Excitation energy transfer in condensed media

被引:175
作者
Hsu, CP [1 ]
Fleming, GR
Head-Gordon, M
Head-Gordon, T
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Lab, Phys Biosci Div, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Chem Sci, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA
关键词
D O I
10.1063/1.1338531
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
We derive an expression for resonance energy transfer between a pair of chromophores embedded in a condensed medium by considering the energy splitting of the chromophores from their resonant excited states. We employ time-dependent density functional response theory in our derivation. The linear response theory treatment is rigorous within the framework of time-dependent density functional theory, while in obtaining the energy transfer coupling, the standard first-order approximation is used. The density response function for the medium, which can be replaced by the macroscopic dielectric susceptibility, enables the inclusion of the medium influence on the energy transfer coupling between the donor and acceptor. We consider the Coulomb coupling, and determine that our result is isomorphic to the Coulomb interaction between two charge densities inside a dielectric medium. The isomorphism we found not only provides a general and useful expression for applications, but additionally offers a basis for the extension of the dielectric response model to energy transfer coupling, which has been implicitly used earlier. An illustrative model shows that for two separated molecules, the medium adds a dielectric screening effect to the Coulomb coupling of their transitions. However, if the two molecules are so closely spaced that they effectively reside in a single cavity, the medium can enhance or reduce the strength of the coupling depending on the orientation and the alignment of the two chromophores. (C) 2001 American Institute of Physics.
引用
收藏
页码:3065 / 3072
页数:8
相关论文
共 52 条
[1]  
AGRANOVICH VM, 1982, ELECT EXCITATION ENE, P13
[2]   Calculations of spectroscopic properties of the LH2 bacteriochlorophyll - Protein antenna complex from Rhodopseudomonas acidophila [J].
Alden, RG ;
Johnson, E ;
Nagarajan, V ;
Parson, WW ;
Law, CJ ;
Cogdell, RG .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (23) :4667-4680
[3]   Recent advances in the description of solvent effects with the polarizable continuum model [J].
Amovilli, C ;
Barone, V ;
Cammi, R ;
Cancès, E ;
Cossi, M ;
Mennucci, B ;
Pomelli, CS ;
Tomasi, J .
ADVANCES IN QUANTUM CHEMISTRY, VOL 32: QUANTUM SYSTEMS IN CHEMISTRY AND PHYSICS, PT II, 1998, 32 :227-261
[4]   A QED THEORY OF INTERMOLECULAR ENERGY-TRANSFER IN DIELECTRIC MEDIA [J].
ANDREWS, DL ;
JUZELIUNAS, G .
JOURNAL OF LUMINESCENCE, 1994, 60-1 :834-837
[5]   Treatment of electronic excitations within the adiabatic approximation of time dependent density functional theory [J].
Bauernschmitt, R ;
Ahlrichs, R .
CHEMICAL PHYSICS LETTERS, 1996, 256 (4-5) :454-464
[6]  
Bottcher C. J. F., 1973, THEORY ELECTRIC POLA, V1, P129
[7]  
Casida M. E., 1995, RECENT ADV DENSITY F, V1, P155, DOI [10.1142/9789812830586_0005, DOI 10.1142/9789812830586_0005]
[8]  
Chance R. R., 1978, ADV CHEM PHYS, V37, P1, DOI DOI 10.1002/9780470142561.CH1
[9]   COMMENTS ON CLASSICAL THEORY OF ENERGY-TRANSFER [J].
CHANCE, RR ;
PROCK, A ;
SILBEY, R .
JOURNAL OF CHEMICAL PHYSICS, 1975, 62 (06) :2245-2253
[10]   EXCITATION TRANSFER IN THE VICINITY OF A DIELECTRIC SURFACE [J].
CHO, M ;
SILBEY, RJ .
CHEMICAL PHYSICS LETTERS, 1995, 242 (03) :291-296