Monodisperse Six-Armed Starbursts based on Truxene-Cored Multibranched Oligofluorenes: Design,Synthesis, and Stabilized Lasing Characteristics

A series of monodisperse six-armed conjugated starbursts ( Tr1F , Tr2F , and Tr3F ) containing a truxene core and multibranched oligofluorene bridges capped with diphenylamine (DPA) units has been designed, synthesized, and investigated as robust gain media for organic semiconductor lasers (OSLs). The influence of electron-rich DPA end groups on their optoelectronic characteristics has been discussed at length. DPA cappers effectively raise HOMO levels of the starbursts, thus enhancing the hole injection and transport ability. Solution-processed electroluminescence devices based on the resulting six-armed starbursts exhibited efficient deep-blue electroluminescence with clear reduced turn-on voltages (3.2–3.5 V). Moreover, the resulting six-armed molecules showed stabilized electroluminescence and amplified spontaneous emission with low thresholds (27.4–63.9 nJ pulse⁻¹), high net gain coefficients (80.1–101.3 cm⁻¹), and small optical loss (2.6–4.4 cm⁻¹). Distributed feedback OSLs made from Tr3F exhibited a low lasing threshold of 0.31 kW cm⁻² (at 465 nm). The results suggest that the construction of truxene-centered six-armed conjugated starbursts with the incorporation of DPA units can effectively enhance EL properties by precisely regulating the HOMO energy levels, and further optimizing their optical gain properties.     

Enhancing light-extraction efficiency of OLEDs with high- and low-refractive-index organic–inorganic hybrid materials

High- and low-refractive-index hybrid materials were prepared by an in situ acid-free sol–gel process for internal and external light-extraction layers in organic light-emitting diodes (OLEDs). A random copolymer of methyl methacrylate (MMA) and 3-(trimethoxysilyl) propyl methacrylate (MSMA), poly(MMA-co-MSMA), which was capped with trialkoxysilane in MSMA units, was used as a precursor. The precursor was further reacted with titanium(IV) isopropoxide (TTIP) and tetraethyl orthosilicate (TEOS) to synthesize the high- and low-refractive-index hybrid materials, respectively, in which TiO₂ and SiO₂ nanoparticles were well dispersed, respectively, in the polymer matrix. After the reactions with TTIP and TEOS, the refractive index increased to 1.81 and decreased to 1.44 from 1.50 of the precursor, respectively. The luminance, power, and current efficiency of the OLED with an external light-extraction layer were enhanced by 21.3, 28.6, and 29.1%, respectively, those of the OLED with an internal light-extraction layer were increased by 62.4, 76.9, and 59.2%, respectively, and those of the device with combined ELEL and ILEL were enhanced by 62.7, 77.2, and 59.3%, respectively, when compared to values for the reference OLED without an internal or external light-extraction layer. These results indicate that high- and low-refractive-index materials are desirable for enhancement in light-extraction efficiency, and they can provide practical solutions for various applications such as OLED displays and lighting.     

Air‐Stable Spirofluorene‐Containing Ladder‐Type Bis(alkynyl)borane Compounds with Readily Tunable Full Color Emission Properties

A series of air‐stable spiro‐fused ladder‐type boron(III) compounds has been designed, synthesized, and the electrochemistry and photophysical behavior have been characterized. By simply varying the substituents on the pyridine ring and extending the π‐conjugation of the spiro framework, the emission color of these compounds can be easily fine‐tuned spanning the visible spectrum from blue to red. All compounds exhibit a broad and structureless emission band across the entire visible region, assigned as an intramolecular charge‐transfer transition originating from the thiophene of the spiro framework to the pyridine‐borane moieties. In addition, these compounds demonstrate high photoluminescence quantum yields of up to 0.81 in dichloromethane solution and 0.86 in doped thin films. Some of the compounds have also been employed as emissive materials, in which solution‐processed organic light‐emitting devices (OLEDs) with tunable emission colors spanning the visible spectrum from blue, green to red have been realized, demonstrating the potential applications of these boron compounds in OLEDs.     

