ABSTRACT
This study addresses the challenge of incomplete separation of mechanically recovered residual films and impurities in cotton fields, examining their impact on resource utilization and environmental pollution. It introduces an innovative screening method that combines pneumatic force and mechanical vibration for processing crushed film residue mixtures. A double-action screening device integrating pneumatic force and a key-type vibrating screen was developed. The working characteristics of this device were analyzed to explore the dynamic characteristics and kinematic laws of the materials using theoretical analysis methods. This led to the revelation of the screening laws of residual films and impurities. Screening tests were conducted using the Central Composite Design method, considering factors such as fan outlet, fan speed, vibration frequency of the screen, and feeding amount, with the impurity-rate-in-film (Q) and film-content-in-impurity (W) as evaluation indexes. The significant influence of each factor on the indexes was determined, regression models between the test factors and indexes were established, and the effect laws of key parameters and their significant interaction terms on the indexes were interpreted. The optimal combination of working parameters for the screening device was identified through multivariable optimization methods. Validation tests under this optimal parameters combination showed that the impurity-rate-in-film was 3.08% and the film-content-in-impurity was 1.94%, with average errors between the test values and the predicted values of 3.36% and 5.98%, respectively, demonstrating the effectiveness of the proposed method. This research provides a novel method and technical reference for achieving effective separation of residual film and impurities, thereby enhancing resource utilization.
Subject(s)
Gossypium , Cotton Fiber/analysis , Environmental Pollution/prevention & controlABSTRACT
Halide perovskite materials have rapidly emerged as outstanding optoelectronic materials for solar cells, light-emitting diodes (LEDs), and lasers. Compared to hybrid organic-inorganic perovskites, all-inorganic perovskites have shown unique merits that may contribute to the ultimate goal of developing electrically-pumped lasers. In this paper, we demonstrate a distributed feedback (DFB) resonator using an all-inorganic perovskite thin film as the gain medium. The film has a gain coefficient of 161.1 cm-1 and a loss coefficient of 30.9 cm-1. Excited by picosecond pulses, the microstructured all-inorganic perovskite film exhibits a single-mode emission at 654 nm with a threshold of 33 µJ/cm2. The facile fabrication process provides a promising route towards low-cost single-mode visible lasers for many practical applications.
ABSTRACT
Visible light communication (VLC) is a promising candidate for high-speed wireless communication with numerous unlicensed spectrum. To achieve high-speed data communication, it requires intense light signals concentrated on a tiny fast photodiode. The common way of using focusing optics reduces the field of view (FoV) of the photodiode due to the conservation of étendue. Luminescent solar concentrators (LSC) provide a solution to enhance the signals without affecting the FoV. In this paper we demonstrate nanopatterned LSCs fabricated on flexible plastics that achieve a doubling of optical gain compared to its traditional rectangular counterparts. These LSCs can free VLC detectors from complex active pointing and tracking systems, making them compatible with smart mobile terminals in a simple fashion.
ABSTRACT
High-efficiency blue perovskite emitters with fast fluorescence radiation are not only crucial to achieving high-quality displays but also highly desired for optical wireless communications and quantum information technologies. Here, we demonstrate the preparation of blue-emitting Eu3+-, Sb3+-, and Ba2+-induced CsPbBr3 nanoplatelets with narrow spectral widths. Among them, Sb3+-doped CsPbBr3 NPLs can reach a photoluminescence quantum yield of 95%, with a very short fluorescence lifetime of 1.48 ns and greatly reduced ligand dosage. Through nuclear magnetic resonance analysis and density functional theory calculations, we find that the dopant-ligand interaction and dopant-induced growth energy barrier decide the growth kinetics of doped nanoplatelets. These mechanisms offer a fresh route to controlling the dimension of nanoscale perovskite emitters and benefit the development of fast-radiative perovskite emitters.
