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Register a new userHyperfine interaction and coherence time of praseodymium ions at the site 2 in yttrium orthosilicate
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Praseodymium (Pr$^{3+}$) ions doped in the site 1 of yttrium orthosilicate (Y$_2$SiO$_5$) has been widely employed as the photonic quantum memory due to their excellent optical coherence and spin coherence. While praseodymium ions occupying the site 2 in Y$_2$SiO$_5$ crystal have better optical coherence as compared with those at site 1, which may enable better performance in quantum memory. Here we experimentally characterize the hyperfine interactions of the ground state $^3$H$_4$ and excited state $^1$D$_2$ of Pr$^{3+}$ at site 2 in Y$_2$SiO$_5$ using Raman heterodyne detected nuclear magnetic resonance. The Hamiltonians for the hyperfine interaction are reconstructed for both ground state $^3$H$_4$ and excited state $^1$D$_2$ based on the Raman heterodyne spectra in 201 magnetic fields. The two-pulse spin-echo coherence lifetime for the ground state is measured to be 2.6$pm$0.1 ms at site 2 with zero magnetic field, which is more than five times longer than that at site 1. The magnetic fields with zero first order Zeeman shift in the hyperfine transition for Pr$^{3+}$ at site 2 in Y$_2$SiO$_5$ are identified.
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Doping of substrates at desired locations is a key technology for spin-based quantum memory devices. Focused ion beam implantation is well-suited for this task due to its high spacial resolution. In this work, we investigate ion-beam implanted erbium ensembles in Yttrium Orthosilicate crystals by means of confocal photoluminescence spectroscopy. The sample temperature and the post-implantation annealing step strongly reverberate in the properties of the implanted ions. We find that hot implantation leads to a higher activation rate of the ions. At high enough fluences, the relation between the fluence and final concentration of ions becomes non-linear. Two models are developed explaining the observed behaviour.
The coherence of a hyperfine-state superposition of a trapped $^{9}$Be$^+$ ion in the presence of off-resonant light is experimentally studied. It is shown that Rayleigh elastic scattering of photons that does not change state populations also does not affect coherence. Coherence times exceeding the average scattering time of 19 photons are observed. This result implies that, with sufficient control over its parameters, laser light can be used to manipulate hyperfine-state superpositions with very little decoherence.
We present a detailed study of the lifetime of optical spectral holes due to population storage in Zeeman sublevels of Nd$^{3+}$:Y$_2$SiO$_5$. The lifetime is measured as a function of magnetic field strength and orientation, temperature and Nd$^{3+}$ doping concentration. At the lowest temperature of 3 K we find a general trend where the lifetime is short at low field strengths, then increases to a maximum lifetime at a few hundreds of mT, and then finally decays rapidly for high field strengths. This behaviour can be modelled with a relaxation rate dominated by Nd$^{3+}$-Nd$^{3+}$ cross relaxation at low fields and spin lattice relaxation at high magnetic fields. The maximum lifetime depends strongly on both the field strength and orientation, due to the competition between these processes and their different angular dependencies. The cross relaxation limits the maximum lifetime for concentrations as low as 30 ppm of Nd$^{3+}$ ions. By decreasing the concentration to less than 1 ppm we could completely eliminate the cross relaxation, reaching a lifetime of 3.8 s at 3~K. At higher temperatures the spectral hole lifetime is limited by the magnetic-field independent Raman and Orbach processes. In addition we show that the cross relaxation rate can be strongly reduced by creating spectrally large holes of the order of the optical inhomogeneous broadening. Our results are important for the development and design of new rare-earth-ion doped crystals for quantum information processing and narrow-band spectral filtering for biological tissue imaging.
A complete effective Hamiltonian for relativistic corrections at orders $malpha^6$ and $malpha^6(m/M)$ in a one-electron molecular system is derived from the NRQED Lagrangian. It includes spin-independent corrections to the energy levels and spin-spin scalar interactions contributing to the hyperfine splitting, both of which had been studied previously. In addition, corrections to electron spin-orbit and spin-spin tensor interactions are newly obtained. This allows improving the hyperfine structure theory in the hydrogen molecular ions. Improved values of the spin-orbit hyperfine coefficient are calculated for a few transitions of current experimental interest.
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