Structure and Dynamics in Supercritical Fluids

Supercritical fluids (SCFs) are currently receiving much industrial and scientific interest as a result of their unique physical properties. The most characteristic features of SCFs are liquid-like densities, gas-like viscosities, and diffusivities that are intermediate between typical gas and liquid values. The resulting combination of high dissolving power and enhanced mass-transfer rates makes SCFs attractive alternatives to liquid solvents for a variety of industrial applications, such as extraction, separation and reaction processes. In addition, the high compressibility of SCFs in the near-critical region allows one to tune their properties to desired values by applying small changes in pressure, which in turn makes it possible to tailor the rates and selectivities of chemical processes. Since the aforementioned applications of SCFs generally involve dilute solutions, it is essential to develop a microscopic understanding of the structure and dynamics of a supercritical solvent in the vicinity of a solute.

We use the methods of classical statistical mechanics, such as integral equation theory and mode coupling theory, to study structural and dynamical properties of supercritical solutions. Some of the problems we address are as follows. How does the solvent-solute and solute-solute clustering affect the rates and equilibrium constants of chemical reactions in SCFs? How does the proximity to the critical point affect the transport properties and what are the ramifications for diffusion controlled chemical reactions? How is preferential solvation manifested in local composition effects in dilute supercritical solutions? The answers to these questions should help us shed further light on fundamental properties of SCFs and their practical applications.

Quantum and Semiclassical Many-Body Dynamics

Numerous problems in chemical physics involve calculations of quantum time correlation functions (TCFs) in many-body systems. Particular examples include: medium-induced electron transfer, dissipative tunneling, radiationless processes, and electronic spectroscopy of chromophores in crystals and in liquids. While certain systems require a fully quantum mechanical treatment, there exists a large class of systems of chemical interest for which classical mechanics provides a reasonably good approximation. An appealing approach to the calculation of TCFs for such systems involves using semiclassical methods, which are generally based on the assumption that quantum effects can be taken into account by introducing relatively small corrections to the classical results. However, the shorter the time scale on which the behavior is analyzed, the more important quantum corrections may become, even for systems which are classical as far as their static and low-frequency dynamical properties are concerned. One of the research projects in our group involves developing a systematic procedure for including quantum effects into the results for TCFs obtained from classical simulations.

An alternative approach to study quantum dynamics in condensed phases involves calculating imaginary-time correlation functions using path integral Monte Carlo (PIMC) method and performing analytic continuation to the real-time axis. Unfortunately, analytic continuation is numerically unstable, and therefore leads to uncontrollable amplification of statistical noise unavoidable in PIMC simulations. In our group we employ the information theory and the methodology from the field of inverse problems in order to develop various techniques, such as Maximum Entropy and Singular Value Decomposition, for stabilizing the procedure of analytic continuation of quantum imaginary-time TCFs.

Recent Publications

Stiffness-Guided Motion of a Droplet on a Solid Substrate. Theodorakis PE, Egorov SA, Milchev A. J Chem Phys. Jun 28; 146(24):244705 (2017).

Conformations and Orientational Ordering of Semiflexible Polymers in Spherical Confinement.

Milchev A, Egorov SA, Nikoubashman A, Binder K. J Chem Phys. May 21;146(19):194907 (2017).

Semiflexible Polymers Confined in a Slit Pore with Attractive Walls: Two-Dimensional Liquid Crystalline Order Versus Capillary Nematization. Milchev A, Egorov SA, Binder K. Soft Matter. Mar 1; 13(9):1888-1903 (2017).

Theoretical and Experimental Investigation of Microphase Separation in Mixed Thiol Monolayers on Silver Nanoparticles.  Merz SN, Farrell ZJ, Dunn CJ, Swanson RJ, Egorov SA, Green DL. ACS Nano. Nov 22; 10(11):9871-9878 (2016).

Concentration-Induced Planar-to-Homeotropic Anchoring Transition of Stiff Ring Polymers on Hard Walls. Poier P, Egorov SA, Likos CN, Blaak R. Soft Matter. Sep 28; 12(38):7983-7994 (2016).

Elasticity of polymeric nanocolloidal particles. Riest J, Athanasopoulou L, Egorov SA, Likos CN, Ziherl P. Sci Rep. Nov 2; 5:15854 (2015).

Semiflexible Polymer Brushes and the Brush-Mushroom Crossover. Egorov SA, Hsu HP, Milchev A, Binder K. Soft Matter. Apr 7; 11(13):2604-16 (2015).

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First Name: 
Sergei A.
People Type: 
Computing ID: 
Office Address: 
Room 155, Chemistry Building

B.Sc. Leningrad University, 1987

Ph.D. University of Wisconsin, 1996

Postdoctoral Research Associate, Columbia University,1996-1997

Research Interests: 
Theoretical chemical physics