ACS Photonics,
Год журнала:
2024,
Номер
11(4), С. 1491 - 1501
Опубликована: Март 13, 2024
Quasi-2D
metal
halide
perovskites
are
highly
promising
next-generation
luminescent
materials
with
extremely
favorable
photoelectric
characteristics.
Nevertheless,
the
performance
and
stability
of
perovskite
light-emitting
diodes
could
potentially
be
seriously
impacted
by
inefficient
energy
transfer
arising
from
coexistence
multidimensional
phases
presence
a
significant
number
defects
at
grain
boundaries
or
interfaces.
In
present
research,
to
address
these
challenges,
modification
layer
utilizing
thermally
activated
delayed
fluorescent
(TADF)
DTC-mBPSB
BTBC-DPS
was
achieved.
These
effectively
suppress
small
n-phase,
while
Förster
channel
efficiently
facilitates
carriers
large
promoting
radiative
recombination.
Additionally,
uncoordinated
Pb2+
can
passivated
passivation
group
(S=O),
resulting
in
notable
reduction
nonradiative
recombination
losses.
This
comprehensive
approach,
encompassing
optimization,
balanced
carrier
transport,
improved
film
morphology,
defect
passivation,
exhibits
excellent
effectiveness.
As
result,
we
have
achieved
outstanding
device
performance,
current
efficiencies
(and
EQE
values)
44.72
cd/A
(DTC-mBPSB,
=
11.77%)
68.18
(BTBC-DPS,
17.94%),
correspondingly.
Nature Photonics,
Год журнала:
2024,
Номер
18(6), С. 554 - 561
Опубликована: Фев. 13, 2024
Abstract
Blue
organic
light-emitting
diode
(OLED)
technology
requires
further
advancements,
and
hyperfluorescent
(HF)
OLEDs
have
emerged
as
a
promising
solution
to
address
stability
colour-purity
concerns.
A
key
factor
influencing
the
performance
of
HF-OLEDs
is
Förster
resonance
energy
transfer
(FRET).
Here
we
investigate
FRET
mechanism
in
blue
using
contrasting
thermally
activated
delayed
fluorescence
(TADF)
sensitizers.
We
demonstrate
that
molecular
structure
sensitizer
profoundly
impacts
efficiency,
exemplified
by
spiro-linked
TADF
molecule
ACRSA,
which
suppresses
dihedral-angle
inhomogeneity
any
lower-energy
conformers
exhibit
minimal
terminal
emitter.
Consequently,
efficiency
can
be
optimized
nearly
100%.
Further,
how
properties
near-ideal
diverge
from
ideal
emitters.
As
result,
utilizing
greenish
remarkable
tripling
external
quantum
(~30%)
compared
with
non-HF
devices.
This
new
understanding
opens
avenues
for
design,
indicating
green
sensitizers
efficiently
pump
emitters,
thereby
reducing
device
exciton
energies
improving
OLED
stability.
Angewandte Chemie International Edition,
Год журнала:
2023,
Номер
62(32)
Опубликована: Июнь 10, 2023
Developing
double
boron-based
emitters
with
extremely
narrow
band
spectrum
and
high
efficiency
in
organic
light-emitting
diodes
(OLEDs)
is
crucial
challenging.
Herein,
we
report
two
materials,
NO-DBMR
Cz-DBMR,
hinge
on
polycyclic
heteraborin
skeletons
based
role-play
of
the
highest
occupied
molecular
orbital
(HOMO)
energy
levels.
The
contains
an
oxygen
atom,
whereas
Cz-DBMR
has
a
carbazole
core
boron-embedded
ν-DABNA
structure.
synthesized
materials
resulted
unsymmetrical
pattern
for
surprisingly
symmetrical
Cz-DBMR.
Consequently,
both
showed
full
width
at
half
maximum
(FWHM)
14
nm
hypsochromic
(pure
blue)
bathochromic
(Bluish
green)
shifted
emission
without
losing
their
color
fidelity.
