Quantum effects in energy and charge transfer in an artificial photosynthetic complex

被引:37
作者
Ghosh, Pulak Kumar [1 ]
Smirnov, Anatoly Yu. [1 ,2 ]
Nori, Franco [1 ,2 ]
机构
[1] RIKEN, Adv Sci Inst, Wako, Saitama 3510198, Japan
[2] Univ Michigan, Dept Phys, Ann Arbor, MI USA
基金
美国国家科学基金会;
关键词
charge exchange; fullerenes; molecule-photon collisions; organic compounds; photosynthesis; reaction kinetics theory; PHOTOINDUCED ELECTRON-TRANSFER; PHYSIOLOGICAL TEMPERATURE; COHERENCE; MIGRATION; DYNAMICS; SYSTEM;
D O I
10.1063/1.3600341
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 investigate the quantum dynamics of energy and charge transfer in a wheel-shaped artificial photosynthetic antenna-reaction center complex. This complex consists of six light-harvesting chromophores and an electron-acceptor fullerene. To describe quantum effects on a femtosecond time scale, we derive the set of exact non-Markovian equations for the Heisenberg operators of this photosynthetic complex in contact with a Gaussian heat bath. With these equations we can analyze the regime of strong system-bath interactions, where reorganization energies are of the order of the intersite exciton couplings. We show that the energy of the initially excited antenna chromophores is efficiently funneled to the porphyrin-fullerene reaction center, where a charge-separated state is set up in a few picoseconds, with a quantum yield of the order of 95%. In the single-exciton regime, with one antenna chromophore being initially excited, we observe quantum beatings of energy between two resonant antenna chromophores with a decoherence time of similar to 100 fs. We also analyze the double-exciton regime, when two porphyrin molecules involved in the reaction center are initially excited. In this regime we obtain pronounced quantum oscillations of the charge on the fullerene molecule with a decoherence time of about 20 fs (at liquid nitrogen temperatures). These results show a way to directly detect quantum effects in artificial photosynthetic systems. (C) 2011 American Institute of Physics. [doi: 10.1063/1.3600341]
引用
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页数:13
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