No Arabic abstract
Recently, the production of ultrahigh-density (~10^{19}cm^{-3}) spin-polarized deuterium (SPD) atoms was demonstrated, from the photodissociation of deuterium iodide, but the upper density limit was not determined. Here, we present studies of spin-polarized hydrogen (SPH) densities up to 10^{20} cm^{-3}, by photodissociating 5 bar of hydrogen chloride with a focused 213 nm, 150 ps laser pulse. We extract the depolarization cross-section of hydrogen and chlorine atom collisions, which is the main depolarization mechanism at this high-density regime, to be {sigma}_{HCl} = 7(2) x 10^{-17}cm^2. We discuss the conditions under which the ultrahigh SPH and SPD densities can be reached, and the potential applications to ultrafast magnetometry, laser-ion acceleration, and tests of polarized nuclear fusion.
We measure nuclear and electron spin-polarized H and D densities of at least 10$^{19}, cm^{-3}$ with $sim$10 ns lifetimes, from the photodissociation of HBr and DI with circularly-polarized UV light pulses. This density is $sim$6 orders of magnitude higher than that produced by conventional continuous-production methods, and, surprisingly, at least 100 times higher than expected densities for this photodissociation method. We observe the hyperfine quantum beating of the H and D magnetization with a pick-up coil, i.e., the respective 0.7 and 3 ns periodic transfer of polarization from the electrons to the nuclei and back. The $rm{10^{19},cm^{-3}}$ spin-polarized H and D density is sufficient for laser-driven ion acceleration of spin polarized electrons, protons, or deuterons, the preparation of nuclear-spin-polarized molecules, and for the demonstration of spin-polarized D-T or D-$rm{{^3He}}$ laser fusion, for which a reactivity enhancement of $rm{sim50%}$ is expected.
Simulations of the generation of the atomic polarization is necessary for interpreting the second solar spectrum. For this purpose, it is important to rigorously determine the effects of the isotropic collisions with neutral hydrogen on the atomic polarization of the neutral atoms, ionized atoms and molecules. Our aim is to treat in generality the problem of depolarizing isotropic collisions between singly ionized atoms and neutral hydrogen in its ground state. Using our numerical code, we computed the collisional depolarization rates of the $p$-levels of ions for large number of values of the effective principal quantum number $n^{*}$ and the Unsold energy $E_p$. Then, genetic programming has been utilized to fit the available depolarization rates. As a result, strongly non-linear relationships between the collisional depolarization rates, $n^{*}$ and $E_p$ are obtained, and are shown to reproduce the original data with accuracy clearly better than 10%. These relationships allow quick calculations of the depolarizing collisional rates of any simple ion which is very useful for the solar physics community. In addition, the depolarization rates associated to the complex ions and to the hyperfine levels can be easily derived from our results. In this work we have shown that by using powerful numerical approach and our collisional method, general model giving the depolarization of the ions can be obtained to be exploited for solar applications.
In a recent publication [arXiv:2010.14579], we introduced a new type of atomic magnetometer, which relies on hydrohalide photo-dissociation to create high-density spin-polarized hydrogen. Here, we extend our previous work and present a detailed theoretical analysis of the magnetometer signal and its dependence on time. We also derive the sensitivity for a spin-projection noise limited magnetometer, which can be applied to an arbitrary magnetic field waveform.
We present a new evaluation of an 87Sr optical lattice clock using spin polarized atoms. The frequency of the 1S0-3P0 clock transition is found to be 429 228 004 229 873.6 Hz with a fractional accuracy of 2.6 10^{-15}, a value that is comparable to the frequency difference between the various primary standards throughout the world. This measurement is in excellent agreement with a previous one of similar accuracy.
We present calculations of spin-relaxation rates of alkali-metal atoms due to the spin-axis interaction acting in binary collisions between the atoms. We show that for the high-temperature conditions of interest here, the spin relaxation rates calculated with classical-path trajectories are nearly the same as those calculated with the distorted-wave Born approximation. We compare these calculations to recent experiments that used magnetic decoupling to isolate spin relaxation due to binary collisions from that due to the formation of triplet van-der-Waals molecules. The values of the spin-axis coupling coefficients deduced from measurements of binary collision rates are consistent with those deduced from molecular decoupling experiments. All the experimental data is consistent with a simple and physically plausible scaling law for the spin-axis coupling coefficients.