DIFFUSION-INFLUENCED REVERSIBLE TRANSFER OF ELECTRONIC EXCITATION-ENERGY IN LIQUID SOLUTION BY LONG-RANGE INTERACTION

Authors
Citation
T. Bandyopadhyay, DIFFUSION-INFLUENCED REVERSIBLE TRANSFER OF ELECTRONIC EXCITATION-ENERGY IN LIQUID SOLUTION BY LONG-RANGE INTERACTION, The Journal of chemical physics, 106(12), 1997, pp. 5049-5061
Citations number
42
Categorie Soggetti
Physics, Atomic, Molecular & Chemical
ISSN journal
00219606
Volume
106
Issue
12
Year of publication
1997
Pages
5049 - 5061
Database
ISI
SICI code
0021-9606(1997)106:12<5049:DRTOEE>2.0.ZU;2-#
Abstract
An approach to donor-acceptor kinetics in the presence of diffusion an d reversible energy transfer due to microscopic interaction is describ ed. A set of coupled dynamic equations for the reduced distribution fu nctions of reactant molecules in forward and reverse steps is presente d on the basis of a hierarchical system of many-body Smoluchowski equa tions. With a view toward treating long-range dipolar interaction medi ated energy transfer kinetics, this formalism is generalized to incorp orate unimolecular decay pathways. Numerical calculations of this set of equations for the excited donor decay after a delta pulse show the dependence of the result on acceptor concentration, forward and back t ransfer distance-dependent rates, donor and acceptor lifetime, and on their diffusive motion. Comparison with the corresponding forward and irreversible reactive dynamics provides detailed insights into the tim e dependence of flow of electronic excitation in donors and accepters. The irreversible Smoluchowski limit is only recovered when both the f orward and the reverse reactive systems are undergoing fast molecular motion (slow reaction). In the donor-donor case the temporal profile o f the excited donor decay and the evolution of ground state donor (tha t receives energy from the initially excited donor) is presented, alon g with the total excitation that resides in these two kind of donors. The total excitation in this situation is found to follow a monotonic exponential decay with its characteristic natural lifetime, as expecte d in a lifetime measurement experiment. (C) 1997 American Institute of Physics.