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Flavio Soldera

Publications and source records attributed to Flavio Soldera.

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Grain boundary defects induced Tc increment in MnSi

The rapid advancement of digital technologies necessitates significant progress in functional materials, which are often derived from scarce elements and involve complex manufacturing processes. Additionally, the trend towards miniaturization in high-tech devices has heightened the demand for extremely small components with tailored functionalities. In the domains of ferromagnetic materials, the market is mostly dominated by rare-earth elements-based structures, which are also limited in abundance. In this work, we focus on the microstructure and properties of MnSi. It is a ferromagnetic material with a relatively low Curie temperature (TC) of 30 K. However, our study demonstrates that Tc can be increased by a factor of 4 through careful control of the crystal size. MnSi thin films were synthesized by combining two non-equilibrium techniques: magnetron sputtering and laser annealing. Laser annealing provoked the crystallinity evolution, by heat accumulation, of the barely crystallized films deposited by magnetron sputtering. The laser beam scanning parameters were adjusted to achieve different fluence values, pulse numbers, and pulse frequencies at each point of the film. Films with a crystal size of around 20 nm exhibited a TC of up to 120 K. These properties were obtained under conditions of low fluence and a high number pulse. Local laser impacts were applied to as-deposited samples, enabling spatially controlled crystallization. The interface between the poorly and well-crystallized regions was showcased using high-resolution transmission electron microscopy (HR-TEM). A spatial resolution of approximately 100 {\mu}m was achieved. These results demonstrate the strong potential of laser annealing as a versatile and promising approach for the fabrication of miniaturized devices.

cond-mat.mtrl-sci

Elemental depth profiling of fluoridated hydroxyapatite by X-ray photoelectron spectroscopy

Structural and chemical changes that arise from a fluoridation of synthetic hydroxyapatite in neutral and acidic fluoridation agents are investigated. For synthetic hydroxyapatite (Ca5(PO4)3OH = HAp), the elemental depth profiles were determined by X-ray photoelectron spectroscopy (XPS) to reveal the effect of fluoridation in nearly neutral (pH = 6.2) and acidic agents (pH = 4.2). Due to the high surface sensitivity of the technique, the depth profiles have a resolution on the nm scale. With respect to the chemical composition and the crystal structure XPS depth profiling revealed very different effects of the two treatments. In both cases, however, the fluoridation affects the surface only on the nm scale which is in contrast to recent literature, where a penetration depth up to several microns was reported. Moreover, evidence is given that the actual fluoridation depth depends on the pH value. Recently, a qualitative three layer model was proposed for the fluoridation of HAp in an acidic agent. In addition to the elemental depth profile, as presented also by various other authors, we present a quantitative depth profile of the compounds CaF2, Ca(OH)2 and fluorapatite (FAp) that are predicted by the three layer model. The analysis of our experimental data exactly reproduces the structural order of the model, however, on a scale that differs by nearly two orders of magnitude from previous predictions. Our results also reveal that the amount of Ca(OH)2 and FAp is small as compared to that of CaF2. Therefore, it has to be questioned whether such narrow Ca(OH)2 and FAp layers really can act as protective layers for the enamel.

cond-mat.mtrl-sci