Furthermore,
show
photoluminescence
quantum
yield
(PLQY)
over
82
%,
small
singlet-triplet
gap
(ΔEST
)
0.04
eV,
resulting
reverse
intersystem
crossing
process
(kRISC
105
s-1
.
Due
to
efficient
thermally
activated
delayed
fluorescence
(TADF)
characteristics,
fabricated
OLEDs
these
heteraborins
manifested
external
(EQEmax
33.7
29.8
%
respectively.
This
first
work
reported
this
type
strategy
achieving
emissions
similar
skeleton.
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Июль 22, 2024
Abstract
Multi-resonance
thermally
activated
delayed
fluorophores
have
been
actively
studied
for
high-resolution
photonic
applications
due
to
their
exceptional
color
purity.
However,
these
compounds
encounter
challenges
associated
with
the
inefficient
spin-flip
process,
compromising
device
performance.
Herein,
we
report
two
pure-blue
emitters
based
on
an
organoboron
multi-resonance
core,
incorporating
a
conformationally
flexible
donor,
10-phenyl-5
H
-phenophosphazinine
10-oxide
(or
sulfide).
This
design
concept
selectively
modifies
orbital
type
of
high-lying
excited
states
charge
transfer
configuration
while
simultaneously
providing
necessary
conformational
freedom
enhance
density
without
sacrificing
We
show
that
different
embedded
phosphorus
motifs
(phosphine
oxide/sulfide)
donor
can
finely
tune
electronic
structure
and
freedom,
resulting
in
accelerated
process
through
intense
spin-vibronic
coupling,
achieving
over
20-fold
increase
reverse
intersystem
crossing
rate
compared
parent
emitter.
Utilizing
emitters,
achieve
high-performance
organic
light-emitting
diodes,
showcasing
top-tier
external
quantum
efficiency
37.6%
reduced
roll-offs.
proposed
strategy
not
only
conventional
notion
electron-donors
are
undesirable
constructing
narrowband
but
also
offer
pathway
designing
efficient
narrow-spectrum
blue
diodes.
Advanced Materials,
Год журнала:
2024,
Номер
36(30)
Опубликована: Май 2, 2024
Abstract
Ultrapure
deep‐blue
emitters
are
in
high
demand
for
organic
light‐emitting
diodes
(OLEDs).
Although
color
coordinates
serve
as
straightforward
parameters
assessing
purity,
precise
control
over
the
maximum
wavelength
and
full‐width
at
half‐maximum
is
necessary
to
optimize
OLED
performance,
including
luminance
efficiency
luminous
efficacy.
Multiple‐resonance
(MR)
promising
candidates
achieving
ideal
luminescence
properties;
consequently,
a
wide
variety
of
MR
frameworks
have
been
developed.
However,
most
these
experience
displacement
from
color,
which
limits
their
practical
applicability.
Therefore,
molecular
design
that
compatible
with
modulating
energy
levels
output
particularly
valuable.
Here,
it
demonstrated
azepine
donor
unit
induces
an
appropriate
blue‐shift
emission
while
maintaining
efficient
characteristics,
photoluminescence
quantum
yield,
narrow
emission,
fast
reverse
intersystem
crossing
rate.
OLEDs
using
newly
developed
based
on
ν
‐DABNA
framework
simultaneously
exhibit
≈30%,
efficacy
≈20
lm
W
−1
,
exceptional
purity
Commission
Internationale
de
l’Éclairage
low
(0.14,
0.06),
notably
operational
stability.
These
results
demonstrate
unprecedentedly
compared
those
observed
previously
reported
emitters.
Nature Communications,
Год журнала:
2025,
Номер
16(1)
Опубликована: Янв. 4, 2025
1,4-Azaborine-based
arenes
are
promising
electroluminescent
emitters
with
thermally
activated
delayed
fluorescence
(TADF),
offering
narrow
emission
spectra
and
high
quantum
yields
due
to
a
multi-resonance
(MR)
effect.
However,
their
practical
application
is
constrained
by
limited
operational
stability.
