Tuning the structure and magnetic behavior of Ni-Ir-based nanoparticles in ionic liquids
Fecha
2018Autor
Abarca, Gabriel [Univ Mayor, Fac Ciencias, Ctr Nanotecnol Aplicada]
da Silva, Kacris I. M.
Bernardi, Fabiano
Baptista, Daniel L.
Leite Santos, Marcos José
Fernández Barquin, Luis
Dupont, Jairton
de Pedro, Imanol
Ubicación geográfica
Notas
HERRAMIENTAS
Resumen
We report on a simple preparation of extremely small diameter (ca. 2 nm) Ni-Ir-based NPs using Ni(COD)(2) and [Ir(COD)OCH3](2) in 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (BMImNTf(2)). The prepared NPs had either core-shell-like or alloy-like structures with the presence of Ni,Ir-oxides, depending on the synthetic approach. X-ray diffraction (XRD), Rutherford backscattering spectrometry (RBS), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), extended X-ray absorption fine structure (EXAFS), and magnetic measurements are combined to describe the influence of nanostructure on the magnetic behavior of these nanosystems. The present findings reveal that the alloy NPs display a disordered magnetic state, similar to a spin glass (SG)-like system (T-f = 7.2 K). Core-shell NPs are formed by a magnetically blocked/unblocked core with a magnetically disordered shell as deduced from the two magnetic responses peaking at T-B = 75 K and T-f = 5.8 K. Coupling at the core-shell interface leads to an exchange bias revealed at low temperature as horizontal shifts in the hysteresis loops of 0.12 kOe at 2 K.
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