Dual Sulfone-Bridged Triphenylamine Heteroaromatics for High-Performance Blue Organic Electroluminescence.

Polycyclic heteroaromatics (PHAs) are a highly versatile class of functional materials, especially applicable as efficient luminophores in organic light-emitting diodes (OLEDs). Those constructed by tethered phenyl surrounding the main group center attract extensive attention due to their excellent OLED device performance. However, the development of such a class of emitters is often limited to boron, nitrogen-doped π-conjugated heterocycles.

Boosting External Quantum Efficiency to 12.0 % of an Ultraviolet OLED by Engineering the Horizontal Dipole Orientation of a Hot Exciton Emitter.

Currently, much research effort has been devoted to improving the exciton utilization efficiency and narrowing the emission spectra of ultraviolet (UV) fluorophores for organic light-emitting diode (OLED) applications, while almost no attention has been paid to optimizing their light out-coupling efficiency. Here, we developed a linear donor-acceptor-donor (D-A-D) triad, namely CDFDB, which possesses high-lying reverse intersystem crossing (hRISC) property. Thanks to its integrated narrowband UV photoluminescence (PL) (λ: 397 nm; FWHM: 48 nm), moderate PL quantum yield (ϕ: 72 %, Tol), good triplet hot exciton (HE) conversion capability, and large horizontal dipole ratio (Θ: 92 %), the OLEDs based on CDFDB not only can emit UV electroluminescence with relatively good color purity (λ: 398 nm; CIE: 0.

Understanding the degradation mechanism of TTA-based blue fluorescent OLEDs by exciton dynamics and transient electroluminescence measurements.

The lifetime of blue organic light-emitting diodes (OLEDs) has always been a big challenge in practical applications. Blue OLEDs based on triplet-triplet annihilation (TTA) up-conversion materials have potential to achieve long lifetimes due to fusing two triplet excitons to one radiative singlet exciton, but there is a lack of an in-depth understanding of exciton dynamics on degradation mechanisms. In this work, we established a numerical model of exciton dynamics to study the impact factors in the stability of doped blue OLEDs based on TTA up-conversion hosts.

Extremely Stable Perylene Bisimide-Bridged Regioisomeric Diradicals and Their Redox Properties.

Excellent stability is an essential premise for organic diradicals to be used in organic electronic and spintronic devices. We have attached two tris(2,4,6-trichlorophenyl)methyl (TTM) radical building blocks to the two sides of perylene bisimide (PBI) bridges and obtained two regioisomeric diradicals (1,6-TTM-PBI and 1,7-TTM-PBI). Both of the isomers show super stability rather than the monomeric TTM under ambient conditions, due to the increased conjugation and the electron-withdrawing effects of the PBI bridges.

Exciton dynamics of an aggregation-induced delayed fluorescence emitter in non-doped OLEDs and its application as host for high-efficiency red phosphorescent OLEDs.

Aggregation-induced delayed fluorescence (AIDF) materials have great potential in non-doped OLEDs due to their high photoluminescence (PL) quantum efficiency in film, high exciton utilization in the aggregated state and negligible efficiency roll-off at high luminance. However, their efficient mechanism in OLEDs is not yet well understood. Here, the exciton dynamics are used to investigate the electroluminescence (EL) mechanism of an AIDF emitter (4-(10-phenoxazin-10-yl)phenyl)-(9-phenyl-9-carbazol-3-yl)methanone (CP-BP-PXZ) in detail.

A Nitroxide Radical Conjugated Polymer as an Additive to Reduce Nonradiative Energy Loss in Organic Solar Cells.

Nonfullerene-acceptor-based organic solar cells (NFA-OSCs) are now set off to the 20% power conversion efficiency milestone. To achieve this, minimizing all loss channels, including nonradiative photovoltage losses, seems a necessity. Nonradiative recombination, to a great extent, is known to be an inherent material property due to vibrationally induced decay of charge-transfer (CT) states or their back electron transfer to the triplet excitons.

Increasing the operating lifetime of green phosphorescent organic light emitting diodes by reducing charge accumulation at the interface.

The stability and degradation mechanism of phosphorescent organic light emitting diodes (OLEDs) has been an unresolved problem in the past decades. Here, we found that electron accumulation at the interface between the electron blocking layer and the emitting layer is one of the reasons for device degradation. By inserting a thin layer with a shallower LUMO level than that of the electron transporting layer between the emitting layer and the electron transporting layer, we successfully reduced the density of electrons at the interface and greatly improved the lifetime of the resulting green phosphorescent OLEDs.

Improved transient electroluminescence technique based on time-correlated single-photon counting technology to evaluate organic mobility.

