Elastic and spin-changing inelastic collision cross sections are presented for cold and ultracold magnetically trapped NH. The cross sections are obtained from coupled-channel scattering calculations as a function of energy and magnetic field. We specifically investigate the influence of the intramolecular spin-spin, spin-rotation, and intermolecular magnetic dipole coupling on the collision dynamics. It is shown that $^{15}\mathrm{N}$ H is a very suitable candidate for evaporative cooling experiments. The dominant trap-loss mechanism in the ultracold regime originates from the intermolecular dipolar coupling term. At higher energies and fields, intramolecular spin-spin coupling becomes increasingly important. Our qualitative results and conclusions are fairly independent of the exact form of the potential and of the size of the channel basis set.Elastic and spin-changing inelastic collision cross sections are presented for cold and ultracold magnetically trapped NH. The cross sections are obtained from coupled-channel scattering calculations as a function of energy and magnetic field. We specifically investigate the influence of the intramolecular spin-spin, spin-rotation, and intermolecular magnetic dipole coupling on the collision dynamics. It is shown that $^{15}\mathrm{N}$H is a very suitable candidate for evaporative cooling experiments. The dominant trap-loss mechanism in the ultracold regime originates from the intermolecular dipolar coupling term. At higher energies and fields, intramolecular spin-spin coupling becomes increasingly important. Our qualitative results and conclusions are fairly independent of the exact form of the potential and of the size of the channel basis set.

arXiv:1012.2814Physical Review AFeb 28, 201142 citations

Quantum Reactive Scattering of Ultracold NH(X Σ−3) Radicals in a Magnetic Trap

Liesbeth M. C. Janssen, Ad van der Avoird, Gerrit C. Groenenboom

We investigate the ultracold reaction dynamics of magnetically trapped NH(X (3)Σ(-)) radicals using rigorous quantum scattering calculations involving three coupled potential energy surfaces. We find that the reactive NH+NH cross section is driven by a short-ranged collisional mechanism, and its magnitude is only weakly dependent on magnetic field strength. Unlike most ultracold reactions observed so far, the NH+NH scattering dynamics is nonuniversal. Our results indicate that chemical reactions can cause more trap loss than spin-inelastic NH+NH collisions, making molecular evaporative cooling more difficult than previously anticipated.We investigate the ultracold reaction dynamics of magnetically trapped NH(X (3)Σ(-)) radicals using rigorous quantum scattering calculations involving three coupled potential energy surfaces. We find that the reactive NH+NH cross section is driven by a short-ranged collisional mechanism, and its magnitude is only weakly dependent on magnetic field strength. Unlike most ultracold reactions observed so far, the NH+NH scattering dynamics is nonuniversal. Our results indicate that chemical reactions can cause more trap loss than spin-inelastic NH+NH collisions, making molecular evaporative cooling more difficult than previously anticipated.

arXiv:1301.1931Physical Review LettersFeb 4, 201364 citations

^{15}\mathrm{N}

H is a very suitable candidate for evaporative cooling experiments. The dominant trap-loss mechanism in the ultracold regime originates from the intermolecular dipolar coupling term. At higher energies and fields, intramolecular spin-spin coupling becomes increasingly important. Our qualitative results and conclusions are fairly independent of the exact form of the potential and of the size of the channel basis set.