5 years ago

N\'{e}el Spin Orbit Torque driven antiferromagnetic resonance in Mn$_{2}$Au probed by time-domain THz spectroscopy.

M. Obergfell, D. Dominko, J. Cao, J. Sinova, M. Kläui, S.Y. Agustsson, V.Yu. Grigorev, M. Jourdan, S.Yu. Bodnar, J. Demsar, H.-J. Elmers, O. Gomonay, N. Bhattacharjee, A.A. Sapozhnik

We observe the excitation of collective modes in the THz range driven by the recently discovered N\'{e}el spin-orbit torques (NSOT) in the metallic antiferromagnet Mn$_{2}$Au. Temperature dependent THz spectroscopy reveals a strong absorption mode centered near 1 THz, which upon heating from 4 K to 450 K softens and looses intensity. Comparison with the estimated eigenmode frequencies implies that the observed mode is an in-plane antiferromagnetic resonance (AFMR) mode. The AFMR absorption strength exceeds those found in antiferromagnetic insulators, driven by the magnetic field of the THz radiation, by three orders of magnitude. Based on this and the agreement with our theory modelling, we infer that the driving mechanism for the observed mode is the current induced NSOT. This electric manipulation of the Ne\'{e}l order parameter at high frequencies makes Mn$_{2}$Au a prime candidate for AFM ultrafast memory applications.

Publisher URL: http://arxiv.org/abs/1802.03199

DOI: arXiv:1802.03199v1

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.