Carbon Encapsulation of High Entropy Alloy Nanoparticles with Extraordinary Coercivity and Saturation at Room Temperature

Owing to their unique properties and technological potential, high entropy alloys (HEAs) have become the subject of great interest in the materials science community. HEAs consist of more than four principle elements in equimolar ratio so their configurational entropy is intrinsically greater than one-principle element based. The increasing surface energy and chemical tendency toward clustering of like atoms at low dimension, however, make production of HEA-nanoparticles (HEA-NPs) extremely difficult. A facile production of HEA-NPs inside carbon nanotubes and nanoparticles is demonstrated in this work. Electron microscopic and elemental analyses confirm encapsulated to be solution phase; some embrace carbides and form multidomains with chemical composition ranging from quaternary to quinary phase. Multidomains and nonmagnetic centers create hardening thus promoting coercivity significantly at room temperature. Alloying induces electron redistribution into high spin states, accounting for observed high saturation. Configurational entropy of encapsulated HEA-NPs lies on a range comparable with bulk.     

Effects of exchanged surfactant cations on the pore structure and adsorption characteristics of montmorillonite

Ca-montmorillonite (Ca-Mont) was exchanged with two quaternary amines, tetramethylammonium (TMA) chloride and hexadecyltrimethylammonium (HDTMA) bromide, to study the surfactant ion exchange effect on the pore structure, surface characteristics, and adsorption properties of montmorillonite. The revolution of both the surface area and pore structure of montmorillonite was characterized based on classical and fractal analyses of the nitrogen isotherms as well as the XRD patterns. The change of surface characteristics was identified from FTIR patterns and zeta-potential plots. The adsorption isotherms of acid dye, Amido Naphthol Red G (AR1), were then measured to identify the effects of the ion-exchange process on the adsorption properties of montmorillonite. It was found that the exchange processes might induce an increase or decrease in the surface area, pore size, pore volume, and surface fractal dimension D of montmorillonite, depending on the size, the molecular arrangement, and the degree of hydration of the exchanged ion in the clay. On the other hand, it was also found that the hydrophobic bonding by conglomeration of large C(16) alkyl groups associated with HDTMA could cause positive charge development on the surface of montmorillonite, which was not observed for TMA-modified montmorillonite (TMM). The effects of the alteration of the surface characteristics of montmorillonites on their adsorption selectivity for acid dye were discussed.     

Thermally-induced order-order transition of DNA-cationic surfactant complexes

Polyanionic DNA interacts with cationic amphiphiles to form electrostatic complexes exhibiting rich self-assembled structures. This type of complex has been considered as a nonviral carrier in gene therapy and as a template for nanostructure construction. Here we report a thermally-induced phase transition of the complexes of DNA with the mixtures of a cationic surfactant, dodecyltrimethyl bromide (DTAB), and a neutral lipid, dioleoylphosphatidylethanolamine (DOPE), in fully hydrated state. An order-order transition between a multilamellar (L(c)alpha) phase and an inverted hexagonal (H(c)II) phase was found to occur with the transition temperature adjustable by the DTAB-to-DNA base pair molar ratio (x) and DOPE-to-DTAB molar ratio (m). The stability of the L(c)alpha phase was enhanced at lower m and x, as the L(c)alpha-to-H(c)II transition temperature increased with the decreases of these two parameters. The suppression of -to- transition at lower x was attributed to the lower entropic gain from the counterion release due to the presence of uncomplexed DNA in the bulk solution.     

Kinetics of regioselective acetolysis of epichlorohydrin

The liquid phase acetolysis of epichlorohydrin (ECH) with acetic acid was studied over bentonite clay catalysts and was found to be very active for the selective formation of 1-acetoxy-3-chloro-2-propanol. The reaction followed first order kinetics with respect to epichlorohydrin and obeyed the Langmuir-Hinshelwood mechanism.     

Single-longitudinal-mode linear-cavity fiber laser using multiple subring-cavities

A single-longitudinal-mode selection is realized in a linear-cavity fiber laser construction using a loop-back optical circulator and a partial reflectance fiber Bragg grating as the cavity ends. At 1551 nm wavelength, the measured signal-to-noise-ratio is 56 dB and with a line width less than 1 MHz obtained using multiple subring cavities as mode filters. The pumping efficiency is 10% improved by recycling the residual pump power to gain medium.     