The transient electroluminescence (EL) technique is widely used to evaluate the carrier mobility in the field of organic light emitting diodes. The traditional analog detection strategy using oscilloscopes is generally limited since the background noise causes an underestimation of the mobility value. In this paper, we utilize time-correlated single-photon counting (TCSPC) to probe the transient EL for mobility calculation.

Suppressing singlet-triplet annihilation processes to achieve highly efficient deep-blue AIE-based OLEDs.

Aggregation-induced emission (AIE) materials are attractive for the fabrication of high efficiency organic light-emitting diodes (OLEDs) by harnessing "hot excitons" from the high-lying triplet exciton states (T, ≥ 2) and high photoluminescence (PL) quantum efficiency in solid films. However, the electroluminescence (EL) efficiency of most AIE-based OLEDs does not meet our expectation due to some unrevealed exciton loss processes. Herein, we further enhance the efficiency of blue AIE-based OLEDs, and find experimentally and theoretically that the serious exciton loss is caused by the quenching of radiative singlet excitons and long-lived triplet excitons [singlet-triplet annihilation (STA)].

Converting molecular luminescence to ultralong room-temperature phosphorescence the excited state modulation of sulfone-containing heteroaromatics.

Manipulating the molecular orbital properties of excited states and the subsequent relaxation processes can greatly alter the emission behaviors of luminophores. Herein we report a vivid example of this, with luminescence conversion from thermally activated delayed fluorescence (TADF) to ultralong room-temperature phosphorescence (URTP) a facile substituent effect on a rigid benzothiazino phenothiazine tetraoxide (BTPO) core. Pristine BTPO with multiple heteroatoms shows obvious intramolecular charge transfer (ICT) excited states with small exchange energy, featuring TADF.

Exceptionally efficient deep blue anthracene-based luminogens: design, synthesis, photophysical, and electroluminescent mechanisms.

Achieving high-efficiency deep blue emitter with CIE < 0.06 (CIE, Commission Internationale de L'Eclairage) and external quantum efficiency (EQE) >10% has been a long-standing challenge for traditional fluorescent materials in organic light-emitting diodes (OLEDs). Here, we report the rational design and synthesis of two new deep blue luminogens: 4-(10-(4'-(9H-carbazol-9-yl)-2,5-dimethyl-[1,1'-biphenyl]-4-yl)anthracen-9-yl)benzonitrile (2M-ph-pCzAnBzt) and 4-(10-(4-(9H-carbazol-9-yl)-2,5-dimethylphenyl)anthracen-9-yl)benzonitrile (2M-pCzAnBzt).

Evolution of the electronic structure in open-shell donor-acceptor organic semiconductors.

Most organic semiconductors have closed-shell electronic structures, however, studies have revealed open-shell character emanating from design paradigms such as narrowing the bandgap and controlling the quinoidal-aromatic resonance of the π-system. A fundamental challenge is understanding and identifying the molecular and electronic basis for the transition from a closed- to open-shell electronic structure and connecting the physicochemical properties with (opto)electronic functionality. Here, we report donor-acceptor organic semiconductors comprised of diketopyrrolopyrrole and naphthobisthiadiazole acceptors and various electron-rich donors commonly utilized in constructing high-performance organic semiconductors.

Unraveling the Important Role of High-Lying Triplet-Lowest Excited Singlet Transitions in Achieving Highly Efficient Deep-Blue AIE-Based OLEDs.

Aggregation-induced emission (AIE) materials are attractive for achieving highly efficient nondoped organic light-emitting diodes (OLEDs) owing to their strong luminescence in the solid state. However, the electroluminescence efficiency of most AIE-based OLEDs remains low owing to the waste of triplet excitons. Here, using theoretical calculations, photophysical dynamics, and magnetoluminescence measurements, the spin conversion process is demonstrated between the high-lying triplet state (T ) and the lowest excited singlet state (S ) in AIE materials.

Correlated magnetic field effects on carriers and excitons in single-carrier exciplex-based organic photodiodes.

Magnetic field effects in nonmagnetic organic semiconductors (OMFEs) are attracting increasing attention because of the fingerprint characteristics of their line shapes when they are used to analyze the dynamic processes of organic photodiodes. However, the origin and correlation of OMFEs on carriers and excitons are currently still major challenges for researchers. In this study, we strategically designed exciplex-based single-carrier devices to effectively separate carriers and excitons and investigate their OMFEs and relationships.

Superior Efficiency and Low-Efficiency Roll-Off White Organic Light-Emitting Diodes Based on Multiple Exciplexes as Hosts Matched to Phosphor Emitters.

