Reversible electric-field manipulation of the adsorption morphology and magnetic anisotropy of small Fe and Co clusters on graphene

First-principles electronic calculations show how the adsorption morphology, orbital magnetism, and magnetic anisotropy energy (MAE) of small CoN and FeN clusters (N≤3) on graphene (G) can be reversibly controlled under the action of an external electric field (EF). A variety of cluster-specific and...

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Bibliographic Details
Published in:Physical review. B 2017-12, Vol.96 (22), Article 224413
Main Authors: Tanveer, M., Dorantes-Dávila, J., Pastor, G. M.
Format: Article
Language:English
Subjects:
Adsorption
Anisotropy
Clusters
Coercivity
Dimers
Dipole moments
Electric fields
First principles
Graphene
Magnetic anisotropy
Magnetic properties
Magnetism
Magnetization reversal
Morphology
Trimers
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Summary:First-principles electronic calculations show how the adsorption morphology, orbital magnetism, and magnetic anisotropy energy (MAE) of small CoN and FeN clusters (N≤3) on graphene (G) can be reversibly controlled under the action of an external electric field (EF). A variety of cluster-specific and EF-induced effects are revealed, including (i) perpendicular or canted adsorption configurations of the dimers and trimers, (ii) significant morphology-dependent permanent dipole moments and electric susceptibilities, (iii) EF-induced reversible transitions among the different metastable adsorption morphologies of Fe3 and Co3 on graphene, (iv) qualitative changes in the MAE landscape driven by structural changes, (v) colossal values of the magnetic anisotropy ΔE≃45 meV per atom in Co2/G, (vi) EF-induced spin-reorientation transitions in Co3/G, and (vii) reversibly tunable coercive field and blocking temperatures, which in some cases allow a barrierless magnetization reversal of the cluster. These remarkable electric and magnetic fingerprints open new possibilities of characterizing and exploiting the size- and structural-dependent properties of magnetic nanostructures at surfaces.
ISSN:2469-9950
2469-9969
DOI:10.1103/PhysRevB.96.224413