Antiphase resonance at X-ray irradiated microregions in amorphous Fe80B20 stripes
We report on the induction, through X-ray irradiation, of local anisotropy modifications in amorphous Fe80B20 stripes prepared by laser lithography from 15 nm thick films deposited by pulsed laser ablation. Those anisotropy modifications, taking place in a zone having a dimension of 15 μm around the...
| Autores: | , , , , , , , , , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2021 |
| País: | España |
| Institución: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositorio: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/377529 |
| Acceso en línea: | http://hdl.handle.net/10261/377529 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85084797767&doi=10.1016%2fj.jmmm.2020.167017&partnerID=40&md5=10be198c0826cf952fb6eb4b96341849 |
| Access Level: | acceso abierto |
| Palabra clave: | Amorphous Fe80B20 Anisotropy induction Ferromagnetic resonance Kerr microscopy inhomogeneous X-ray irradiation |
| Sumario: | We report on the induction, through X-ray irradiation, of local anisotropy modifications in amorphous Fe80B20 stripes prepared by laser lithography from 15 nm thick films deposited by pulsed laser ablation. Those anisotropy modifications, taking place in a zone having a dimension of 15 μm around the X-ray beam (2 µm width) incidence area center point, lead to an effective transverse-to-the-stripe long axis local magnetic easy axis that can be exploited to stably localize a 180° domain wall, in remanence after saturation with a transverse-to the stripe easy axis dc field. Upon stabilizing that wall it is possible to excite spatially inhomogeneous ferromagnetic resonances nearby the irradiated region (IR). The time dependencies of the magnetization precession at both sides of the IR exhibit a uniform phase shift of 180° over distances of the order of 20 μm from the stabilized domain wall. © 2020 Elsevier B.V. |
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