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Compared to conventional heating techniques, the carbon carrier-based rapid Joule heating (CJH) method is a new class of technologies that offer significantly higher heating rates and ultra-high temperatures. Over the past few decades, CJH technology has spawned several techniques with similar principles for different application scenarios, including ultra-fast high temperature sintering (UHS), carbon thermal shock (CTS), and flash Joule heating (FJH), which have been widely used in material preparation research studies. Functional nanomaterials are a popular direction of research today, mainly including nanometallic materials, nanosilica materials, nanoceramic materials and nanocarbon materials. These materials exhibit unique physical, chemical, and biological properties, including a high specific surface area, strength, thermal stability, and biocompatibility, making them ideal for diverse applications across various fields. The CJH method is a remarkable approach to producing functional nanomaterials that has attracted attention for its significant advantages. This paper aims to delve into the fundamental principles of CJH and elucidate the efficient preparation of functional nanomaterials with superior properties using this technique. The paper is organized into three sections, each dedicated to introducing the process and characteristics of CJH technology for the preparation of three distinct material types: carbon-based nanomaterials, inorganic non-metallic materials, and metallic materials. We discuss the distinctions and merits of the CJH method compared to alternative techniques in the preparation of these materials, along with a thorough examination of their properties. Furthermore, the potential applications of these materials are highlighted. In conclusion, this paper concludes with a discussion on the future research trends and development prospects of CJH technology.
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The field of microsystems is a rapidly evolving area with a wide range of applications in the field of electronics [...].
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Tandem structures with different subpixels are promising for perovskite-based multicolor electroluminescence (EL) devices in ultra-high-resolution full-color displays; however, realizing excellent luminance- and color-independent tunability considering the low brightness and stability of blue perovskite light-emitting diodes (PeLEDs) remains a challenge. Herein, a bright and stable blue gallium nitride (GaN) LED is utilized for vertical integration with a green MAPbBr3 PeLED, successfully achieving a Pe-GaN tandem LED with independently tunable luminance and color. The electronic and photonic co-excitation (EPCE) effect is found to suppress the radiative recombination and current injection of PeLEDs, leading to degraded luminance and current efficiency under direct current modulation. Accordingly, the pulse-width modulation is introduced to the tandem device with a negligible EPCE effect, and the average hybrid current efficiency is significantly improved by 139.5%, finally achieving a record tunable luminance (average tuning range of 16631 cd m-2 at an arbitrary color from blue to green) for perovskite-based multi-color LEDs. The reported excellent independent tunability can be the starting point for perovskite-based multicolor EL devices, enabling the combination with matured semiconductor technologies to facilitate their commercialization in advanced display applications with ultra-high resolution.
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In this work, a phosphor converter with small thickness and low concentration, based on a micro-angle tunable tilted filter (ATFPC), was proposed for hybrid-type laser lighting devices to solve the problem of silicone phosphor converters' carbonizing under high-energy density. Taking advantage of the filter and the scattering characteristics of microphosphors, two luminous areas are generated on the converter. Compared with conventional phosphor converters (CPCs), the lighting effects of ATFPCs are adjustable using tilt angles. When the tilt angle of the micro filter is 20°, the luminous flux of the ATPFCs is increased by 11.5% at the same concentration; the maximum temperature (MT) of ATFPCs is reduced by 22.8% under the same luminous flux and the same correlated color temperature (CCT) 6500 K. This new type of lighting device provides an alternative way to improve the luminous flux and heat dissipation of laser lighting.
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Laser-driven illumination has unique advantages in high-power applications. Taking advantage of the valuable experience of light-emitting diodes (LED) development, phosphor in silicone (PiS) is considered to be one of the most potential commercial phosphor converter solutions for laser-driven illumination. However, the thermal quenching of the PiS converter is a bottleneck problem. Herein, a boron nitride (BN)-coated copper foam strategy is introduced for the laser-driven illumination system. The phosphor/silicone is embedded in the designed BN/copper foam to form a phosphor in metal (PiM) converter. Copper foam serves as an internal connected heat transfer channel; the BN coating solves the light absorption problem of the copper foam effectively. Based on this PiM(BN/copper foam) design, the heat dissipation is effectively improved. Under high-power laser excitation (8.13 W), the PiS converter cannot reach thermal equilibrium, and therefore the temperature increases sharply up to 660 °C. In comparison, the thermal performance of an optimized PiM(BN/copper foam) converter is able to maintain excellent stability, where the maximum temperature is only 166.5 °C. The proposed PiM strategy has a maximum temperature that is 493.5 °C lower than that of the reference PiS solution. Due to the superior thermal management, the luminous efficiency of the illumination system is constantly stable at 254 lm/W, though with less phosphor mass; and the related color temperature is about 6000 K all the time. This provides a practical and feasible heat-dissipation solution for high-power laser-driven illumination.
