Rare-earth ion-doped crystals are of great interest for quantum memories, a central component in future quantum repeaters. To assess the promise of 1 % Tm ³⁺-doped yttrium gallium garnet (Tm:YGG), we report measurements of optical coherence and energy-level lifetimes of its ³H 6 ↔ 3 H ₄ transition at a temperature of around 500 mK and various magnetic fields. Using spectral hole burning (SHB), we find hyperfine ground-level (Zeeman level) lifetimes of several minutes at magnetic fields of less than 1000 G. We also measure coherence time exceeding one millisecond using two-pulse photon echoes. Three-pulse photon echo and SHB measurements reveal that due to spectral diffusion, the effective coherence time reduces to a few µs over a timescale of around two hundred seconds. Finally, temporal and frequency-multiplexed storage of optical pulses using the atomic frequency comb protocol is demonstrated. Our results suggest Tm:YGG to be promising for multiplexed photonic quantum memory for quantum repeaters.

Here, we discuss our experimental efforts toward building an alignment-free, long-lived, and efficient cavity-enhanced quantum memory in a thulium-doped crystal. A significant step forward for creating efficient quantum memories with long optical storage times.

The creation of well-understood structures using spectral hole burning is an important task in the use of technologies based on rare-earth ion-doped crystals. We apply a series of different techniques to model and improve the frequency dependent population change in the atomic level structure of thulium yttrium gallium garnet (Tm:YGG). In particular we demonstrate that, at zero applied magnetic field, numerical solutions to frequency-dependent three-level rate equations show good agreement with spectral hole-burning results. This allows us to predict spectral structures given a specific hole-burning sequence, the underpinning spectroscopic material properties, and the relevant laser parameters. This enables us to largely eliminate power-dependent hole broadening through the use of adiabatic hole-burning pulses. Although this system of rate equations shows good agreement at zero field, the addition of a magnetic field results in unexpected spectral diffusion proportional to the induced Tm ion magnetic-dipole moment and average magnetic-field strength, which, through the quadratic Zeeman effect, dominates the optical spectrum over long timescales. Our results allow optimization of the preparation process for spectral structures in a large variety of rare-earth ion-doped materials for quantum memories and other applications.

We develop a theoretical model for a cavity-enhanced atomic frequency comb quantum memory and demonstrate good agreement with experimental results.

In this work, we fabricate a multimode quantum memory out of a thulium-doped crystal and demonstrate storage of laser pulses of up to 100 µsec. A significant step forward for creating quantum memories with long optical storage times.

Long optical storage times are an essential requirement to establish high-rate entanglement distribution over large distances using memory-based quantum repeaters. Rare earth ion-doped crystals are arguably well-suited candidates for building such quantum memories. Toward this end, we investigate the 795.32 nm ³H₆ ↔ ³H₄ transition of 1% thulium-doped yttrium gallium garnet crystal (Tm³⁺:Y₃Ga₅O₁₂ : Tm³⁺:YGG). Most essentially, we find that the optical coherence time can reach 1.1 ms, and, using laser pulses, we demonstrate optical storage based on the atomic frequency comb (AFC) protocol up to 100 µs. In addition, we demonstrate multiplexed storage, including feed-forward selection, shifting, and filtering of spectral modes, as well as quantum state storage using members of non-classical photon pairs. Our results show that Tm:YGG can be a potential candidate for creating multiplexed quantum memories with long optical storage times.

We characterize the magnetic properties for thulium ion energy levels in the (Tm:YGG) lattice with the goal to improve decoherence and reduce linewidth broadening caused by local host spins and crystal imperfections. More precisely, we measure hyperfine tensors for the lowest level of and excited states using a combination of spectral hole burning, absorption spectroscopy, and optically detected nuclear magnetic resonance. By rotating the sample through a series of angles with an applied external magnetic field, we measure and analyze the orientation dependence of the ion's spin Hamiltonian. Using this spin Hamiltonian, we propose a set of orientations to improve material properties that are important for light-matter interaction and quantum information applications. Our results yield several important external field directions: some to extend optical coherence times, another to improve spin inhomogeneous broadening, and yet another that maximizes mixing of the spin states for specific sets of ions, which allows improving optical pumping and creation of lambda systems in this material.

We argue that long optical storage times are required to establish entanglement at high rates over large distances using memory-based quantum repeaters. Triggered by this conclusion, we investigate the 795.325 nm3 H6↔H34 transition of Tm:Y3Ga5O12 (Tm:YGG). Most importantly, we find that the optical coherence time can reach 1.1 ms, and, using laser pulses, we demonstrate optical storage based on the atomic frequency comb protocol during up to 100 μs as well as a memory decay time Tm of 13.1 μs. Possibilities of how to narrow the gap between the measured value of Tm and its maximum of 275 μs are discussed. In addition, we demonstrate multiplexed storage, including with feed-forward selection, shifting and filtering of spectral modes, as well as quantum state storage using members of nonclassical photon pairs. Our results show the potential of Tm:YGG for creating multiplexed quantum memories with long optical storage times, and open the path to repeater-based quantum networks with high entanglement distribution rates.

We design and implement an atomic frequency comb quantum memory for 793-nm wavelength photons using a monolithic cavity based on a thulium- (Tm-) doped Y3Al5O12 crystal. Approximate impedance matching results in the absorption of 90% of input photons and a memory efficiency of (27.5±2.7)% over a 500-MHz bandwidth. The cavity enhancement leads to a significant improvement over the previous efficiency in Tm-doped crystals using a quantum memory protocol. In turn, this allows us to store and recall quantum states of light in such a memory. Our results demonstrate progress toward efficient and faithful storage of single-photon qubits with a large time-bandwidth product and multimode capacity for quantum networking.

Entangling quantum systems with different characteristics through the exchange of photons is a prerequisite for building future quantum networks. Proving the presence of entanglement between quantum memories for light working at different wavelengths furthers this goal. Here, we report on a series of experiments with a thulium-doped crystal, serving as a quantum memory for 794-nm photons, an erbium-doped fiber, serving as a quantum memory for telecommunication-wavelength photons at 1535 nm, and a source of photon pairs created via spontaneous parametric down-conversion. Characterizing the photons after re-emission from the two memories, we find nonclassical correlations with a cross-correlation coefficient of g12(2)=53±8; entanglement preserving storage with input-output fidelity of FIO≈93±2%; and nonlocality featuring a violation of the Clauser-Horne-Shimony-Holt Bell inequality with S=2.6±0.2. Our proof-of-principle experiment shows that entanglement persists while propagating through different solid-state quantum memories operating at different wavelengths.