Individually addressed Er 3+ ions in solid-state hosts are promising resources for quantum repeaters, because of their direct emission in the telecom band and their compatibility with silicon photonic devices.While the Er 3+ electron spin provides a spin-photon interface, ancilla nuclear spins could enable multiqubit registers with longer storage times.In this work, we demonstrate coherent coupling between the electron spin of a single Er 3+ ion and a single I = 1/2 nuclear spin in the solid-state host crystal, which is a fortuitously located proton ( 1 H).We control the nuclear spin using dynamical-decoupling sequences applied to the electron spin, implementing one-and two-qubit gate operations.Crucially, the nuclear spin coherence time exceeds the electron coherence time by several orders of magnitude, because of its smaller magnetic moment.These results provide a path toward combining long-lived nuclear spin quantum registers with telecom-wavelength emitters for long-distance quantum repeaters.
The ability to coherently control and read out qubits with long coherence times in a scalable system is a crucial requirement for any quantum processor. Nuclear spins in the solid state have shown great promise as long-lived qubits. Control and readout of individual nuclear spin qubit registers has made major progress in the recent years using individual electron spin ancilla addressed either electrically or optically. Here, we present a new platform for quantum information processing, consisting of
183W nuclear spin qubits adjacent to an Er
3+ impurity in a CaWO
4 crystal, interfaced via a superconducting resonator and detected using a microwave photon counter at 10mK. We study two nuclear spin qubits with
T2∗ of
0.8(2) s and
1.2(3) s,
T2 of
3.4(4) s and
4.4(6) s, respectively. We demonstrate single-shot quantum non-demolition readout of each nuclear spin qubit using the Er
3+ spin as an ancilla. We introduce a new scheme for all-microwave single- and two-qubit gates, based on stimulated Raman driving of the coupled electron-nuclear spin system. We realize single- and two-qubit gates on a timescale of a few milliseconds, and prepare a decoherence-protected Bell state with 88% fidelity and
T2∗ of
1.7(2) s. Our results are a proof-of-principle demonstrating the potential of solid-state nuclear spin qubits as a promising platform for quantum information processing. With the potential to scale to tens or hundreds of qubits, this platform has prospects for the development of scalable quantum processors with long-lived qubits.
Entanglement between photons and a quantum memory is a key component of quantum repeaters, which allow long-distance quantum entanglement distribution in the presence of fiber losses. Spin-photon entanglement has been implemented with a number of different atomic and solid-state qubits with long spin coherence times, but none directly emit photons into the 1.5 − μ m telecom band where losses in optical fibers are minimized. Here, we demonstrate spin-photon entanglement using a single rare earth ion in the solid-state Er 3 + coupled to a silicon nanophotonic cavity, which directly emits photons at 1532.6 nm. We infer an entanglement fidelity of 73(3)% after propagating through 15.6 km of optical fiber. This work opens the door to large-scale quantum networks based Er 3 + ions, leveraging scalable silicon device fabrication and spectral multiplexing.
Rare-earth related electron spins in crystalline hosts are unique material systems, as they can potentially provide a direct interface between telecom band photons and long-lived spin quantum bits. Specifically, their optically accessible electron spins in solids interacting with nuclear spins in their environment are valuable quantum memory resources. Detection of nearby individual nuclear spins, so far exclusively shown for few dilute nuclear spin bath host systems such as the nitrogen-vacancy center in diamond or the silicon vacancy in silicon carbide, remained an open challenge for rare earths in their host materials, which typically exhibit dense nuclear spin baths. Here, we present the electron spin spectroscopy of single Ce^{3+} ions in a yttrium orthosilicate host, featuring a coherence time of T_{2}=124 μs. This coherent interaction time is sufficiently long to isolate proximal ^{89}Y nuclear spins from the nuclear spin bath of ^{89}Y. Furthermore, it allows for the detection of a single nearby ^{29}Si nuclear spin, native to the host material with ∼5% abundance. This study opens the door to quantum memory applications in rare-earth ion related systems based on coupled environmental nuclear spins, potentially useful for quantum error correction schemes.
Rare-earth-ion-doped crystals has emerged as a promising platform for quantum technologies, owing to their narrow telecom-band optical emission, long spin memory, and compatibility with silicon integrated photonic architectures. However, the realization of scalable quantum devices requires host materials with intrinsically dilute spin environments to suppress decoherence. In this context, erbium (Er
3+) doped cerium oxide (CeO
2) is an attractive candidate due to the ultra-low concentration of nuclear spins in the host matrix and its compatibility with silicon-based technologies. Here we perform a comprehensive investigation of the coherence properties of Er
3+ electron spin qubit in CeO
2 via semiclassical as well as detailed cluster correlation expansion simulations. By systematically exploring magnetic field strength, pulse sequences, erbium concentration, and spin temperature, we identify regimes where decoherence from the spin bath is strongly suppressed. Our investigations illustrate that at dilute doping concentration (of the order of 10 ppb) and sub-Kelvin temperatures, operation near clock transitions enables Hahn-echo coherence times to approach the second timescale even at natural isotopic abundance. Importantly, from a practical standpoint, coherence times on the order of
∼10 ms are expected even at liquid helium temperature (about 2 K) for similar concentrations. Moreover, we demonstrate that an additional enhancement can be obtained with conventional multi-
π-pulse dynamical decoupling protocols. Thus, our findings establish Er
3+ doped CeO
2 as a front-runner for realizing spin qubits, quantum memories, and integrated quantum networks.
Robust spin-photon interfaces with optical transitions in the telecommunication band are essential for quantum networking technologies. Erbium (Er) ions are the ideal candidate with environmentally protected transitions in telecom-C band. Finding the right technologically compatible host material to enable long-lived spins remains a major hurdle. We introduce a new platform based on Er ions in cerium dioxide (CeO 2 ) as a nearly-zero nuclear spin environment (0.04%) epitaxially grown on silicon, offering silicon compatibility for opto-electrical devices. Our studies focus on Er 3+ ions and show a narrow homogeneous linewidth of 440 kHz with an optical coherence time of 0.72 μs at 3.6 K. The reduced nuclear spin noise enables a slow spin-lattice relaxation with a spin relaxation time up to 2.5 ms and an electron spin coherence time of 0.66 μs (in the isolated ion limit) at 3.6 K. These findings highlight the potential of Er 3+ :CeO 2 platform for quantum networks applications.
Abstract Doping erbium ions into europium-based hosts offers a promising platform for quantum repeater nodes, combining europium’s exceptional coherence properties for long-term quantum storage with erbium’s microwave compatibility and direct telecom-band emission for efficient optical interfacing. In this work, we investigated erbium-doped EuCl3 · 6H2O stoichiometric crystals as a candidate for such nodes. We demonstrate that erbium doping shifts the optical transition frequencies of nearby Eu3+ ions, producing well resolved satellite lines in the inhomogeneous absorption profile. We experimentally probe the coupling between Er3+ and Eu3+ ions under varying temperature and magnetic field conditions, quantifying the interaction strength, which ranges from tens to hundreds of kilohertz, depending on field orientation, magnitude, and the lattice position of the Eu3+ ions. At 60 mK and a moderate magnetic field of 0.1 T, we observed a strong frozen core effect from Er3+ spins, substantially extending the Eu3+ optical coherence time from 62 us to 162 us, approaching the lifetime limit, and enabling hour-long hyperfine state lifetimes. These results underscore the potential of dual-species rare-earth systems for photonic quantum technologies and highlight their promise for precise quantum control.