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Ferroelectric control of magnetocrystalline anisotropy at cobalt/poly(vinylidene fluoride) interfaces.

ACS nano (2012-10-09)
Pavel V Lukashev, Tula R Paudel, Juan M López-Encarnación, Shireen Adenwalla, Evgeny Y Tsymbal, Julian P Velev
RESUMEN

Electric field control of magnetization is one of the promising avenues for achieving high-density energy-efficient magnetic data storage. Ferroelectric materials can be especially useful for that purpose as a source of very large switchable electric fields when interfaced with a ferromagnet. Organic ferroelectrics, such as poly(vinylidene fluoride) (PVDF), have an additional advantage of being weakly bonded to the ferromagnet, thus minimizing undesirable effects such as interface chemical modification and/or strain coupling. In this work we use first-principles density functional calculations of Co/PVDF heterostructures to demonstrate the effect of ferroelectric polarization of PVDF on the interface magnetocrystalline anisotropy that controls the magnetization orientation. We show that switching of the polarization direction alters the magnetocrystalline anisotropy energy of the adjacent Co layer by about 50%, driven by the modification of the screening charge induced by ferroelectric polarization. The effect is reduced with Co oxidation at the interface due to quenching the interface magnetization. Our results provide a new insight into the mechanism of the magnetoelectric coupling at organic ferroelectric/ferromagnet interfaces and suggest ways to achieve the desired functionality in practice.

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Sigma-Aldrich
Poly(vinylidene fluoride), average Mw ~534,000 by GPC, powder
Sigma-Aldrich
Poly(vinylidene fluoride), average Mw ~180,000 by GPC, average Mn ~71,000, beads or pellets
Sigma-Aldrich
Poly(vinylidene fluoride), average Mw ~530,000, pellets
Sigma-Aldrich
Poly(vinylidene fluoride), average Mw ~275,000 by GPC, average Mn ~107,000, pellets