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Amorphous magnetic microwires can be suitable for a variety of technological applications due to their excellent magnetic softness and giant magnetoimpedance (GMI) effect. Several approaches for optimization of soft magnetic properties and GMI effect of magnetic microwires covered with an insulating, flexible, and biocompatible glass coating with tunable magnetic properties are overviewed. The high GMI effect and soft magnetic properties, achieved even in as-prepared Co-rich microwires with a vanishing magnetostriction coefficient, can be further improved by appropriate heat treatment (including stress-annealing and Joule heating). Although as-prepared Fe-rich amorphous microwires exhibit low GMI ratio and rectangular hysteresis loops, stress-annealing, Joule heating, and combined stress-annealed followed by conventional furnace annealing can substantially improve the GMI effect (by more than an order of magnitude).

Amorphous magnetic microwires can be suitable for a variety of technological applications due to their excellent magnetic softness and giant magnetoimpedance (GMI) effect. Several approaches for optimization of soft magnetic properties and GMI effect of magnetic microwires covered with an insulating, flexible, and biocompatible glass coating with tunable magnetic properties are overviewed. The high GMI effect and soft magnetic properties, achieved even in as-prepared Co-rich microwires with a vanishing magnetostriction coefficient, can be further improved by appropriate heat treatment (including stress-annealing and Joule heating). Although as-prepared Fe-rich amorphous microwires exhibit low GMI ratio and rectangular hysteresis loops, stress-annealing, Joule heating, and combined stress-annealed followed by conventional furnace annealing can substantially improve the GMI effect (by more than an order of magnitude). [ABSTRACT FROM AUTHOR]

Thiols and selenides bind to the surface of gold nanoparticles (AuNPs) and thus provide suitable platforms for the fabrication of sensors. However, the co-existence of adsorbed citrate on the surface of the nanoparticles can influence their functionalization behavior and potentially their sensing performance measured by the extent of particle aggregation. In this study, the functionalization of purchased (7.3 ± 1.2 nm) and in-house prepared AuNPs (13.8 ± 1.2 nm), under the same experimental conditions with either cysteamine (Cys), 3-mercaptopropionic acid (3-MPA), or l-selenocystine (SeCyst) was investigated. 1H-NMR measurements showed distinct citrate signatures on the in-house synthesized citrate-stabilized AuNPs, while no citrate signals were detected on the purchased AuNPs other than evidence of the presence of α-ketoglutaric acid. Carboxylate-containing species attributed to either citrate or α-ketoglutaric acid were identified in all functionalized AuNPs. ATR-FTIR spectroscopy confirmed the functionalization of AuNPs with Cys and 3-MPA, and energy dispersive X-ray (EDX) spectroscopy measurements suggested the formation of SeCyst functionalized AuNPs. Co-adsorption rather than displacement by the functionalizing agents and carboxylate-containing molecules was indicated, which for Cys and SeCyst functionalized AuNPs was also the aggregation limiting factor. In contrast, the behavior of 3-MPA functionalized AuNPs could be attributed to electrostatic repulsions between the functionalized groups. [ABSTRACT FROM AUTHOR]