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While visible light communication (VLC) has become the candidate for the wireless technology of the 21st century due to its inherent advantages, VLC based positioning also has a great chance of becoming the standard approach to positioning. Within the last few years, many studies on VLC based positioning have been published, but there are not many survey works in this field. In this paper, an in-depth survey of VLC based positioning systems is provided. More than 100 papers ranging from pioneering papers to the state-of-the-art in the field were collected and classified based on the positioning algorithms, the types of receivers, and the multiplexing techniques. In addition, current issues and research trends in VLC based positioning are discussed.

Quantum dot (QD) light-emitting diodes (LEDs) are ideal for large-panel displays because of their excellent efficiency, colour purity, reliability and cost-effective fabrication 1 – 4 . Intensive efforts have produced red-, green- and blue-emitting QD-LEDs with efficiencies of 20.5 per cent 4 , 21.0 per cent 5 and 19.8 per cent 6 , respectively, but it is still desirable to improve the operating stability of the devices and to replace their toxic cadmium composition with a more environmentally benign alternative. The performance of indium phosphide (InP)-based materials and devices has remained far behind those of their Cd-containing counterparts. Here we present a synthetic method of preparing a uniform InP core and a highly symmetrical core/shell QD with a quantum yield of approximately 100 per cent. In particular, we add hydrofluoric acid to etch out the oxidative InP core surface during the growth of the initial ZnSe shell and then we enable high-temperature ZnSe growth at 340 degrees Celsius. The engineered shell thickness suppresses energy transfer and Auger recombination in order to maintain high luminescence efficiency, and the initial surface ligand is replaced with a shorter one for better charge injection. The optimized InP/ZnSe/ZnS QD-LEDs showed a theoretical maximum external quantum efficiency of 21.4 per cent, a maximum brightness of 100,000 candelas per square metre and an extremely long lifetime of a million hours at 100 candelas per square metre, representing a performance comparable to that of state-of-the-art Cd-containing QD-LEDs. These as-prepared InP-based QD-LEDs could soon be usable in commercial displays. A method of engineering efficient and stable InP/ZnSe/ZnS quantum dot light-emitting diodes (QD-LEDs) has improved their performance to the level of state-of-the-art cadmium-containing QD-LEDs, removing the problem of the toxicity of cadmium in large-panel displays.

Red and near‐infrared (NIR) organic light‐emitting diodes (OLED) have gained remarkable interest due to their numerous applications. However, the construction of highly emissive emitters is hampered by the energy‐gap law and aggregation‐caused quenching (ACQ) effect. Whereas, aggregation‐induced emission (AIE) materials could avoid the undesirable ACQ effect and emit bright light in aggregated state, which is one class of the most promising materials to fabricate high‐performance OLED with a high external quantum efficiency and low efficiency roll‐off. This review summarizes recent advances in red and NIR OLED with AIE property, including the traditional fluorescence, thermally activated delayed fluorescence, and hybridized local and charge transfer compounds. Meanwhile, the emphasis attention is paid to the molecular design principles, as well as the molecular structure‐photophysical characteristics. We also briefly further outlook the challenges and perspective of red and NIR AIE luminogens. In the field of organic light‐emitting diodes (OLED), red and near‐infrared (NIR) emitter with aggregation‐induced emission (AIE) effect can be divided into fluorescence, thermally activated delayed fluorescence (TADF), and hybridized local and charge transfer (HLCT) according to emission mechanism.

Organic light-emitting diodes (OLEDs) promise highly efficient lighting and display technologies. We introduce a new class of linear donor-bridge-acceptor light-emitting molecules, which enable solution-processed OLEDs with near-100% internal quantum efficiency at high brightness. Key to this performance is their rapid and efficient utilization of triplet states. Using time-resolved spectroscopy, we establish that luminescence via triplets occurs within 350 nanoseconds at ambient temperature, after reverse intersystem crossing to singlets. We find that molecular geometries exist at which the singlet-triplet energy gap (exchange energy) is close to zero, so that rapid interconversion is possible. Calculations indicate that exchange energy is tuned by relative rotation of the donor and acceptor moieties about the bridge. Unlike other systems with low exchange energy, substantial oscillator strength is sustained at the singlet-triplet degeneracy point.

In the present time, organic light-emitting diode (OLED) is a very promising participant over light-emitting diodes (LEDs), liquid crystal display (LCD), and also another solid-state lighting device due to its low cost, ease of fabrication, brightness, speed, wide viewing angle, low power consumption, and high contrast ratio. The most prominent layer of OLED is the emissive layer because the device emission color, contrast ratio, and external efficiency depend of this layer’s materials. This review ruminates on the basics of OLEDs, different light emission mechanisms, OLEDs achievements, and different types of challenges revealed in the field of OLEDs. This review’s primary intention is to broadly discuss the synthesizing methods, physicochemical properties of conducting polymer polymethyl methacrylate (PMMA), and its polymeric nanocomposite-based emissive layer materials for OLEDs application. It also discusses the most extensively used OLED fabrication techniques. PMMA-based polymeric nanocomposites revealed good transparency properties, good thermal stability, and high electrical conductivity, making suitable materials as an emissive layer for OLED applications.

