Laboratoire de Spectroscopie Ultrarapide, Ecole Polytechnique Fédérale de Lausanne, ISIC, SB, Switzerland.
J Phys Chem A. 2010 Sep 2;114(34):9034-42. doi: 10.1021/jp101778u.
We report on an ultrafast experimental and simulations study of the early relaxation events of photoexcited tryptophan in water. Experimentally, we used fluorescence up-conversion in both polychromatic and single wavelength detection modes in the 300-480 nm range with polarization dependence. We report on the time evolution of the Stokes shift, bandwidth, and anisotropy from tens of femtoseconds to picoseconds. These observables contain signatures of the simultaneous occurrence of intramolecular and solvent-molecule interactions, which we disentangle with the help of nonequilibrium molecular dynamics simulations. We also observe a breakdown of the linear response approximation to describe our results.
我们报告了一项超快实验和模拟研究,研究了色氨酸在水中的光激发后的早期弛豫事件。实验中,我们使用多色和单波长检测模式的荧光上转换,在 300-480nm 范围内进行,具有偏振依赖性。我们报告了斯托克斯位移、带宽和各向异性从几十飞秒到皮秒的时间演化。这些可观测到的特征包含了分子内和溶剂分子相互作用的同时发生的信号,我们借助非平衡分子动力学模拟来分离这些信号。我们还观察到线性响应近似无法描述我们的结果。