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arXiv:2308.00888 · Journal of Physics B Atomic Molecular and Optical Physics

Hyperfine transition induced by atomic motion above a paraffin-coated magnetic film

Naota Sekiguchi, Hiroaki Usui, A. Hatakeyama

Published Sep 27, 2023• 2 citations
arXivHTMLPDF

Abstract

Abstract We measured transitions between the hyperfine levels of the electronic ground state of potassium-39 atoms (transition frequency: 460 MHz) as the atoms moved through a periodic magneto-static field produced above the magnetic-stripe domains of a magnetic film. The period length of the magnetic field was 3.8 µm. The atoms were incident to the field as an impinging beam with the most probable velocity of 550 m s−1 and experienced a peak oscillating field of 20 mT. Unwanted spin relaxation caused by the collisions of the atoms with the film surface was suppressed by the paraffin coating on the film. We observed increasing hyperfine transition probabilities as the frequency of the field oscillations experienced by the atoms increased from 0 to 140 MHz for the atomic velocity of 550 m s−1, by changing the incident angle of the atomic beam with respect to the stripe domains. Numerical calculation of the time evolution of the hyperfine states revealed that the oscillating magnetic field experienced by the atoms induced the hyperfine transitions, and the main process was not a single-quantum transition but rather multi-quanta transitions.

DOI
10.1088/1361-6455/acfde5

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Abstract We measured transitions between the hyperfine levels of the electronic ground state of potassium-39 atoms (transition frequency: 460 MHz) as the atoms moved through a periodic magneto-static field produced above the magnetic-stripe domains of a magnetic film. The period length of the magnetic field was 3.8 µm. The atoms were incident to the field as an impinging beam with the most probable velocity of 550 m s−1 and experienced a peak oscillating field of 20 mT. Unwanted spin relaxation caused by the collisions of the atoms with the film surface was suppressed by the paraffin coating on the film. We observed increasing hyperfine transition probabilities as the frequency of the field oscillations experienced by the atoms increased from 0 to 140 MHz for the atomic velocity of 550 m s−1, by changing the incident angle of the atomic beam with respect to the stripe domains. Numerical calculation of the time evolution of the hyperfine states revealed that the oscillating magnetic field experienced by the atoms induced the hyperfine transitions, and the main process was not a single-quantum transition but rather multi-quanta transitions.
Nonlinear magneto-optical Faraday rotation (NMOR) on the potassium D1 and D2 lines was used to study Zeeman relaxation rates in an antirelaxation paraffin-coated $3\text{\ensuremath{-}}\mathrm{cm}$-diameter potassium vapor cell. Intrinsic Zeeman relaxation rates of ${\ensuremath{\gamma}}^{NMOR}∕2\ensuremath{\pi}=2.0(6)\phantom{\rule{0.3em}{0ex}}\mathrm{Hz}$ were observed. The relatively small hyperfine intervals in potassium lead to significant differences in NMOR in potassium compared to rubidium and cesium. Using laser optical pumping, widths and frequency shifts were also determined for transitions between ground-state hyperfine sublevels of 39K^{39}\mathrm{K}39K atoms contained in the same paraffin-coated cell. The intrinsic hyperfine relaxation rate of ${\ensuremath{\gamma}}_{\mathit{expt}}^{\mathit{hf}}∕2\ensuremath{\pi}=10.6(7)\phantom{\rule{0.3em}{0ex}}\mathrm{Hz}$ and a shift of $\ensuremath{-}9.1(2)\phantom{\rule{0.3em}{0ex}}\mathrm{Hz}$ were observed. These results show that adiabatic relaxation gives only a small contribution to the overall hyperfine relaxation in the case of potassium, and the relaxation is dominated by other mechanisms similar to those observed in previous studies with rubidium.
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An atom moving in a spatially periodic field experiences a temporally periodic perturbation and undergoes a resonance transition between atomic internal states when the transition frequency is equal to the atomic velocity divided by the field period. We demonstrated that spin nutation was induced by this resonant transition in a polarized rubidium (Rb) atomic beam passing through a magnetic lattice. The lattice was produced by current flowing through an array of parallel wires crossing the beam. This array structure, reminiscent of a multiwire chamber for particle detection, allowed the Rb beam to pass through the lattice at a variety of incident angles. The dephasing of spin nutation was reduced by varying the incident angle.
Abstract Selective reflection of a laser radiation from an interface formed by a dielectric window and a potassium atomic vapour confined in a nano-cell with 350 nm gap thickness is implemented for the first time to study the atomic transitions of K D 2 line in external magnetic fields. In moderate B -fields, there are 44 individual Zeeman transitions which reduce to two groups (one formed by σ + , the other one by σ − circularly-polarised light), each containing eight atomic transitions, as the magnetic field increases. Each of these groups contains one so-called ‘guiding’ transition whose particularities are to have a probability (intensity) as well as a frequency shift slope (in MHz G −1 ) that are constant in the whole range of 0–10 kG magnetic fields. In the case of π -polarised laser radiation, among eight transitions, two are forbidden at B = 0, yet their probabilities undergo a giant modification under the influence of a magnetic field. We demonstrate that for B -fields > 165 G a complete hyperfine Paschen–Back regime is observed. Other peculiarities of K D 2 line behaviour in magnetic field are also presented. We show a very good agreement between theoretical calculations and experiments. The recording of the hyperfine Paschen–Back regime of K D 2 line with high spectral resolution is demonstrated for the first time.
We demonstrate that transitions between Zeeman-split sublevels of Rb atoms are resonantly induced by the motion of the atoms (velocity: approximately 100 m/s) in a periodic magnetostatic field (period: 1 mm) when the Zeeman splitting corresponds to the frequency of the magnetic field experienced by the moving atoms. A circularly polarized laser beam polarizes Rb atoms with a velocity selected using the Doppler effect and detects their magnetic resonance in a thin cell, to which the periodic field is applied with the arrays of parallel current-carrying wires.
Abstract The “mixing” of magnetic sublevels of the ground and excited levels of an atomic transition with magnetic sublevels of a nearby transition (in the hyperfine structure of atoms of alkali metals) is responsible for a strong modification of its probability. A dramatic manifestation of this mixing effect is a huge increase in the probability of the atomic transition in magnetic fields that is forbidden by selection rules in zero magnetic field B = 0; the latter is called a magnetically induced (MI) transition. Two MI transitions with different dependences on B have been studied. Another dramatic manifestation of the mixing effect is that there are atomic transitions whose frequency is practically fixed in a wide range of magnetic fields, i.e., the slope S [MHz/G] of the frequency shifts as a function of B is practically zero, with the transition probability being significant. We call these transitions “unmoved” transitions (UTs). We have studied the UTs of 87Rb atoms, the D2 line, |1, +1〉 → |1', +1'〉 and Cs atoms, the D2 line, |3, –3〉 → |5', –4'〉, where the quantum numbers F and mF of the excited and ground levels are marked with and without primes, respectively. We show that in the range B = 180–705 G for 87Rb, the D2 line, |S| ≤ 0.03 MHz/G; for comparison, S ≈ 3.6 MHz/G for 87Rb in the same B range for the MI transition |1, +1〉 → |3', +2'〉 is greater by a factor of 120. A second laser was used to control the UT amplitude. Our theoretical model describes well the experiment.