ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

Ultrafast underdamped solvation: Agreement between computer simulation and various theories of solvation dynamics

Roy, Srabani and Bagchi, Biman (1993) Ultrafast underdamped solvation: Agreement between computer simulation and various theories of solvation dynamics. In: Journal of Chemical Physics, The, 99 (2). pp. 1310-1319.

[img] PDF
Ultrafast.pdf - Published Version
Restricted to Registered users only

Download (870kB) | Request a copy
Official URL: http://jcp.aip.org/resource/1/jcpsa6/v99/i2/p1310_...


A theoretical analysis of the three currently popular microscopic theories of solvation dynamics, namely, the dynamic mean spherical approximation (DMSA), the molecular hydrodynamic theory (MHT), and the memory function theory (MFT) is carried out. It is shown that in the underdamped limit of momentum relaxation, all three theories lead to nearly identical results when the translational motions of both the solute ion and the solvent molecules are neglected. In this limit, the theoretical prediction is in almost perfect agreement with the computer simulation results of solvation dynamics in the model Stockmayer liquid. However, the situation changes significantly in the presence of the translational motion of the solvent molecules. In this case, DMSA breaks down but the other two theories correctly predict the acceleration of solvation in agreement with the simulation results. We find that the translational motion of a light solute ion can play an important role in its own solvation. None of the existing theories describe this aspect. A generalization of the extended hydrodynamic theory is presented which, for the first time, includes the contribution of solute motion towards its own solvation dynamics. The extended theory gives excellent agreement with the simulations where solute motion is allowed. It is further shown that in the absence of translation, the memory function theory of Fried and Mukamel can be recovered from the hydrodynamic equations if the wave vector dependent dissipative kernel in the hydrodynamic description is replaced by its long wavelength value. We suggest a convenient memory kernel which is superior to the limiting forms used in earlier descriptions. We also present an alternate, quite general, statistical mechanical expression for the time dependent solvation energy of an ion. This expression has remarkable similarity with that for the translational dielectric friction on a moving ion.

Item Type: Journal Article
Additional Information: Copyright of this article belongs to American Institute of Physics.
Department/Centre: Division of Chemical Sciences > Solid State & Structural Chemistry Unit
Depositing User: Ms TV Yashodha
Date Deposited: 26 Apr 2011 10:27
Last Modified: 26 Apr 2011 10:27
URI: http://eprints.iisc.ac.in/id/eprint/36443

Actions (login required)

View Item View Item