Luminescence enhancement by symmetry-breaking in the excited state in radical organic light-emitting diodes.
Ontology highlight
ABSTRACT:
SUBMITTER: Ohisa S
PROVIDER: S-EPMC10622504 | biostudies-literature | 2023 Nov
REPOSITORIES: biostudies-literature
Publications
Luminescence enhancement by symmetry-breaking in the excited state in radical organic light-emitting diodes.
Ohisa Satoru S Honda Satoshi S
Communications chemistry 20231102 1
Similar Datasets
Project description:Since their introduction over 15 years ago, the operational lifetime of blue phosphorescent organic light-emitting diodes (PHOLEDs) has remained insufficient for their practical use in displays and lighting. Their short lifetime results from annihilation between high-energy excited states, producing energetically hot states (>6.0 eV) that lead to molecular dissociation. Here we introduce a strategy to avoid dissociative reactions by including a molecular hot excited state manager within the device emission layer. Hot excited states transfer to the manager and rapidly thermalize before damage is induced on the dopant or host. As a consequence, the managed blue PHOLED attains T80=334±5 h (time to 80% of the 1,000 cd m-2 initial luminance) with a chromaticity coordinate of (0.16, 0.31), corresponding to 3.6±0.1 times improvement in a lifetime compared to conventional, unmanaged devices. To our knowledge, this significant improvement results in the longest lifetime for such a blue PHOLED.
| S-EPMC5460033 | biostudies-literature
Project description:Organic light-emitting diodes (OLEDs) under constant current operation suffer from a decrease of luminance accompanied by an increase of driving voltage. We report a way to greatly improve the stability of OLEDs having a green emitter exhibiting thermally activated delayed fluorescence (TADF), (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl) isophthalonitrile (4CzIPN), by introducing ultrathin (1 to 3?nm) interlayers of 8-hydroxyquinolinato lithium (Liq) between hole-blocking layer and its surrounding emissive and electron-transport layers. Under constant current operation starting at a luminescence of 1,000 cd/m(2), the time to reach 90% of initial luminance (LT90) increased eight times, resulting in LT90?=?1,380?hours after insertion of the interlayers. Combining this new concept and mixed host system, LT95 was further extended to 1315?hours that is 16 times of reference device. This is the best value reported for TADF-based OLEDs and is comparable to the operational lifetimes of well-established phosphorescence-based OLEDs. Thermally stimulated current measurements showed that the number of deep charge traps was reduced with the insertion of the ultrathin Liq interlayer, indicating that reducing the number of deep traps is important for improving the operational lifetime and that exciton-polaron annihilation may be a source of the device degradation.
| S-EPMC4772539 | biostudies-literature
Project description:It is a long-standing scientific controversy to achieve anti-Kasha-type multiple emissions by tuning the structures at a molecular level. Although it is known that some conjugated structures have excitation-dependent multiple emissions, no all-benzenoid molecules have yet been reported, the emissions of which originate from different excited states. Herein, we report the design of two symmetry-breaking heterogeneous carbon bisnanohoops that in solution become multiple fluorescent emitters with unusual anti-Kasha characteristics. This phenomenon can be spectroscopically and theoretically explained and will find applications in a wide range of sensing and imaging technologies.
| S-EPMC10973529 | biostudies-literature
Project description:Metal-halide perovskite nanocrystals have demonstrated excellent optoelectronic properties for light-emitting applications. Isovalent doping with various metals (M2+) can be used to tailor and enhance their light emission. Although crucial to maximize performance, an understanding of the universal working mechanism for such doping is still missing. Here, we directly compare the optical properties of nanocrystals containing the most commonly employed dopants, fabricated under identical synthesis conditions. We show for the first time unambiguously, and supported by first-principles calculations and molecular orbital theory, that element-unspecific symmetry-breaking rather than element-specific electronic effects dominate these properties under device-relevant conditions. The impact of most dopants on the perovskite electronic structure is predominantly based on local lattice periodicity breaking and resulting charge carrier localization, leading to enhanced radiative recombination, while dopant-specific hybridization effects play a secondary role. Our results suggest specific guidelines for selecting a dopant to maximize the performance of perovskite emitters in the desired optoelectronic devices.
| S-EPMC9437917 | biostudies-literature
Project description:π-Helical push-pull dyes were prepared and their (chir)optical properties were investigated both experimentally and computationally. Specific fluorescent behaviour of bis-substituted system was observed with unprecedented solvent effect on the intensity of circularly polarized luminescence (CPL, dissymmetry factor decreasing from 10-2 to 10-3 with an increase in solvent polarity) that was linked to a change in symmetry of chiral excited state and suppression of interbranched exciton coupling. The results highlight the potential of CPL spectroscopy to study and provide a deeper understanding of electronic photophysical processes in chiral π-conjugated molecules.
