Skandary Sepideh, Hussels Martin, Konrad Alexander, Renger Thomas, Müh Frank, Bommer Martin, Zouni Athina, Meixner Alfred J, Brecht Marc
†IPTC and Lisa+ Center, Universität Tübingen, Tübingen, Germany.
‡Institut für Theoretische Physik, Johannes Kepler Universität, Linz, Austria.
J Phys Chem B. 2015 Mar 19;119(11):4203-10. doi: 10.1021/jp510631x. Epub 2015 Mar 10.
The spectral properties and dynamics of the fluorescence emission of photosystem II core complexes are investigated by single-molecule spectroscopy at 1.6 K. The emission spectra are dominated by sharp zero-phonon lines (ZPLs). The sharp ZPLs are the result of weak to intermediate exciton-vibrational coupling and slow spectral diffusion. For several data sets, it is possible to surpass the effect of spectral diffusion by applying a shifting algorithm. The increased signal-to-noise ratio enables us to determine the exciton-vibrational coupling strength (Huang-Rhys factor) with high precision. The Huang-Rhys factors vary between 0.03 and 0.8. The values of the Huang-Rhys factors show no obvious correlation between coupling strength and wavelength position. From this result, we conclude that electrostatic rather than exchange or dispersive interactions are the main contributors to the exciton-vibrational coupling in this system.
在1.6 K温度下,通过单分子光谱法研究了光系统II核心复合物荧光发射的光谱特性和动力学。发射光谱主要由尖锐的零声子线(ZPLs)主导。尖锐的ZPLs是弱到中等激子 - 振动耦合以及缓慢光谱扩散的结果。对于几个数据集,通过应用移位算法可以超越光谱扩散的影响。信噪比的提高使我们能够高精度地确定激子 - 振动耦合强度(黄 - 里斯因子)。黄 - 里斯因子在0.03至0.8之间变化。黄 - 里斯因子的值在耦合强度和波长位置之间没有明显的相关性。从这个结果,我们得出结论,静电相互作用而非交换或色散相互作用是该系统中激子 - 振动耦合的主要贡献因素。