I. de Pedro

Long-range magnetic ordering in magnetic ionic liquid: Emim[FeCl4].

Up to now most of the magnetic ionic liquids containing tetrachloroferrate ion FeCl(4) have evidenced a paramagnetic temperature dependence of the magnetic susceptibility, with only small deviations from the Curie law at low temperatures. However, we report on the physical properties of 1-ethyl-3-methylimidazolium tetrachloroferrate Emim[FeCl(4)], that clearly shows a long-range antiferromagnetic ordering below the Néel temperature T(N)≈3.8 K. In addition, the field dependence of the magnetization measured at 2 K is characterized by a linear behaviour up to around 40 kOe, while above this field the magnetization becomes saturated with a value of 4.3 μ(B)/Fe, which is near the expected fully saturated value of 5 μ(B)/Fe for an Fe(3+) ion.

Interacting Superparamagnetic Iron(II) Oxide Nanoparticles: Synthesis and Characterization in Ionic Liquids

Interacting superparamagnetic iron(II) oxide nanoparticles (NPs) with sizes of 5.3 ± 1.6 nm were prepared by simple decomposition of [Fe(COT)2] (COT = 1,3,5,7-cyclooctatetraene) with 5 bar of H2 in 1-n-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (BMI·NTf2) ionic liquid (IL). The static and dynamic magnetic characterization revealed a superparamagnetic behavior with weak dipolar interactions of these NPs. In situ structural studies by X-ray absorption spectroscopy demonstrated that they consist of nanostructured FeO. This approach is an appropriate method to prepare and stabilize nanostructured FeO particles, where the presence of an IL proved to be fundamental to suppress the aggregation and usual overoxidation of the FeO NPs.

On the exchange bias effect in NiO nanoparticles with a core(antiferromagnetic)/shell (spin glass) morphology

The unexpected appearance of magnetic hysteresis and exchange bias effects in nominally antiferromagnetic NiO nanoparticles is usually explained in terms of a core/shell morphology, where a spin glass-like shell is exchange coupled to an antiferromagnetic core. However, recent studies have challenged the validity of this assumption for small enough NiO nanoparticles. In this work we present proof of the core/shell model for NiO nanoparticles with sizes below 10 nm by combining neutron powder diffraction and magnetic measurements. In addition, we have verified that the exchange bias effect persists even when the particle size is reduced down to 4 nm.

Collective magnetic behaviors of Fe–Ag nanostructured thin films above the percolation limit

The magnetic behavior of sputtered and pulsed laser deposited (PLD) FexAg100−x thin films with 27≤x≤55 has been studied by means of ac and dc magnetic measurements. Sputtered samples present a continuous decrease in the magnetization, down to 310 K for x=30, where a magnetic transition into a superparamagnetic state with the presence of dipolar interactions is observed. The ac susceptibility measurements indicate that this transition resembles that of three dimensional glassy systems. Sputtered samples with higher concentration of Fe present a similar but slower thermal evolution of magnetization. PLD samples with x≥50 show a Curie–Weiss-type transition above ∼200 K triggered by direct exchange interactions. As the temperature decreases, the system behaves like a ferromagnet and below ∼75 K, a transition into a cluster-glass state appears. As the composition decreases, these phenomena vanish.

Low Temperature Magnetic Ordering of the Magnetic Ionic Plastic Crystal, Choline[FeCl4]

We report on the nature of the low temperature magnetic ordering of a magnetic ionic plastic crystal, Choline[FeCl4]. This investigation was carried out using heat capacity measurements, neutron diffraction experiments and muon spin relaxation (μSR) spectroscopy. The calorimetric measurements show the onset of an unusual magnetic ordering below 4 K with a possible second magnetic phase transition below 2 K. Low temperature neutron diffraction data reveal a three dimensional antiferromagnetic ordering at 2 K compatible with the previous magnetometry results. The analysis of μSR spectra indicates a magnetic phase transition below 2.2 K. At 1.6 K, the analysis of the shape of the μSR spectra suggests the existence of an additional magnetic phase with features of a possible incommensurate magnetic structure.

Neutron Powder Diffraction study of the Magnetic Ionic Liquid Emim[FeCL4] and its deuterated phase

A magnetic ionic liquid comprising 1-ethyl-3 methylimidazolium (Emim) cations and tetraclhoroferrate(III) (FeCl4) anions and its deuterated phase were synthetized and characterized magnetically. In both materials, the low temperature dependence of the magnetic susceptibility presents a maximum (around 4 K) related to an antiferromagnetic ordering, but the ordering temperatures are slightly shifted and the curves display different shapes. In addition, the magnetization of the deuterated phase tends to saturate at higher values than that corresponding to the non-deuterated analogue. A comparison of the neutron diffraction patterns above and below the magnetic transition clearly shows that the crystal and magnetic structures of these materials are different. Therefore, the present findings clearly prove that the magnetic exchange interactions that induce three-dimensional magnetic ordering are modified after the deuteration process.