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T. Hartmann

Publications and source records attributed to T. Hartmann.

6 recordsLinked to original sources
arXiv2021

Probing photoinduced two-body loss of ultracold non-reactive bosonic $^{23}$Na$^{87}$Rb and $^{23}$Na$^{39}$K molecules

We probe photo-induced loss for chemically stable bosonic $^{23}$Na$^{87}$Rb and $^{23}$Na$^{39}$K molecules in chopped optical dipole traps where the molecules spend a significant time in the dark. We expect the effective two-body decay to be largely suppressed in chopped traps due to the small expected complex lifetimes of about $13\mu$s and $6\mu$s for $^{23}$Na$^{87}$Rb and $^{23}$Na$^{39}$K respectively. However, instead we do observe near-universal loss even at the lowest chopping frequencies we can probe. Our data thus either suggest a so far unknown loss mechanism or a drastic underestimation of the complex lifetime by at least one to two orders of magnitude.

physics.atom-ph↗
arXiv2016

Versatile electric fields for the manipulation of ultracold NaK molecules

In this paper, we present an electrode geometry for the manipulation of ultracold rovibrational ground state NaK molecules. The electrode system allows to induce a dipole moment in trapped diatomic NaK molecules with a magnitude up to $68 \%$ of their internal dipole moment along any direction in a given two-dimensional plane. The strength, the sign and the direction of the induced dipole moment is therefore fully tunable. Furthermore, the possibility to create strong electric field gradients provides the opportunity to address molecules in single layers of an optical lattice. The maximal relative variation of the electric field over the trapping volume is below $10^{-6}$. At the desired electric field value of 10 kV/cm this corresponds to a deviation of 0.01 V/cm. The electrode structure is made of transparent indium tin oxide and combines large optical access for sophisticated optical dipole traps and optical lattice configurations with the possibility to create versatile electric field configurations.

cond-mat.quant-gas↗
arXiv2013

Multi-channel modeling and two photon coherent transfer paths in NaK

We explore possible pathways for the creation of ultracold polar NaK molecules in their absolute electronic and rovibrational ground state starting from ultracold Feshbach molecules. In particular, we present a multi-channel analysis of the electronic ground and K(4p)+Na(3s) excited state manifold of NaK, analyze the spin character of both the Feshbach molecular state and the electronically excited intermediate states and discuss possible coherent two-photon transfer paths from Feshbach molecules to rovibronic ground state molecules. The theoretical study is complemented by the demonstration of STIRAP transfer from the X^1Σ^+ (v=0) state to the a^3Σ^+ manifold on a molecular beam experiment.

physics.atom-ph↗
arXiv2001

Measurement of the (gamma,n) reaction rates of the nuclides 190Pt, 192Pt, and 198Pt in the astrophysical gamma-process

The nucleosynthesis of heavy neutron-deficient nuclei in a stellar photon bath at the temperatures relevant for the astrophysical gamma process was investigated. In order to derive (gamma,n) cross sections and reaction rates, the stellar photon bath was simulated by the superposition of several bremsstrahlung spectra with different endpoint energies. As a first test for this method, the (gamma,n) reaction rates of the platinum isotopes 190Pt, 192Pt, and 198Pt were derived. The results are compared to other experimental data and theoretical calculations.

astro-ph↗