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Physical Review A

Polarization transfer in a spin-exchange optical-pumping experiment

Jyrki Rantaharju, Matti Hanni, Juha Vaara

Published Sep 14, 2020• 5 citations
Publisher

Abstract

Spin-exchange optical pumping (SEOP) enables hyperpolarization of magnetic noble gas nuclei and allows enormously enhanced signal in nuclear magnetic resonance studies in materials, biosciences, and medicine. We model the dynamics of the SEOP process taking place in a $\mathrm{Rb}\ensuremath{-}^{129}\mathrm{Xe}$ gas mixture and shed light on how the different microscopic processes influence the macroscopic polarization transfer. For each Rb-Xe collision taking place in simulated molecular dynamics trajectory, we sample a time series of quantum-chemically preparametrized Hamiltonians. Combined electron and nuclear spin dynamics of each event is propagated by solving the corresponding Liouville--von Neumann equation. The rarely occurring, long-lived van der Waals molecules are seen to give the most significant contribution to polarization transfer under the simulated conditions ($T=300$ K, $p=2.4$ bar), in agreement with earlier findings. Besides the lifetime of the collision complex, the average and minimum Rb-Xe interatomic distances characterize the efficiency of the polarization transfer events. We obtain insight into magnetization transfer in both individual binary collisions and van der Waals complexes and demonstrate a stepwise buildup of $^{129}\mathrm{Xe}$ spin polarization upon bond-length oscillations in the latter.

DOI
10.1103/physreva.102.032813

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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

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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 $\hatρ(t)$ 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 $\hatρ(t)$ 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.

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Efficiency of Spin Exchange between Rubidium Spins and Xe129 Nuclei in a Gas

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Theory of spin-exchange optical pumping of 3 He and 129 Xe

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We present a comprehensive theory of nuclear spin polarization of ${}^{3}\mathrm{He}$ and ${}^{129}\mathrm{Xe}$ gases by spin-exchange collisions with optically pumped alkali-metal vapors. The most important physical processes considered are (1) spin-conserving spin-exchange collisions between like or unlike alkali-metal atoms; (2) spin-destroying collisions of the alkali-metal atoms with each other and with buffer-gas atoms; (3) electron-nuclear spin-exchange collisions between alkali-metal atoms and ${}^{3}\mathrm{He}$ or ${}^{129}\mathrm{Xe}$ atoms; (4) spin interactions in van der Waals molecules consisting of a Xe atom bound to an alkali-metal atom; (5) optical pumping by laser photons; (6) spatial diffusion. The static magnetic field is assumed to be small enough that the nuclear spin of the alkali-metal atom is well coupled to the electron spin and the total spin is very nearly a good quantum number. Conditions appropriate for the production of large quantities of spin-polarized ${}^{3}\mathrm{He}$ or ${}^{129}\mathrm{Xe}$ gas are assumed, namely, atmospheres of gas pressure and nearly complete quenching of the optically excited alkali-metal atoms by collisions with ${\mathrm{N}}_{2}$ or ${\mathrm{H}}_{2}$ gas. Some of the more important results of this work are as follows: (1) Most of the pumping and relaxation processes are sudden with respect to the nuclear polarization. Consequently, the steady-state population distribution of alkali-metal atoms is well described by a spin temperature, whether the rate of spin-exchange collisions between alkali-metal atoms is large or small compared to the optical pumping rate or the collisional spin-relaxation rates. (2) The population distributions that characterize the response to sudden changes in the intensity of the pumping light are not described by a spin temperature, except in the limit of very rapid spin exchange. (3) Expressions given for the radio-frequency (rf) resonance linewidths and areas can be used to make reliable estimates of the local spin polarization of the alkali-metal atoms. (4) Diffusion effects for these high-pressure conditions are mainly limited to thin layers at the cell surface and at internal resonant surfaces generated by radio-frequency magnetic fields when the static magnetic field has substantial spatial inhomogeneities. The highly localized effects of diffusion at these surfaces are described with closed-form analytic functions instead of the spatial eigenmode expansions that are appropriate for lower-pressure cells.

