Publications by authors named "Markus Deiss"

We explore the physical origin and the general validity of a propensity rule for the conservation of the hyperfine spin state in three-body recombination. This rule was recently discovered for the special case of ^{87}Rb with its nearly equal singlet and triplet scattering lengths. Here, we test the propensity rule for ^{85}Rb for which the scattering properties are very different from ^{87}Rb.

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We extend state-to-state chemistry to a realm where besides vibrational, rotational, and hyperfine quantum states magnetic quantum numbers are also resolved. For this, we make use of the Zeeman effect, which energetically splits levels of different magnetic quantum numbers. The chemical reaction which we choose to study is three-body recombination in an ultracold quantum gas of ^{87}Rb atoms forming weakly bound Rb_{2} molecules.

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Experimental investigation of chemical reactions with full quantum state resolution for all reactants and products has been a long-term challenge. Here we prepare an ultracold few-body quantum state of reactants and demonstrate state-to-state chemistry for the recombination of three spin-polarized ultracold rubidium (Rb) atoms to form a weakly bound Rb molecule. The measured product distribution covers about 90% of the final products, and we are able to discriminate between product states with a level splitting as small as 20 megahertz multiplied by Planck's constant.

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Exploring and controlling inelastic and reactive collisions on the quantum level is a main goal of the developing field of ultracold chemistry. For this, the preparation of precisely defined initial atomic and molecular states in tailored environments is necessary. Here we present experimental studies of inelastic collisions of metastable ultracold Rb molecules in an array of quasi-1D potential tubes.

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We present a novel method for probing the alignment of the molecular axis of an ultracold, nonpolar dimer. These results are obtained using diatomic ^{87}Rb_{2} molecules in the vibrational ground state of the lowest triplet potential a^{3}Σ_{u}^{+} trapped in a 3D optical lattice. We measure the molecular polarizabilities, which are directly linked to the alignment, along each of the x, y, and z directions of the lab coordinate system.

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