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Reducing spin decoherence in a Tm3+:YAG crystal by dynamical decoupling

R.-C. Tongning, M. F. Pascual-Winter, T. Chanelière, J.-L. Le Gouët

Published Jan 1, 2013• 0 citations
Publisher

Abstract

We extend Tm3+ nuclear spin coherence lifetime to ∼ 230 ms. This 450-fold gain is achieved within the quantum memory context, involving spin hyperpolarization by optical pumping, dynamical decoupling and optical detection of Tm3+ ions.
DOI
10.1364/cleo_qels.2013.jth2a.96

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We report a high fidelity optical memory in which dynamical decoupling is used to extend the storage time. This is demonstrated in a rare-earth doped crystal in which optical coherences were transferred to nuclear spin coherences and then protected against environmental noise by dynamical decoupling, leading to storage times of up to 4.2 ms. An interference experiment shows that relative phases of input pulses are preserved through the whole storage and retrieval process with a visibility ≈1, demonstrating the usefulness of dynamical decoupling for extending the storage time of quantum memories. We also show that dynamical decoupling sequences insensitive to initial spin coherence increase retrieval efficiency.
A thulium-doped crystal is experimentally shown to be an excellent candidate for broadband quantum storage in a solid-state medium. The nuclear spin coherence is optically excited, detected, and characterized in such a crystal. The lifetime of the spin coherence---the potential storage entity---is measured by means of a new Raman echo protocol to be about $300\text{ }\ensuremath{\mu}\text{s}$ over a wide range of ground state splittings. This flexibility, which is attractive for broadband operation and well fitted to existing quantum sources, results from the simple hyperfine structure, which contrasts to Pr- and Eu-doped crystals.
We report on spin coherence lifetime extension in Tm3+{}^{3+}3+:YAG obtained through dynamically decoupling the thulium spins from their magnetic environment. The coherence lifetime reached with a Carr-Purcell-Meiboom-Gill sequence revealed a 450-fold extension [$\ensuremath{\sim}$$(230\ifmmode\pm\else\textpm\fi{}30)$ ms] with respect to previously measured values. Comparison to a simple theoretical model allowed us to estimate the correlation time of the fluctuations of the ground-level transition frequency to $(172\ifmmode\pm\else\textpm\fi{}30)$ $\ensuremath{\mu}$s at 1.7 K. For attaining efficient decoupling sequences, we developed a strategy inspired by the zero-first-order Zeeman effect to minimize the large inhomogeneous broadening of the ground-level spin transition.
In low-concentration Tm3+{}^{3+}3+:YAG, we observe efficient adiabatic rapid passage (ARP) of thulium nuclear spin over flipping times much longer than T2{T}_{2}T2​. Efficient ARP with long flipping time has been observed in monoatomic solids for decades and has been analyzed in terms of spin temperature and of the thermodynamic equilibrium of a coupled spin ensemble. In low-concentration impurity-doped crystals the spin temperature concept may be questioned. A single spin model should be preferred since the impurity ions are weakly coupled together but interact with the numerous off-resonant matrix ions that originate the spin-spin relaxation. The experiment takes place in the context of quantum information investigation, involving impurity-doped crystals, spin hyperpolarization by optical pumping, and optical detection of the spin evolution.
Methods that preserve coherence broadly impact all quantum information processing and metrology applications. Dynamical decoupling methods accomplish this by protecting qubits in noisy environments but are typically constrained to the limit where the qubits themselves are non-interacting. Here we consider the alternate regime wherein the inter-qubit couplings are of the same order as dephasing interactions with the environment. We propose and demonstrate a multi-pulse protocol that protects transverse spin states by suitably Hamiltonian engineering the inter-spin coupling while simultaneously suppressing dephasing noise on the qubits. We benchmark the method on 13C nuclear spin qubits in diamond, dipolar coupled to each other and embedded in a noisy electronic spin bath, and hyperpolarized via optically pumped NV centers. We observe effective state lifetimes of 13C nuclei $T_2^{\prime}\approx$2.5s at room temperature, an extension of over 4700-fold over the conventional T2∗T_2^{\ast}T2∗​ free induction decay. The spins are continuously interrogated during the applied quantum control, resulting in 13C NMR line narrowing and an $>$500-fold boost in SNR due to the lifetime extension. Together with hyperpolarization spin interrogation is accelerated by >1011>10^{11}>1011 over conventional 7T NMR. This work suggests strategies for the dynamical decoupling of coupled qubit systems with applications in a variety of experimental platforms.
Eu3+{\mathrm{Eu}}^{3+}Eu3+:Y2SiO5{\mathrm{Y}}_{2}{\mathrm{SiO}}_{5}Y2​SiO5​ crystals are promising candidates for quantum memories because their nuclear spin coherence lifetime can be extended to 47 seconds at a particular magnetic field. Although an extended coherence lifetime of 6 hours can be achieved with a large number of dynamic decoupling sequences, these pulses will also introduce unwanted noise. To realize quantum storage with a lifetime of hours, it is necessary to quantitatively characterize the spin decoherence process of Eu3+{\mathrm{Eu}}^{3+}Eu3+ ions to guide the experimental efforts. In practice, a number of limiting factors could impose a limit on the achievable spin coherence lifetime, which includes the spin inhomogeneous broadening of the Eu3+{\mathrm{Eu}}^{3+}Eu3+ ensemble and the homogeneity and stability of the external magnetic field. Here, we provide a Monte Carlo simulation model of the nuclear spin decoherence process of Eu3+{\mathrm{Eu}}^{3+}Eu3+ ions in Y2SiO5{\mathrm{Y}}_{2}{\mathrm{SiO}}_{5}Y2​SiO5​ crystals, and these limiting factors are considered to provide an accurate prediction of the spin coherence lifetimes. This method is universal and can be applied to other rare-earth-ion-doped crystals.