Mapping of Lattice Strain in 4H-SiC Crystals by Synchrotron Double-Crystal X-ray Topography

The presence of lattice strain in n-doped 4H-SiC substrate crystals grown by a physical vapor transport method can strongly influence the performance of related power devices that are fabricated on them. Information on the level and the variation of lattice strain in these wafer crystals is thus important. In this study, a non-destructive method is developed based on synchrotron double-crystal x-ray topography to map lattice strains in 4H-SiC wafers. Measurements are made on two 4H-SiC substrate crystals—one is an unprocessed commercial wafer while the other was subject to a post-growth high-temperature heat treatment. Maps of different strain components are generated from the equi-misorientation contour maps recorded using synchrotron monochromatic radiation. The technique is demonstrated to be a powerful tool in estimating strain fields in 4H-SiC crystals. Analysis of the strain maps also shows that the normal strain components vary much more significantly than do the shear/rotation components, indicating that lattice dilation/compression rather than lattice tilt is the major type of deformation caused by both the incorporation of nitrogen dopants and the nucleation of basal plane dislocations.     

Isometry in mechanism designIsometrie in der getriebesynthese

Isometric designs are those that carry the same linear dimensions. Unique specification of the motion requirements of a mechanism between skew axes, with the help of a suitable set of conventions, removes all alternative designs isometric to the original mechanism, with one exception: an isometric design satisfying exactly the same motion requirements is available but with the algebraic sign of the axis distance changed. The transformation is one of reflection and is called an opposite isometry. Extending the use of unique specification of motion requirements to the special case of two-position design with identical specification of motion derivatives at the two positions (as in the case of a crank-rocker design), one is left with an alternative isometric design, without change of sign of axis distance. The device consists of a change of direction of motion of the mechanism, coupled with an interchange of mechanism positions that correspond to the two distinct positions on the curve of motion relationship. There is, in this case, what is called a direct isometry. The two transformations are shown to be useful: (i) in reducing the extent of design cataloguing, and (ii) in reducing the area of search for suitable mechanism designs.     

Experimental investigation of lift enhancement by suction-assisted delayed separation of the boundary layer on NACA 0012 airfoil

In the aerodynamic industry, one of the major problems of interest is the lift enhancement without any increase in the drag. In this paper, an attempt is made to increase the lift coefficient by delayed boundary layer separation using suction at various points, also the study is carried out to identify the optimum location for suction which provides maximum lift augmentation. The experiment is conducted with selected suction pressures of 60, 70, 80, 90?kN/m² at different locations in the range of 40–75% of the chord length of the airfoil. Among the selected pressures, the lowest one at the 70% length provides maximum performance. The critical Reynolds number occurs at around 95% of the length instead of 45% of the length when the same experiment is conducted without suction. The suction also assists in the heat transfer enhancement over the airfoil surface.     

Electrochemical cell current requirements for toxic organic waste destruction in Ce(IV)-mediated electrochemical oxidation process

The electrochemical cell for cerium oxidation and reactor for organic destruction are the most important operation units for the successful working mediated electrochemical oxidation (MEO) process. In this study, electrochemical cells with DSA electrodes of two types, single stack and double stack connected in series, were used. The performances towards the electrochemical generation of Ce(IV) in nitric acid media at 80 °C were studied. The current-voltage curves and cerium electrolysis kinetics showed the dependence on number of cell stacks needed to be connected in series for the destruction of a given quantity of organic pollutant. The presence of an optimum region for Ce(III) oxidation with a contribution of oxygen evolution, especially at low Ce(III) concentration (high conversion ratios), was found. The cells were applied for the Ce(IV) regeneration during the organic destruction. The cell and reactor processes were fitted in a simple model proposed and used to calculate the current needed in terms of Ce(III) oxidation rate and the number of cell stacks required for maintaining Ce(IV)/Ce(III) ratio at the same level during the organic destruction. This consideration was based on the kinetic model previously developed by us for the organic destruction in the MEO process.     

Mn4+-activated KLaMgWO6: A new high-efficiency far-red phosphor for indoor plant growth LEDs

Novel Mn⁴⁺-activated KLaMgWO₆ red phosphors with different Mn⁴⁺ concentrations were successfully synthesized via a high-temperature solid-state reaction method. The phase formation, microstructure, photoluminescence properties, decay lifetimes and internal quantum efficiency were discussed to analyze the properties of the as-prepared phosphors. The samples belonged to monoclinic crystal system with enough WO₆ octahedrons that provided suitable sites for Mn⁴⁺ ions. Upon the excitation of 348?nm, KLaMgWO₆:Mn⁴⁺ phosphors gave bright far-red emission around 696?nm due to the ²E_g→⁴A_2g transition of Mn⁴⁺ ions. The critical concentration of Mn⁴⁺ was 0.6?mol% and the concentration quenching mechanism belonged to electric multipolar interaction. Besides, the CIE chromaticity coordinates of the KLaMgWO₆:0.6%Mn⁴⁺ phosphor were (0.7205, 0.2794) which located in deep red range, and its color purity reached up to 96.6%. The KLaMgWO₆:0.6%Mn⁴⁺ sample also exhibited high internal quantum efficiency of 43%. All of the admirable optical properties indicate that the KLaMgWO₆:Mn⁴⁺ phosphors can be applied to indoor plant growth illumination.     

