Electron-vibrational coupling decreases trapping by low-energy states in photosynthesis

被引:5
|
作者
Maly, Pavel [1 ,2 ,4 ]
Novoderezhkin, Vladimir, I [3 ]
van Grondelle, Rienk [2 ]
Mancal, Tomas [1 ,4 ]
机构
[1] Charles Univ Prague, Fac Math & Phys, Ke Karlovu 5, CR-12116 Prague, Czech Republic
[2] Vrije Univ Amsterdam, Fac Sci, De Boelelaan 1081, NL-1081 HV Amsterdam, Netherlands
[3] Moscow MV Lomonosov State Univ, AN Belozersky Inst Physicochem Biol, Moscow 119992, Russia
[4] Univ Wurzburg, Inst Phys & Theoret Chem, D-97074 Wurzburg, Germany
基金
俄罗斯基础研究基金会;
关键词
LIGHT-HARVESTING COMPLEX; PHOTOSYSTEM-I; CHARGE SEPARATION; REDFIELD EQUATION; FAR-RED; DYNAMICS; FLUORESCENCE; COHERENCE; EXCITON; CHLOROPHYLLS;
D O I
10.1016/j.chemphys.2019.02.011
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
In photosynthetic light harvesting, states with energy well below that needed for charge separation can be found in abundance. They do not hinder the quantum efficiency of the primary processes; on the contrary, they can be highly functional, extending the absorption towards the red. Although many properties of these states are well described based on spectroscopic and theoretical studies, the physical mechanisms underlying their working are not known. Here we propose a mechanism which utilizes high-frequency vibrations of the photosynthetic pigments and the combined spatio-energetic aspect of the excitation dynamics. We present numerical calculations of the excitation dynamics in explicit electron-vibrational basis, with parameters based on photosynthetic complexes such as the Lhca4 complex of higher plants. The electron-vibrational states have two roles. For the trapped, low-energy excitation they provide a thermally populated ladder out of the trap. And for the high-energy excitation they provide local-bath states, effectively forming a bridge over the trap.
引用
收藏
页码:69 / 76
页数:8
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