California Institute for Quantitative Biosciences and Department of Chemistry, University of California, Berkeley, USA.
Acc Chem Res. 2009 Sep 15;42(9):1352-63. doi: 10.1021/ar9001075.
The properties of molecular aggregates, coupled clusters of small molecules, are often challenging to unravel because of their inherent complexity and disordered environments. Their structure-function relationships are often far from obvious. However, their ability to efficiently channel excitation energy over remarkable distances, as is the case in photosynthetic light harvesting, is a compelling motivation to investigate them. Understanding and subsequently mimicking the processes in photosynthesis, for example, will set the stage for considerable advances in using light harvesting to fuel renewable energy technologies. Two-dimensional (2D) electronic spectroscopy is emerging as a nonlinear optical technique that provides significant insight into the interactions and dynamics of complex molecular systems. In addition to spectrally resolving excitation and emission energies over significant bandwidths with femtosecond resolution, this technique has already enabled discoveries about the structure and dynamics of photosynthetic light-harvesting complexes and other aggregates. Multiple capabilities unique to 2D electronic spectroscopy enable such findings. For example, the spectral resolution of excitation and emission combined with the ability to eliminate the effects of static disorder can reveal the homogeneous line width of a transition and the different dynamic contributions to it. Two dimensional spectroscopy is also sensitive to electronic coherence and has been employed to identify and characterize coherent excitation energy transfer dynamics in photosynthetic systems and conjugated polymers. The presence of cross-peaks, signals for which excitation and emission occur at different wavelengths, provides multiple forms of information. First, it allows the identification of states in congested spectra and reveals correlations between them. Second, we can track excitation energy flow from origin to terminus through multiple channels simultaneously. Finally, 2D electronic spectroscopy is uniquely sensitive to intermolecular electronic coupling through the sign and amplitude of the cross-peaks. This feature makes it possible to reveal spatial molecular configurations by probing electronic transitions. Another means of "resolving" these angstrom-scale arrangements is to manipulate the probing laser pulse polarizations. In this way, we can isolate and modulate specific processes in order to retrieve structural information. In this Account, we demonstrate these capabilities through a close collaboration between experiments and modeling on isolated photosynthetic pigment-protein complexes and also on J-aggregates. Each of the probed systems we describe offers insights that have both increased the utility of 2D electronic spectroscopy and led to discoveries about the molecular aggregates' dynamics and underlying structure.
分子聚集体、小分子的耦合簇的性质通常具有挑战性,因为它们具有内在的复杂性和无序环境。它们的结构-功能关系往往不明显。然而,它们能够有效地在显著的距离上传递激发能量,就像光合作用中的光捕获一样,这是研究它们的一个令人信服的动机。例如,理解和随后模仿光合作用中的过程,将为利用光捕获来为可再生能源技术提供燃料奠定基础。二维(2D)电子光谱学作为一种非线性光学技术,正在兴起,它为复杂分子系统的相互作用和动力学提供了重要的见解。除了以飞秒分辨率在显著的带宽上光谱分辨激发和发射能量外,该技术已经使人们对光合作用光捕获复合物和其他聚集体的结构和动力学有了新的认识。二维电子光谱学具有多种独特的能力,使其能够实现这些发现。例如,激发和发射的光谱分辨率与消除静态无序影响的能力相结合,可以揭示跃迁的均匀线宽及其对其不同的动态贡献。二维光谱学也对电子相干性敏感,并已被用于识别和表征光合作用系统和共轭聚合物中相干激发能量转移动力学。交叉峰的存在,即激发和发射在不同波长处发生的信号,提供了多种形式的信息。首先,它允许在拥挤的光谱中识别状态,并揭示它们之间的相关性。其次,我们可以同时通过多个通道跟踪激发能量从起点到终点的流动。最后,二维电子光谱学通过交叉峰的符号和幅度对分子间电子耦合具有独特的敏感性。这一特性使得通过探测电子跃迁来揭示空间分子构型成为可能。“解析”这些埃级排列的另一种方法是操纵探测激光脉冲的偏振。通过这种方式,我们可以隔离和调制特定的过程,以获取结构信息。在本报告中,我们通过在孤立的光合作用色素-蛋白复合物以及 J-聚集体上进行实验和建模之间的密切合作,展示了这些能力。我们描述的每个被探测的系统都提供了一些见解,这些见解既增加了二维电子光谱学的实用性,又揭示了分子聚集体的动力学和基础结构。