47 research outputs found
ChemInform Abstract: Evolution of Emission Manners of Organic Light-Emitting Diodes: From Emission of Singlet Exciton to Emission of Doublet Exciton
Up to 100% Formation Ratio of Doublet Exciton in Deep-Red Organic Light-Emitting Diodes Based on Neutral π‑Radical
In a neutral π-radical-based
organic light-emitting diode (OLED), although the emission comes from
the doublet excitons and their transition to the ground state is spin-allowed,
the upper limit of internal quantum efficiency (IQE) is not clear,
50% or 100%? In this work, the deep-red OLEDs based on a neutral π-radical
were fabricated. Up to 100% doublet exciton formation ratio was obtained
through rational designing device structure and host–guest
doping system. This indicates the IQE of neutral π-radical-based
OLEDs will reach 100% if the nonradiative pathways of radicals can
be suppressed. The maximum external quantum efficiency of the optimized
device is as high as 4.3%, which is among the highest values of deep-red/near-infrared
OLEDs with nonphosphorescent materials as emitters. Our results also
indicate that using partially reduced radical mixture as emitter may
be a way to solve aggregation-caused quenching in radical-based OLEDs
Doublet–Triplet Energy Transfer-Dominated Photon Upconversion
Stable
luminescent π-radicals with doublet emission have
aroused a growing interest for functional molecular materials. We
have demonstrated a neutral Ď€-radical dye (4-<i>N</i>-carbazolyl-2,6-dichlorophenyl)ÂbisÂ(2,4,6-trichlorophenyl)-methyl
(TTM-1Cz) with remarkable doublet emission, which could be used as
triplet sensitizer to initiate the photophysical process of triplet–triplet
annihilation photon upconversion (TTA-UC). Dexter-like excited doublet-triplet
energy transfer (DTET) was confirmed by theoretical calculation. With
the same sensitizer, a mixed solution of TTM-1Cz and aromatic emitters
could upconvert red light (λ = 635 nm) to blue or cyan light.
An anti-Stokes energy shift as large as 0.92 eV was observed from
red to blue light upconversion. This finding of DTET phenomena offers
a new kind of triplet sensitizer for TTA-UC
White Organic Light-Emitting Diodes Using Exciplex Emission with Multiple Emitting Layers
Highly Efficient Nondoped Near-Ultraviolet Electroluminescence with an External Quantum Efficiency Greater Than 6.5% Based on a Carbazole-Triazole Hybrid Molecule with High and Balanced Charge Mobility
A pure red luminescent β-carboline-substituted biphenylmethyl radical: photophysics, stability and OLEDs
Novel Luminescent Benzimidazole-Substituent Tris(2,4,6-trichlorophenyl)methyl Radicals: Photophysics, Stability, and Highly Efficient Red-Orange Electroluminescence
Luminescent
radicals have various applications because they simultaneously
possess optoelectronic, electronic, and magnetic properties. Despite
the development of some luminescent trisÂ(2,4,6-trichlorophenyl)Âmethyl
(TTM)-based radicals, all the substituents directly attached to the
TTM skeleton are electron-donating groups. Herein, the electron-withdrawing
group is first attached to a p carbon of the parent TTM radical, and
two novel stable open-shell adducts based on the benzimidazole unit
with red-orange emission are obtained. Their photophysical properties,
photochemical stabilities, and electroluminescent performances are
fully investigated. Because of the introduction of the benzimidazole
unit, the intramolecular charge transfer property of D–A type
molecules is suppressed to a large extent, and the delocalization
of the sole electron is strengthened. Both radicals exhibit largely
improved photostability compared to that of the TTM core. High PL
quantum yields (Φ<sub>F</sub>) of 0.39 and 0.36 in doped films
are achieved, which are among the highest values for luminescent radicals.
Extremely high-voltage-durable characteristic is demonstrated in the
organic light-emitting diodes utilizing them as emitters. One device
has a maximal external quantum efficiency that even exceeds the classical
theoretical upper limit of 5%