)
28.7%
low
roll-off,
maintaining
EQEs
27.2
20.8%
even
brightnesses
100
1000
cd
m–2
without
sensitizer.
These
outcomes
indicate
promise
this
molecular
design
strategy
obtain
color
purity
efficiency.
Advanced Optical Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 17, 2024
Abstract
Organic
light‐emitting
diodes
(OLEDs)
using
a
simple
solution‐processing
approach
have
natural
advantages
in
cost‐effective
commercialization.
However,
solution‐processed
deep‐red
OLEDs
are
rarely
reported
due
to
the
scarcity
of
efficient
purely
organic
narrowband
red
emitters
with
commendable
film‐forming
capabilities.
Herein,
strategy
is
proposed
develop
molecules
emission
by
expanding
rigid
conjugated
frame
block
rotation
α
position
boron‐dipyrromethene
(BODIPY)
core
restricted
twisting
vibration.
Furtherly,
introducing
moderate
donor
meso‐position
BODIPY
core,
bathochromic‐shifted
can
be
achieved
without
sacrificing
narrow
full‐width
at
half‐maximum
(FWHM)
increasing
electron
density
whole
molecule
and
repulsive
force
distal
units
suppress
stretching/scissoring
By
employing
developed
BODIPY‐derived
materials
as
terminal
thermally
activated
delayed
fluorescence
material
assistant
host
fabricate
OLED
devices,
maximum
external
quantum
efficiency
16.43%
an
peak
672
nm
FWHM
28
nm.
This
work,
according
knowledge,
represents
best
instance
based
on
typical
fluorescent
emitters.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 7, 2024
Multi-resonance
thermally
activated
delayed
fluorescence
(MR-TADF)
emitters
offer
natural
advantages
for
creating
power-efficient,
wide-color-gamut
OLEDs.
However,
current
green
MR-TADF
face
challenges
in
simultaneously
achieving
high
color
purity
and
efficient
reverse
inter-system
crossing
(RISC),
leading
to
suboptimal
device
performance.
In
this
study,
we
propose
a
synergistic
molecular
design
approach
that
combines
π-extension
peripheral
locking
address
these
challenges.
This
allows
the
construction
of
quadruple
borylated
not
only
deliver
precisely
tuned
pure-green
emission
with
narrow
full
width
at
half
maximum
(FWHM)
15
nm,
but
also
exhibit
close-to-unity
quantum
yield,
rapid
RISC,
optimal
horizontal
dipole
orientation.
The
resulting
sensitizer-free
OLED
approaches
BT.2020
standard
CIE
coordinates
(0.18,
0.74)
demonstrates
impressive
external
efficiency
(EQE)
36.6
%
31.8
1000
cd
m
Advanced Optical Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 16, 2024
Abstract
High‐efficiency
multi‐resonance
thermally
activated
delayed
fluorescence
(MR‐TADF)
emitters
with
narrowband
emission
show
great
potential
for
organic
light‐emitting
diodes
(OLEDs).
However,
their
inherent
planar
rigid
structures
often
lead
to
intractable
challenges
of
spectral
broadening,
self‐quenching,
and
low
device
efficiency
at
high
dopant
concentrations.
Herein,
two
steric
isomers,
BN‐1TPh
BN‐2TPh,
are
designed
by
incorporating
bulky
shielding
unit
(1,3,5‐triphenylbenzene)
the
para‐
position
B
atom
in
MR
skeleton
hinder
intermolecular
interactions.
They
both
enhanced
photoluminescence
quantum
yields
(PLQYs)
as
compared
model
compound
BCzBN.
The
corresponding
OLEDs
based
on
BN‐2TPh
display
maximum
external
(EQE
max
)
values
up
30.8%
30.4%
narrow
full
width
half
(FWHM)
bands
27
28
nm,
respectively.
It
is
worth
noting
that
even
doping
ratio
20%,
EQEs
still
maintained
24.8%
25.7%
almost
unchanged
spectra.
These
results
segregating
MR‐TADF
spatial
structure
can
weaken
interaction,
which
one
effective
ways
resist
aggregation‐caused
quenching
effect
achieve
high‐efficiency
concentration‐indispensible
OLEDs.