Deposition and electrostatic removal of gaseous organic contaminants on substrate surfaces

The adhesion behavior of di-n-butyl phthalate (DBP) onto different substrates (quartz, glass, and silicon) used as wafer surfaces was studied by using an in situ UV spectrophotometric technique. The results from the closed cell experiments revealed that greatest extent of DBP adhesion occurred on the quartz chip (0.154 μg cm⁻²), followed in the order by the glass (0.054 μg cm⁻²) and silicon (0.039 μg cm⁻²). By means of the in situ spectrophotometric observation, application of an electrical field at 290 V cm⁻¹ in the cell proved to be effective in inducing charging of DBP aerosols, which were consequently attracted towards the electrodes. This method can be applied to wafer storage and transport equipments to prevent wafer contamination from material outgassing representative by DBP.     

Effect of graded triple delta-doped sheets on the performance of GaAs based dual channel pseudomorphic high electron mobility transistors

The characteristics of InGaP/InGaAs/GaAs dual channel pseudomorphic high electron mobility transistors (DCPHEMTs) with different graded triple delta-doped sheets are investigated and experimentally demonstrated. Based on a two-dimensional simulator of ATLAS, the band diagrams, electron densities and DC characteristics of studied devices are comprehensively analyzed. Due to the use of properly graded triple delta-doped sheets, good pinch-off and saturation characteristics, improved transport properties and wide current swing are obtained. For comparison, a practical DCPHEMT with good device performances is fabricated as well. It is found that the simulated data are in good agreement with experimental results.     

Impact of an indium oxide/indium-tin oxide mixed structure for GaN-based light-emitting diodes

An interesting GaN-based light emitting diode (LED) using a 50 nm indium oxide (In₂O₃)/250 nm indium-tin oxide (ITO) mixed structure to replace the commonly used ITO (250 nm) current spreading layer is fabricated and studied. Use of the In₂O₃ layer could reduce the contact resistance of p-GaN in LEDs. In addition, this highly-resistive In₂O₃ layer, below the ITO layer could improve the current spreading performance. Experimentally, at room temperature, using this mixed structure, the luminous and EL intensities are enhanced by 17.7 and 17.1%, respectively.     

Bio-inspired and Eco-friendly Synthesis of 3D Spongy Meso-Microporous Carbons from CO2 for Supercapacitors

Inspired by the spongy bone structures, three-dimensional (3D) sponge-like carbons with meso-microporous structures are synthesized through one-step electro-reduction of CO₂ in molten carbonate Li₂CO₃−Na₂CO₃−K₂CO₃ at 580 °C. SPC4-0.5 (spongy porous carbon obtained by electrolysis of CO₂ at 4 A for 0.5 h) is synthesized with the current efficiency of 96.9 %. SPC4-0.5 possesses large electrolyte ion accessible surface area, excellent wettability and electronical conductivity, ensuring the fast and effective mass and charge transfer, which make it an advcanced supercapacitor electrode material. SPC4-0.5 exhibits a specific capacitance as high as 373.7 F g⁻¹ at 0.5 A g⁻¹, excellent cycling stability (retaining 95.9 % of the initial capacitance after 10000 cycles at 10 A g⁻¹), as well as high energy density. The applications of SPC4-0.5 in quasi-solid-state symmetric supercapacitor and all-solid-state flexible devices for energy storage and wearable piezoelectric sensor are investigated. Both devices show considerable capacitive performances. This work not only presents a controllable and facile synthetic route for the porous carbons but also provides a promising way for effective carbon reduction and green energy production.     

Novel conjugated copolymers based on dithiafulvalene moiety for bulk heterojunction solar cells

New conjugated copolymers, P1‐P3 , based on dithiafulvalene‐fused entity and different conjugated segments have been synthesized. Incorporation of electron‐deficient conjugated segments into the conjugated copolymers results in red shifting the absorption band and lowering the hole mobility. Bulk heterojunction solar cells using on these polymers as the donor and [6,6]‐phenyl‐C61 ‐butyric acid methyl ester (PC₆₁BM) as the acceptor were fabricated by solution process. The cells based on the blend of P1‐P3 /PC₆₁BM (1:1, w/w) have power conversion efficiencies (PCEs) ranging from 0.53 to 0.93%. Among these, the cell of P1 /PC₆₁BM exhibited the highest open‐circuit voltage at 0.85 V, and the cell of P3/PC₆₁BM exhibited the best PCE at 0.93% with the short‐circuit current (J_SC) of 4.88 mA/cm². © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012