Non-Hermitian exciton dynamics in a photosynthetic unit system

被引:16
|
作者
Thilagam, A. [1 ]
机构
[1] Univ S Australia, Mawson Inst, Div ITEE, Adelaide, SA 5095, Australia
来源
JOURNAL OF CHEMICAL PHYSICS | 2012年 / 136卷 / 06期
关键词
LIGHT-HARVESTING COMPLEX; GREENS-FUNCTION APPROACH; ENERGY-TRANSFER; QUANTUM COHERENCE; ELECTRON-TRANSFER; SUPERRADIANCE; SPECTRA;
D O I
10.1063/1.3684654
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 non-Hermitian quantum dynamics of excitonic energy transfer in photosynthetic systems is investigated using a dissipative two-level dimer model. The approach is based on Green's function formalism which permits consideration of decoherence and intersite transfer processes on comparable terms. The results indicate a combination of coherent and incoherent behavior at higher temperatures with the possibility of exceptional points occurring at the coherent-incoherent crossover regime at critical temperatures. When each dimer site is coupled equally to the environmental sources of dissipation, the excitonic wavepacket evolves with time with a coherent component, which can be attributed to the indistinguishability of the sources of dissipation. The time evolution characteristics of the B850 Bchls dimer system is analysed using typical parameter estimates in photosynthetic systems, and the quantum brachistochrone passage times are obtained for a range of parameters. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.3684654]
引用
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页数:9
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