Magnetic Resonance Study of Fe-Implanted TiO2 Rutile

Single-crystal (100) and (001) TiO 2 rutile substrates have been implanted with 40 keV Fe + at room temperature with high doses in the range of (0.5–1.5) × 10 17 ions/cm 2 . A ferromagnetic resonance (FMR) signal has been observed for all samples with the intensity and the out-of-plane anisotropy in...

Full description

Saved in:
Bibliographic Details
Published inApplied magnetic resonance Vol. 48; no. 4; pp. 347 - 360
Main Authors Okay, C., Vakhitov, I. R., Valeev, V. F., Khaibullin, R. I., Rameev, B.
Format Journal Article
LanguageEnglish
Published Vienna Springer Vienna 01.04.2017
Springer Nature B.V
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Single-crystal (100) and (001) TiO 2 rutile substrates have been implanted with 40 keV Fe + at room temperature with high doses in the range of (0.5–1.5) × 10 17 ions/cm 2 . A ferromagnetic resonance (FMR) signal has been observed for all samples with the intensity and the out-of-plane anisotropy increasing with the implantation dose. The FMR signal has been related to the formation of a percolated metal layer consisting of close-packed iron nanoparticles in the implanted region of TiO 2 substrate. Electron spin resonance (ESR) signal of paramagnetic Fe 3+ ions substituting Ti 4+ positions in the TiO 2 rutile structure has been also observed. The dependences of FMR resonance fields on the DC magnetic field orientation reveal a strong in-plane anisotropy for both (100) and (001) substrate planes. An origin of the in-plane anisotropy of FMR signal is attributed to the textured growth of the iron nanoparticles. As result of the nanoparticle growth aligned with respect to the structure of the rutile host, the in-plane magnetic anisotropy of the samples reflects the symmetry of the crystal structure of the TiO 2 substrates. Crystallographic directions of the preferential growth of iron nanoparticles have been determined by computer modeling of anisotropic ESR signal of substitutional Fe 3+ ions.
ISSN:0937-9347
1613-7507
DOI:10.1007/s00723-017-0868-y