Brian B. Laird

Professor and Associate Chair for Graduate Studies

1251 Wescoe Hall Drive Malott Hall Room 6084 University of Kansas Lawrence, KS 66045 Phone: (785) 864-4632 Fax: (785) 864-5396 Email: blaird@ku.edu

Theoretical and computational chemistry

The ultimate goal of materials chemistry is the understanding of the macroscopic properties of materials in terms of the microscopic molecular interactions. This is a common theme in all of the natural sciences. The differences between the various scientific disciplines (chemistry, biology, physics, materials sciences, etc.) often disappear as the traditional macroscopic phenomenology is replaced by a more molecular approach. At present, most of what is known about the chemical and physical properties of materials is still largely empirical, especially in the case of amorphous, macromolecular or interfacial systems. The development of a microscopic theoretical description for a variety of such complex systems is the primary focus of our research. Several representative projects are listed below. They are all projects in which great advantage will be gained by exploiting the natural symbiosis between analytical and computer-simulation techniques.

1) Crystal-melt interfaces of complex systems: The structure and dynamics of an interface between a crystal and its melt are of paramount importance in studies of crystal growth and nucleation. Experimental study is difficult as such an interface lies sandwiched between two dense phases, and experimental data is lacking, increasing the value of computer simulations to the study of such systems.  Most previous studies have involved simple, one-component model systems. Using molecular-dynamics computer simulations and classical density-functional theories, we are currently concentrating on more complex systems such as multicomponent systems (for example, alloys) and molecular systems, such as succinonitrile  and pivalic acid, for which extensive data relating to crystal growth and interfacial properties have been collected from microgravity experiments aboard the Space Shuttle.

2) Fundamental Investigations into Gas Expanded Solvent Media for Green Chemistry:  This project is part of the research mission of the newly formed Center for Environmentally Beneficial Catalysis, an NSF funded Engineering Research Center headquartered at the University of Kansas. In this project we seek a fundamental understanding, through molecular simulation, of the thermodynamics, transport properties and molecular-level structure of gas-expanded solvent systems - a new class of solvent media in which a traditional industrial organic solvents, such as acetonitrile, are expanded by an order of magnitude in volume (without phase separation) by the addition of a large amount of miscible gas - primarily CO_2.

In these new media, dense CO₂ significantly replaces the traditional solvent (up to 80% by volume), such that the retained solvent maintains the catalyst solubility and other advantages provided by the traditional solvent (for example, rate enhancement due to polarity). Further, solubility is increased for O₂   Thus, gas-expanded solvents combine the environmentally beneficial nature of supercritical (sc) solvents (such as sc-CO₂) and the advantages of traditional solvents in an optimal manner, thereby deriving many reaction and environmental/economic advantages not possible with either the neat solvent or sc-fluid.  Due to their novelty, these gas-expanded solvent systems have received little attention from the molecular simulation community. To complement the current experimental effort, this project represents a parallel program of modeling efforts to

• gain a fundamental molecular-level understanding of the physico-chemical properties of gas-expanded solvents, with particular attention to those systems utilizing CO₂ as the expansion gas. provide guidance to the experimental program to rationally chose optimum solvents
  
• provide guidance to the experimental program in the optimization of catalyst performance in expanded media.

3) Algorithms for Molecular Modeling: Molecular-dynamics computer simulation has become an invaluable tool in chemistry, chemical engineering, physics, materials science and biology; however, its uses are still limited by the relatively small system sizes and short time scales that can be simulated at present.  Progress in this area therefore comes from advances in computer technology and in the development of efficient and stable algorithms.  The latter is the goal of an ongoing multidisciplinary project in collaboration with Prof. Ben Leimkuhler, an applied mathematician at the University of Leicester.

Selected Publications

"Calculation of the kinetic coefficient for the hard-sphere crystal-melt interface", M. Amini and B.B. Laird, Phys. Rev. Lett. 97 216102 (4 pages) (2006).

"Phase Equilibria in Carbon-Dioxide Expanded Solvents: Experiments and Molecular Simulations", Y. Houndonougbo, J. Hong, B. Rajagopalan, K. Wong, K. Kuczera, B. Subramaniam, and B.B. Laird, J. Phys. Chem. B., 110 13195-13202 (2006).

"Monte Carlo Simulations of CO2-expanded Acetonitrile", Y. Houndonougbo, J-X Guo, G.H. Lushington and B. Laird, Mol. Phys., 104, 2955-2960 (2006).

"The anisotropic hard-sphere crystal-melt interfacial free energy from fluctuations" , R.L. Davidchack, J.R. Morris and B.B. Laird, J.Chem. Phys. 125,094710 (7 pages) (2006).

"Calculation of the crystal-melt interfacial free energy of succinonitrile from molecular simulation", X. Feng and B.B. Laird,
J. Chem. Phys, 124 , 044707 (8 pages) (2006).

"Direct calculation of the crystal-melt interfacial free energy via molecular-dynamics computer simulation", B.B. Laird and R.L. Davidchack, J. Phys. Chem. B, 109 17802-17812 (2005). [Feature Article]

"A 6-site model for succinonitrile", X.-B. Feng and B.B. Laird, Molecular Physics 103, 2795 - 2801 (2005).

Crystal structure and interaction dependence of the crystal-melt interfacial free energy" , R.L Davidchack and B.B. Laird, Phys. Rev. Lett., 94 , 086102 (2005).