| S-EPMC7069512 | biostudies-literature
Project description:Crystalline white organic light-emitting diodes (C-WOLEDs) are promising candidates for lighting and display applications. It is urgently necessary, however, to develop energy-saving and high-efficiency C-WOLEDs that have stable and powerful emission to meet commercial demands. Here, we report a crystalline host matrix (CHM) with embedded nanoaggregates (NA) structure for developing high-performance C-WOLEDs by employing a thermally activated delayed fluorescence (TADF) material and orange phosphorescent dopants (Phos.-D). The CHM-TADFNA-D WOLED exhibit a remarkable EQE of 12.8%, which is the highest performance WOLEDs based on crystalline materials. The device has a quick formation of excitons and a well-designed energy transfer process, and possesses a fast ramping of luminance and current density. Compared to recently reported high-performance WOLEDs based on amorphous material route, the C-WOLED achieves a low series-resistance Joule-heat loss ratio and an enhanced photon output, demonstrating its significant potential in developing the next-generation WOLEDs.
| S-EPMC11001915 | biostudies-literature
Project description:White organic light-emitting diodes (WOLEDs) have several desirable features, but their commercialization is hindered by the poor stability of blue light emitters and high production costs due to complicated device structures. Herein, we investigate a standard blue emitting hole transporting material (HTM) N,N'-bis(naphthalen-1-yl)-N,N'-bis(phenyl)benzidine (NPB) and its exciplex emission upon combining with a suitable electron transporting material (ETM), 3-(biphenyl-4-yl)-5-(4-tert-butylphenyl)-4-phenyl-4H-1,2,4-triazole (TAZ). Blue and yellow OLEDs with simple device structures are developed by using a blend layer, NPB:TAZ, as a blue emitter as well as a host for yellow phosphorescent dopant iridium (III) bis(4-phenylthieno[3,2-c]pyridinato-N,C2')acetylacetonate (PO-01). Strategic device design then exploits the ambipolar charge transport properties of tetracene as a spacer layer to connect these blue and yellow emitting units. The tetracene-linked device demonstrates more promising results compared to those using a conventional charge generation layer (CGL). Judicious choice of the spacer prevents exciton diffusion from the blue emitter unit, yet facilitates charge carrier transport to the yellow emitter unit to enable additional exciplex formation. This complementary behavior of the spacer improves the blue emission properties concomitantly yielding reasonable yellow emission. The overall white light emission properties are enhanced, achieving CIE coordinates (0.36, 0.39) and color temperature (4643 K) similar to daylight. Employing intermolecular exciplex emission in OLEDs simplifies the device architecture via its dual functionality as a host and as an emitter.
| S-EPMC10721783 | biostudies-literature
Project description:Donor-spacer-acceptor (D-π-A) materials CAPI and CCAPI, with hybridized local and charge transfer (HLCT) emissive states, have been synthesized. The twisting D-π-A architecture promotes the partial separation of HOMO and LUMO, leading to an enhanced % CT component, and the anthracene moiety in CAPI and CCAPI increases the conjugation length, leading to an enhanced % LE component. The non-doped device with CCAPIb shows the blue emission (450 nm) with maximum current efficiency (η c), power efficiency (η p), and external quantum efficiency (η ex) of 16.83 cd A-1, 15.32 lm W-1, and 12.0%, respectively, as well as exciton utilization efficiency (EUE) of 95% with a luminance of 32 546 cd m-2 and a roll-off efficiency of 0.53%. The new design strategy has great potential for developing high-performance blue electroluminescent materials.
| S-EPMC8695226 | biostudies-literature
Project description:We report an effective and rare-earth free light conversion material synthesized via a facile fabrication route, in which organic fluorescent dyes, i.e. Rhodamine B (RhB) and fluorescein isothiocyanate (FITC) are embedded into activated boron nitride (αBN) to form a composite phosphor. The composite phosphor shows highly efficient Förster resonance energy transfer and greatly improved thermal stability, and can emit at broad visible wavelengths of 500-650 nm under the 466 nm blue-light excitation. By packaging of the composite phosphors and a blue light-emitting diode (LED) chip with transparent epoxy resin, white LED with excellent thermal conductivity, current stability and optical performance can be realized, i.e. a thermal conductivity of 0.36 W/mk, a Commission Internationale de 1'Eclairage color coordinates of (0.32, 0.34), and a luminous efficiency of 21.6 lm·W(-1). Our research opens the door toward to the practical long-life organic fluorescent dyes-based white LEDs.
| S-EPMC4329563 | biostudies-literature
Project description:The efficiencies of green and red perovskite light-emitting diodes (PeLEDs) have been increased close to their theoretical upper limit, while the efficiency of blue PeLEDs is lagging far behind. Here we report enhancing the efficiency of sky-blue PeLEDs by overcoming a major hurdle of low photoluminescence quantum efficiency in wide-bandgap perovskites. Blending phenylethylammonium chloride into cesium lead halide perovskites yields a mixture of two-dimensional and three-dimensional perovskites, which enhances photoluminescence quantum efficiency from 1.1% to 19.8%. Adding yttrium (III) chloride into the mixture further enhances photoluminescence quantum efficiency to 49.7%. Yttrium is found to incorporate into the three-dimensional perovskite grain, while it is still rich at grain boundaries and surfaces. The yttrium on grain surface increases the bandgap of grain shell, which confines the charge carriers inside grains for efficient radiative recombination. Record efficiencies of 11.0% and 4.8% were obtained in sky-blue and blue PeLEDs, respectively.
| S-EPMC6904584 | biostudies-literature