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Currently, laser-driven lighting based on phosphor-in-glass (PIG) has drawn much interest in solid state lighting due to its high electro-optical efficiency and high-power density. However, the fabrication of PIG requires expensive equipment, long sintering time, and high cost. In this work, we utilized a simple, fast, and high temperature Joule heating process to make phosphor-in-glass bulk sintered in less than 20 s, which greatly improved the production efficiency. The PIG converters sintered under different sintering temperatures were investigated experimentally. The optimized PIG converter exhibited high and robust luminous efficacy (164.24 lm/W), a high radiant flux, and a small CCT deviation at 3.00 W. Moreover, the optimized sample also showed high temperature resistance at 3.00 W, robust temperature management during normal working. These results indicated that the optimized PIG converter sintered by the Joule heating process could offer great potential for the application in high-power laser-driven white lighting.
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In this study, we analyze the influence of the pore structure of an SBA-15 particle on the light emission from its inner adsorbed quantum dots (QDs) and outer light-emitting diode (LED) chips. It is found that the particle features of a high refractive index, comparable feature size of pore structure, and lower amount of QD adsorption help with QD light extraction, demonstrating a mechanism to suppress QD light propagating through pores and thus reducing the reabsorption loss. We consequently developed highly efficient QD white LEDs with wet-mixing QD/SBA-15 nanocomposite particles (NPs) by further optimizing the packaging methods and the introduced NP mass ratio. The LEDs demonstrated a record luminous efficacy (the ratio of luminous flux to electrical power) of 206.8 (entrusted test efficiency of 205.8 lm W-1 certificated by China National Accreditation Service) and 137.6 lm W-1 at 20 mA for white LEDs integrating only green QDs and green-red QD color convertors, respectively, with improved operating stability. These results are comparable to conventional phosphor-based white LEDs, which can be a starting point for white LEDs only using QDs as convertors toward commercialization in the near future.
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Inspired by the porous scale of the bright white beetle Cyphochilus, a polymerization-induced phase separation method is proposed to fabricate bioinspired high-scattering polymer films with porous structures. With an optimized formulation, the porous films with a mean pore size of â¼200nm feature a broadband reflectance of â¼71% at a thickness of 16 µm and are measured to have a transport mean free path of â¼3µm. The porous films with high reflectivity enable the application on light-emitting diodes and have great potential in other similar optoelectronic fields.
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Disordered porous polymer structures have gained tremendous attention due to their wide applications in various fields. As a simple yet versatile technique, supercritical CO2 microcellular foaming has been proposed to fabricate highly scattering porous polymer films, which have been used to enhance the efficiency of quantum dots (QDs) films. In the foaming process, numerous enclosed pores are generated, which induce significant scattering, underpinning the efficiency enhancement in optoelectronic devices. However, the scattering property of foamed porous structures has still not been well investigated, and effective guidelines for engineering the porous structures are still not available. In this work, we use Mie scattering theory and ray-tracing simulation to analyze the optical property of a single pore, pore assembly, and porous film. Furthermore, it is demonstrated that the scattering scheme in the porous QD films leads to a large enhancement of excitation light absorption and QD emission extraction. It is envisioned that our work will contribute to the engineering guidelines of porous structures and boost the application of porous structures in similar fields.
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Whiteness is an intriguing property in some creature surfaces and usually originates from broadband multi-scattering by the refined structures. In this article, we report that Boehmeria nivea, a widely distributed tropical and subtropical plant, has a highly reflective layer on the lower surface of the leaf. Morphological characterization demonstrates that the layer consists of numerous wrinkled micro-filaments, forming a disordered porous network to efficiently scatter visible light. Moreover, the white layer is shown to exhibit a protection function by reflecting incident light when exposed to high radiation. The reflective layer can slightly improve the absorption by the leaves when light is incident on the upper surface of the leaves. In addition, the porous layer shows hydrophobicity. To mimic the white layer, a well-established electrospinning process is used to fabricate porous polymeric membranes, consisting of nano-wrinkled filaments with micro-sized diameter. Finally, the artificial membranes are demonstrated to have a light-shielding function in a photo-chromic experiment and a light-management ability for quantum dot film.
