Optically induced anisotropy in time-resolved scattering: Imaging molecular scale structure and dynamics in disordered media with experiment and theory
arXiv:2202.03562 · doi:10.1103/PhysRevLett.129.056001
Abstract
Time-resolved scattering experiments enable imaging of materials at the molecular scale with femtosecond time resolution. However, in disordered media they provide access to just one radial dimension thus limiting the study of orientational structure and dynamics. Here we introduce a rigorous and practical theoretical framework for predicting and interpreting experiments combining optically induced anisotropy and time-resolved scattering. Using impulsive nuclear Raman and ultrafast X-ray scattering experiments of chloroform and simulations, we demonstrate that this framework can accurately predict and elucidate both the spatial and temporal features of these experiments.
References in corpus (6)
- Canonical sampling through velocity-rescaling
- Imaging electronic quantum motion with light
- Femtosecond X-Ray Scattering Study of Ultrafast Photoinduced Structural Dynamics in Solvated [Co(terpy)2]2+
- Basis set effects on the hyperpolarizability of CHCl_3: Gaussian-type orbitals, numerical basis sets and real-space grids
- Anisotropy enhanced X-ray scattering from solvated transition metal complexes
- Resolving Multiphoton Processes with High-Order Anisotropy Ultrafast X-ray Scattering