No Arabic abstract
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.
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 demonstrate detection of a weak alternate-current magnetic field by application of the spin echo technique to F = 2 Bose-Einstein condensates. A magnetic field sensitivity of 12 pT/Hz^1/2 is attained with the atom number of 5*10^3 at spatial resolution of 99 mu m^2. Our observations indicate magnetic field fluctuations synchronous with the power supply line frequency. We show that this noise is greatly suppressed by application of a reverse phase magnetic field. Our technique is useful in order to create a stable magnetic field environment, which is an important requirement for atomic experiments which require a weak bias magnetic field.
We report the production of highly spin-polarized Deuterium atoms via photodissociation of deuterium iodide at 270 nm. The velocity distribution of both the deuterium and iodine photodissociation products is performed via velocity mapping slice-imaging. Additionally, the angular momentum polarization of the iodine products is studied using polarization-sensitive ionization schemes. The results are consistent with excitation of the $A^1Pi_1$ state followed by adiabatic dissociation. The process produces $sim$100% electronically polarized deuterium atoms at the time of dissociation, which is then converted to $sim 60%$ nuclear D polarization after $sim 1.6$ ns. These production times for hyperpolarized deuterium allow collision-limited densities of $sim 10^{18}$ cm$^{-3}$, which is $sim 10^6$ times higher than conventional (Stern-Gerlach separation) methods. We discuss how such high-density hyperpolarized deuterium atoms can be combined with laser fusion to measure polarized D-D fusion cross sections.
Optical properties of compressed fluid hydrogen in the region where dissociation and metallization is observed are computed by ab-initio methods and compared to recent experimental results. We confirm that above 3000 K both processes are continuous while below 1500K the first order phase transition is accompanied by a discontinuity of the DC conductivity and the thermal conductivity, while both the reflectivity and absorption coefficient vary rapidly but continuously. Our results support the recent analysis of NIF experiments (P. Celliers et al, Science 361, 677-682 (2018)) which assigned the inception of metallization to pressures where the reflectivity is about 0.3. Our results also support the conclusion that the temperature plateau seen in laser-heated DAC experiments at temperatures higher than 1500 K corresponds to the onset of of optical absorption, not to the phase transition.
Dissociation of molecular hydrogen by secondary electrons produced by cosmic ray or X-ray ionization plays a crucial role in the chemistry of the densest part of molecular clouds. Here we study the effect of the mean kinetic energy of secondary electrons on this process. We compare predictions using a range of secondary electron energies and predictions of the cross-sections with the values in the UMIST database. We find that the predicted column densities change by nearly one dex.