In situ X-ray absorption spectroscopy study of the thermal behaviour of giant magnetoresistance CoxAg1-x and NixAg1-x heterogeneous alloys

Citation
O. Proux et al., In situ X-ray absorption spectroscopy study of the thermal behaviour of giant magnetoresistance CoxAg1-x and NixAg1-x heterogeneous alloys, EPJ-APPL PH, 9(2), 2000, pp. 115-124
Citations number
26
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science
Journal title
EUROPEAN PHYSICAL JOURNAL-APPLIED PHYSICS
ISSN journal
12860042 → ACNP
Volume
9
Issue
2
Year of publication
2000
Pages
115 - 124
Database
ISI
SICI code
1286-0042(200002)9:2<115:ISXASS>2.0.ZU;2-D
Abstract
Heterogeneous CoxAg1-x and NixAg1-x alloys have giant magnetoresistance pro perties. Such alloys, with atomic concentrations x = 0.20 and 0.37, were st udied by transmission X-ray Absorption Spectroscopy at the Co or Ni K-edge after in situ thermal annealing. For alloys as-deposited and annealed at 20 0 degrees C, Extended X-ray Absorption Fine Structure analysis displays bot h Go-Co (Ni-Ni) bonds related to Co (Ni) atoms agglomerated in magnetic par ticles and Co-Ag (Ni-Ag) bonds related to Co (Ni) atoms in substitutional s ites in the Ag matrix. At the same alloy concentration, the miscibility in the Ag matrix is found larger for Ni than for Co. After annealing around 25 0 degrees C, the marked decrease of the Ag neighbour peak corresponds to a diffusion of magnetic atoms outside the Ag matrix. The Go-Co coordination n umber increases regularly with annealing temperatures up to 450 degrees C r eflecting a progressive expansion of Co particles. On the contrary, for Ni alloys, no further particle expansion has been observed in the same anneali ng range. This different behaviour may be linked both to the difference bet ween the as-deposited structural states and to the Co/Ag and Ni/Ag interfac es energies. Using a simple model, evolution of the mean particle size has been estimated as a function of annealing.