Jørgen Johansen Rørstad

arXiv2018

Attosecond transient-absorption spectroscopy of polar molecules

We apply attosecond transient absorption spectroscopy (ATAS) to explore the effects of a nonzero permanent dipole on electron dynamics at the subfemtosecond scale, exemplified in the polar LiF molecule. In contrast with nonpolar systems, a familiar feature of the ATA spectra--the light-induced structures--are observed adjacent to a bright state. Moreover, a previously unobserved ladder structure is identified. The new observations are analyzed in the context of a model based on fixed-nuclei adiabatic states, supported by full numerical simulations. Analytic calculations originating in the adiabatic model shed light on the nature and origins of the new findings.

physics.atom-ph↗

arXiv2017

Analytic modeling of structures in attosecond transient-absorption spectra

Attosecond transient-absorption spectroscopy (ATAS) is an established method for exploring electron dynamics on the subfemtosecond time-scale. ATAS spectra contain certain ubiquitous features, such as oscillating fringes, light-induced structures and hyperbolic sidebands, representing physical processes. We derive closed analytical expressions describing these features, based on a three-level system responding adiabatically to the influence of an infrared field in conjunction with an extreme ultraviolet pulse, and use He to illustrate the theory. The validity of the formulas is substantiated by comparing their predictions with spectra calculated numerically by the time-dependent Schrödinger equation. The closed analytical forms and the details of their derivation resolve the origins of the features.

physics.atom-ph↗