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arXiv:2106.09293 · Quantum Science and Technology

Shortcuts to adiabatic rotation of a two-ion chain

Ander Tobalina, Juan Gonzalo Muga, Ion Lizuain, Mikel Palmero

Published Aug 16, 2021• 3 citations
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Abstract

Abstract We inverse engineer fast rotations of a transversally tight, linear trap with two ions for a predetermined rotation angle and time, avoiding final excitation. Different approaches are analyzed and compared when the ions are of the same species or of different species. The separability into dynamical normal modes for equal ions in a harmonic trap, or for different ions in non-harmonic traps with up to quartic terms allows for simpler computations of the rotation protocols. For non-separable scenarios, in particular for different ions in harmonic traps, rotation protocols are also found using more costly numerical optimisations.

DOI
10.1088/2058-9565/ac1e01

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Abstract We inverse engineer fast rotations of a transversally tight, linear trap with two ions for a predetermined rotation angle and time, avoiding final excitation. Different approaches are analyzed and compared when the ions are of the same species or of different species. The separability into dynamical normal modes for equal ions in a harmonic trap, or for different ions in non-harmonic traps with up to quartic terms allows for simpler computations of the rotation protocols. For non-separable scenarios, in particular for different ions in harmonic traps, rotation protocols are also found using more costly numerical optimisations.
We design fast protocols to separate or recombine two ions in a segmented Paul trap. By inverse engineering the time evolution of the trapping potential composed of a harmonic and a quartic term, it is possible to perform these processes in a few microseconds without final excitation. These times are much shorter than the ones reported so far experimentally. The design is based on dynamical invariants and dynamical normal modes. Anharmonicities beyond the harmonic approximation at potential minima are taken into account perturbatively. The stability versus an unknown potential bias is also studied.
We investigate the dynamics of mixed-species ion crystals during transport between spatially distinct locations in a linear Paul trap in the diabatic regime. In a general mixed-species crystal, all degrees of freedom along the direction of transport are excited by an accelerating well, so unlike the case of same-species ions, where only the center-of-mass mode is excited, several degrees of freedom have to be simultaneously controlled by the transport protocol. We design protocols that lead to low final excitations in the diabatic regime using invariant-based inverse engineering for two different-species ions and also show how to extend this approach to longer mixed-species ion strings. Fast transport of mixed-species ion strings can significantly reduce the operation time in certain architectures for scalable quantum-information processing with trapped ions.
We study the fast transport of a particle or a Bose-Einstein condensate in a harmonic potential. An exact expression for the final excitation energy in terms of the Fourier transform of the trap acceleration is used to engineer optimal transport protocols (with no final excitation) that are robust with respect to spring-constant errors. The same technique provides a way to design the simultaneous and robust transport of a few noninteracting species that experience different harmonic trap frequencies in the same trap.