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Register a new userEfficient optical pumping of Zeeman spin levels in Nd3+:YVO4
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We demonstrate that Zeeman ground-state spin levels in Nd3+:YVO4 provides the possibility to create an efficient lambda-system for optical pumping experiments. The branching ratio R in the lambda-system is measured experimentally via absorption spectroscopy and is compared to a theoretical model. We show that R can be tuned by changing the orientation of the magnetic field. These results are applied to optical pumping experiments, where significant improvement is obtained compared to previous experiments in this system. The tunability of the branching ratio in combination with its good coherence properties and the high oscillator strength makes Nd3+:YVO4 an interesting candidate for various quantum information protocols.
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Efficient optical pumping is an important tool for state initialization in quantum technologies, such as optical quantum memories. In crystals doped with Kramers rare-earth ions, such as erbium and neodymium, efficient optical pumping is challenging due to the relatively short population lifetimes of the electronic Zeeman levels, of the order of 100 ms at around 4 K. In this article we show that optical pumping of the hyperfine levels in isotopically enriched $^{145}$Nd$^{3+}$:Y$_2$SiO$_5$ crystals is more efficient, owing to the longer population relaxation times of hyperfine levels. By optically cycling the population many times through the excited state a nuclear-spin flip can be forced in the ground-state hyperfine manifold, in which case the population is trapped for several seconds before relaxing back to the pumped hyperfine level. To demonstrate the effectiveness of this approach in applications we perform an atomic frequency comb memory experiment with 33% storage efficiency in $^{145}$Nd$^{3+}$:Y$_2$SiO$_5$, which is on a par with results obtained in non-Kramers ions, e.g. europium and praseodymium, where optical pumping is generally efficient due to the quenched electronic spin. Efficient optical pumping in neodymium-doped crystals is also of interest for spectral filtering in biomedical imaging, as neodymium has an absorption wavelength compatible with tissue imaging. In addition to these applications, our study is of interest for understanding spin dynamics in Kramers ions with nuclear spin.
We report measurements of the optical properties of the 1042 nm transition of negatively-charged Nitrogen-Vacancy (NV) centers in type 1b diamond. The results indicate that the upper level of this transition couples to the m_s=+/-1 sublevels of the {^3}E excited state and is short-lived, with a lifetime <~ 1 ns. The lower level is shown to have a temperature-dependent lifetime of 462(10) ns at 4.4 K and 219(3) ns at 295 K. The light-polarization dependence of 1042 nm absorption confirms that the transition is between orbitals of A_1 and E character. The results shed new light on the NV level structure and optical pumping mechanism.
The realization of a future quantum Internet requires processing and storing quantum information at local nodes, and interconnecting distant nodes using free-space and fibre-optic links. Quantum memories for light are key elements of such quantum networks. However, to date, neither an atomic quantum memory for non-classical states of light operating at a wavelength compatible with standard telecom fibre infrastructure, nor a fibre-based implementation of a quantum memory has been reported. Here we demonstrate the storage and faithful recall of the state of a 1532 nm wavelength photon, entangled with a 795 nm photon, in an ensemble of cryogenically cooled erbium ions doped into a 20 meter-long silicate fibre using a photon-echo quantum memory protocol. Despite its currently limited efficiency and storage time, our broadband light-matter interface brings fibre-based quantum networks one step closer to reality. Furthermore, it facilitates novel tests of light-matter interaction and collective atomic effects in unconventional materials.
Solid-state electronic spins are extensively studied in quantum information science, as their large magnetic moments offer fast operations for computing and communication, and high sensitivity for sensing. However, electronic spins are more sensitive to magnetic noise, but engineering of their spectroscopic properties, e.g. using clock transitions and isotopic engineering, can yield remarkable spin coherence times, as for electronic spins in GaAs, donors in silicon and vacancy centres in diamond. Here we demonstrate simultaneously induced clock transitions for both microwave and optical domains in an isotopically purified $^{171}$Yb$^{3+}$:Y$_2$SiO$_5$ crystal, reaching coherence times of above 100 $mu$s and 1 ms in the optical and microwave domain, respectively. This effect is due to the highly anisotropic hyperfine interaction, which makes each electronic-nuclear state an entangled Bell state. Our results underline the potential of $^{171}$Yb$^{3+}$:Y$_2$SiO$_5$ for quantum processing applications relying on both optical and spin manipulation, such as optical quantum memories, microwave-tooptical quantum transducers, and single spin detection, while they should also be observable in a range of different materials with anisotropic hyperfine interaction.
We propose a new method for generating programmable interactions in one- and two-dimensional trapped-ion quantum simulators. Here we consider the use of optical tweezers to engineer the sound-wave spectrum of trapped ion crystals. We show that this approach allows us to tune the interactions and connectivity of the ion qubits beyond the power-law interactions accessible in current setups. We demonstrate the experimental feasibility of our proposal using realistic tweezer settings and experimentally relevant trap parameters to generate the optimal tweezer patterns to create target spin-spin interaction patterns in both one- and two-dimensional crystals. Our approach will advance quantum simulation in trapped-ion platforms as it allows them to realize a broader family of quantum spin Hamiltonians.
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