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arXiv:physics/0205020 · Physical Review Letters

Rotational Feshbach Resonances in Ultracold Molecular Collisions

John L. Bohn, А. V. Avdeenkov, Michael P. Deskevich

Published Oct 28, 2002• 38 citations
arXivHTMLPDF

Abstract

In collisions at ultralow temperatures, molecules will possess Feshbach resonances, foreign to ultracold atoms, whose virtual excited states consist of rotations of the molecules. We estimate the mean spacing and mean widths of these resonant states, exploiting the fact the molecular collisions at low energy display chaotic motion. As examples, we consider the experimentally relevant molecules O2, OH, and PbO. Especially for polar species, the density of s-wave resonant states is quite high, implying potentially disastrous consequences for trapped molecules.

DOI
10.1103/physrevlett.89.203202

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In collisions at ultralow temperatures, molecules will possess Feshbach resonances, foreign to ultracold atoms, whose virtual excited states consist of rotations of the molecules. We estimate the mean spacing and mean widths of these resonant states, exploiting the fact the molecular collisions at low energy display chaotic motion. As examples, we consider the experimentally relevant molecules O2, OH, and PbO. Especially for polar species, the density of s-wave resonant states is quite high, implying potentially disastrous consequences for trapped molecules.
Compared to purely atomic collisions, ultracold molecular collisions potentially support a much larger number of Fano-Feshbach resonances due to the enormous number of rovibrational states available. In fact, for alkali-metal dimers we find that the resulting density of resonances cannot be resolved at all, even on the sub-$\ensuremath{\mu}$K temperature scale of ultracold experiments. As a result, all observables become averaged over many resonances and can effectively be described by simpler, nonresonant scattering calculations. Two particular examples are discussed: nonchemically reactive RbCs and chemically reactive KRb. In the former case, the formation of a long-lived collision complex may lead to the ejection of molecules from a trap. In the latter case, chemical reactions broaden the resonances so much that they become unobservable.
Compared to purely atomic collisions, ultracold molecular collisions potentially support a much larger number of Fano-Feshbach resonances due to the enormous number of ro-vibrational states available. In fact, for alkali-metal dimers we find that the resulting density of resonances cannot be resolved at all, even on the sub-μμμK temperature scale of ultracold experiments. As a result, all observables become averaged over many resonances and can effectively be described by simpler, non-resonant scattering calculations. Two particular examples are discussed: non-chemically reactive RbCs and chemically reactive KRb. In the former case, the formation of a long-lived collision complex may lead to the ejection of molecules from a trap. In the latter case, chemical reactions broaden the resonances so much that they become unobservable.
With the creation of ultracold atoms and molecules, a new type of chemistry---``resonance'' chemistry---emerges: chemical reactions can occur when the energy of colliding atoms and molecules matches a bound state of the combined molecule (Feshbach resonance). This chemistry is rather similar to reactions that take place in nuclei at low energies. In this paper we suggest some problems for future experimental and theoretical work related to the resonance chemistry of ultracold molecules. Molecular Bose-Einstein condensates are particularly interesting because in this system collisions and chemical reactions are extremely sensitive to weak fields; also, a preferred reaction channel may be enhanced due to a finite number of final states. The sensitivity to weak fields arises due to the high density of narrow compound resonances and the macroscopic number of molecules with kinetic energy E=0E=0E=0 (in the ground state of a mean-field potential). The high sensitivity to the magnetic field may be used to measure the distribution of energy intervals, widths, and magnetic moments of compound resonances and study the onset of quantum chaos. A difference in the production rate of right-handed and left-handed chiral molecules may be produced by external electric E\mathbf{E}E and magnetic B\mathbf{B}B fields and the finite width $\ensuremath{\Gamma}$ of the resonance (correlation $\ensuremath{\Gamma}\mathbf{E}∙\mathbf{B}$). The same effect may be produced by the parity-violating energy difference in chiral molecules.
We investigate interactions and ultracold collisions of high-spin but spherical atoms with closed-shell atoms, focusing on the example of Cr with Yb. Such a combination has only one potential energy curve but gives rise to a substantial intra-atomic spin–spin interaction, which causes Feshbach resonances due to rotationally excited states. We find such resonances are guaranteed below 250 G and can reach widths of tens of G in favorable circumstances. We study the effect of hyperfine structure, which can create additional wide resonances at low fields. Finally, we consider isotopic substitution and show that for any realistic potential it is very likely that at least one combination of commonly used isotopes will have resonances with experimentally favorable properties. Thus, this is a promising system for both molecule formation and studying quantum mixtures including dipolar species. Published by the American Physical Society 2024
A detailed study is made of the nature of rotational Feshbach resonances in the elastic scattering of extremely-low-energy electrons by diatomic polar molecules. The bound-state properties of an electron in the field of a dipole rotator, determined previously, are used in establishing the resonance behavior of elastic-scattering phase shifts in the energy region below the first rotational excitation threshold. Feshbach resonances of very narrow widths are found in partial-wave scattering channels with total angular momenta greater than zero when the strength of the interaction potentials is somewhat less than that necessary to yield bound states of the same symmetry type, and very much less than those necessary to yield a "bound state" of the projected Hamiltonian QHQ\mathrm{QHQ}QHQ. The latter implies a non-negligible value of the resonance energy shift for polar molecules.
Abstract : We explored Feshbach resonances in the collision between ultracold highly-magnetic dysprosium and erbium atoms. The resonance density is orders of magnitude larger than seen in any other previously studied atomic system. Moreover, we showed that these resonance can only exist because of the anisotropic nature of the atom-atom potentials. Analysis of nearest-neighbor spacings between Feshbach resonances shows a chaotic distribution that one would expect from random-matrix theory. We explained these statistics as originating from the large strength of the anisotropy. We demonstrated that the vibrational motion of BaCl+ molecules is quenched by collisions with ultracold calcium atoms at a rate comparable to the Langevin rate. This is over four orders of magnitude more efficient than traditional sympathetic cooling schemes. In addition, we calculated the electronic structure of BaCl+ and other molecular ions. Based on these results we found unusually-large rates for cold charge-transfer reactions between neutral and ionic atoms.