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Materiales Biomiméticos , Boehmeria/ultraestructura , Materiales Biomiméticos/química , Color , Interacciones Hidrofóbicas e Hidrofílicas , Membranas Artificiales , Hojas de la Planta/ultraestructura , Porosidad , Dispersión de RadiaciónRESUMEN
All-inorganic cesium lead halide perovskite CsPbX3 (X = Cl, Br, I) nanocrystals (NCs) have attracted significant attention owing to their fascinating electronic and optical properties. However, researchers still face challenges to achieve highly stable and photoluminescent CsPbX3 NCs at room temperature by the direct-synthesis method. Herein, we synthesize CsPbX3 NCs by a facile and environmentally friendly method, which uses an aqueous solution of metal halides to react with Cs4PbBr6 NCs via interfacial anion exchange reactions and without applying any pretreatment. This method produces monodisperse and air-stable CsPbX3 NCs with tunable spectra covering the entire visible range, narrow photoluminescence emission bandwidth, and high photoluminescence quantum yield (PL QY, 80%). In addition, the chemical transformation mechanism between Cs4PbBr6 NCs and CsPbX3 NCs was investigated. The Cs4PbBr6 NCs were converted to CsPbBr3 NCs first by stripping CsBr, and then, the as-prepared CsPbBr3 NCs reacted with metal halides to form CsPbX3 NCs. This work takes advantage of the chemical transformation mechanism of Cs4PbBr6 NCs and provides an efficient and environmentally friendly way to synthesize CsPbX3 NCs.
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Light-emitting diode (LED) combined with quantum dots (QDs) is an important candidate for next-generation high-quality semiconductor devices. However, the effect of the excitation wavelength on their optical performance has not been fully explored. In this study, green and red QDs are applied to LEDs of different excitation wavelengths from 365 to 455 nm. The blue light is recommended for exciting QDs from the perspective of energy utilization. However, QD LEDs excited at 365 nm have unique advantages in eliminating the original peaks from the LED chip. Moreover, the green or red light excited by ultraviolet light has an advantage in colorimetry. Even for the 455 nm LED with the highest QD concentration at 7.0 wt%, the color quality could not compete with the 365 nm LED with the lowest QD concentration at 0.2 wt%. A 117.5% (NTSC1953) color gamut could be obtained by the 365 nm-excited RGB system, which is 32.6% higher than by the 455 nm-excited solution, and this can help expand the color gamut of LED devices. Consequently, this study provides an understanding of the properties of QD-converted LEDs under different wavelength excitations, and offers a general guide to selecting a pumping source for QDs.
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Ultrathin transition metal carbides with high capacity, high surface area, and high conductivity are a promising family of materials for applications from energy storage to catalysis. However, large-scale, cost-effective, and precursor-free methods to prepare ultrathin carbides are lacking. Here, we demonstrate a direct pattern method to manufacture ultrathin carbides (MoCx, WCx, and CoCx) on versatile substrates using a CO2 laser. The laser-sculptured polycrystalline carbides (macroporous, ~10-20 nm wall thickness, ~10 nm crystallinity) show high energy storage capability, hierarchical porous structure, and higher thermal resilience than MXenes and other laser-ablated carbon materials. A flexible supercapacitor made of MoCx demonstrates a wide temperature range (-50 to 300 °C). Furthermore, the sculptured microstructures endow the carbide network with enhanced visible light absorption, providing high solar energy harvesting efficiency (~72 %) for steam generation. The laser-based, scalable, resilient, and low-cost manufacturing process presents an approach for construction of carbides and their subsequent applications.
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We demonstrate an ultrasonication-assisted synthesis without polar solvent of CsPbBr3 and Cs4PbBr6 perovskite nanocrystals (PNCs) and their reversible transformation. The as-prepared CsPbBr3 PNCs and Cs4PbBr6 PNCs exhibit different optical properties that depend on their morphology, size, and structure. The photoluminescence (PL) emission and quantum yield (QY) of the CsPbBr3 PNCs can be tuned by changing the ultrasound power, radiation time, and the height of the vibrating spear. The optimized CsPbBr3 PNCs show a good stability and high PL QY of up to 85%. In addition, the phase transformation between CsPbBr3 PNCs and Cs4PbBr6 PNCs can be obtained through varying the amount of oleylamine (OAm) and water. The mechanism of this transformation between the CsPbBr3 PNCs and Cs4PbBr6 PNCs and their morphology change are studied, involving ions equilibrium, anisotropic growth kinetics, and CsBr-stripping process.
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Quantum-dot (QD) white light-emitting diodes (LEDs) are promising for illumination and display applications due to their excellent color quality. Although they have a high quantum yield close to unity, the reabsorption of QD light leads to high conversion loss, significantly reducing the luminous efficacy and stability of QD white LEDs. In this report, SBA-15 mesoporous particles (MPs) with two-dimensional hexagonal pore structures (2D-HPS) are utilized to largely enhance the luminous efficacy and color-conversion efficiency of QD white LEDs in excess of 50%. The reduction in conversion loss also helps QD white LEDs to achieve a lifetime 1.9 times longer than that of LEDs using QD-only composites at harsh aging conditions. Simulation and testing results suggest that the waveguide effect of 2D-HPS helps in reducing the reabsorption loss by constraining the QD light inside the wall of 2D-HPS, decreasing the probability of being captured by QDs inside the hole of 2D-HPS. As such, materials and mechanisms like SBA-15 MPs with 2D-HPS could provide a new path to improve the photon management of QD light, comprehensively enhancing the performances of QD white LEDs.
