In this work, we report the influence of single-ionized oxygen vacancies ($$V^{\prime}_{{\text{O}}}$$ V O ′ ) as a spin ½ system in the ferromagnetic response of undoped and Cr-doped SnO2 nanowires. For this study, undoped and Cr-doped SnO2 nanowires were synthesized by a thermal evaporation method. Raman, Auger, and X-ray photoelectron spectroscopies confirmed the incorporation of Cr3+ ions in the SnO2 lattice. Electron paramagnetic resonance measurements demonstrated the presence of single-ionized oxygen vacancies ($$V^{\prime}_{{\text{O}}}$$ V O ′ ) in undoped and Cr-doped nanowires. Complementarily, cathodoluminescence measurements confirmed the presence of VO defects in the samples. Magnetic measurements revealed FM behavior from the undoped SnO2 and Cr-doped SnO2 nanowires, showing magnetization saturation values (MS) of ± 1 × 10–3 and ± 1.6 × 10–3 emu/g, respectively, and magnetic coercivity values (HC) of 180 and 200 Oe. We assign the FM response of nanowires to the presence of single ionized $$V^{\prime}_{{\text{O}}}$$ V O ′ acting as a spin ½ system and to the alignment of magnetic moments of Cr3+ ions, finding that $$V^{\prime}_{{\text{O}}}$$ V O ′ defects dominate in the FM generation.
IntroductionAluminum-based metal matrix composites (MMC) reinforced with ceramic particles are demanded because of their low density and high specific stiffness . Dispersion strengthened materials belong to the group of composite materials, which are made mainly by the techniques of Powder Metallurgy (PM). Their microstructure is composed by a polycrystalline matrix, in which dispersed particles are incorporated (mainly oxides, carbides and nitrides). The Mechanical Alloying (MA) and Mechanical Milling (MM) processes have been widely recognized as alternative routes for the formation of metastable phases for selected applications. On the other hand, the interactions between the hardening particles and the matrix include atomic-level effects that are responsible for the new and novel properties of composites. By using Electron Energy Loss Spectroscopy (EELS), it is possible to characterize the materials from the electronic point of view. The raw materials were Al powders (99.5 % purity, mesh -325) and pre-milled graphite with Cu. The mixtures of pure Al, Al-C, Al-Cu and Al-C-Cu were employed to produce the composites. Each one was mechanically processed in a high energy SPEX mill for 4 h. Argon was used as the milling atmosphere. Consolidated samples were pressure-less sintered for 1 h at 823 K under vacuum (∼ 1 Torr). Figure 1 shows a typical HRTEM micrograph of the Al-C-Cu composite in the as milled condition. Graphite nanoparticles are present in the Al matrix whose dimensions are ~ 2 nm in thickness and ~10-15 nm in length. Figure 2 shows typical nanofibers found in the Al-CCu composite in the as-sintered condition. Nanofibers show asymmetrical shape, irregular surface and the dimensions are ~20-40 nm in thickness and ~200-300 nm in length. During the sintering process Al react with O and form Al 2 O 3 which present a fiber shape. Additionally to HRTEM characterization, EELS analyses were carried out for all Al-based composites. Figures 3 and 4 show the Al-K ionization edge for metallic Al, Al-C and Al-CCu composites in the as-milled and sintered condition respectively. Figure 3(b) and (c) present changes with respect to metallic Al, 3(a). It is expected C have two routes of reaction during milling and sintering process, one of them is a preferential reaction with oxidized shell in aluminum powders and the second one is the reaction with aluminum matrix to crystallize Al 3 C 4 . By comparing Figures 4(a) and 3(a), was found that Figure 4(a) presents Al 2 O 3 presence which is not perceptible in Figure 4(a), this means Al and oxygen still react during sintering process to crystallize Al 2 O 3 . Analyzing Figure 3(b) and 4(b) were found differences in the Al-K ionization edge of Al-C components, these differences could be the result of changes in Al 2 O 3 structures. An analysis by HRTEM, developed on the alumina nanofibers in the as-sintered samples revealed that alumina is Al 2 O 3 -κ type. We assume that the alumina formed during the milling is Al 2 O 3 -α and it is transformed in the metastable Al 2 O 3 -κ.
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