ABSTRACT
The lack of highly efficient, durable, and cost-effective electrocatalysts for the hydrogen evolution reaction (HER) working at high current densities poses a significant challenge for the large-scale implementation of hydrogen production from renewable energy. Herein, amorphous molybdenum tungsten sulfide/nitrogen-doped reduced graphene oxide nanocomposites (a-MoWSx /N-RGO) are synthesized by plasma treatment for use as high-performance HER catalysts. By adjusting the plasma treatment duration and chemical composition, an optimal a-MoWSx /N-RGO catalyst is obtained, which exhibits a low overpotential of 348 mV at a current density of 1000 mA cm-2 and almost no decay after 24 h of working at this current density, outperforming commercial platinum/carbon (Pt/C) and previously reported heteroatom-doped MoS2 -based catalysts. Based on density functional theory (DFT) calculations, it is found that with a reasonable tungsten doping level, the catalytic active site (2S2 - ) shows excellent catalytic performance working at high current densities because extra electrons preferentially fill at 2S2 - . The introduction of tungsten tends to lower the electronic structure energy, resulting in a closer-to-zero positive Δ G H ∗ $\Delta {G}_{{{\rm{H}}}^{\rm{*}}}$ . Excessive tungsten introduction, however, can lead to structural damage and a worse HER performance under high current densities. The work provides a route towards rationally designing high-performance catalysts for the HER at industrial-level currents using earth-abundant elements.
ABSTRACT
At present, mainstream neuromorphic hardware is based on artificial synapses; however, an engram, instead of a synapse, has recently been confirmed as the basic unit of memory, which verifies the engram theory proposed by Richard Semon in 1904. Here, we demonstrate an artificial engram device based on a nanoimprinted curable resin. The variation in the relative diffraction efficiency based on the asymmetric reversible topological change of the nanoimprinted resin enables the device to meet all the requirements for artificial engrams, including synaptic plasticity, long memory storage time, asymmetric memorizing-forgetting behaviour and measurable changes and responses. On this basis, we demonstrate the concept of realizing memory formation, memory manipulation and implantation, and memory consolidation using our artificial engram device in comparison with its biological counterpart.
Subject(s)
Memory Consolidation , Neuronal Plasticity , SynapsesABSTRACT
Colloidal CsPbX3 (X = Br, Cl, and I) perovskite nanocrystals exhibit tunable bandgaps over the entire visible spectrum and high photoluminescence quantum yields in the green and red regions. However, the lack of highly efficient blue-emitting perovskite nanocrystals limits their development for optoelectronic applications. Herein, neodymium (III) (Nd3+) doped CsPbBr3 nanocrystals are prepared through the ligand-assisted reprecipitation method at room temperature with tunable photoemission from green to deep blue. A blue-emitting nanocrystal with a central wavelength at 459 nm, an exceptionally high photoluminescence quantum yield of 90%, and a spectral width of 19 nm is achieved. First principles calculations reveal that the increase in photoluminescence quantum yield upon doping is driven by an enhancement of the exciton binding energy due to increased electron and hole effective masses and an increase in oscillator strength due to shortening of the Pb-Br bond. Putting these results together, an all-perovskite white light-emitting diode is successfully fabricated, demonstrating that B-site composition engineering is a reliable strategy to further exploit the perovskite family for wider optoelectronic applications.
ABSTRACT
Raspberry-like structure, providing a high degree of symmetry and strong interparticle coupling, has received extensive attention from the community of functional material synthesis. Such structure constructed in the nanoscale using gold nanoparticles has broad applicability due to its tunable collective plasmon resonances, while the synthetic process with precise control of the morphology is critical in realizing its target functions. Here, we demonstrate a synthetic strategy of seed-mediated space-confined self-assembly using the virus-like silica (V-SiO2) nanoparticles as the templates, which can yield gold nanoraspberries (AuNRbs) with uniform size and controllable morphology. The spikes on V-SiO2 templates serve dual functions of providing more growth sites for gold nanoseeds and activating the space-confined effect for gold nanoparticles. AuNRbs with wide-range tunability of plasmon resonances from the visible to near infrared (NIR) region have been successfully synthesized, and how their geometric configurations affect their optical properties is thoroughly discussed. The close-packed AuNRbs have also demonstrated huge potential in Raman sensing due to their abundant "built-in" hotspots. This strategy offers a new route towards synthesizing high-quality AuNRbs with the capability of engineering the morphology to achieve target functions, which is highly desirable for a large number of applications.