Department of Physics and Astronomy, VU University Amsterdam, Amsterdam, The Netherlands.
Departamento de física aplicada, Universidad Politécnica de Cartagena, Cartagena, Spain.
Sci Rep. 2017 Jun 6;7(1):2890. doi: 10.1038/s41598-017-02906-7.
Experimental/theoretical evidence for sustained vibration-assisted electronic (vibronic) coherence in the Photosystem II Reaction Center (PSII RC) indicates that photosynthetic solar-energy conversion might be optimized through the interplay of electronic and vibrational quantum dynamics. This evidence has been obtained by investigating the primary charge separation process in the PSII RC by two-dimensional electronic spectroscopy (2DES) and Redfield modeling of the experimental data. However, while conventional Fourier transform analysis of the 2DES data allows oscillatory signatures of vibronic coherence to be identified in the frequency domain in the form of static 2D frequency maps, the real-time evolution of the coherences is lost. Here we apply for the first time wavelet analysis to the PSII RC 2DES data to obtain time-resolved 2D frequency maps. These maps allow us to demonstrate that (i) coherence between the excitons initiating the two different charge separation pathways is active for more than 500 fs, and (ii) coherence between exciton and charge-transfer states, the reactant and product of the charge separation reaction, respectively; is active for at least 1 ps. These findings imply that the PSII RC employs coherence (i) to sample competing electron transfer pathways, and ii) to perform directed, ultrafast and efficient electron transfer.
实验/理论证据表明,在光合作用系统 II 反应中心 (PSII RC) 中存在持续的振动辅助电子(振动协同)相干,这表明光合作用太阳能转换可能通过电子和振动量子动力学的相互作用得到优化。这一证据是通过二维电子光谱 (2DES) 研究 PSII RC 中的初级电荷分离过程以及对实验数据的 Redfield 建模获得的。然而,尽管 2DES 数据的传统傅里叶变换分析允许以静态 2D 频率图的形式在频域中识别振动协同相干的振荡特征,但相干的实时演化却丢失了。在这里,我们首次将小波分析应用于 PSII RC 2DES 数据,以获得时间分辨的 2D 频率图。这些图谱使我们能够证明 (i) 引发两种不同电荷分离途径的激子之间的相干性活跃超过 500 fs,以及 (ii) 激子和电荷转移态之间的相干性,分别是电荷分离反应的反应物和产物;活跃至少 1 ps。这些发现意味着 PSII RC 采用相干性 (i) 来采样竞争电子转移途径,以及 (ii) 进行定向、超快和有效的电子转移。