Technical University of Denmark, Department of Physics, Fysikvej 307, DK-2800 Kongens Lyngby, Denmark.
Technical University of Denmark, Department of Chemistry, Kemitorvet 207, DK-2800 Kongens Lyngby, Denmark.
Phys Rev Lett. 2019 Feb 15;122(6):063001. doi: 10.1103/PhysRevLett.122.063001.
We report x-ray free electron laser experiments addressing ground-state structural dynamics of the diplatinum anion Pt_{2}POP_{4} following photoexcitation. The structural dynamics are tracked with <100 fs time resolution by x-ray scattering, utilizing the anisotropic component to suppress contributions from the bulk solvent. The x-ray data exhibit a strong oscillatory component with period 0.28 ps and decay time 2.2 ps, and structural analysis of the difference signal directly shows this as arising from ground-state dynamics along the PtPt coordinate. These results are compared with multiscale Born-Oppenheimer molecular dynamics simulations and demonstrate how off-resonance excitation can be used to prepare a vibrationally cold excited-state population complemented by a structure-dependent depletion of the ground-state population which subsequently evolves in time, allowing direct tracking of ground-state structural dynamics.
我们报告了 X 射线自由电子激光实验结果,该实验研究了光激发后二铂阴离子 Pt_{2}POP_{4}的基态结构动力学。通过 X 射线散射,利用各向异性分量抑制了来自体相溶剂的贡献,以 <100 fs 的时间分辨率跟踪结构动力学。X 射线数据显示出强烈的振荡分量,其周期为 0.28 ps,衰减时间为 2.2 ps,差分信号的结构分析直接表明这是由 PtPt 坐标上的基态动力学引起的。这些结果与多尺度 Born-Oppenheimer 分子动力学模拟进行了比较,并展示了如何使用离共振激发来制备振动冷的激发态,同时伴随着与结构相关的基态的耗散,随后随时间演化,从而可以直接跟踪基态结构动力学。