Photomultiplication-Type Organic Photodetectors for Near-Infrared Sensing with High and Bias-Independent Specific Detectivity.

Highly responsive organic photodetectors allow a plethora of applications in fields like imaging, health, security monitoring, etc. Photomultiplication-type organic photodetectors (PM-OPDs) are a desirable option due to their internal amplification mechanism. However, for such devices, significant gain and low dark currents are often mutually excluded since large operation voltages often induce high shot noise. Here, a fully vacuum-processed PM-OPD is demonstrated using trap-assisted electron injection in BDP-OMe:C60 material system. By applying only -1 V, compared with the self-powered working condition, the responsivity is increased by one order of magnitude, resulting in an outstanding specific detectivity of ≈1013  Jones. Remarkably, the superior detectivity in the near-infrared region is stable and almost voltage-independent up to -10 V. Compared with two photovoltaic-type photodetectors, these PM-OPDs exhibit the great potential to be easily integrated with state-of-the-art readout electronics in terms of their high responsivity, fast response speed, and bias-independent specific detectivity. The employed vacuum fabrication process and the easy-to-adapt PM-OPD concept enable seamless upscaling of production, paving the way to a commercially relevant photodetector technology.

Organic Dye-Doped PMMA Lasing.

Organic thin-film lasers gain interest as potential light sources for application in diverse fields. With the current development, they hold variety of benefits such as: low-cost, high-performance, and color-tunability. Meanwhile, the production is not complicated because both the resonator and the gain medium can be assembled by solution-processable organic materials. To our knowledge, information about using poly(methyl methacrylate) (PMMA) as a matrix for organic dye lasers was insubstantial. Herein, the feasibility of using organic dye-doped PMMA as an organic dye laser was tested. Six different sample designs were introduced to find out the best sample model. The most optimum result was displayed by the sample design, in which the gain medium was sandwiched between the substrate and the photoresist layer with grating structure. The impact of dye concentration and grating period on peak wavelength was also investigated, which resulted in a shift of 6 nm and 25 nm, respectively. Moreover, there were in total six various organic dyes that could function well with PMMA to collectively perform as 'organic dye lasers', and they emitted in the range of 572 nm to 609 nm. Besides, one of the samples was used as a sensor platform. For instance, it was used to detect the concentration of sugar solutions.

High-Efficiency Red Organic Light-Emitting Diodes with External Quantum Efficiency Close to 30% Based on a Novel Thermally Activated Delayed Fluorescence Emitter.

Researchers have spared no effort to design new thermally activated delayed fluorescence (TADF) emitters for high-efficiency organic light-emitting diodes (OLEDs). However, efficient long-wavelength TADF emitters are rarely reported. Herein, a red TADF emitter, TPA-PZCN, is reported, which possesses a high photoluminescence quantum yield (ΦPL ) of 97% and a small singlet-triplet splitting (ΔEST ) of 0.13 eV. Based on the superior properties of TPA-PZCN, red, deep-red, and near-infrared (NIR) OLEDs are fabricated by utilizing different device structure strategies. The red devices obtain a remarkable maximum external quantum efficiency (EQE) of 27.4% and an electroluminescence (EL) peak at 628 nm with Commission Internationale de L'Eclairage (CIE) coordinates of (0.65, 0.35), which represents the best result with a peak wavelength longer than 600 nm among those of the reported red TADF devices. Furthermore, an exciplex-forming cohost strategy is adopted. The devices achieve a record EQE of 28.1% and a deep-red EL peak at 648 nm with the CIE coordinates of (0.66, 0.34). Last, nondoped devices exhibit 5.3% EQE and an NIR EL peak at 680 nm with the CIE coordinates of (0.69, 0.30).

Tailor-made nanostructures bridging chaos and order for highly efficient white organic light-emitting diodes.

Organic light-emitting diodes (OLEDs) suffer from notorious light trapping, resulting in only moderate external quantum efficiencies. Here, we report a facile, scalable, lithography-free method to generate controllable nanostructures with directional randomness and dimensional order, significantly boosting the efficiency of white OLEDs. Mechanical deformations form on the surface of poly(dimethylsiloxane) in response to compressive stress release, initialized by reactive ions etching with periodicity and depth distribution ranging from dozens of nanometers to micrometers. We demonstrate the possibility of independently tuning the average depth and the dominant periodicity. Integrating these nanostructures into a two-unit tandem white organic light-emitting diode, a maximum external quantum efficiency of 76.3% and a luminous efficacy of 95.7 lm W-1 are achieved with extracted substrate modes. The enhancement factor of 1.53 ± 0.12 at 10,000 cd m-2 is obtained. An optical model is built by considering the dipole orientation, emitting wavelength, and the dipole position on the sinusoidal nanotexture.

High-performance organic light-emitting diodes comprising ultrastable glass layers.

Organic light-emitting diodes (OLEDs) are one of the key solid-state light sources for various applications including small and large displays, automotive lighting, solid-state lighting, and signage. For any given commercial application, OLEDs need to perform at their best, which is judged by their device efficiency and operational stability. We present OLEDs that comprise functional layers fabricated as ultrastable glasses, which represent the thermodynamically most favorable and, thus, stable molecular conformation achievable nowadays in disordered solids. For both external quantum efficiencies and LT70 lifetimes, OLEDs with four different phosphorescent emitters show >15% enhancements over their respective reference devices. The only difference to the latter is the growth condition used for ultrastable glass layers that is optimal at about 85% of the materials' glass transition temperature. These improvements are achieved through neither material refinements nor device architecture optimization, suggesting a general applicability of this concept to maximize the OLED performance, no matter which specific materials are used.

In vivo animal trials with a scanning CO2 laser osteotome.

BACKGROUND AND OBJECTIVES: We report first results of animal trials using an improved laser osteotomy technique. This technique allows effective bone cutting without the usual thermal tissue damage. STUDY DESIGN/MATERIALS AND METHODS: A comparative in vivo study on mandibles of seven canines was done with a mechanical saw and a CO(2) laser based osteotome with a pulse duration of 80 microseconds. The laser incisions were performed in a multipass mode using a PC-controlled galvanic beam scanner and an assisting water spray. RESULTS: A complete healing through a whole bony rearrangement of the osteotomy gap with newly build lamellar Haversian bone was observed 22 days after the laser operations under optimal irradiation conditions. CONCLUSIONS: An effective CO(2) laser osteotomy without aggravating thermal side effects and healing delay is possible using the described irradiation technique. It allows an arbitrary cut geometry and may result in new advantageous bone surgery procedures.