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arXiv:2601.20062

Comment on "Determining angle of arrival of radio-frequency fields using subwavelength, amplitude-only measurements of standing waves in a Rydberg atom sensor"

M. Chilcott, N. Kjærgaard

quant-phphysics.atom-phSubmitted Jan 27, 2026• Announced Jan 29, 2026
v1 · Jan 27, 2026v2 · Jun 9, 2026
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Abstract

We discuss the consequence of excluding allowed RF-transition between substates of a field-dressed Rydberg manifold when predicting the spectrum that will be observed if the dressed system is probed in an optical EIT scheme.
Journal reference
Journal of Applied Physics 139, 226101 (2026)
DOI
10.1063/5.0310791
Comments
Comment on arXiv:2502.09835 published in J. Appl. Phys. 138, 114402 (2025). The following article has been submitted to Journal of Applied Physics

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We demonstrate a method for determining the magnitude of the angle of arrival (AoA) of a linearly polarized radio-frequency (RF) field using the angle-dependent spectral amplitudes of AC Stark-shifted electromagnetically induced transparency (EIT) resonances. An off-resonant RF field produces distinct Stark shifts of the ∣mJ∣|m_J|∣mJ​∣ sublevels, while their relative excitation strengths depend strongly on the relative orientation of the RF and optical polarizations. Under the controlled polarization geometry considered here, this dependence enables determination of the AoA magnitude without requiring RF phase measurements or spatially separated sensing locations. We experimentally demonstrate the method at RF frequencies of 1.27 GHz, 2 GHz, 3 GHz, and 4 GHz using a subwavelength cesium vapor cell. Within the 20∘−40∘20^\circ-40^\circ20∘−40∘ region of highest angular sensitivity, the estimated repeatability-based 1σ1σ1σ AoA uncertainty ranges from approximately 0.6∘0.6^\circ0.6∘ to 2∘2^\circ2∘ across the investigated RF frequencies. A model combining Floquet-Shirley calculations of the RF-dressed Rydberg states with a coherent hyperfine-to-fine-structure optical excitation model qualitatively reproduces the experimental observations. These results establish a path toward compact, phase-independent AoA sensing using spatially localized Rydberg-atom spectroscopy.