Triarylphosphine oxide–phenanthroline molecular conjugate as a promising doped electron-transport layer for organic light-emitting diodes

Over the past three decades, transparent high electron mobility molecular materials have attracted intensive research efforts for organic light-emitting diodes as electron-transport layer for the sake of low working voltage, high power efficiency and operational stability. However, developing high-performing electron-transport materials presents a demanding challenge owing to difficulties in synthesis, purification and/or processing. In this contribution, we show that n-doping a simple and facilely available phenanthroline derivative, namely 3-(6-diphenylphosphinylnaphth-2-yl)-1,10-phenanthroline Phen-NaDPO with a high T_g of 116 °C, is capable of greatly increasing the electron conductivity up to 3.3 × 10⁻⁴ S m⁻¹. The characterization of the blue sky fluorescent and green phosphorescent OLEDs involving this doped electron-transport layer Phen-NaDPO:50% wt Cs₂CO₃ revealed comparable performances to the analogue BPhen (T_g ≈ 66 °C) OLEDs. For instance, the resulting sky blue fluorescent OLEDs provided ca. 15 cd/A, 13 lm/W @1000 cd m⁻² & t₉₅ ≈ 167 h @1000 cd m⁻². The present finding shows that the doped Phen-NaDPO may be a robust electron-transport material for optoelectronics.     

High-performance and current crowding-free InGaN-GaNbased LEDs integrated by an electrically-reverse-connected Schottky diode and a Mg-delta doped p-GaN

This work demonstrates high-performance and current crowding-free InGaN/GaN light-emitting diodes (LEDs) using an electrically-reverse-connected Schottky diode (SD) and an Mg-delta (δ) doped layer.Poss...     

On the exciton profile in OLEDs-seamless optical and electrical modeling

We present a comprehensive model to simulate organic light-emitting devices (OLEDs) that includes a seamless coupling of charges, excitons and photons. The comprehensive model accounts for the position dependent exciton lifetime due to the optical environment in the multilayer OLED structures. We first study the effect of different charge mobilities and quantum efficiencies of the light-emitting material on the exciton profiles. Moreover, we discuss the extension of an optical model to account for the exciton dynamics. This comprehensive optical model is validated and justified on the basis of consistency checks. Namely, we show that our comprehensive optical model can take the cavity effects as seen in simulation results of the comprehensive electrical model into account. The advantage of the comprehensive optical model is a quick and accurate insight into the exciton physics if applied together with a nonlinear least square (NLSQ) fitting method. Finally, we apply the comprehensive optical model with the NLSQ-method in order to extract the exciton profiles from emission spectra of a blue light-emitting polymer diode (PLED) measured at different current levels.     

Ge quantum dots light-emitting devices

Si photonics becomes one of the research focuses in the field of photonics.Si-based light-emitting devices are one of the most important devices in this field.In this paper,we review the Si-based light...     

Optimizing Optoelectronic Properties of Pyrimidine‐Based TADF Emitters by Changing the Substituent for Organic Light‐Emitting Diodes with External Quantum Efficiency Close to 25 % and Slow Efficiency Roll‐Off

A series of green butterfly‐shaped thermally activated delayed fluorescence (TADF) emitters, namely PXZPM , PXZMePM , and PXZPhPM , are developed by integrating an electron‐donor (D) phenoxazine unit and electron‐acceptor (A) 2‐substituted pyrimidine moiety into one molecule via a phenyl‐bridge π linkage to form a D –π–A–π–D configuration. Changing the substituent at pyrimidine unit in these emitters can finely tune their emissive characteristics, thermal properties, and energy gaps between the singlet and triplet states while maintaining frontier molecular orbital levels, and thereby optimizing their optoelectronic properties. Employing these TADF emitters results in a green fluorescent organic light‐emitting diode (OLED) that exhibits a peak forward‐viewing external quantum efficiency (EQE) close to 25 % and a slow efficiency roll‐off characteristic at high luminance.     

Realizing improved performance of down-conversion white organic light-emitting diodes by localized surface plasmon resonance effect of Ag nanoparticles

Down-conversion structure white organic light-emitting diodes (WOLEDs), in which white light is generated by a blue emission organic light-emitting diodes (OLEDs) in combination with a color conversion layer (CCL) outside the substrate, has attracted extensive interest due to its significant advantages in low cost and stabilized white-light emissions. However, low color-conversion efficiency of CCL is still a bottleneck for the performance improvement of down-conversion WOLEDs. Here, we demonstrate an approach to enhance the color-conversion efficiency of CCL-WOLEDs by localized surface plasmon resonance (LSPR) effect. In this approach, a blend of Ag nanoparticles and polyvinyl alcohol (PVA) is solution-deposited between the blue organic light emitting diodes and color-conversion layer. Based on the LSPR effect of this modified structure, the color conversion efficiency has improved 32%, from 45.4% to 60%, resulting a 14.4% enhancement of the current efficiency, from 9.73 cd/A to 11.14 cd/A. Our work provides a simple and low-cost way to enhance the performance of down-conversion WOLEDs, which highlights its potential in illumination applications.