Role of the interfaces in the crystallization and hysteresis mechanisms of amorphous Fe-B thin films
Creators
- 1. POEMMA-CEMDATIC, Escuela Técnica Superior de Ingenieros de Telecomunicación-Universidad Politécnica de Madrid, 28040 Madrid (Spain)
- 2. Instituto de Ciencia de Materiales de Madrid (ICMM), A.E. Consejo Superior de Investigaciones Científicas (CSIC), 28049 Madrid (Spain)
- 3. Laboratorio de Microscopias Avanzadas (LMA), Universidad de Zaragoza, 50018 Zaragoza (Spain)
- 4. Instituto de Nanociencia y Materiales de Aragon (INMA), A.E. Consejo Superior de Investigaciones Científicas (CSIC), Universidad de Zaragoza, 50009 Zaragoza (Spain)
- 5. Institute of Natural Sciences, Ural Federal University, 620002 Ekaterinburg (Russian Federation)
- 6. Leibniz Institute for Solid State and Materials Research (IFW) Dresden, Institute for Metallic Materials, Helmholtzstrasse 20, D-01069 Dresden (Germany)
- 7. Institute for Material Science, TU Dresden, 01062 Dresden (Germany)
Description
Highlights: • Amorphous Fe‐B thin films deposited by pulsed laser ablation for the first time. • Highly homogeneous, weak magnetic anisotropy. • No pinning involved in the magnetization reversal mechanism. • Crystallization temperature 150–250 °C lower than other Fe‐B alloys. • Negligible coercivity increase during the early crystallization stages. -- Abstract: In this work we study the crystallization processes of two sets of amorphous Fe80B20 films fabricated by Pulsed Laser Ablation Deposition on substrates with different nature, Corning glass® and MgO(001). We analyze their magnetic hysteresis mechanisms by means of magneto-optic techniques and Transmission Electron Microscopy. The as-deposited amorphous films present a highly homogeneous uniaxial magnetic anisotropy with the easy axis orientation dependent on the type of substrate and much weaker than that of bulk alloys with similar composition. The onset of crystallization for the films deposited on glass and MgO appears, respectively, at temperatures 150 °C and 250 °C below that of their bulk counterparts. We study the role of the substrate in the crystallization mechanism and the resulting nanostructure of the magnetic films. While the crystallization of the MgO-deposited films proceeds in a broad front growing from the substrate to the surface, that of the glass-deposited films takes place through the nucleation and growth of isolated crystallites. We analyze the evolution of the coercivity during the crystallization of the films. It follows a similar trend for both types, remaining in values close to those of the amorphous precursors until it rises steeply at a given annealing temperature. The threshold of the steep coercivity increase of the glass-deposited films is shifted to lower temperatures with respect to the MgO ones, in spite of the higher crystallization onset temperature of the former. The coercivity mechanisms have been analyzed, correlated to the films interfacial characteristics and compared to those of bulk alloys.
Additional details
Identifiers
- DOI
- 10.1016/j.jallcom.2021.159276;
- PII
- S0925838821006848;
Publishing Information
- Journal Title
- Journal of Alloys and Compounds
- Journal Volume
- 869
- Journal Page Range
- vp.
- ISSN
- 0925-8388
- CODEN
- JALCEU
INIS
- Country of Publication
- Switzerland
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 55033911
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- ALLOYS; COERCIVE FORCE; CRYSTAL GROWTH; CRYSTALLIZATION; DEPOSITION; DEPOSITS; HYSTERESIS; IRON; MAGNESIUM OXIDES; MAGNETIZATION; SUBSTRATES; THIN FILMS; TRANSMISSION ELECTRON MICROSCOPY
- Descriptors DEC
- ALKALINE EARTH METAL COMPOUNDS; CHALCOGENIDES; ELECTRON MICROSCOPY; ELEMENTS; FILMS; MAGNESIUM COMPOUNDS; METALS; MICROSCOPY; OXIDES; OXYGEN COMPOUNDS; PHASE TRANSFORMATIONS; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2021 Elsevier B.V. All rights reserved.