This
study
investigates
the
degradation
mechanism
of
MR-TADF
molecules.
Electroluminescent
devices
incorporating
these
compounds
display
varied
lifetimes,
uncorrelated
excitonic
stability
or
external
efficiency
roll-off.
Bulk
electrolysis
reveals
significant
instability
in
radical
cationic
forms
compounds,
device
lifetime
linked
Faradaic
yield
oxidation.
Comprehensive
chemical
analyses
corroborate
that
byproducts
originated
from
intramolecular
cyclization
cation,
followed
hydrogen
atom
transfer.
The
further
supported
enhanced
observed
deuterated
emitter,
attributed
secondary
kinetic
isotope
These
findings
provide
insights
into
stabilizing
effects
deuteration
mechanism-driven
strategies
for
designing
improved
longevity.
often
constrains
application.
Here,
authors
report
direct
correlation
between
oxidative
emitter
Advanced Optical Materials,
Год журнала:
2023,
Номер
11(22)
Опубликована: Окт. 4, 2023
Abstract
Over
the
past
decade,
thermally
activated
delayed
fluorescence
(TADF)
emitters
have
garnered
tremendous
impetus
because
of
their
ability
to
harvest
100%
excitons
for
light
emission
in
organic
emitting
diodes
(OLEDs).
However,
despite
superior
external
quantum
efficiencies
(>
35%),
broad
spectra
with
associated
full‐width‐at‐half
maximum
(FWHM
>
70
nm)
present
a
limiting
factor
that
must
be
solved.
Recently,
multiple‐resonance
TADF
(MR‐TADF)
materials
based
on
heteroatom
doped
polyaromatic
hydrocarbons
gained
astonishing
attention
owing
remarkable
narrowband
<
30
nm).
majority
reported
MR‐TADF
falls
blue/green
region,
which
inevitably
jeopardizes
application
full‐color
OLEDs.
Therefore,
there
is
an
urgent
need
develop
new
molecular
designs
expanding
color‐gamut
emitters,
i.e.,
λ
em
550
nm
without
compromising
emission.
To
best
current
knowledge,
no
detailed
reviews
focusing
different
design
strategies
producing
long‐wavelength
been
date.
this
end,
review
highlighting
recent
advances
constructing
presented,
and
photophysics
OLED
performance
discussed.
Finally,
status
future
prospects
are
Frontiers in Chemistry,
Год журнала:
2023,
Номер
11
Опубликована: Июнь 12, 2023
Over
the
decade,
there
have
been
developments
in
purely
organic
thermally
activated
delayed
fluorescent
(TADF)
materials
for
light-emitting
diodes
(OLEDs).
However,
achieving
narrow
full
width
at
half
maximum
(FWHM)
and
high
external
quantum
efficiency
(EQE)
is
crucial
real
display
industries.
To
overcome
these
hurdles,
hyperfluorescence
(HF)
technology
was
proposed
next-generation
OLEDs.
In
this
technology,
TADF
material
considered
a
sensitizing
host,
so-called
sensitized
host
(TSH),
use
of
triplet
excitons
via
reverse
intersystem
crossing
(RISC)
pathway.
Since
most
show
bipolar
characteristics,
electrically
generated
singlet
exciton
energies
can
be
transported
to
final
emitter
(FE)
through
Förster
resonance
energy
transfer
(FRET)
rather
than
Dexter
(DET).
This
mechanism
possible
from
S
1
state
TSH
dopant
(FD)
as
long-range
transfer.
Considering
this,
some
reports
are
available
based
on
OLEDs,
but
detailed
analysis
highly
efficient
stable
devices
commercialization
unclear.
So
herein,
we
reviewed
relevant
factors
recent
advancements
build
system.
The
include
an
spectral
overlapping,
requirements,
electroluminescence
study
exciplex
polarity
system,
shielding
effect,
DET
suppression,
FD
orientation.
Furthermore,
outlook
future
positives
with
new
directions
were
discussed
high-performance