Based on exciplexes as hosts, the monochromatic organic light-emitting diodes (OLEDs) have achieved high power and external quantum efficiencies. However, the high-quality white OLEDs (WOLEDs) with high color rendering index (CRI) have the unsatisfactory efficiencies at high luminance, particularly in terms of power efficiency (PE), resulting in high energy consumption. Here, a new design concept using multiple exciplexes as hosts to match different phosphors has been demonstrated to develop high-performance WOLEDs.

Efficient Deep-Blue Fluorescent OLEDs with a High Exciton Utilization Efficiency from a Fully Twisted Phenanthroimidazole-Anthracene Emitter.

A novel, efficient, deep-blue fluorescent emitter mPAC, with a meta-connected donor-acceptor structure containing phenanthroimidazole (PPI) as the donor and phenylcarbazole-substituted anthracene (An-CzP) as the acceptor, was designed and synthesized. The meta-linkage provided a highly twisted molecular conformation, which efficiently interrupts the intramolecular π-conjugation, resulting in a deep-blue emission. The optimized nondoped device based on mPAC displayed a deep-blue emission with a narrow full width at half-maximum of 56 nm and Commission Internationale de L'Eclairage coordinates of (0.

Strategic-tuning of radiative excitons for efficient and stable fluorescent white organic light-emitting diodes.

The emerging thermally activated delayed fluorescence materials have great potential for efficiencies in organic light-emitting diodes by optimizing molecular structures of the emitter system. However, it is still challenging in the device structural design to achieve high efficiency and stable device operation in white organic light-emitting diodes. Here we propose a universal design strategy for thermally activated delayed fluorescence emitter-based fluorescent white organic light-emitting diodes, establishing an advanced system of "orange thermally activated delayed fluorescence emitter sensitized by blue thermally activated delayed fluorescence host" combined with an effective exciton-confined emissive layer.

Highly Efficient Blue Fluorescent OLEDs Based on Upper Level Triplet-Singlet Intersystem Crossing.

Purely organic electroluminescent materials, such as thermally activated delayed fluorescent (TADF) and triplet-triplet annihilation (TTA) materials, basically harness triplet excitons from the lowest triplet excited state (T ) to realize high efficiency. Here, a fluorescent material that can convert triplet excitons into singlet excitons from the high-lying excited state (T ), referred to here as a "hot exciton" path, is reported. The energy levels of this compound are determined from the sensitization and nanosecond transient absorption spectroscopy measurements, i.

Trap-Assisted Enhanced Bias Illumination Stability of Oxide Thin Film Transistor by Praseodymium Doping.

Praseodymium-doped indium zinc oxide (PrIZO) has been employed as the channel layer of thin-film transistors (TFTs). The TFTs with Pr doping exhibited a remarkable suppression of the light-induced instability. A negligible photo-response and remarkable enhancement in negative gate bias stress under illumination (NBIS) were achieved in the PrIZO-TFTs.

High efficiency hybrid white organic light-emitting diodes based on a simple and efficient exciton regulation emissive layer structure.

It is well-known that hybrid white organic light-emitting diodes (WOLEDs) are constructed by blue fluorophors and red-green or orange phosphors, therefore, theoretically exhibiting the advantages of long lifetime and high efficiency. However, the efficiency is far from reaching the expected values. Here, we designed a simple and efficient exciton regulation emissive layer (EML) structure to fabricate high efficiency hybrid WOLEDs.

Efficient Room-Temperature Phosphorescence from Organic-Inorganic Hybrid Perovskites by Molecular Engineering.

Solution-processed organic-inorganic hybrid perovskites are promising emitters for next-generation optoelectronic devices. Multiple-colored, bright light emission is achieved by tuning their composition and structures. However, there is very little research on exploring optically active organic cations for hybrid perovskites.

Responses of holocyclic and anholocyclic populations to low-temperature and short-photoperiod induction.

The different life cycles of aphid species make these organisms good models for studying the short-term consequences of sex. The bird cherry-oat aphid has a wide geographic distribution and correspondingly different life cycles. In this study, the life cycles of collected from six different regions in China were characterized experimentally by comparing the responses of holocyclic and anholocyclic populations to low-temperature and short-photoperiod induction.

Managing Excitons and Charges for High-Performance Fluorescent White Organic Light-Emitting Diodes.

The simultaneous realization of high efficiency, stable spectra, high color rendering index (CRI), and low-efficiency roll-off in a fluorescent white organic light-emitting diode (WOLED) still remains a big challenge. Here, we demonstrate high-performance conventional fluorescent-dopant-based WOLEDs by strategic management of singlet and triplet excitons within an efficient emissive zone. This design consists of two separated red/green sub-EMLs with ultralow doping concentration and a sandwiched sub-EML doped with red and green fluorescent dyes at a relatively high concentration, which can harness all electrogenerated excitons and reduce the energy loss to the utmost extent.