Beyond the Forster theory of excitation energy transfer: importance of higher-order processes in supramolecular antenna systems

被引:23
|
作者
May, Volkhard [1 ]
机构
[1] Humboldt Univ, Inst Phys, D-12489 Berlin, Germany
关键词
LASER-PULSE CONTROL; TRANSFER DYNAMICS; ELECTRON-TRANSFER; EXCITON DYNAMICS; SPECTRAL DENSITY; REDFIELD; COMPLEX; PHEOPHORBIDE; MIGRATION; STATES;
D O I
10.1039/b908567j
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Electronic excitation energy transfer in molecular systems is connected with the de-excitation of one molecule and the excitation of the other. Mostly, it can be understood in terms of Forster (or fluorescence) resonance energy transfer. An increasing interest in the optimization of artificial light harvesting systems, however, requires a more detailed study going beyond the standard Forster scheme. There are two main routes to do this. Considering a Coulombic less-strongly coupled system first, coherences among different chromophores may be considered in the framework of perturbation theory with higher-order mechanisms correcting the standard second-order description. Secondly, if inter-chromophore coherences are dominant and delocalized Frenkel-exciton states are formed, it becomes of some importance to study their decay due to the coupling to vibrational degrees of freedom. While we will also comment on this latter mechanism, the first description based on localized excitations will be the main focus. A general higher-order theory resulting in respective transition rates and rate equations is utilized. Its capability is demonstrated when presenting a systematic description of short-range and long-range corrections to the basic Forster mechanism. Accordingly, a unique description of bridge-mediated and photon-mediated long-range electronic excitation energy transfer is offered. Moreover, short-range excitation energy transfer appearing as a two electron exchange is also discussed. And, the exciton-exciton annihilation process present at higher optical excitation intensities is described as a direct higher-order transition. The related higher-order vibrational correlation functions are presented and estimated for the reference case where the coupling to vibrational degrees of freedom either of intra-molecular or inter-molecular type is reduced to a simple electronic state dephasing process.
引用
收藏
页码:10086 / 10105
页数:20
相关论文
共 6 条
  • [1] A Mixed Quantum-Classical Description of Excitation Energy Transfer in Supramolecular Complexes: Forster Theory and beyond
    Megow, Joerg
    Roeder, Beate
    Kulesza, Alexander
    Bonacic-Koutecky, Vlasta
    May, Volkhard
    CHEMPHYSCHEM, 2011, 12 (03) : 645 - 656
  • [2] Generalized quantum kinetic expansion: Higher-order corrections to multichromophoric Forster theory
    Wu, Jianlan
    Gong, Zhihao
    Tang, Zhoufei
    JOURNAL OF CHEMICAL PHYSICS, 2015, 143 (07)
  • [3] Excitation energy-transfer in functionalized nanoparticles: Going beyond the Forster approach
    Gil, G.
    Corni, S.
    Delgado, A.
    Bertoni, A.
    Goldoni, G.
    JOURNAL OF CHEMICAL PHYSICS, 2016, 144 (07)
  • [4] Combined Forster-Redfield Theory for Modeling Energy Transfer in Plant Photosynthetic Antenna Complexes
    Novoderezhkin, V. I.
    BIOLOGICHESKIE MEMBRANY, 2012, 29 (05): : 367 - 373
  • [5] General theory of excitation energy transfer in donor-mediator-acceptor systems
    Kimura, Akihiro
    JOURNAL OF CHEMICAL PHYSICS, 2009, 130 (15)
  • [6] Quantum-Chemical Studies on Excitation Energy Transfer Processes in BODIPY-Based Donor-Acceptor Systems
    Spiegel, J. Dominik
    Kleinschmidt, Martin
    Larbig, Alexander
    Tatchen, Joerg
    Marian, Christel M.
    JOURNAL OF CHEMICAL THEORY AND COMPUTATION, 2015, 11 (09) : 4316 - 4327