Abstract

Recently, we experimentally demonstrated that the nucleation and annihilation of µm-sized skyrmions in Pt/Co/AlOx trilayers can be controlled by tuning the perpendicular magnetic anisotropy with electric field gating [1]. Here, we show our present efforts to extend this concept to smaller skyrmions, down to 50 nm lateral size. Two trilayer systems, in which sub-100 nm skyrmions were observed at room temperature, were studied: Pt/Co/MgO [2] and Pt/Co/TbOx. The stacks were patterned by electron beam lithography and ion beam etching into stripes (1 – 50 µm width) then covered with a 10 nm thick ZrO2 dielectric layer and a 6 nm thick Pt top electrode to form capacitor-like structures, Fig (a). Using Magnetic Force Microscopy, Fig (b-c), we show that in both stacks, starting from a stable skyrmion network, a positive electric field (EF) leads to the increase of the PMA and to the annihilation of the skyrmion phase. We attribute this to the EF-induced migration of oxygen towards the top Co interface. This result is confirmed by the variation of the hysteresis loops taken with polar Magneto-Optical Kerr Effect, Fig (d). This new state persists after removing the EF i.e. EF-gating leads to a non-volatile effect. In the Pt/Co/MgO trilayer, the application of a negative EF shows no effect on the magnetic anisotropy, preventing us to renucleate the skyrmions. This irreversible process is probably due to the stabilization of the stochiometric MgO phase induced by oxygen ion migration towards the Co/MgO interface when a positive gating is applied. On the contrary, for Pt/Co/TbOx trilayers, the application of a negative EF triggered the oxygen ion migration away from the top Co interface. This allows us to tune reversibly the magnetic anisotropy, and therefore to reproducibly nucleate and annihilate 50 nm size skyrmions. This is an easily integrable and energetically efficient solution that might ease the use of magnetic skyrmions as information carriers in future spintronic devices.

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