Physical Review A•Aug 1, 1998•443 citations
Spin-exchange optical pumping (SEOP) enables hyperpolarization of magnetic noble gas nuclei and allows enormously enhanced signal in nuclear magnetic resonance studies in materials, biosciences, and medicine. We model the dynamics of the SEOP process taking place in a Rb\ensuremath−129Xe\mathrm{Rb}\ensuremath{-}^{129}\mathrm{Xe}Rb\ensuremath−129Xe gas mixture and shed light on how the different microscopic processes influence the macroscopic polarization transfer. For each Rb-Xe collision taking place in simulated molecular dynamics trajectory, we sample a time series of quantum-chemically preparametrized Hamiltonians. Combined electron and nuclear spin dynamics of each event is propagated by solving the corresponding Liouville--von Neumann equation. The rarely occurring, long-lived van der Waals molecules are seen to give the most significant contribution to polarization transfer under the simulated conditions (T=300T=300T=300 K, p=2.4p=2.4p=2.4 bar), in agreement with earlier findings. Besides the lifetime of the collision complex, the average and minimum Rb-Xe interatomic distances characterize the efficiency of the polarization transfer events. We obtain insight into magnetization transfer in both individual binary collisions and van der Waals complexes and demonstrate a stepwise buildup of 129Xe^{129}\mathrm{Xe}129Xe spin polarization upon bond-length oscillations in the latter.
Analytical model for polarization transfer during gas-phase collision events in spin-exchange optical pumping: Spin-12\frac{1}{2}21​ 129^{129}129Xe versus spin-32\frac{3}{2}23​ 131^{131}131Xe
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=1/2I = 1/2I=1/2 nuclei, such as 129Xe, is relatively well understood, that of spin I>1/2I > 1/2I>1/2 nuclei, such as 131Xe (I=3/2I = 3/2I=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 ρ^(t)\hatρ(t)ρ^​(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 ρ^(t)\hatρ(t)ρ^​(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.
Abstract Efficient production of hyperpolarized 129 Xe at clinically relevant output levels remains an important challenge for spin-exchange optical pumping (SEOP). In this work, we report a comparative experimental study of Cs– 129 Xe and Rb– 129 Xe SEOP. The spin-exchange and spin-relaxation rates are measured and separated into binary-collision and van der Waals (vdW) molecular contributions. The resulting parameter set shows that long-lived vdW interactions enhance the intrinsic spin-exchange efficiency within a narrow pressure window, with Cs exhibiting a modest advantage over Rb under comparable conditions. Using these experimentally constrained quantities in a device-level model, we predict that clinically relevant 129 Xe polarization levels and throughput could be achievable at pump powers near 5 W.
We experimentally study the Rb-Xe spin-exchange optical pumping process. The dependence of the spin-exchange rate on the intensity of the pumping light is measured at different temperatures under low magnetic fields. We demonstrate that the spin-exchange rate will decrease as the Rb spin polarization increases, which agrees well with the theoretical prediction. In our measurement, three spin exchange and spin relaxation mechanisms, namely, the spin exchange rates between Rb and Xe atoms caused by van der Waals molecule (${\mathrm{\ensuremath{\Gamma}}}_{\mathrm{vdW}}$) and binary collision (${\mathrm{\ensuremath{\Gamma}}}_{\mathrm{bin}}$) processes, and the spin relaxation rate due to the wall collision of Xe atoms (${\mathrm{\ensuremath{\Gamma}}}_{\mathrm{w}}$), have comparable magnitudes. These rates are extracted separately from the measured data with different Rb spin polarization at various temperatures. Our work provides a comprehensive confirmation of the physical picture of the spin-exchange optical pumping process.
