Qiming Wu

Trapped ions provide a high-fidelity platform for quantum information processing, yet delivery of multiple, distinct wavelengths across large networks of interaction zones remains a bottleneck. Conventional free-space light delivery lacks scalability, while on-chip grating couplers suffer from narrow operational bandwidth that increases circuit footprint and optical interfacing complexity. Here we show a broadband photonic integrated circuit capable of addressing individual ions. The circuit combines a planar waveguide lens with a micromirror fabricated using two-photon polymerization at wafer scale. This implementation can address three individual ions from $λ$ = 405 - 880 nm with -27 dB average intensity crosstalk at $5\,μ\mathrm{m}$ pitch. We trap $^{40}\mathrm{Ca}^{+}$ and $^{138}\mathrm{Ba}^{+}$ ions above such devices, characterize optical crosstalk with barium ions, and demonstrate individual repumping of calcium ions. This monolithic photonic architecture brings broadband addressing in an on-chip modality to trapped-ion technology. More generally, integrating additive manufacturing into quantum devices is poised to unlock expanded design space for implementing novel quantum architectures.

Synchronization is a hallmark of collective behavior that emerges when nonlinear systems interact, spanning scales from mechanical oscillators to planetary orbits. As a universal phenomenon it underpins the study of complex systems and has far-reaching technological implications. While classical synchronization has a long and rich history, it has not been observed experimentally between multiple quantum limit-cycle oscillators despite a decade of theoretical investigations. We realize synchronization between two quantum van der Pol oscillators by engineering dissipation in a mixed-isotope trapped-ion quantum simulator. The synchronized state is encoded in a fixed relative phase between the oscillators that is inaccessible to local measurements and only revealed through joint readout of both oscillators, in stark contrast to the classical case where synchronization can be observed via individual phase measurements. We further show that the relative phase can be precisely controlled, and that the chain of two oscillators can synchronize to an external field, suggesting applications in sensing. Our results provide a promising pathway for studying more complex synchronized quantum dynamics beyond two oscillators, where a theoretical treatment becomes increasingly challenging, and it remains to be understood whether genuinely quantum features persist in such cases.

Trapped-ion quantum computing requires precise optical control for individual qubit manipulation. However, conventional free-space optics face challenges in alignment stability and scalability as the number of qubits increases. Integrated photonics offers a promising alternative, providing miniaturized optical systems on a chip. Here, we propose a design for a multimode photonic circuit integrated with a surface-electrode ion trap capable of targeted and reconfigurable light delivery. Three closely positioned ions can be addressed using a focusing grating coupler that emits multimode light through electrode openings to ions trapped 80 $μ$m above the chip. Simulations show that the couplers achieve diffraction-limited spot with a 4.3 $μ$m beam waist along the trap axis and 2.2 $μ$m perpendicular to the trap axis. Controlled interference of the TE$_{\text{10}}$ and TE$_{\text{20}}$ modes results in crosstalk of -20 dB to -30 dB at ion separations of 5-8 $μ$m when addressing ions individually, and down to -60 dB when two of the three ions are addressed simultaneously. Additionally, the higher-order TE modes can offer a novel mechanism for driving spin-motion coupling transitions, potentially enabling alternative approaches to quantum gates and simulations. The proposed integrated platform offers a viable path for constructing large-scale trapped-ion systems, leveraging the benefits of nanophotonic design for precise and reliable ion manipulation.

