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Kylie Gannan

Publications and source records attributed to Kylie Gannan.

2 recordsLinked to original sources

Attosecond Transient Polarimetry

We introduce elliptical-dichroic attosecond transient absorption spectroscopy (eDATAS), an ultrafast attosecond spectroscopy technique in which an atomic gas is probed by elliptically polarized attosecond and near-infrared pulses with an arbitrary angle between the polarization ellipses and a varying time-delay. Using perturbation theory, we show that the transient absorption signal factorizes into form factors whose dependence on pulse ellipticities and polarization-ellipse orientations are governed entirely by dipole selection rules: ellipticity sets the amplitudes of the interfering multiphoton pathways, while the relative orientations of the ellipses control the phase. We reinterpret circular- and linear-dichroic attosecond transient absorption spectroscopy as limiting cases of eDATAS, and validate the theory through an eDATAS measurement in helium, finding excellent agreement. Finally, we demonstrate that eDATAS can also serve as an in situ measurement of the polarization state of the XUV field, avoiding the need for a dedicated XUV polarimeter.

physics.atom-ph

Attosecond Optical Orientation

Circularly polarized light offers opportunities to probe symmetry-dependent properties of matter such as chirality and spin. Circular dichroism measurements typically require further intrinsic or extrinsic breaking of symmetry by e.g. enantiomeric excess, orientation, magnetic fields or direction-sensitive detectors. Here we introduce circular-dichroic attosecond transient absorption spectroscopy by leveraging the angular momentum of two circular-polarized pulses, both pump and probe, in an isotropic medium, optically orienting the angular momentum of excited states on an attosecond timescale. We investigate a circular-dichroic measurement of the attosecond transient absorption of He Rydberg states. By limiting the allowed pathways via dipole selection rules for co- and counter-rotating circular polarized NIR and XUV pulses, different spectral reshapings of the XUV transient absorption due to the AC Stark effect are observed. Paired with time-dependent Schrödinger equation calculations, the results show the role of selection and propensity rules and open up new opportunities to study coupling pathways of excited states as well as spin-dependent dynamics in atoms and beyond via attosecond optical orientation.

physics.atom-ph