Damping and higher multipole effects in the quantum electrodynamical model for electronic energy transfer in the condensed phase

被引:62
作者
Scholes, GD [1 ]
Andrews, DL [1 ]
机构
[1] UNIV E ANGLIA,SCH CHEM SCI,NORWICH NR4 7TJ,NORFOLK,ENGLAND
关键词
D O I
10.1063/1.475145
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The interplay between electronic coupling, spectral linewidth, and rate of electronic energy transfer between chromophores is examined in the context of a quantum electrodynamical (QED) model. The QED framework properly allows us to identify the partitioning between the near and far zone mechanisms for transfer of energy between chromophores dispersed in condensed phase (liquid or solid) host media. The extent to which coupling is modified by the medium is investigated. A general QED treatment of higher multipole contributions to the coupling between transition moments is also derived, whence interactions involving electric dipole, quadrupole and octopole as well as magnetic dipole and quadrupole interactions are examined explicitly. A new formulation is presented wherein expressions for the multipolar coupling tensors are obtained in terms of spherical Bessel functions, providing a clear, compact representation of the retarded coupling interaction and its distance-dependence. The irreducible tensor formulation of the coupling is discussed, highlighting features concerning the exact form of the orientation factors that have often in the past escaped notice. The detailed method of implementing a rotational averaging of the resultant interaction tensors is demonstrated, finally leading to a novel and concise representation for multipolar couplings of arbitrary order. The coupling between bacteriochlorophyll a chromophores is discussed as an example. (C) 1997 American Institute of Physics.
引用
收藏
页码:5374 / 5384
页数:11
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共 78 条
[51]  
Mukamel S., 1995, Principles of Nonlinear Optical Spectroscopy
[52]   Exchange-induced resonance energy transfer [J].
Naqvi, K. Razi ;
Steel, Colin .
CHEMICAL PHYSICS LETTERS, 1970, 6 (01) :29-32
[53]   QUANTUM ELECTRODYNAMICS WITH NON-RELATIVISTIC SOURCES .3. INTERMOLECULAR INTERACTIONS [J].
POWER, EA ;
THIRUNAMACHANDRAN, T .
PHYSICAL REVIEW A, 1983, 28 (05) :2671-2675
[54]   A new generalization of the Casimir-Polder potential to higher electric multipole polarizabilities [J].
Salam, A ;
Thirunamachandran, T .
JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (13) :5094-5099
[55]   RATE EXPRESSIONS FOR EXCITATION TRANSFER .4. ENERGY MIGRATION AND SUPEREXCHANGE PHENOMENA [J].
SCHOLES, GD ;
GHIGGINO, KP .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (20) :8873-8883
[56]   ELECTRONIC INTERACTIONS AND INTERCHROMOPHORE EXCITATION TRANSFER [J].
SCHOLES, GD ;
GHIGGINO, KP .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (17) :4580-4590
[57]   RATE EXPRESSIONS FOR EXCITATION TRANSFER .1. RADIATIONLESS TRANSITION THEORY PERSPECTIVE [J].
SCHOLES, GD ;
GHIGGINO, KP .
JOURNAL OF CHEMICAL PHYSICS, 1994, 101 (02) :1251-1261
[58]   ON THE RATE OF RADIATIONLESS INTERMOLECULAR ENERGY-TRANSFER [J].
SCHOLES, GD ;
CLAYTON, AHA ;
GHIGGINO, KP .
JOURNAL OF CHEMICAL PHYSICS, 1992, 97 (10) :7405-7413
[59]   Energy transfer and spectroscopic characterization of multichromophoric assemblies [J].
Scholes, GD .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (48) :18731-18739
[60]   Configuration interaction and the theory of electronic factors in energy transfer and molecular exciton interactions [J].
Scholes, GD ;
Harcourt, RD .
JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (13) :5054-5061