Atom-cavity systems offer unique advantages for building large-scale distributed quantum computers by providing strong atom-photon coupling while allowing for high-fidelity local operations of atomic qubits. However, in prevalent schemes where the photonic state is encoded in polarization, cavity birefringence introduces an energy splitting of the cavity eigenmodes and alters the polarization states, thus limiting the fidelity of remote entanglement generation. To address this challenge, we propose a scheme that encodes the photonic qubit in the frequency degree-of-freedom. The scheme relies on resonant coupling of multiple transverse cavity modes to different atomic transitions that are well-separated in frequency. We numerically investigate the temporal properties of the photonic wavepacket, two-photon interference visibility, and atom-atom entanglement fidelity under various cavity polarization-mode splittings and find that our scheme is less affected by cavity birefringence. Finally, we propose practical implementations in two trapped ion systems, using the fine structure splitting in the metastable D state of $\mathrm{^{40}Ca^{+}}$, and the hyperfine splitting in the ground state of $\mathrm{^{225}Ra^{+}}$. Our study presents an alternative approach for cavity-based quantum networks that is less sensitive to birefringent effects, and is applicable to a variety of atomic and solid-state emitter-cavity interfaces.

High-rate remote entanglement between photon and matter-based qubits is essential for distributed quantum information processing. A key technique to increase the modest entangling rates of existing long-distance quantum networking approaches is multiplexing. Here, we demonstrate a temporally multiplexed ion-photon interface via rapid transport of a chain of nine calcium ions across 74 $\mathrm{μm}$ within 86 $\mathrm{μs}$. The non-classical nature of the multiplexed photons is verified by measuring the second-order correlation function with an average value of $g^{(2)}(0)$ = 0.060(13), indicating negligible crosstalk between the multiplexed modes. In addition, we characterize the motional degree-of-freedom of the ion crystal after transport and find that it is coherently excited to as much as $\bar{n}_α\approx 110$ for the center-of-mass mode. Our proof-of-principle implementation paves the way for large-scale quantum networking with trapped ions, but highlights some challenges that must be overcome.

Geometry and dimensionality have played crucial roles in our understanding of the fundamental laws of nature, with examples ranging from curved space-time in general relativity to modern theories of quantum gravity. In quantum many-body systems, the entanglement structure can change if the constituents are connected differently, leading to altered bounds for correlation growth and difficulties for classical computers to simulate large systems. While a universal quantum computer can perform digital simulations, an analog-digital hybrid quantum processor offers advantages such as parallelism. Here, we engineer a class of high-dimensional Ising interactions using a linear one-dimensional (1D) ion chain with up to 8 qubits through stroboscopic sequences of commuting Hamiltonians. %with a thorough understanding of the error sources and deviation from the target Hamiltonian. In addition, we extend this method to non-commuting circuits and demonstrate the quantum XY and Heisenberg models using Floquet periodic drives with tunable symmetries. The realization of higher dimensional spin models offers new opportunities ranging from studying topological phases of matter or quantum spin glasses to future fault-tolerant quantum computation.

We report continuous Raman sideband cooling (CRSC) of a long ion chain to the motional ground state beyond the Lamb-Dicke (LD) regime. By driving multiple sideband transitions simultaneously, we show that nearly all axial modes of a 24-ion chain are cooled to the ground state, with an LD parameter as large as $η= 1.3$, spanning a frequency bandwidth of 4 MHz. Compared to traditional ground-state cooling methods such as pulsed sideband cooling or electromagnetic-induced-transparency (EIT) cooling, our method offers two key advantages: robustness to timing errors; and an ultra-wide bandwidth unlimited by the number of ions. This technique contributes as a crucial step for large-scale quantum information processing with linear ion chains and higher dimensions alike, and can be readily generalized to other atomic and molecular systems.

Trapped atomic ions find wide applications ranging from precision measurement to quantum information science and quantum computing. Among the different atomic species employed, beryllium ions are widely used due to its light mass and convenient atomic structure. However, the ion loading process requires a high temperature for sufficient vapor pressure, generating undesirable gas load for the background vacuum and limiting the lifetime of a long ion chain. Here, we demonstrate a simple method to rapidly produce pure linear chains of beryllium ions with pulsed laser ablation, serving as a starting point for large-scale quantum information processing. Our method is fast compared to thermal ovens; reduces the vacuum load to only 10^(-12) Torr level; yields a short recovery time of a few seconds; and also eliminates the need for a deep ultraviolet laser for photo-ionization. In addition, we apply feedback control to obtain defect-free ion arrays with desirable lengths.