William Cody Burton

We report on Quantinuum Helios, a 98-qubit trapped-ion quantum processor based on the quantum charge-coupled device (QCCD) architecture. Helios features $^{137}$Ba$^{+}$ hyperfine qubits, all-to-all connectivity enabled by a rotatable ion storage ring connecting two quantum operation regions by a junction, speed improvements from parallelized operations, and a new software stack with real-time compilation of dynamic programs. Averaged over all operational zones in the system, we achieve average infidelities of $2.5(1)\times10^{-5}$ for single-qubit gates, $7.9(2)\times10^{-4}$ for two-qubit gates, and $4.8(6)\times10^{-4}$ for state preparation and measurement, none of which are fundamentally limited and likely able to be improved. These component infidelities are predictive of system-level performance in both random Clifford circuits and random circuit sampling, the latter demonstrating that Helios operates well beyond the reach of classical simulation and establishes a new frontier of fidelity and complexity for quantum computers.

Quantum processors based on linear arrays of trapped ions have achieved exceptional performance, but scaling to large qubit numbers requires realizing two-dimensional ion arrays as envisioned in the quantum charge-coupled device (QCCD) architecture. Here we present a scalable method for the control of ion crystals in a grid-based surface-electrode Paul trap and characterize it in the context of transport operations that sort and reorder multispecies crystals. By combining cowiring of control electrodes at translationally symmetric locations in each grid site with the sitewise ability to exchange the voltages applied to two special electrodes gated by a binary input, site dependent operations can be achieved using only a fixed number of analog voltage signals and a single digital input per site. In two separate experimental systems containing nominally identical grid traps, one using $^{171}\mathrm{Yb}^{+}$-$^{138}\mathrm{Ba}^{+}$ crystals and the other $^{137}\mathrm{Ba}^{+}$-$^{88}\mathrm{Sr}^{+}$, we demonstrate this method by characterizing the conditional intrasite crystal reorder and the conditional exchange of ions between adjacent sites on the grid. Averaged across a multisite region of interest, we measure subquanta motional excitation in the axial in-phase and out-of-phase modes of the crystals following these operations at exchange rates of 2.5 kHz. In this initial demonstration, the logic controlling the voltage exchange occurs in software, but the applied signals mimic a proposed hardware implementation using crossover switches. These techniques can be further extended to implement other conditional operations in the QCCD architecture such as gates, initialization and measurement.

We report on the first demonstration of transport of a multispecies ion crystal through a junction in an RF Paul trap. The trap is a two-dimensional surface-electrode trap with an X junction and segmented control electrodes to which time-varying voltages are applied to control the shape and position of potential wells above the trap surface. We transport either a single $^{171}$Yb$^+$ ion or a crystal composed of a $^{138}$Ba$^+$ ion cotrapped with the $^{171}$Yb$^+$ ion to any port of the junction. We characterize the motional excitation by performing multiple round-trips through the junction and back to the initial well position without cooling. The final excitation is then measured using sideband asymmetry. For a single $^{171}$Yb$^+$ ion, transport with a $4\;\mathrm{m/s}$ average speed induces between $0.013\pm0.001$ and $0.014\pm0.001$ quanta of excitation per round trip, depending on the exit port. For a Ba-Yb crystal, transport at the same speed induces between $0.013\pm0.001$ and $0.030\pm0.002$ quanta per round trip of excitation to the axial center of mass mode. Excitation in the axial stretch mode ranges from $0.005\pm0.001$ to $0.021\pm0.001$ quanta per round trip.