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Register a new userTrapped Rydberg Ions: From Spin Chains to Fast Quantum Gates
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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.
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Control over physical systems at the quantum level is a goal shared by scientists in fields as diverse as metrology, information processing, simulation and chemistry. For trapped atomic ions, the quantized motional and internal degrees of freedom can be coherently manipulated with laser light. Similar control is difficult to achieve with radio frequency or microwave radiation because the essential coupling between internal degrees of freedom and motion requires significant field changes over the extent of the atoms motion. The field gradients are negligible at these frequencies for freely propagating fields; however, stronger gradients can be generated in the near-field of microwave currents in structures smaller than the free-space wavelength. In the experiments reported here, we coherently manipulate the internal quantum states of the ions on time scales of 20 ns. We also generate entanglement between the internal degrees of freedom of two atoms with a gate operation suitable for general quantum computation. We implement both operations through the magnetic fields from microwave currents in electrodes that are integrated into the micro-fabricated trap structure and create an entangled state with fidelity 76(3) %. This approach, where the quantum control mechanism is integrated into the trapping device in a scalable manner, can potentially benefit quantum information processing, simulation and spectroscopy.
We implement faster-than-adiabatic two-qubit phase gates using smooth state-dependent forces. The forces are designed to leave no final motional excitation, independently of the initial motional state in the harmonic, small-oscillations limit. They are simple, explicit functions of time and the desired logical phase of the gate, and are based on quadratic invariants of motion and Lewis-Riesenfeld phases of the normal modes.
We study the speed/fidelity trade-off for a two-qubit phase gate implemented in $^{43}$Ca$^+$ hyperfine trapped-ion qubits. We characterize various error sources contributing to the measured fidelity, allowing us to account for errors due to single-qubit state preparation, rotation and measurement (each at the $sim0.1%$ level), and to identify the leading sources of error in the two-qubit entangling operation. We achieve gate fidelities ranging between $97.1(2)%$ (for a gate time $t_g=3.8mu$s) and $99.9(1)%$ (for $t_g=100mu$s), representing respectively the fastest and lowest-error two-qubit gates reported between trapped-ion qubits by nearly an order of magnitude in each case.
Generating quantum entanglement in large systems on time scales much shorter than the coherence time is key to powerful quantum simulation and computation. Trapped ions are among the most accurately controlled and best isolated quantum systems with low-error entanglement gates operated via the vibrational motion of a few-ion crystal within tens of microseconds. To exceed the level of complexity tractable by classical computers the main challenge is to realise fast entanglement operations in large ion crystals. The strong dipole-dipole interactions in polar molecule and Rydberg atom systems allow much faster entangling gates, yet stable state-independent confinement comparable with trapped ions needs to be demonstrated in these systems. Here, we combine the benefits of these approaches: we report a $700,mathrm{ns}$ two-ion entangling gate which utilises the strong dipolar interaction between trapped Rydberg ions and produce a Bell state with $78%$ fidelity. The sources of gate error are identified and a total error below $0.2%$ is predicted for experimentally-achievable parameters. Furthermore, we predict that residual coupling to motional modes contributes $sim 10^{-4}$ gate error in a large ion crystal of 100 ions. This provides a new avenue to significantly speed up and scale up trapped ion quantum computers and simulators.
Thermodynamics is one of the oldest and well-established branches of physics that sets boundaries to what can possibly be achieved in macroscopic systems. While it started as a purely classical theory, it was realized in the early days of quantum mechanics that large quantum devices, such as masers or lasers, can be treated with the thermodynamic formalism. Remarkable progress has been made recently in the miniaturization of heat engines all the way to the single Brownian particle as well as to a single atom. However, despite several theoretical proposals, the implementation of heat machines in the fully quantum regime remains a challenge. Here, we report an experimental realization of a quantum absorption refrigerator in a system of three trapped ions, with three of its normal modes of motion coupled by a trilinear Hamiltonian such that heat transfer between two modes refrigerates the third. We investigate the dynamics and steady-state properties of the refrigerator and compare its cooling capability when only thermal states are involved to the case when squeezing is employed as a quantum resource. We also study the performance of such a refrigerator in the single shot regime, and demonstrate cooling below both the steady-state energy and the benchmark predicted by the classical thermodynamics treatment.
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