Ta/Ti/Ni/Ceramic Multilayered Composites by Combustion Synthesis: Microstructure and Mechanical Properties

Ta/Ti/Ni/ceramic multilayered composites were successfully prepared by combustion synthesis. Laminated composites Ti–Ta–(Ti + 0.65C)–Ni–(Ti + 1.7B)–(Ti + 1.7B)–Ta–Ni-Ti and 3(Ti + 1.7B)–Ta–(5Ti + 3Si)–Ta–(Ti + 1.7B)–Ta–(5Ti + 3Si)–Ta–3(Ti + 1.7B) were combustion synthesized in an Ar atmosphere using (1) metallic foils (Ti, Ta, Ni) and (2) reactive tapes (Ti + 0.65C), (Ti + 1.7B), and (5Ti + 3Si), which, upon combustion, yielded ceramic layers as starting materials. The microstructure, crystal structure, and chemical composition of multilayered composites were characterized by SEM, EDX, and XRD. Their flexural strength was measured at 1100 °C. Upon combustion, Ta foils turned strongly joined with Ti ones due to the development of high temperature in the reactive layers yielding TiCx and TiBy. The formation of a liquid phase between metallic foils and reactive tapes and mutual interdiffusion between melted components during combustion favored strong joining between refractory metallic foils. Good joining between metals and ceramics is reached due to the formation of thin interfacial layers in the form of cermets and eutectic solutions.

Directional manipulation of diffusio-osmosis flow by design of solute-wall and solvent-wall interactions

Understanding of the diffusio-osmosis, the flow induced by a solute gradient acting in narrow interfacial layers at nanoscale solid-liquid interface, is of great value in view of the increasing importance of micro- and nano-fluidic devices and self-propelling particle. Here, using molecular dynamics simulations, we develop a numerical method for direct simulation of diffusio-osmosis flows mimicking the realistic experiment without any assumed external forces. It allows us to obtain reliable flow details which is however hard to get in experiments. We found that the solvent-wall interaction, previously overlooked in classical paradigm, plays a critical role in diffusio-osmosis process. In particular, diffusio-osmosis is controlled by the interaction difference between solute-wall and solvent-wall. When solute-than solvent-wall, a surface excess (depletion) of solute particles on solid-liquid interface is formed which induces diffusio-osmosis flow towards low (high) concentration. We modified the classical Derjaguin expression to include the effect of nanoscale hydrodynamics boundary conditions for the accurate prediction of diffusio-osmosis characteristics. Overall, our results provide the clear guidance for controlling fluids flow and manipulating motion of colloids under tunable solute concentrations.

DFT-Based Studies on Carbon Adsorption on the wz-GaN Surfaces and the Influence of Point Defects on the Stability of the Diamond–GaN Interfaces

Integration of diamond with GaN-based high-electron-mobility transistors improves thermal management, influencing the reliability, performance, and lifetime of GaN-based devices. The current GaN-on-diamond integration technology requires precise interface engineering and appropriate interfacial layers. In this respect, we performed first principles calculation on the stability of diamond–GaN interfaces in the framework of density functional theory. Initially, some stable adsorption sites of C atoms were found on the Ga- and N-terminated surfaces that enabled the creation of a flat carbon monolayer. Following this, a model of diamond–GaN heterojunction with the growth direction [111] was constructed based on carbon adsorption results on GaN{0001} surfaces. Finally, we demonstrate the ways of improving the energetic stability of diamond–GaN interfaces by means of certain reconstructions induced by substitutional dopants present in the topmost GaN substrate’s layer.

Engineering of Fe-pnictide heterointerfaces by electrostatic principles

Interface-related phenomena have great potential to control the superconducting state in Fe-based superconductors. We propose a comprehensive classification of Fe-pnictide heterointerfaces based on electrostatic principles that allow the prediction of the interface microstructure, in particular, distinguishing between clean heterointerfaces and the formation of interfacial layers. The concept was successfully tested on a novel LnOFeAs/BaFe2As2 (Ln = La, Sm) Fe-pnictide heterostructure. With the addition of different cations/anions, it is possible to produce clean interfaces or interfacial layers. The impact of the microstructure on superconductivity in the Fe-pnictide heterostructures is discussed.

Effects of Surfactant Volume Fraction on the Antioxidant Efficiency and on The Interfacial Concentrations of Octyl and Tetradecyl p-Coumarates in Corn Oil-in-Water Emulsions

Surfactants have been used for decades in the food industry for the preparation of lipid-based emulsified food stuffs. They play two main roles in the emulsification processes: first they decrease the interfacial tension between the oil and water, facilitating droplet deformation and rupture; second, they reduce droplet coalescence by forming steric barriers. However, addition of surfactants to binary oil-water mixtures also brings up the formation of three-dimensional interfacial layers, surrounding each emulsion droplet, that significantly alter chemical reactivity. This is the case, for instance, in the inhibition reaction between antioxidants and the lipid radicals formed in the course of the spontaneous oxidation reaction of unsaturated lipids, which are commonly employed in the preparation of food-grade emulsions. The rate of the inhibition reaction depends on the effective concentrations of antioxidants, which are mostly controlled by the amount of surfactant employed in the preparation of the emulsion. In this work, we analyze the effects of the surfactant Tween 20 on the oxidative stability and on the effective concentrations of two model antioxidants derived from cinnamic acid, determining their interfacial concentrations in the intact emulsions to avoid disrupting the existing equilibria and biasing results. For this purpose, a recently developed methodology was employed, and experimental results were interpreted on the grounds of a pseudophase kinetic model.