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Anisotropic particles are widely presented in nature, from colloidal to bacterial systems, and control over their interactions is of crucial importance for many applications, from self-assembly of novel materials to microfluidics. Placed in rapidly rotating external electric fields, colloidal particles attain a tunable long-range and many-body part in their interactions. For spherical colloids, this approach has been shown to offer rich capabilities to construct the tunable interactions via designing the internal structure of particles and spatial hodographs of external rotating fields, but in the case of anisotropic particles, the interactions remain poorly understood. Here, we show that tunable interactions between anisotropic rod-like and spheroidal colloidal particles in rotating electric or magnetic fields can be calculated and analyzed with the diagrammatic technique we developed in the present work. With this technique, we considered an in-plane rotating electric field, obtained the long-range asymptotics of the anisotropic interactions, calculated the tunable interactions between particles rotating synchronously, and found conditions for rotator repulsion. We compared the mechanisms providing tunable interactions to those for orientational (Keesom), induction (Debye), and dispersion (London) interactions in molecular systems and found that the tunable interactions between anisotropic particles represent a novel kind of dipole-like interaction. The method can be directly generalized for magnetically induced interactions, 3D systems, and fields with spatial hodographs. The results provide significant advance in theoretical methods for tunable interactions in colloids and, therefore, are of broad interest in condensed matter, chemical physics, physical chemistry, materials science, and soft matter. [ABSTRACT FROM AUTHOR]

Tunable interactions between colloidal particles, governed by external rotating electric or magnetic fields, yield rich capabilities for prospective self-assembly technologies of materials and fundamental particle-resolved studies of phase transitions and transport phenomena in soft matter. However, the role of the internal structure of colloidal particles in the tunable interactions has never been systematically investigated. Here, we study the tunable interactions between composite particles with core–shell structure in a rotating electric field and show that the engineering of their internal structure provides an effective tool for designing the interactions. We generalized an integral theory and studied the tunable interactions between core–shell particles with homogeneous cores (layered particles) and cores with nano-inclusions to reveal the main trends in the interactions influenced by the structure. We found that depending on the materials of the core, shell, and solvent, the interactions with the attractive pairwise part and positive or negative three-body part can be obtained, as well as pairwise repulsion with attractive three-body interactions (for triangular triplets). The latter case is observed for the first time, being unattainable for homogeneous particles but feasible with core–shell particles: Qualitatively similar interactions are inherent to charged colloids (repulsive pairwise and attractive three-body energies), known as a model system of globular proteins. The methods and conclusions of our paper can be generalized for magnetic and 3D colloidal systems. The results make a significant advance in the analysis of tunable interactions in colloidal systems, which are of broad interest in condensed matter, chemical physics, physical chemistry, materials science, and soft matter. [ABSTRACT FROM AUTHOR]

Tunable interactions in colloids, induced by rotating electric or magnetic fields, provide a flexible and promising tool for self-assembly of soft materials, as well as for fundamental particle-resolved studies of phase transitions and other generic phenomena in condensed matter. In the case of two-dimensional systems and the in-plane rotating fields, the interactions are known to have a long-range (dipolar) attraction and an expressed three-body part at short distances, but still remain poorly understood. Here, we show that the interactions and polarization mechanisms governing the tunable interactions can be described, calculated, and analyzed in detail with the diagrammatic method we proposed. The diagrams yield a clear illustration of different polarization processes contributing to the Keesom, Debye, London, self, and external energies, classified in colloids similarly to intermolecular interactions. The real tunable interactions, obtained with the boundary element method, can be simply and accurately interpolated with the set of basis of the diagrams attributed to different physically clear polarization processes. Calculation of large-distance behavior and interpolation of the many-body interactions (and analysis of the leading mechanisms contributing to them) excellently illustrate that the diagrammatic method provides deep insights into the nature of tunable interactions. The method can be generalized for multicomponent systems, suspensions of particles with a composite structure and a complicated shape. The results provide significant advance in theoretical methods for detailed analysis of tunable interactions in colloids and, therefore, the method is of broad interest in condensed matter, chemical physics, physical chemistry, materials science, and soft matter. [ABSTRACT FROM AUTHOR]

Silicon carbide (SiC) possesses a unique combination of properties such as high mechanical strength at elevated temperatures, wear resistance, low thermal expansion coefficient, high temperature oxidation resistance, corrosion stability, radiation hardness, high chemical inertness, and thermal conductivity. Unfortunately, SiC is very brittle and cannot, therefore, be used "as is". SiC's crack resistance, due to the prevention of crack propagation, can be increased by the reinforcing of SiC. In this paper, a novel method for manufacturing SiC-based composites reinforced with Mo wire is developed. The composites are produced by infiltrating porous carbon blanks with molten silicon. The molten silicon reacts with the molybdenum wire embedded in the carbon blanks. As a result, a complex interfacial silicide layer with a predominant MoSi2 phase is formed on the surface of the Mo wire. In addition, a thin layer of Mo5Si3 is formed between the residual metal in the core of the wire and the disilicide. A stable bond of the interfacial layer with both the residual metal and the SiC-based ceramic matrix is observed. Mechanical tests on the obtained samples for three-point bending at 20 and 1500 °C showed quasi-plastic damage. The reinforcing elements act as stoppers for propagating cracks in the event of a matrix failure. The developed method for producing composites with a ceramic matrix reinforced with metal wire makes it possible to reduce the cost of machining and manufacturing products with complex geometric shapes. It also opens the way for broader applications of SiC-based composites. [ABSTRACT FROM AUTHOR]

The heat capacity of classical crystals is determined by the Dulong–Petit value CV ≃ D (where D is the spatial dimension) for softly interacting particles and has the gas-like value CV ≃ D/2 in the hard-sphere limit, while deviations are governed by the effects of anharmonicity. Soft- and hard-sphere interactions, which are associated with the enthalpy and entropy of crystals, are specifically anharmonic owing to violation of a linear relation between particle displacements and corresponding restoring forces. Here, we show that the interplay between these two types of anharmonicities unexpectedly induces two possible types of heat capacity anomalies. We studied thermodynamics, pair correlations, and collective excitations in 2D and 3D crystals of particles with a limited range of soft repulsions to prove the effect of interplay between the enthalpy and entropy types of anharmonicities. The observed anomalies are triggered by the density of the crystal, changing the interaction regime in the zero-temperature limit, and can provide about 10% excess of the heat capacity above the Dulong–Petit value. Our results facilitate understanding effects of complex anharmonicity in molecular and complex crystals and demonstrate the possibility of new effects due to the interplay between different types of anharmonicities. [ABSTRACT FROM AUTHOR]

The amplification of surface acoustic waves (SAWs) by a multilayer graphene (MLG)-based amplifier is studied. The conductivity of massless carriers (electrons or holes) in graphene in an external drift electric field is calculated using Boltzmann's equation. At some carrier drift velocities, the real part of the variable conductivity becomes negative and MLG can be employed in SAW amplifiers. Amplification of Blustein's and Rayleigh's SAWs in CdS, a piezoelectric hexagonal crystal of the symmetry group C6v, is considered. The corresponding equations for SAW propagation in the device are derived and can be applied to other substrate crystals of the same symmetry. The results of the paper indicate that MLG can be considered as a perspective material for SAW amplification and related applications. [ABSTRACT FROM AUTHOR]