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Cooling of a Zero-Nuclear-Spin Molecular Ion to a Selected Rotational State
We demonstrate rotational cooling of the silicon monoxide cation via optical pumping by a spectrally filtered broadband laser. Compared with diatomic hydrides, SiO\+ is more challenging to cool because of its smaller rotational interval. However, the rotational level spacing and large dipole moment...
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Published in: | arXiv.org 2020-07 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | We demonstrate rotational cooling of the silicon monoxide cation via optical pumping by a spectrally filtered broadband laser. Compared with diatomic hydrides, SiO\+ is more challenging to cool because of its smaller rotational interval. However, the rotational level spacing and large dipole moment of SiO\+ allows direct manipulation by microwaves, and the absence of hyperfine structure in its dominant isotopologue greatly reduces demands for pure quantum state preparation. These features make \(^{28}\)Si\(^{16}\)O\+ a good candidate for future applications such as quantum information processing. Cooling to the ground rotational state is achieved on a 100 ms time scale and attains a population of 94(3)\%, with an equivalent temperature \(T=0.53(6)\) K. We also describe a novel spectral-filtering approach to cool into arbitrary rotational states and use it to demonstrate a narrow rotational population distribution (\(N\pm1\)) around a selected state. |
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ISSN: | 2331-8422 |
DOI: | 10.48550/arxiv.2005.06638 |