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Enhanced magnetism derived from pore-edge spins in thin FeGeTenanomeshes. | LitMetric

Enhanced magnetism derived from pore-edge spins in thin FeGeTenanomeshes.

Nanotechnology

Faculty of Science and Engineering, Aoyama Gakuin University, 5-10-1 Fuchinobe, Sagamihara, Kanagawa 252-5258, Japan.

Published: September 2024

AI Article Synopsis

  • The emergence of two-dimensional van der Waals magnetic materials like FeGeTe (FGT) offers exciting prospects for new physical phenomena and applications.
  • Researchers have created a honeycomb-like nanomesh structure with zigzag pore edges on thin FGT flakes, which significantly boosts ferromagnetism compared to bulk flakes.
  • The study shows that non-oxidized edges enhance ferromagnetic behavior, while oxidized edges can induce antiferromagnetism, suggesting that FGT nanomeshes could be valuable in magnetic and spintronic technologies.

Article Abstract

The growth of two-dimensional van der Waals magnetic materials presents attractive opportunities for exploring new physical phenomena and valuable applications. Among these materials, FeGeTe(FGT) exhibits a variety of remarkable properties and has garnered significant attention. Herein, we have for the first time created a nanomesh structure-a honeycomb-like array of hexagonal nanopores-with the zigzag pore-edge atomic structure on thin FGT flakes with and without oxidation of the pore edges. It is revealed that the magnitude of ferromagnetism (FM) significantly increases in both samples compared with bulk flakes without nanomeshes. Critical temperature annealing results in the formation of zigzag pore edges and interpore zigzag-edge nanoribbons. We unveil that the non-oxide (O) termination of the Fe dangling bonds on these zigzag edges enhances FM behavior, while O-termination suppresses this FM by introducing antiferromagnetic behavior through edge O-Fe coupling. FGT nanomeshes hold promise for the creation of strong FM and their effective application in magnetic and spintronic systems.

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Source
http://dx.doi.org/10.1088/1361-6528/ad6fa2DOI Listing

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