Effective manipulation of the magnetic properties of nanostructured metallic alloys, exhibiting intergrain porosity (i.e., channels) and conformally coated with insulating oxide nanolayers, with an electric field is demonstrated. Nanostructured Co-Pt films are grown by electrodeposition (ED) and subsequently coated with either AlOx or HfOx by atomic layer deposition (ALD) to promote magneto-ionic effects (i.e., voltage-driven ion migration) during electrolyte gating. Pronounced variations in coercivity (HC) and magnetic moment at saturation (mS) are found at room temperature after biasing the heterostructures. The application of a negative voltage results in a decrease of HC and an increase of mS, whereas the opposite trend is achieved for positive voltages. Although magneto-ionic phenomena are already observed in uncoated Co-Pt films (because of the inherent presence of oxygen), the ALD oxide nanocoatings serve to drastically enhance the magneto-ionic effects because of partially reversible oxygen migration, driven by voltage, across the interface between AlOx or HfOx and the nanostructured Co-Pt film. Co-Pt/HfOx heterostructures exhibit the most significant magneto-electric response at negative voltages, with an increase of mS up to 76% and a decrease of HC by 58%. The combination of a nanostructured magnetic alloy and a skinlike insulating oxide nanocoating is shown to be appealing to enhance magneto-ionic effects, potentially enabling electrolyte-gated magneto-ionic technology.
English
Magneto-ionic effects; Ion migration; Voltage control of magnetism; Co-Pt; Nanostructured material
European Commission 648454
Ministerio de Economía y Competitividad MAT2017-86357-C3-1-R
Ministerio de Economía y Competitividad MAT2017-83169-R
Ministerio de Economía y Competitividad SEV-2015-0496
Agència de Gestió d'Ajuts Universitaris i de Recerca 2017/SGR-292
Agència de Gestió d'Ajuts Universitaris i de Recerca 2017/SGR-1519
European Commission 665919
ACS applied materials & interfaces ; Vol. 12, Issue 12 (March 2020), p. 14484-14494
open access
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