We present a design for a spin-exchange optical pumping system to produce large quantities of highly polarized 129Xe and 131Xe. Low xenon concentrations in the flowing gas mixture which allow the laser to maintain high Cs polarization. The large spin-exchange rate between Cs and Xe through the long-lived van der Waals molecules at low pressure, combined with a high flow rate, results in large production rates of hyperpolarized xenon. The fast rates make it possible to obtain large nuclear polarizations after several minutes of optical pumping with a laser.At high Xe pressures. According to the theory, the longitudinal spin-elaxation rate 1T1 of Xe in a high-pressure sample containing only Xe and Cs vapor has the simple form is the velocity averaged binary spin-exchange cross section, It is the relaxation rate due to wall collisions and perhaps magnetic field inhomogeneities. Our results complement earlier studies performed at 129Xe pressures of about 20 Torr and 131Xe pressures of about 20 Torr and N2 pressures of 600 Torr . This work is useful for predicting spin-exchange rates between polarized Cs atoms and Xe nuclei.
By directly observing the nuclear polarization of 129Xe^{129}\mathrm{Xe}129Xe, the efficiency $\ensuremath{\eta}$ of spin exchange between optically pumped Rb spins and 129Xe^{129}\mathrm{Xe}129Xe nuclei has been measured. It is found that $\frac{1}{\ensuremath{\eta}}=23\ifmmode\pm\else\textpm\fi{}4$ rubidium D1{D}_{1}D1​ resonance-line photons are required to polarize a 129Xe^{129}\mathrm{Xe}129Xe nucleus when long-lived van der Waals molecules are unimportant. The binary spin-exchange cross section deduced from our measurements is ${\ensuremath{\sigma}}_{\mathrm{ex}}=(7.3\ifmmode\pm\else\textpm\fi{}1.1)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}21}$ cm2{\mathrm{cm}}^{2}cm2.
We present a comprehensive theory of nuclear spin polarization of 3He{}^{3}\mathrm{He}3He and 129Xe{}^{129}\mathrm{Xe}129Xe gases by spin-exchange collisions with optically pumped alkali-metal vapors. The most important physical processes considered are (1) spin-conserving spin-exchange collisions between like or unlike alkali-metal atoms; (2) spin-destroying collisions of the alkali-metal atoms with each other and with buffer-gas atoms; (3) electron-nuclear spin-exchange collisions between alkali-metal atoms and 3He{}^{3}\mathrm{He}3He or 129Xe{}^{129}\mathrm{Xe}129Xe atoms; (4) spin interactions in van der Waals molecules consisting of a Xe atom bound to an alkali-metal atom; (5) optical pumping by laser photons; (6) spatial diffusion. The static magnetic field is assumed to be small enough that the nuclear spin of the alkali-metal atom is well coupled to the electron spin and the total spin is very nearly a good quantum number. Conditions appropriate for the production of large quantities of spin-polarized 3He{}^{3}\mathrm{He}3He or 129Xe{}^{129}\mathrm{Xe}129Xe gas are assumed, namely, atmospheres of gas pressure and nearly complete quenching of the optically excited alkali-metal atoms by collisions with N2{\mathrm{N}}_{2}N2​ or H2{\mathrm{H}}_{2}H2​ gas. Some of the more important results of this work are as follows: (1) Most of the pumping and relaxation processes are sudden with respect to the nuclear polarization. Consequently, the steady-state population distribution of alkali-metal atoms is well described by a spin temperature, whether the rate of spin-exchange collisions between alkali-metal atoms is large or small compared to the optical pumping rate or the collisional spin-relaxation rates. (2) The population distributions that characterize the response to sudden changes in the intensity of the pumping light are not described by a spin temperature, except in the limit of very rapid spin exchange. (3) Expressions given for the radio-frequency (rf) resonance linewidths and areas can be used to make reliable estimates of the local spin polarization of the alkali-metal atoms. (4) Diffusion effects for these high-pressure conditions are mainly limited to thin layers at the cell surface and at internal resonant surfaces generated by radio-frequency magnetic fields when the static magnetic field has substantial spatial inhomogeneities. The highly localized effects of diffusion at these surfaces are described with closed-form analytic functions instead of the spatial eigenmode expansions that are appropriate for lower-pressure cells.