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  Magnetization switching in ferromagnets by adsorbed chiral molecules without current or external magnetic field

Ben Dor, O., Yochelis, S., Radko, A., Vankayala, K., Capua, E., Capua, A., et al. (2017). Magnetization switching in ferromagnets by adsorbed chiral molecules without current or external magnetic field. Nature Communications, 8: 14567. doi:10.1038/ncomms14567.

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Ben Dor, O.1, Author
Yochelis, S.1, Author
Radko, A.1, Author
Vankayala, K.1, Author
Capua, E.1, Author
Capua, A.1, Author
Yang, S. H.1, Author
Baczewski, L. T.1, Author
Parkin, Stuart Stephen Papworth2, Author                 
Naaman, R.1, Author
Paltiel, Y.1, Author
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1External Organizations, ou_persistent22              
2Nano-Systems from Ions, Spins and Electrons, Max Planck Institute of Microstructure Physics, Max Planck Society, ou_3287476              

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 Abstract: Ferromagnets are commonly magnetized by either external magnetic fields or spin polarized currents. The manipulation of magnetization by spin-current occurs through the spin-transfer-torque effect, which is applied, for example, in modern magnetoresistive random access memory. However, the current density required for the spin-transfer torque is of the order of 1 × 106 A·cm−2, or about 1 × 1025 electrons s−1 cm−2. This relatively high current density significantly affects the devices’ structure and performance. Here we demonstrate magnetization switching of ferromagnetic thin layers that is induced solely by adsorption of chiral molecules. In this case, about 1013 electrons per cm2 are sufficient to induce magnetization reversal. The direction of the magnetization depends on the handedness of the adsorbed chiral molecules. Local magnetization switching is achieved by adsorbing a chiral self-assembled molecular monolayer on a gold-coated ferromagnetic layer with perpendicular magnetic anisotropy. These results present a simple low-power magnetization mechanism when operating at ambient conditions.

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 Dates: 2017-02-23
 Publication Status: Published online
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 Identifiers: BibTex Citekey: P13164
DOI: 10.1038/ncomms14567
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Title: Nature Communications
  Abbreviation : Nat. Commun.
Source Genre: Journal
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Publ. Info: London : Nature Publishing Group
Pages: - Volume / Issue: 8 Sequence Number: 14567 Start / End Page: - Identifier: ISSN: 2041-1723
CoNE: https://pure.mpg.de/cone/journals/resource/2041-1723