Electrochemical oxidation of boron containing compounds on titanium carbide and its implications to direct fuel cells

Electrochemical oxidation of sodium borohydride (NaBH₄) and ammonia borane (NH₃BH₃) (AB) have been studied on titanium carbide electrode. The oxidation is followed by using cyclic voltammetry, chronoamperometry and polarization measurements. A fuel cell with TiC as anode and 40 wt% Pt/C as cathode is constructed and the polarization behaviour is studied with NaBH₄ as anodic fuel and hydrogen peroxide as catholyte. A maximum power density of 65 mW cm⁻² at a load current density of 83 mA cm⁻² is obtained at 343 K in the case of borhydride-based fuel cell and a value of 85 mW cm⁻² at 105 mA cm⁻² is obtained in the case of AB-based fuel cell at 353 K.     

Mid‐IR transparent TeO2‐TiO2‐La2O3 glass and its crystallization behavior for photonic applications

In this report, effect of enhanced rare earth (La₂O₃) concentration on substitution of TeO₂ within ternary TeO₂‐TiO₂‐La₂O₃ (TTL) glass system has been studied with respect to its thermal, structural, mechanical, optical, and crystallization properties with an aim to achieve glass and glass‐ceramics having rare‐earth‐rich crystalline phase for nonlinear optical and infrared photonic applications. DSC analysis (10°C/min) demonstrates a progressive increase in glass‐transition temperature (T_g) from 359 to 452°C with the increase in La₂O₃ content. Continuous glass network modification with transformation of [TeO₄] to [TeO₃/TeO₃₊₁] units is evidenced from Raman spectra which is corroborated with XPS studies. While mechanical properties demonstrate enhancement of cross‐linking density in the network. These glasses exhibit optical transmission window extended from 0.4 to 6 μm with calculated zero dispersion wavelength (λ_ZDW) varying from 2.41 to 2.28 μm depending upon La₂O₃ content. Crystallization kinetics of TTL10 (80TeO₂‐10TiO₂‐10La₂O₃ in mol%) glass has been studied via established models. Activation energy (E_a) has been evaluated and dimensionality of crystal growth (m) suggests formation of surface crystals. Glass‐ceramic with crystalline phase of La₂Te₆O₁₅ has been realized in heat‐treated TTL10 glass samples (at 450°C). As predicted from DSC analysis, FESEM study unveils the formation of surface crystallized glass‐ceramics.     

High-efficiency Silicon Solar Cells: A Review

Over the past few decades, crystalline silicon solar cells have been extensively studied due to their high efficiency, high reliability, and low cost. In addition, these types of cells lead the industry and account for more than half of the market. For the foreseeable future, Si will still be a critical material for photovoltaic devices in the solar cell industry. In this paper, we discuss key issues, cell concepts, and the status of recent high-efficiency crystalline silicon solar cells.     

Stability of SiN<Subscript>X</Subscript>/SiN<Subscript>X</Subscript> double stack antireflection coating for single crystalline silicon solar cells

Double stack antireflection coatings have significant advantages over single-layer antireflection coatings due to their broad-range coverage of the solar spectrum. A solar cell with 60-nm/20-nm SiN_X:H double stack coatings has 17.8% efficiency, while that with a 80-nm SiN_X:H single coating has 17.2% efficiency. The improvement of the efficiency is due to the effect of better passivation and better antireflection of the double stack antireflection coating. It is important that SiN_X:H films have strong resistance against stress factors since they are used as antireflective coating for solar cells. However, the tolerance of SiN_X:H films to external stresses has never been studied. In this paper, the stability of SiN_X:H films prepared by a plasma-enhanced chemical vapor deposition system is studied. The stability tests are conducted using various forms of stress, such as prolonged thermal cycle, humidity, and UV exposure. The heat and damp test was conducted for 100 h, maintaining humidity at 85% and applying thermal cycles of rapidly changing temperatures from -20°C to 85°C over 5 h. UV exposure was conducted for 50 h using a 180-W UV lamp. This confirmed that the double stack antireflection coating is stable against external stress.     

Electric field strength effects on time-dependent passivation of metal surfaces

This paper presents further results and extensions of our previous point defect model for time-dependent growth of passive oxide films on metal surfaces. Specifically, by accounting for vacancies as material species rather than just holes in the oxide lattice, the model incorporates more plausible expressions for interfacial reactions and associated kinetic rate expressions. We use the model to explore the general effects of varying metal valence and electrolyte pH on passive film growth. Furthermore, we examine key assumptions concerning the thickness dependence of the electric field within the film. When the electric field inside the film remains constant and the rate constant for oxygen vacancy production varies with applied potential, the model predicts trends in thickness versus potential in reasonable agreement with experimental data for a variety of metal/metal oxide systems. This represents a considerable improvement upon the previous ‘high-field’ form of the model which assumed rate constants independent of potential and electric field in the film varying with thickness.