Oliver Alexander,Felix Egun,Douglas Garratt,Laura Rego,James Patrick Cryan,Taran Driver,J. P. Marangos
出处
期刊:日期:2023-06-26卷期号:: 1-1
标识
DOI:10.1109/cleo/europe-eqec57999.2023.10232835
摘要
X-ray Raman scattering can be used to excite to valence states of neutral atoms in molecules. In the impulsive case, this is faster than the electronic response of the system and can be used to excite coherent charge wavepackets. It is therefore a highly anticipated tool for the study of attosecond charge dynamics [1], which is typically restricted to cationic wavepackets created via strong-field or impulsive ionisation. With the recent development of attosecond soft X-ray pulses above$1\times 10^{17}\ \text{W cm}^{-2}$at XFELs, the nonlinear regime of impulsive X-ray Raman is achievable, and has been demonstrated in simple gas molecules [2].