Long-baseline precision tests based on atom interferometry require drastic control over the initial external degrees of freedom of atomic ensembles to reduce systematic effects. The use of optical lattices (OLs) is a highly accurate method to manipulate atomic states in position and momentum allowing excellent control of the launch in atomic fountains. The simultaneous lattice launch of two atomic species, as required in a quantum test of the equivalence principle, is however problematic due to crosstalk effects. In this article, we propose to selectively address two species of alkalines by applying two OLs at or close to magic-zero wavelengths of the atoms. The proposed scheme applies in general for a pair of species with a vastly different ac Stark shift to a laser wavelength. We illustrate the principle by studying a fountain launch of condensed ensembles of 87 Rb and 41 K initially co-located. Numerical simulations confirm the fidelity of our scheme up to few nm and nm s −1 in inter-species differential position and velocity, respectively. This result is a pre-requisite for the next performance level in precision tests.
Using a quantum wave packet simulation including the nuclear and electronic degrees of freedom, we investigate the femtosecond and picosecond energy- and angle-resolved photoelectron spectra of the E(Σg+1) electronic state of Li. We find that the angular distributions of the emitted photoelectrons depend strongly on the pulse duration in the regime of ultrashort laser pulses. This effect is illustrated by the extraction of a time-dependent asymmetry parameter whose variation with pulse duration can be explained by an incoherent average over different ion rotational quantum numbers. We then derive for the variation of the asymmetry parameter a simple analytical formula, which can be used to extract the asymptotic CW asymmetry parameters of individual transitions from measurements performed with ultra-short pulses.
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