Core-excited states of SF probed with soft X-ray femtosecond transient absorption of vibrational wavepackets
arXiv:2206.15125 · doi:10.1103/PhysRevA.108.012805
Abstract
A vibrational wavepacket in SF, created by impulsive stimulated Raman scattering with a few-cycle infrared pulse, is mapped onto five sulfur core-excited states using table-top soft X-ray transient absorption spectroscopy between 170-200 eV. The amplitudes of the X-ray energy shifts of the femtosecond oscillations depend strongly on the nature of the state. The prepared wavepacket is controlled with the pump laser intensity to probe the core-excited levels for various extensions of the S-F stretching motion. This allows the determination of the relative core-level potential energy gradients, in good agreement with TDDFT calculations. This experiment demonstrates a new means of characterizing core-excited potential energy surfaces.
References in corpus (7)
- Multi-channel Electronic and Vibrational Dynamics in Polyatomic High-order Harmonic Generation
- Efficient table-top dual-wavelength beamline for ultrafast transient absorption spectroscopy in the soft X-ray region
- Coherent electronic-vibrational dynamics in deuterium bromide probed via attosecond transient absorption spectroscopy
- Source noise suppression in attosecond transient absorption spectroscopy by edge-pixel referencing
- Jahn-Teller Distortion and Dissociation of CCl by Transient X-ray Spectroscopy Simultaneously at the Carbon K- and Chlorine L-Edge
- Attosecond XUV probing of vibronic quantum superpositions in Br
- Transient grating spectroscopy of SF6 molecular vibrations
Cited by in corpus (3)
- Measurement of Coherent Vibrational Dynamics with X-ray Transient Absorption Spectroscopy Simultaneously at the Carbon K- and Chlorine L- Edges
- Attosecond Probing of Coherent Vibrational Dynamics in CBr
- Different Rise Times of Atomic Br M 3d Core Level Absorptions during Br C State Dissociation via Extreme Ultraviolet Transient Absorption Spectroscopy