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arXiv:1208.2863 · Physical Review A

Parallel execution of quantum gates in a long linear ion chain via Rydberg mode shaping

Weibin Li, Alexander W. Glaetzle, Rejish Nath, Igor Lesanovsky

Published May 6, 2013• 27 citations
arXivHTMLPDF

Abstract

We present a mechanism that permits the parallel execution of multiple quantum gate operations within a single long linear ion chain. Our approach is based on large coherent forces that occur when ions are electronically excited to long-lived Rydberg states. The presence of Rydberg ions drastically affects the vibrational mode structure of the ion crystal, giving rise to modes that are spatially localized on isolated subcrystals which can be individually and independently manipulated. We theoretically discuss this Rydberg mode shaping in an experimentally realistic setup and illustrate its power by analyzing the fidelity of two conditional phase flip gates executed in parallel. The ability to dynamically shape vibrational modes on the single-ion level might find applications in quantum simulators and quantum computation architectures.

DOI
10.1103/physreva.87.052304

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We present a mechanism that permits the parallel execution of multiple quantum gate operations within a single long linear ion chain. Our approach is based on large coherent forces that occur when ions are electronically excited to long-lived Rydberg states. The presence of Rydberg ions drastically affects the vibrational mode structure of the ion crystal, giving rise to modes that are spatially localized on isolated subcrystals which can be individually and independently manipulated. We theoretically discuss this Rydberg mode shaping in an experimentally realistic setup and illustrate its power by analyzing the fidelity of two conditional phase flip gates executed in parallel. The ability to dynamically shape vibrational modes on the single-ion level might find applications in quantum simulators and quantum computation architectures.
Fast entangling gate operations are a fundamental prerequisite for quantum simulation and computation. We propose an entangling scheme for arbitrary pairs of ions in a linear crystal, harnessing the high electric polarizability of highly excited Rydberg states. An all-to-all quantum gate connectivity is based on an initialization of a pair of ions to a superposition of ground and Rydberg states by laser excitation, followed by the entangling gate operation, which relies on a state-dependent frequency shift of collective vibrational modes of the crystal. This gate operation requires applying an electric waveform to trap electrodes. Employing transverse collective modes of oscillation, we reveal operation times on the order of microseconds within any of the qubit pairs in a small crystal. In our calculation, we take into account realistic experimental conditions and feasible electric field ramps. The proposed gate operation is ready to be combined with a scalable processor architecture to reconfigure the qubit register, either by shuttling ions or by dynamically controlling optical tweezer potentials.
A universal quantum computer is an ultimate pursuit, which should possess the ability to perform entangling gate operations in parallel with high quality in a scalable fashion. However, for a long trapped-ion chain, the simultaneous implementation of two-qubit quantum gates is a challenging task due to the drastic increase of the crosstalk resulting from the collective motional modes. In this paper, by utilizing the structure of the localized motional modes in the long mixed-species ion chain, we propose a highly efficient linear iterative scheme to eliminate the crosstalk within the neighboring pairs. We show that this scheme allows the realization of high-fidelity, low-crosstalk, scalable, parallel two-qubit gates with only a few pulse segments for the long chain. In addition, by considering the practical experimental feasibility, we optimize the laser power and improve the robustness against the random static drifts of the motional frequencies.
Ion trap quantum computers are based on modulating the Coulomb interaction between atomic ion qubits using external forces. However, the spectral crowding of collective motional modes could pose a challenge to the control of such interactions for large numbers of qubits. Here, we show that high-fidelity quantum gate operations are still possible with very large trapped ion crystals by using a small and fixed number of motional modes, simplifying the scaling of ion trap quantum computers. We present analytical work that shows that gate operations need not couple to the motion of distant ions, allowing parallel entangling gates with a crosstalk error that falls off as the inverse cube of the distance between the pairs. We also experimentally demonstrate high-fidelity entangling gates on a fully connected set of seventeen 171Yb+^{171}\mathrm{Yb}^{+}171Yb+ qubits using simple laser pulse shapes that primarily couple to just a few modes.
Trapped Rydberg ions represent a flexible platform for quantum simulation and information processing that combines a high degree of control over electronic and vibrational degrees of freedom. The possibility to individually excite ions to high-lying Rydberg levels provides a system where strong interactions between pairs of excited ions can be engineered and tuned via external laser fields. We show that the coupling between Rydberg pair interactions and collective motional modes gives rise to effective long-range and multibody interactions consisting of two, three, and four-body terms. Their shape, strength, and range can be controlled via the ion trap parameters and strongly depends on both the equilibrium configuration and vibrational modes of the ion crystal. By focusing on an experimentally feasible quasi one-dimensional setup of ^{88}Sr^{+} Rydberg ions, we demonstrate that multibody interactions are enhanced by the emergence of soft modes associated with, e.g., a structural phase transition. This has a striking impact on many-body electronic states and results-for example-in a three-body antiblockade effect that can be employed as a sensitive probe to detect structural phase transitions in Rydberg ion chains. Our study unveils the possibilities offered by trapped Rydberg ions for studying exotic phases of matter and quantum dynamics driven by enhanced multibody interactions.
We study the dynamics of Rydberg ions trapped in a linear Paul trap, and discuss the properties of ionic Rydberg states in the presence of the static and time-dependent electric fields constituting the trap. The interactions in a system of many ions are investigated and coupled equations of the internal electronic states and the external oscillator modes of a linear ion chain are derived. We show that strong dipole–dipole interactions among the ions can be achieved by microwave dressing fields. Using low-angular momentum states with large quantum defect, the internal dynamics can be mapped onto an effective spin model of a pair of dressed Rydberg states that describes the dynamics of Rydberg excitations in the ion crystal. We demonstrate that excitation transfer through the ion chain can be achieved on a nanosecond timescale and discuss the implementation of a fast two-qubit gate in the ion chain.
A central challenge in developing practical quantum processors is maintaining low control complexity while scaling to large numbers of qubits. Trapped-ion systems excel in small-scale operations and support rapid qubit scaling via long-chain architectures. However, their performance in larger systems is hindered by spectral crowding in radial motional modes, a problem that forces reliance on intricate pulse-shaping techniques to maintain gate fidelities. Here, we overcome this challenge by developing a trapped-ion processor with an individual-addressing system that generates steerable Hermite-Gaussian beam arrays. The transversal gradient of these beams couples qubits selectively to sparse axial motional modes, enabling to isolate a single or few modes as entanglement mediator. Leveraging this capability, we demonstrate addressable two-qubit entangling gates in chains up to six ions, with Bell-state preparation fidelities consistently around 0.97, achieved without complex pulse shaping. Our method substantially reduces control overhead while preserving scalability, providing a crucial advance toward practical large-scale trapped-ion quantum computing.