IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v10y2019i1d10.1038_s41467-019-11761-1.html
   My bibliography  Save this article

Measurement of the variation of electron-to-proton mass ratio using ultracold molecules produced from laser-cooled atoms

Author

Listed:
  • J. Kobayashi

    (Kyoto University
    PRESTO, Japan Science and Technology Agency)

  • A. Ogino

    (University of Tokyo)

  • S. Inouye

    (Osaka City University
    Osaka City University)

Abstract

Experimental techniques to manipulate cold molecules have seen great development in recent years. The precision measurements of cold molecules are expected to give insights into fundamental physics. Here we use a rovibrationally pure sample of ultracold KRb molecules to improve the measurement on the stability of electron-to-proton mass ratio $$\left( {\mu = \frac{{m_{\mathrm{e}}}}{{M_{\mathrm{p}}}}} \right)$$ μ = m e M p . The measurement is based upon a large sensitivity coefficient of the molecular spectroscopy, which utilizes a transition between a nearly degenerate pair of vibrational levels each associated with a different electronic potential. Observed limit on temporal variation of μ is $$\frac{1}{\mu }\frac{{d\mu }}{{dt}} = (0.30 \pm 1.0) \times 10^{ - 14} \, {\mathrm{year}}^{ - 1}$$ 1 μ d μ d t = ( 0.30 ± 1.0 ) × 1 0 - 14 year - 1 , which is better by a factor of five compared with the most stringent laboratory molecular limits to date. Further improvements should be straightforward, because our measurement was only limited by statistical errors.

Suggested Citation

  • J. Kobayashi & A. Ogino & S. Inouye, 2019. "Measurement of the variation of electron-to-proton mass ratio using ultracold molecules produced from laser-cooled atoms," Nature Communications, Nature, vol. 10(1), pages 1-5, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-11761-1
    DOI: 10.1038/s41467-019-11761-1
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-019-11761-1
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-019-11761-1?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-11761-1. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.