Search arXivSearch

arXiv · 1512.06592

Collective modes and thermodynamics of the liquid state

Abstract

Strongly interacting, dynamically disordered and with no small parameter, liquids took a theoretical status between gases and solids. We review different approaches to liquids and propose that liquids do not need classifying in terms of their proximity to gases and solids. Instead, they are a unique system in their own class with a notably mixed dynamical state in contrast to pure dynamical states of solids and gases. We start with explaining how the first-principles approach to liquids is an intractable, exponentially complex problem of coupled non-linear oscillators with bifurcations. This is followed by a reduction of the problem based on liquid relaxation time $τ$ representing non-perturbative treatment of strong interactions. On the basis of $τ$, solid-like high-frequency modes are predicted and we review related recent experiments. We demonstrate how these modes can be derived by generalizing either hydrodynamic or elasticity equations. We comment on the historical trend to approach liquids using hydrodynamics and compare it to an alternative solid-like approach. We subsequently discuss how collective modes evolve with temperature and how this affects liquid energy and other properties such as fast sound. Here, our emphasis is on real, rather than model, liquids. Highlighting the dominant role of high-frequency modes for liquid energy, we review a wide range of liquids: subcritical low-viscous liquids, supercritical state with two different dynamical and thermodynamic regimes separated by the Frenkel line, highly-viscous liquids and liquid-glass transition. We also discuss liquid-liquid phase transitions where the solid-like properties of liquids have become further apparent. We then discuss gas-like and solid-like approaches to quantum liquids and persisting theoretical problems. We list areas where interesting insights may appear and continue the extraordinary liquid story.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

K. Trachenko, V. V. Brazhkin. 2015-12-21. Collective modes and thermodynamics of the liquid state. https://doi.org/10.1088/0034-4885%2F79%2F1%2F016502

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Transient Elasticity -- A Unifying Framework for Thixotropy, Polymers, and Granular Media

Thixotropic yield stress fluids, such as paint or ketchup, are traditionally viewed as elastic structures that, under shear rates, break into viscous liquids with lumps, and reconnect at rest. An alternative framework is presented here: Upon shear, structural destruction is incomplete, leaving sufficient connections. As a result, elasticity fundamentally underlies their non-Newtonian behavior, though they do appear purely viscous under a steady shear, displaying little direct evidence of elastic rebound---same as granular media and polymers. Consequently, all three are described by the same set of evolution equations, differing only in their parameters. These equations are set up by starting from solid dynamics and allowing the elastic strain $\varepsilon^e$ to relax, which in effect interpolates between solid and fluid behavior, appropriate for systems that display both types of behavior. Incorporating in addition a two-temperature framework, tracking how energy is dissipated in two consecutive stages, yields the nonlinear model of Transient Elasticity (TE). It describes an elasticity that is transient in time yet persistent under shear. Previously validated for polymers and granular media, TE is here applied to thixotropic yield-stress fluids. As shown, it successfully accounts for a wide range of characteristic phenomena, including over- and undershoot, viscosity bifurcation, shear banding, and oscillatory rheography. Given its appropriateness across structurally diverse systems, TE offers a unified, surprisingly general account of non-Newtonian phenomena.

cond-mat.soft

Deformation and organization of droplet-encapsulated soft beads

Many biological, culinary, and engineering processes lead to the co-encapsulation of several soft particles within a liquid interface. In these situations the particles are bound together by the capillary forces that deform them and influence their biological or rheological properties. Here, we introduce an experimental approach to encapsulate a controlled number of soft beads within aqueous droplets in oil. These droplet-encapsulated gels are manipulated in a deformable microfluidic device to merge them and modify the liquid fraction. In the dry limit the contact surface between the hydrogels is found to be determined by the elastocapillary number $E_c$, with the contact radius following a $E_c^{1/3}$ dependence, indicating that the deformation increases for soft or small particles. When multiple beads are co-encapsulated within a single droplet they can be arranged into linear or three-dimensional aggregates that remain at a local energy minimum.

cond-mat.soft

Flexoelectricity-driven softening of bend elasticity leads to spontaneous chiral symmetry breaking in a polar fluid

The origin of the recently observed spontaneous chiral symmetry breaking in polar fluids composed of achiral molecules is an unsolved problem, raising fundamental questions about how heliconical structures emerge in such systems. Here, we investigate the pretransitional fluctuations leading to the formation of the spontaneously chiral twist-bend ferroelectric nematic phase using dielectric spectroscopy, light scattering, and small-angle X-ray scattering. We observe simultaneous softening of the bend elastic constant and the emergence of a collective dielectric mode on approaching the transition. By developing a theoretical model, we show that these phenomena are signatures of a flexoelectricity-driven transition arising from the coupling between electric polarization and bend deformation.

cond-mat.soft