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| Autores principales: | , , , , , |
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| Formato: | Preprint |
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2026
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| Acceso en línea: | https://arxiv.org/abs/2605.28509 |
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| author | Frenett, Alexander Gan, Dorothy Emtage, Nicholas Fouad, Monika Miki-Silva, Sebastian Wu, Xing |
| author_facet | Frenett, Alexander Gan, Dorothy Emtage, Nicholas Fouad, Monika Miki-Silva, Sebastian Wu, Xing |
| contents | Optical cycling refers to repeated excitation and spontaneous emission on an electronic transition in an atom or molecule. Optical cycling in molecules can enable a wide range of quantum control and readout techniques, but unfortunately it has only been demonstrated on a small class of alkali-like or alkaline-earth-like molecules. Thorium monoxide (ThO), a molecule used in one of the most precise permanent electron electric dipole moment (eEDM) searches (ACME[1]), does not fall into this category. In this work, we demonstrate the first optical cycling on this non-conventional class over a range of experimental parameter space, including laser intensity, polarization switching rate, and interaction time. We show that both the $J=1,2$ rotational levels of ThO molecule are capable of cycling 11(2) photons on average at 1.9(6) MHz and 2.3(7) MHz scattering rate, respectively, before population is lost to other vibronic levels. We outline a scheme to apply this demonstrated optical cycling in an ACME-style eEDM measurement, improving the detection efficiency by about tenfold compared to non-cycling fluorescence detection. This would lead to a threefold enhancement in the statistical sensitivity of the eEDM search. This optical cycling scheme can be further extended to scatter around 100 photons, which would enable a wider range of quantum control and sensing using ThO molecules.
[1] V. Andreev, D. G. Ang, D. DeMille, J. M. Doyle, G. Gabrielse, J. Haefner, N. R. Hutzler, Z. Lasner, C. Meisenhelder, B. R. O`Leary, C. D. Panda, A. D. West, E. P. West, and X. Wu, Nature 562, 355 (2018). |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2605_28509 |
| institution | arXiv |
| publishDate | 2026 |
| record_format | arxiv |
| spellingShingle | Optical cycling on thorium monoxide (ThO) for an improved test of fundamental symmetries Frenett, Alexander Gan, Dorothy Emtage, Nicholas Fouad, Monika Miki-Silva, Sebastian Wu, Xing Atomic Physics Optical cycling refers to repeated excitation and spontaneous emission on an electronic transition in an atom or molecule. Optical cycling in molecules can enable a wide range of quantum control and readout techniques, but unfortunately it has only been demonstrated on a small class of alkali-like or alkaline-earth-like molecules. Thorium monoxide (ThO), a molecule used in one of the most precise permanent electron electric dipole moment (eEDM) searches (ACME[1]), does not fall into this category. In this work, we demonstrate the first optical cycling on this non-conventional class over a range of experimental parameter space, including laser intensity, polarization switching rate, and interaction time. We show that both the $J=1,2$ rotational levels of ThO molecule are capable of cycling 11(2) photons on average at 1.9(6) MHz and 2.3(7) MHz scattering rate, respectively, before population is lost to other vibronic levels. We outline a scheme to apply this demonstrated optical cycling in an ACME-style eEDM measurement, improving the detection efficiency by about tenfold compared to non-cycling fluorescence detection. This would lead to a threefold enhancement in the statistical sensitivity of the eEDM search. This optical cycling scheme can be further extended to scatter around 100 photons, which would enable a wider range of quantum control and sensing using ThO molecules. [1] V. Andreev, D. G. Ang, D. DeMille, J. M. Doyle, G. Gabrielse, J. Haefner, N. R. Hutzler, Z. Lasner, C. Meisenhelder, B. R. O`Leary, C. D. Panda, A. D. West, E. P. West, and X. Wu, Nature 562, 355 (2018). |
| title | Optical cycling on thorium monoxide (ThO) for an improved test of fundamental symmetries |
| topic | Atomic Physics |
| url | https://arxiv.org/abs/2605.28509 |