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.
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.
Erbium-doped solid-state crystals present an attractive platform for quantum communication, combining the telecom C-band spin–photon interface and long coherence times of erbium (Er3+) with the versatility of solid-state hosts. However, across commonly investigated materials, Er3+ is a “dim” ion, with low optical emission rates of kilohertz at most. This makes implementing quantum information transfer protocols (e.g., quantum teleportation) at usable rates a major challenge. One route to increasing Er3+ radiative rates is by careful selection of crystal hosts: the crystal field around an Er3+ ion may hybridize states of different parity, potentially increasing the radiative rate of its telecom transition. Here, using high-throughput computational methods, the radiative rates of Er3+ embedded in 9215 materials are estimated. The computation shows that careful host selection could increase Er3+ radiative rates by an order of magnitude compared to commonly studied hosts. Calculated results are compared with experimental radiative rates in a subset of materials, finding notable clustering but weak correlation. Nevertheless, the “brightest” candidates combined with suitable nanophotonics engineering could push Er3+-based quantum memories into the megahertz bandwidth regime.
Rare-earth ion dopants in solid-state hosts are ideal candidates for quantum communication technologies, such as quantum memories, due to the intrinsic spin–photon interface of the rare-earth ion combined with the integration methods available in the solid state. Erbium-doped cerium oxide (Er:CeO2) is a particularly promising host material platform for such a quantum memory, as it combines the telecom-wavelength (∼1.5μm) 4f–4f transition of erbium, a predicted long electron spin coherence time when embedded in CeO2, and a small lattice mismatch with silicon. In this work, we report on the epitaxial growth of Er:CeO2 thin films on silicon using molecular beam epitaxy, with controlled erbium concentration between 2 and 130 parts per million (ppm). We carry out a detailed microstructural study to verify the CeO2 host structure and characterize the spin and optical properties of the embedded Er3+ ions as a function of doping density. In as-grown Er:CeO2 in the 2–3 ppm regime, we identify an EPR linewidth of 245(1) MHz, an optical inhomogeneous linewidth of 9.5(2) GHz, an optical excited state lifetime of 3.5(1) ms, and a spectral diffusion-limited homogeneous linewidth as narrow as 4.8(3) MHz. We test the annealing of Er:CeO2 films up to 900 °C, which yields narrowing of the inhomogeneous linewidth by 20% and extension of the excited state lifetime by 40%.
Clock-transition-enabled long electron spin coherence of telecom emitters in CeO2
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 (Er3+) doped cerium oxide (CeO2) 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 Er3+ electron spin qubit in CeO2 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 Er3+ doped CeO2 as a front-runner for realizing spin qubits, quantum memories, and integrated quantum networks.
Optically active solid-state spin qubits thrive as an appealing technology for quantum interconnects and quantum networks, thanks to their atomic size, scalable synthesis, long-lived coherence, and ability to coherently interface with flying qubits. Trivalent erbium dopants, in particular, emerge as an attractive candidate due to their emission in the telecom C band and shielded 4f intra-shell spin and optical transitions. Nevertheless, prevailing top-down architectures for rare-earth qubits and devices have not yet achieved simultaneous long optical and spin coherence, which is necessary for efficient long-distance quantum networks. Here, we demonstrate dual Er3+ telecom spin-photon interfaces in two distinct lattice symmetry sites within an epitaxial thin-film platform. By leveraging high matrix crystallinity, controlled proximity of dopants to surfaces, and exploiting host lattice symmetry, we simultaneously achieve kilohertz-level optical linewidth in a strongly symmetry-protected site, and erbium qubit spin coherence times exceeding 10 milliseconds. Additionally, we realize single-shot readout and microwave coherent control of erbium qubits in a fiber-integrated package, enabling rapid deployment and scalability. These advancements highlight the significant potential of high-quality rare-earth qubits and quantum memories assembled using a bottom-up method, paving the way for scalable development of quantum light-matter interfaces tailored for telecommunication quantum networks. Erbium quantum emitters operating in the telecom C band are promising for spin-photon interfaces but achieving both optical and spin coherence has been challenging. Gupta et al. report two types of erbium dopants in epitaxial Y2O3 thin films occupying distinct lattice sites and exhibiting long spin and optical coherence times
Abstract Quantum memory is a core enabling device for large-scale quantum networks, serving as the fundamental building block for quantum repeaters and transportable quantum memories. Among various physical platforms, rare-earth-ion-doped crystals stand out as one of the most promising solid-state candidates for long-lived photonic quantum memories, owing to their exceptionally long spin coherence time and their compatibility with integration. In this review, we first introduce the physical mechanisms underlying long-lived spin coherence in rare-earth systems, with particular emphasis on the zero-first-order-Zeeman transition and dynamical decoupling techniques. We then review the experimental progress in this field, highlighting three distinct lifetimes—the spin coherence time, the light storage time, and the quantum storage time—and covering experiments that have achieved hour-scale spin coherence, minute- to hour-scale light storage, and minute-scale single-photon-level quantum storage. Finally, we discuss the remaining challenges that hinder the realization of practical long-lived quantum memories, explore potential strategies to overcome these obstacles, and outline the prospects for their future applications in quantum networks.
Optical quantum memories will enable technologies including long distance quantum communication and modular quantum computing. Rare earth ion doped crystals provide an excellent solid state platform for optical quantum memories. Among rare earths, erbium is particularly appealing due to its long-lived telecom-wavelength resonance, allowing integration with silicon photonics and with existing optical communication technology and infrastructure. We present an on-chip all-optical quantum memory at telecom wavelengths using a nanobeam photonic crystal cavity fabricated directly in erbium-167 doped yttrium orthosilicate. Using an atomic frequency comb protocol, we store coherent pulses for memory times as long as 10 µs, albeit with low efficiency. For shorter memory times, we achieve a memory efficiency of 0.4%, which is limited by the coupling rate between the resonator and the ensemble of ions. By working at dilution refrigerator temperatures, we are able to access a regime where the ions have long optical coherence times and good spectral holeburning properties using only a moderate magnetic field applied with permanent magnets. We characterize the multimode properties and fidelity of the quantum memory in this device, and outline a path toward higher efficiency.