Department of Chemistry, University of California, Irvine, CA 92697;
Laboratory of Ultrafast Spectroscopy, École Polytechnique Fédérale de Lausanne, CH-1015 Lausanne, Switzerland.
Proc Natl Acad Sci U S A. 2019 Jan 8;116(2):395-400. doi: 10.1073/pnas.1816730116. Epub 2018 Dec 24.
The ultrafast spontaneous electron-density fluctuation dynamics in molecules is studied theoretically by off-resonant multiple X-ray diffraction events. The time- and wavevector-resolved photon-coincidence signals give an image of electron-density fluctuations expressed through the four-point correlation function of the charge density in momentum space. A Fourier transform of the signal provides a real-space image of the multipoint charge-density correlation functions, which reveal snapshots of the evolving electron density in between the diffraction events. The proposed technique is illustrated by ab initio simulations of the momentum- and real-space inelastic scattering signals from a linear cyanotetracetylene molecule.
本文通过非共振多 X 射线衍射事件理论研究了分子中超快的自发电子密度涨落动力学。时间和波矢分辨的光子符合信号给出了通过动量空间中电荷密度的四点相关函数表示的电子密度涨落的图像。信号的傅里叶变换提供了多点电荷密度相关函数的实空间图像,揭示了衍射事件之间电子密度演变的快照。该技术通过对线性氰基四乙炔分子的动量和实空间非弹性散射信号的从头算模拟进行了说明。