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Phys Rev Lett. 2019 Jan 25;122(3):037202. doi: 10.1103/PhysRevLett.122.037202.

Electric Field Control of Spins in Molecular Magnets.

Physical review letters

Junjie Liu, Jakub Mrozek, William K Myers, Grigore A Timco, Richard E P Winpenny, Benjamin Kintzel, Winfried Plass, Arzhang Ardavan

Affiliations

  1. CAESR, Department of Physics, University of Oxford, The Clarendon Laboratory, Parks Road, Oxford OX1 3PU, United Kingdom.
  2. CAESR, Inorganic Chemistry Laboratory, University of Oxford, South Parks Road, Oxford OX1 3QR, United Kingdom.
  3. School of Chemistry and Photon Science Institute, The University of Manchester, Manchester, M13 9PL, United Kingdom.
  4. Institut für Anorganische und Analytische Chemie, Friedrich-Schiller-Universität Jena, Humboldtstraße 8, 07743 Jena, Germany.

PMID: 30735403 DOI: 10.1103/PhysRevLett.122.037202

Abstract

Coherent control of individual molecular spins in nanodevices is a pivotal prerequisite for fulfilling the potential promised by molecular spintronics. By applying electric field pulses during time-resolved electron spin resonance measurements, we measure the sensitivity of the spin in several antiferromagnetic molecular nanomagnets to external electric fields. We find a linear electric field dependence of the spin states in Cr_{7}Mn, an antiferromagnetic ring with a ground-state spin of S=1, and in a frustrated Cu_{3} triangle, both with coefficients of about 2  rad s^{-1}/V m^{-1}. Conversely, the antiferromagnetic ring Cr_{7}Ni, isomorphic with Cr_{7}Mn but with S=1/2, does not exhibit a detectable effect. We propose that the spin-electric field coupling may be used for selectively controlling individual molecules embedded in nanodevices.

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