Department of Chemistry, University of California, Berkeley, CA 94720, USA.
Philos Trans A Math Phys Eng Sci. 2012 Aug 13;370(1972):3672-91. doi: 10.1098/rsta.2011.0207.
We briefly review the coherent quantum beats observed in recent two-dimensional electronic spectroscopy experiments in a photosynthetic-light-harvesting antenna. We emphasize that the decay of the quantum beats in these experiments is limited by ensemble averaging. The in vivo dynamics of energy transport depends upon the local fluctuations of a single photosynthetic complex during the energy transfer time (a few picoseconds). Recent analyses suggest that it remains possible that the quantum-coherent motion may be robust under individual realizations of the environment-induced fluctuations contrary to intuition obtained from condensed phase spectroscopic measurements and reduced density matrices. This result indicates that the decay of the observed quantum coherence can be understood as ensemble dephasing. We propose a fluorescence-detected single-molecule experiment with phase-locked excitation pulses to investigate the coherent dynamics at the level of a single molecule without hindrance by ensemble averaging. We discuss the advantages and limitations of this method. We report our initial results on bulk fluorescence-detected coherent spectroscopy of the Fenna-Mathews-Olson complex.
我们简要回顾了在光合作用光捕获天线的二维电子光谱实验中观察到的相干量子拍频。我们强调,这些实验中量子拍频的衰减受到系综平均的限制。在体内能量传递的动力学取决于在能量转移时间(几个皮秒)内单个光合作用复合物的局部波动。最近的分析表明,尽管从凝聚相光谱测量和约化密度矩阵获得的直觉相反,但在环境诱导波动的单个实现下,量子相干运动可能仍然稳健。这一结果表明,观察到的量子相干的衰减可以理解为系综去相位。我们提出了一种具有锁定激发脉冲的荧光探测单分子实验,以在没有系综平均干扰的情况下研究单个分子的相干动力学。我们讨论了这种方法的优点和局限性。我们报告了我们在 Fenna-Mathews-Olson 复合物的体荧光探测相干光谱学方面的初步结果。