All Physics Faculty Publications
Document Type
Article
Journal/Book Title/Conference
Physical Review A: Atomic Molecular and Optical
Volume
41
Issue
10
Publication Date
5-1990
First Page
5362
Last Page
5365
Abstract
It has long been known that the time course of a bimolecular reaction occurring in a condensed host depends on the behavior of the nonequilibrium pair-correlation function for reactant pairs. The classical analysis of such reactions has led to a kind of standard rule: The association rate constant for a diffusion-controlled reaction is 4πDR and this rate constant produces the fastest possible kinetics. This result is only (approximately) true for the case of an irreversible reaction, however. Here, we reexamine this old problem, looking closely at the reversible case. We report a result that challenges the standard wisdom: When the reaction is highly reversible the relaxation of the related kinetics to equilibrium can be much faster than the model in which 4πDR is the association rate constant. We suggest that our work provides a natural resolution to a well-known, long-standing controversy in the study of electrically active impurities in silicon grown by the Czochralski method.
Recommended Citation
D. Peak, D.C. Greenlaw*, and L.A. Schick*, "Pair Correlation Kinetics," Physical Review A 41, 5362-5365 (1990). 10.1103/PhysRevA.41.5362
Comments
Published by American Physical Society in Physical Review A. Publisher PDF available for download through link above.