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Register a new userUltra-narrow optical inhomogeneous linewidth in a stoichiometric rare earth crystal
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We have obtained a low optical inhomogeneous linewidth of 25 MHz in the stoichiometric rare earth crystal EuCl3 .6H2 O by isotopically purifying the crystal in 35 Cl. With this linewidth, an important limit for stoichiometric rare earth crystals is surpassed: the hyperfine structure of 153Eu is spectrally resolved, allowing the whole population of 153Eu3+ ions to be prepared in the same hyperfine state using hole burning techniques. This material also has a very high optical density and can have long coherence times when deuterated. This combination of properties offers new prospects for quantum information applications. We consider two of these, quantum memories and quantum many body studies. We detail the improvements in the performance of current memory protocols possible in these high optical depth crystals, and how certain memory protocols, such as off-resonant Raman memories, can be implemented for the first time in a solid state system. We explain how the strong excitation-induced interactions observed in this material resemble those seen in Rydberg systems, and describe how these interactions can lead to quantum many-body states that could be observed using standard optical spectroscopy techniques.
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Rare-earth ions are promising solid state systems to build light-matter interfaces at the quantum level. This relies on their potential to show narrow optical homogeneous linewidths or, equivalently, long-lived optical quantum states. In this letter, we report on europium molecular crystals that exhibit linewidths in the 10s of kHz range, orders of magnitude narrower than other molecular centers. We harness this property to demonstrate efficient optical spin initialization, coherent storage of light using an atomic frequency comb, and optical control of ion-ion interactions towards implementation of quantum gates. These results illustrate the utility of rare-earth molecular crystals as a new platform for photonic quantum technologies that combines highly coherent emitters with the unmatched versatility in composition, structure, and integration capability of molecular materials.
We describe a method for creating small quantum processors in a crystal stoichiometric in an optically active rare earth ion. The crystal is doped with another rare earth, creating an ensemble of identical clusters of surrounding ions, whose optical and hyperfine frequencies are uniquely determined by their spatial position in the cluster. Ensembles of ions in each unique position around the dopant serve as qubits, with strong local interactions between ions in different qubits. These ensemble qubits can each be used as a quantum memory for light, and we show how the interactions between qubits can be used to perform linear operations on the stored photonic state. We also describe how these ensemble qubits can be used to enact, and study, error correction.
We present a quantum repeater scheme that is based on individual erbium and europium ions. Erbium ions are attractive because they emit photons at telecommunication wavelength, while europium ions offer exceptional spin coherence for long-term storage. Entanglement between distant erbium ions is created by photon detection. The photon emission rate of each erbium ion is enhanced by a microcavity with high Purcell factor, as has recently been demonstrated. Entanglement is then transferred to nearby europium ions for storage. Gate operations between nearby ions are performed using dynamically controlled electric-dipole coupling. These gate operations allow entanglement swapping to be employed in order to extend the distance over which entanglement is distributed. The deterministic character of the gate operations allows improved entanglement distribution rates in comparison to atomic ensemble-based protocols. We also propose an approach that utilizes multiplexing in order to enhance the entanglement distribution rate.
We investigate a novel hybrid system composed of an ensemble of room temperature rare-earth ions embedded in a bulk crystal, intrinsically coupled to internal strain via the surrounding crystal field. We evidence the generation of a mechanical response under resonant light excitation. Thanks to an ultra-sensitive time- and space-resolved photodeflection setup, we interpret this motion as the sum of two resonant optomechanical backaction processes: a conservative, piezoscopic process induced by the optical excitation of a well-defined electronic configuration, and a dissipative, non-radiative photothermal process related to the phonons generated throughout the atomic population relaxation. Parasitic heating processes, namely off-resonant dissipative contributions, are absent. This work demonstrates an unprecedented level of control of the conservative and dissipative relative parts of the optomechanical backaction, confirming the potential of rare-earth-based systems as promising hybrid mechanical systems.
All-optical addressing and control of single solid-state based qubits allows for scalable architectures of quantum devices such as quantum networks and quantum simulators. So far, all-optical addressing of qubits was demonstrated only for color centers in diamond and quantum dots. Here, we demonstrate generation of coherent dark state of a single rare earth ion in a solid, namely a cerium ion in yttrium aluminum garnet (YAG). The dark state was formed under the condition of coherent population trapping. Furthermore, high-resolution spectroscopic studies of native and implanted single Ce ions have been performed. They revealed narrow and spectrally stable optical transitions between the spin sublevels of the ground and excited optical states, indicating the feasibility of interfacing single photons with a single electron spin of a cerium ion.
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