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Atomic Spectroscopy with Twisted Photons: Separation of M1--E2 Mixed Multipoles

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arxiv 1801.03227 v1 pith:QQMOXTW2 submitted 2018-01-10 physics.atom-ph physics.opticsquant-ph

Atomic Spectroscopy with Twisted Photons: Separation of M1--E2 Mixed Multipoles

classification physics.atom-ph physics.opticsquant-ph
keywords atomicphotonsangularatommomentummultipolesphotoexcitationposition
verification ladder T0 review T1 audit T2 compute T3 formal T4 reserved
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We analyze atomic photoexcitation into the discrete states by twisted photons, or photons carrying extra orbital angular momentum along their direction of propagation. From the angular momentum and parity considerations, we are able to relate twisted-photon photoexcitation amplitudes to their plane-wave analogues, independently of the details of the atomic wave functions. We analyzed the photo-absorption cross sections of mixed-multipolarity $E2-M1$ transitions in ionized atoms and found fundamental differences coming from the photon topology. Our theoretical analysis demonstrates that it is possible to extract the relative transition rates of different multipolar contributions by measuring the photo-excitation rate as a function of the atom's position (or the impact parameter) with respect to the optical vortex center. The proposed technique for separation of multipoles can be implemented if the target's atom position is resolved with sub-wavelength accuracy, for example, with Paul traps. Numerical examples are presented for Boron-like highly-charged ions (HCI).

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Cited by 1 Pith paper

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  1. An Al$^+$ clock with $1.6\times10^{-18}$ systematic uncertainty and its frequency ratios

    physics.atom-ph 2026-06 unverdicted novelty 5.0

    An Al+ single-ion clock is evaluated at 1.6×10^{-18} systematic uncertainty with absolute frequency 1121015393207859.19(24) Hz and ratio to Sr clock of 2.611701431781462668(36).