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The nanocrystals (NCs) of inorganic perovskites CsPbX3 and Cs4PbX6 (X = Cl, Br, I) are showing a great development potential due to their versatility of crystal structure. Here, we used a microchannel reactor to synthesize both CsPbBr3 NCs (CsPbBr3 NCs) and Cs4PbBr6 NCs with embedded CsPbBr3 (CsPbBr3/Cs4PbBr6 NCs). Via speed control of the precursor, ligands around the surface of NCs were effectively regulated by ethyl acetate, allowing the transformation from CsPbBr3 NCs to CsPbBr3/Cs4PbBr6 NCs in a short time, an outstanding stability of NCs, and a better crosslinking between NCs and polymer for the application of LEDs. Without any protection, the CsPbBr3/Cs4PbBr6 NCs, with a production rate of 28 mg min-1, retain more than 90% of the PL intensity after 84 d. Finally, the CsPbBr3/Cs4PbBr6 NCs were used to produce an LED device, and a wide color gamut of 122.8% NTSC or 91.7% Rec 2020 was attained.
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We develop a facile, fast, and cost-effective method based on the electrowetting effect to fabricate concave microlens arrays (MLA) with a tunable height-to-radius ratio, namely aspect ratio (AR). The electric parameters including voltage and frequency are demonstrated to play an important role in the MLA forming process. With the optimized frequency of 5 Hz, the AR of MLA are tuned from 0.057 to 0.693 for an increasing voltage from 0 V to 180 V. The optical properties of the MLA, including their transmittance and light diffusion capability, are investigated by spectroscopic measurements and ray-tracing simulations. We show that the overall transmittance can be maintained above around 90% over the whole visible range, and that an AR exceeding 0.366 is required to sufficiently broaden the transmitted light angular distribution. These properties enable to apply the developed MLA films to correlated-color-temperature (CCT)-tunable light-emitting-diodes (LEDs) to enhance their angular color uniformity (ACU). Our results show that the ACU of CCT-tunable LEDs is significantly improved while preserving almost the same lumen output, and that the MLA with the highest AR exhibits the best ACU performance.
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Although quantum dots (QDs) have a high quantum yield close to one in a solution, they exhibit low conversion efficiency in a solidification polymer matrix, which hampers the development of QD-based light-emitting diodes (LEDs) with high stability and optical performance. In this study, we proposed a methyl-terminated-polydimethylsiloxane-(PDMS)-based liquid-type packaging structure (LPS) to improve stability and optical performance of QD-based LEDs. Compared with the traditional ethylene-terminated-PDMS-based solid-type packaging structure, the LPS with an optimized kinematic viscosity of 10000 m2/s can provide higher stability and optical performances for QD-based LEDs, including total radiant power and luminous flux. Consequently, the proposed effective and simple strategy has great potential for illumination and display applications.
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We developed a microreactor with porous copper fibers for synthesizing nitrogen-doped carbon dots (N-CDs) with a high stability and photoluminescence (PL) quantum yield (QY). By optimizing synthesis conditions, including the reaction temperature, flow rate, ethylenediamine dosage, and porosity of copper fibers, the N-CDs with a high PL QY of 73% were achieved. The PL QY of N-CDs was two times higher with copper fibers than without. The interrelations between the copper fibers with different porosities and the N-CDs were investigated using X-ray photoelectron spectroscopy (XPS) and Fourier Transform infrared spectroscopy (FTIR). The results demonstrate that the elemental contents and surface functional groups of N-CDs are significantly influenced by the porosity of copper fibers. The N-CDs can be used to effectively and selectively detect Hg2+ ions with a good linear response in the 0~50 µM Hg2+ ions concentration range, and the lowest limit of detection (LOD) is 2.54 nM, suggesting that the N-CDs have great potential for applications in the fields of environmental and hazard detection. Further studies reveal that the different d orbital energy levels of Hg2+ compared to those of other metal ions can affect the efficiency of electron transfer and thereby result in their different response in fluorescence quenching towards N-CDs.
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In this work, we propose a facile method for manufacturing a three-dimensional copper foil-powder sintering current collector (CFSCC) for a silicon-based anode lithium-ion battery. We found that the CFSCC is suitable as a silicon-based paste electrode, and the paste-like electrodes are commonly used in industrial production. Compared with flat current collectors, the CFSCC better constrained the silicon volume change during the charging-discharging process. The capacitance of electrodes with CFSCC remained as high as 92.2% of its second cycle after 40 cycles, whereas that of electrodes with a flat current collector only remained at 50%.