2019
DOI: 10.1134/s0021364019180036
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On the Search for the Electric Dipole Moment of the Electron: P-, T-Odd Faraday Effect on a PbF Molecular Beam

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Cited by 15 publications
(17 citation statements)
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“…We evaluated the effective electric fields for the PbF molecule. The effective electric fields in the PbF molecule were calculated within the relativistic coupled cluster with single, double and noniterative triple cluster amplitudes method using the Dirac-Coulomb Hamiltonian [19]. All electrons were included in the correlation treatment.…”
Section: P T -Odd Faraday Experiments On Moleculesmentioning
confidence: 99%
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“…We evaluated the effective electric fields for the PbF molecule. The effective electric fields in the PbF molecule were calculated within the relativistic coupled cluster with single, double and noniterative triple cluster amplitudes method using the Dirac-Coulomb Hamiltonian [19]. All electrons were included in the correlation treatment.…”
Section: P T -Odd Faraday Experiments On Moleculesmentioning
confidence: 99%
“…For extraction of the eEDM values from the experimental data, accurate theoretical calculations are required. These calculations were performed for Tl [8][9][10][11][12], for YbF [13][14][15][16], for PbF [17][18][19], for ThO [20][21][22][23], and for HfF + [24][25][26][27]. In the same experiments it is possible to search for another P, T -odd effect: P, T -odd electron-nucleus interaction [28][29][30].…”
Section: Introductionmentioning
confidence: 99%
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“…For now, the best experimental bound on the eEDM was obtained for diatomic molecule with closely spaced a) Electronic mail: zakharova.annet@gmail.com b) Electronic mail: igorkurchavov58@gmail.com c) Electronic mail: petrov an@pnpi.nrcki.ru Ω-doublets such as ThO [17][18][19][20][21][22] and HfF +23,24 . These experiments also put constraints on scalar-pseudoscalar nucleon-electron interaction 11,25,26 .…”
mentioning
confidence: 99%
“…Series Expansion and Bond Operator Approach.-For a complementary analysis of the evolution of the quantum disordered phases, starting from the limit of decoupled dimers, J ⊥ → ∞, we use both, series expansion (SE) [68] and bond operator theory (BOT) [56,69,70]. In BOT, spins at the vertices of each dimer are written as…”
mentioning
confidence: 99%