This book is ideal for practicing engineers working in design or packaging at LED companies and graduate students preparing for work in industry. This book also provides a helpful introduction for advanced undergraduates, graduates, researchers, lighting designers, and product managers interested in the fundamentals of LED design and production.

White‐light‐emitting carbon dots (WCDs) show innate advantages as phosphors in white light‐emitting diodes (WLEDs). For WLEDs, the color rendering index (CRI) is the most important metric to evaluate its performance. Herein, WCDs are prepared by a facile one‐step solvothermal reaction of trimellitic acid and o‐phenylenediamine. It consists of four CDs identified by column chromatography as blue, green, yellow, red, and thus white light is a superposition of these four types of light. The mixture of the four CDs undergoes Förster resonance energy transfer to induce the generation of white light. The photoluminescence of WCDs originates from the synergistic effect of carbon core and surface states. Thereinto, the carbon core states dominate in RCDs, and the increase of amide contents and degree of conjugation promote the redshift of the emission spectra, which is further confirmed by theoretical calculations. In addition, a high CRI of 97 is achieved when the WCDs are used as phosphors to fabricate WLEDs, which is almost the highest value up to now. The multicolor LEDs can also be fabricated by using the four multicolor CDs as phosphors, respectively. This work provides a novel approach to explore the rapid preparation of low‐cost, high‐performance WCDs and CDs‐based WLEDs. The white‐light‐emitting carbon dots are synthesized by a one‐step solvothermal method of trimellitic acid and o‐phenylenediamine, which consists of four types of carbon dots emitting blue, green, yellow, and red light. Five kinds of light‐emitting diodes can be prepared using the above carbon dots, among which the color rendering index of white light‐emitting diode is as high as 97.

Virtual reality, augmented reality, quantum dot light-emitting diodes, and organic light-emitting diodes have progressed over the last two years. Key achievements in these displays are discussed in terms of device performance.

High‐pressure chemistry has provided a huge boost to the development of scientific community. Pressure‐induced emission (PIE) in halide perovskites is gradually showing its unique charm in both pressure sensing and optoelectronic device applications. Moreover, the PIE retention of halide perovskites under ambient conditions is of great commercial value. Herein, we mainly focus on the potential applications of PIE and PIE retention in metal halide perovskites for scintillators and solid‐state lighting. Based on the performance requirements of scintillator and single‐component white light‐emitting diodes (WLEDs), the significance of PIE and PIE retention is critically clarified, aiming to design and synthesize materials used for high‐performance optoelectronic devices. This perspective not only demonstrates promising applications of PIE in the fields of scintillators and WLEDs, but also provides potential applications in display imaging and anti‐counterfeiting of PIE materials. Furthermore, solving the scientific disputes that exist under ambient conditions is also simply discussed as an outlook by introducing high‐pressure dimension to produce PIE. Pressure‐induced emission (PIE), which refers to a novel phenomenon whereby a nonluminescent material exhibits emission upon compression, offers a great step forward to light up the better future. PIE materials not only show promising applications in the fields of scintillators and solid‐state lighting, but also provide potential applications in display imaging and anti‐counterfeiting.

Flexible devices mimicking the sensitivity of human skin typically turn pressure stimuli into electronic signals, which must be further processed to be interpreted by the user. By integrating an active matrix of organic light-emitting diodes in these foldable sensors, pressure can now control the brightness of each coloured pixel, enabling the direct visualization and quantification of the applied stimulus. Electronic skin (e-skin) presents a network of mechanically flexible sensors that can conformally wrap irregular surfaces and spatially map and quantify various stimuli 1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 . Previous works on e-skin have focused on the optimization of pressure sensors interfaced with an electronic readout, whereas user interfaces based on a human-readable output were not explored. Here, we report the first user-interactive e-skin that not only spatially maps the applied pressure but also provides an instantaneous visual response through a built-in active-matrix organic light-emitting diode display with red, green and blue pixels. In this system, organic light-emitting diodes (OLEDs) are turned on locally where the surface is touched, and the intensity of the emitted light quantifies the magnitude of the applied pressure. This work represents a system-on-plastic 4 , 13 , 14 , 15 , 16 , 17 demonstration where three distinct electronic components—thin-film transistor, pressure sensor and OLED arrays—are monolithically integrated over large areas on a single plastic substrate. The reported e-skin may find a wide range of applications in interactive input/control devices, smart wallpapers, robotics and medical/health monitoring devices.