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Juha Vaara

Publications and source records attributed to Juha Vaara.

5 recordsLinked to original sources

Analytical model for polarization transfer during gas-phase collision events in spin-exchange optical pumping: Spin-$\frac{1}{2}$ $^{129}$Xe versus spin-$\frac{3}{2}$ $^{131}$Xe

Spin-exchange optical pumping (SEOP) is a method for producing spin-hyperpolarized noble gas nuclei, such as 129Xe and 131Xe, which are used in various magnetic resonance applications from fundamental physics to quantum sensing and medical imaging. In SEOP, optically polarized alkali-metal atoms transfer their spin polarization to the noble gas nuclei in gas-phase collision events via the hyperfine coupling (HFC) between the alkali valence electron and the noble gas nucleus. While the polarization transfer physics of spin $I = 1/2$ nuclei, such as 129Xe, is relatively well understood, that of spin $I > 1/2$ nuclei, such as 131Xe ($I = 3/2$), has been far less studied, and no rigorous theoretical model has been presented to date. To this end, we derive a simple analytical model for the upper limit, neglecting relaxation, of the SEOP polarization transfer, applicable to noble gases with arbitrary nuclear spin. Analytical evaluation of the Baker-Campbell-Hausdorff expansion for the time evolution of the spin density operator $\hat{\rho}(t)$ reveals that only even-order terms in the HFC contribute to the polarization transfer, with the leading-order quadratic term being the most significant. We obtain a result similar to that derived for the spin-exchange cross section by Herman [Phys. Rev. 137, A 1062 (1965)], but in a more general framework for the time evolution of $\hat{\rho}(t)$ that is also more familiar to magnetic resonance researchers. The model is applied to understand the difference in the polarization transfer efficiency between 129Xe and 131Xe, yielding results in agreement with previous experiments. We also validate the model by comparison to detailed numerical multiscale simulations of the SEOP process, where full quantum-chemically computed spin Hamiltonians sampled from molecular dynamics simulations of the gas-phase collision events are used to propagate the spin dynamics.

physics.atom-ph

Calculation of NMR Shielding in Paramagnetic Molecules: Roadmap and Magnetic Couplings

We present a simple derivation of the nuclear shielding in paramagnetic molecules, extendable to strong spin-orbit coupling cases of relevance to lanthanides and actinides, as well as encompassing contributions from excited multiplets. While our general formulation does not need electron paramagnetic resonance parameters, using them a simple and practical expression is obtained for the special case of the zero-field-split ground-state manifold, including magnetic (Zeeman and hyperfine) couplings between the sublevels. The latter method is implemented computationally and applied in the context of first-principles calculations on example Ni(II) and Co(II) complexes.

physics.chem-ph

Precision calculation of scalar nuclear spin-spin coupling in a noble gas mixture

Indirect spin-spin interactions between nuclei bound in a molecule are well-known in nuclear magnetic resonance, but such interactions between unbound atoms are less well studied and are often assumed to be zero. We present the first precision calculation of this interaction between 129Xe and 3He nuclei in a gas. Relativistic, state-of-the-art electronic structure theory is used to compute the scalar coupling constant J(R) and the interatomic potential energy function, V(R), as functions of the Xe-He internuclear distance R. Using virial expansion we find the nuclear spin enhancement factor kappa = -0.0105 +/- 0.0015 in excellent agreement with recent experiments. This interaction is particularly important for precision measurements using nuclear spin co-magnetometers.

physics.atom-ph

Observation of optical chemical shift by precision nuclear spin optical rotation measurements and calculations

Nuclear spin optical rotation (NSOR) is a recently developed technique for detection of nuclear magnetic resonance via rotation of light polarization, instead of the usual long-range magnetic fields. NSOR signals depend on hyperfine interactions with virtual optical excitations, giving new information about the nuclear chemical environment. We use a multi-pass optical cell to perform first precision measurements of NSOR signals for a range of organic liquids and find clear distinction between proton signals for different compounds, in agreement with our earlier predictions. Detailed first principles quantum-mechanical NSOR calculations are found to be in good agreement with the measurements.

physics.chem-ph

Laser-induced splittings in the nuclear magnetic resonance spectra of the rare gases

Circularly polarized laser field causes a shift in the nuclear magnetic resonance (NMR) spectra of all substances. The shift is proportional to the intensity of the laser beam and yields oppositely signed values for left- and right-circularly polarized light, CPL -/+, respectively. Rapid switching -- in the NMR time scale -- between CPL+ and CPL- gives rise to a splitting of the NMR resonance lines. We present uncorrelated and correlated quadratic response calculations of the splitting per unit of beam intensity in the NMR spectra of $^{21}$Ne, $^{83}$Kr, and $^{129}$Xe. We study both the regions far away from and near to optical resonance and predict off-resonance shifts of the order 0.01, 0.1, and $1\times 10^{-6}$ Hz for $^{21}$Ne, $^{83}$Kr, and $^{129}$Xe, respectively, for a beam intensity of 10 W/cm$^2$. Enhancement by several orders of magnitude is predicted as the beam frequency approaches resonance. Only then can the effect on guest $^{129}$Xe atoms be potentially useful as a probe of the properties of the host material.

physics.atom-ph