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Register a new userSolid-Liquid Composites for Soft Multifunctional Materials
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Soft materials with a liquid component are an emerging paradigm in materials design. The incorporation of a liquid phase, such as water, liquid metals, or complex fluids, into solid materials imparts unique properties and characteristics that emerge as a result of the dramatically different properties of the liquid and solid. Especially in recent years, this has led to the development and study of a range of novel materials with new functional responses, with applications in topics including soft electronics, soft robotics, 3D printing, wet granular systems and even in cell biology. Here we provide a review of solid-liquid composites, broadly defined as a material system with at least one, phase-separated liquid component, and discuss their morphology and fabrication approaches, their emergent mechanical properties and functional response, and the broad range of their applications.
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The exotic physical properties of graphene have led to intense research activities on the synthesis and characterization of graphene composites during the last decade. In this article the methods developed for preparation of such materials and the different application areas are reviewed. The composites discussed are of two types, viz; graphene/polymer and inorganic/ graphene. The techniques of ex-situ hybridization and in-situ hybridization have been pointed out. Some of the application areas are batteries and ultracapacitor for energy storage and fuel cell and solar cell for energy generation and some of the possible future directions of research have been discussed.
We report detailed theoretical investigations of the micro-mechanics and bulk elastic properties of composites consisting of randomly distributed stiff fibers embedded in an elastic matrix in two and three dimensions. Recent experiments published in Physical Review Letters [102, 188303 (2009)] have suggested that the inclusion of stiff microtubules in a softer, nearly incompressible biopolymer matrix can lead to emergent compressibility. This can be understood in terms of the enhancement of the compressibility of the composite relative to its shear compliance as a result of the addition of stiff rod-like inclusions. We show that the Poissons ratio $ u$ of such a composite evolves with increasing rod density towards a particular value, or {em fixed point}, independent of the material properties of the matrix, so long as it has a finite initial compressibility. This fixed point is $ u=1/4$ in three dimensions and $ u=1/3$ in two dimensions. Our results suggest an important role for stiff filaments such as microtubules and stress fibers in cell mechanics. At the same time, our work has a wider elasticity context, with potential applications to composite elastic media with a wide separation of scales in stiffness of its constituents such as carbon nanotube-polymer composites, which have been shown to have highly tunable mechanics.
We present an overview of the differential geometry of curves and surfaces using examples from soft matter as illustrations. The presentation requires a background only in vector calculus and is otherwise self-contained.
Yield stress fluids (YSFs) display a dual nature highlighted by the existence of a yield stress such that YSFs are solid below the yield stress, whereas they flow like liquids above it. Under an applied shear rate $dotgamma$, the solid-to-liquid transition is associated with a complex spatiotemporal scenario. Still, the general phenomenology reported in the literature boils down to a simple sequence that can be divided into a short-time response characterized by the so-called stress overshoot, followed by stress relaxation towards a steady state. Such relaxation can be either long-lasting, which usually involves the growth of a shear band that can be only transient or that may persist at steady-state, or abrupt, in which case the solid-to-liquid transition resembles the failure of a brittle material, involving avalanches. Here we use a continuum model based on a spatially-resolved fluidity approach to rationalize the complete scenario associated with the shear-induced yielding of YSFs. Our model provides a scaling for the coordinates of the stress maximum as a function of $dotgamma$, which shows excellent agreement with experimental and numerical data extracted from the literature. Moreover, our approach shows that such a scaling is intimately linked to the growth dynamics of a fluidized boundary layer in the vicinity of the moving boundary. Yet, such scaling is independent of the fate of that layer, and of the long-term behavior of the YSF. Finally, when including the presence of long-range correlations, we show that our model displays a ductile to brittle transition, i.e., the stress overshoot reduces into a sharp stress drop associated with avalanches, which impacts the scaling of the stress maximum with $dotgamma$. Our work offers a unified picture of shear-induced yielding in YSFs, whose complex spatiotemporal dynamics are deeply connected to non-local effects.
We describe a high-resolution, high-bandwidth technique for determining the local viscoelasticity of soft materials such as polymer gels. Loss and storage shear moduli are determined from the power spectra of thermal fluctuations of embedded micron-sized probe particles, observed with an interferometric microscope. This provides a passive, small-amplitude measurement of rheological properties over a much broader frequency range than previously accessible to microrheology. We study both F-actin biopolymer solutions and polyacrylamide (PAAm) gels, as model semiflexible and flexible systems, respectively. We observe high-frequency omega^(3/4) scaling of the shear modulus in F-actin solutions, in contrast to omega^(1/2) scaling for PAAm.
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