EaStCHEM, School of Chemistry, University of Edinburgh, EH9 3FJ Edinburgh, United Kingdom.
Department of Chemistry, Technical University of Denmark, 2800 Lyngby, Denmark.
J Chem Phys. 2019 Nov 7;151(17):174302. doi: 10.1063/1.5110040.
We recast existing theory of ultrafast time-resolved x-ray scattering by molecules in the gas phase into a unified and coherent framework based on first-order time-dependent perturbation theory and quantum electrodynamics. The effect of the detection window is analyzed in detail and the contributions to the total scattering signal are discussed. This includes the coherent mixed component caused by interference between scattering amplitudes from different electronic states. A new, detailed, and fully converged simulation of ultrafast total x-ray scattering by excited H molecules illustrates the theory and demonstrates that the inelastic component can contribute strongly to the total difference scattering signal, i.e., on the same order of magnitude as the elastic component.
我们将气相中分子的超快时间分辨 X 射线散射的现有理论重新构建为基于一阶时间相关微扰理论和量子电动力学的统一连贯框架。详细分析了检测窗口的影响,并讨论了对总散射信号的贡献。这包括不同电子态散射振幅之间干涉引起的相干混合分量。通过激发 H 分子的超快总 X 射线散射的新的、详细的和完全收敛的模拟说明了该理论,并证明了非弹性分量可以强烈地贡献于总差分散射信号,即与弹性分量处于同一数量级。