Surface anisotropy and resonance modes in Co − SiO 2 heterogeneous films
Surface anisotropy and resonance modes in Co − SiO 2 heterogeneous films
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DOI:
10.1103/physrevb.70.054428
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发表时间:
2004-08
影响因子:
3.7
通讯作者:
J. Gómez;A. Butera;J. Barnard
中科院分区:
文献类型:
--
作者:
J. Gómez;A. Butera;J. Barnard
We have studied the magnetic properties of ${\mathrm{Co}\text{\ensuremath{-}}\mathrm{SiO}}_{2}$ films as a function of the $\mathrm{Co}$ concentration. Films were prepared using rf sputtering and $\mathrm{Co}$ volume concentrations in the range $0.18\ensuremath{\leqslant}x\ensuremath{\leqslant}0.62$ were obtained. The samples were measured using ferromagnetic resonance at X-band $(\ensuremath{\nu}=9.5\phantom{\rule{0.3em}{0ex}}\mathrm{GHz})$ and Q-band $(\ensuremath{\nu}=35\phantom{\rule{0.3em}{0ex}}\mathrm{GHz})$. A main absorption associated to the uniform precession of the magnetic moments was observed in all films. From this resonance field we have evaluated an effective anisotropy field $({H}_{\mathrm{eff}})$ as a function of $x$. For low $\mathrm{Co}$ concentrations the shape anisotropy is the major contribution to ${H}_{\mathrm{eff}}$. However, above a critical concentration ${x}_{p}\ensuremath{\sim}0.37$ (coincident with the percolation of the $\mathrm{Co}$ granules) it is necessary to assume the presence of an additional anisotropy to explain the experimental data. At this same concentration the resonance spectra change with the appearance of an extra absorption at fields higher than that of the uniform resonance mode. For larger $\mathrm{Co}$ concentrations another absorption is observed at intermediate fields. We have analyzed these extra lines using the surface inhomogeneity model that takes into account the different environment of the surface moments. The surface anisotropy was determined as a function of $x$ with a behavior quite similar to the additional anisotropy obtained from ${H}_{\mathrm{eff}}$. In situ annealing studies support the assumption that the observed behavior originates in the effects of the surface and suggest the nonequivalence of both film surfaces.