Single-ion magnets (SIMs) are potential building blocks of novel quantum computing devices. Unique magnetic properties of SIMs require effective separation of magnetic ions and can be tuned by even slight changes in their coordination sphere geometry. We show that an additional level of tailorability in the design of SIMs can be achieved by organizing magnetic ions into supramolecular architectures, resulting in gaining control over magnetic ion packing. Here, γ-cyclodextrin was used to template magnetic Co(II) and nonmagnetic auxiliary Li(+) ions to form a heterometallic {Co, Li, Li}4 ring. In the sandwich-type complex [(γ-CD)2Co4Li8(H2O)12] spatially separated Co(II) ions are prevented from superexchange magnetic coupling. Ac/dc magnetic and EPR studies demonstrated that individual Co(II) ions with positive zero-field splitting exhibit field-induced slow magnetic relaxation consistent with the SIMs' behavior, which is exceptional in complexes with easy-plane magnetic anisotropy.

SummaryThe main goal of this work is to study the structural and magnetic properties of iron nanowires and iron nanoparticles, which have been fabricated in almost the same processes. The only difference in the synthesis is an application of an external magnetic field in order to form the iron nanowires. Both nanomaterials have been examined by means of transmission electron microscopy, energy dispersive X-ray spectrometry, X-ray diffractometry and Mössbauer spectrometry to determine their structures. Structural investigations confirm that obtained iron nanowires as well as nanoparticles reveal core–shell structures and they are composed of crystalline iron cores that are covered by amorphous or highly defected phases of iron and iron oxides. Magnetic properties have been measured using a vibrating sample magnetometer. The obtained values of coercivity, remanent magnetization, saturation magnetization as well as Curie temperature differ for both studied nanostructures. Higher values of magnetizations are observed for iron nanowires. At the same time, coercivity and Curie temperature are higher for iron nanoparticles.

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The iron crosslinked chitosan (Ch-Fe-CL) and N-carboxylmethyl chitosan (N-CM-Ch-Fe) complexes were studied by complementary techniques: structurally sensitive Mössbauer and X-ray absorption methods, as well as static magnetic measurements. A detailed and consistent description of these complexes including, besides the overall magnetic behavior, the spin ordering and local atomic structure around Fe ions is presented. Fe atoms in the investigated samples are mostly penta-coordinated and appear in a high spin Fe (3+) ionic state. In Ch-Fe-CL, two kinds of Fe near neighbors are equally probable and several Fe atoms are situated in the second coordination sphere. The magnetic interactions between these Fe ions lead to a sperimagnetic-like ordering. In N-CM-Ch-Fe, only one Fe neighborhood was found. Other Fe atoms were identified neither in the first nor in the second coordination sphere, but the third coordination sphere indicates the presence of Fe atoms. The magnetic coupling between these atoms is antiferromagnetic, but the dominant part of Fe in this sample remains in a paramagnetic state.

Two sets of core/shell magnetic nanoparticles, CoFe2O4/Fe3O4 and Fe3O4/CoFe2O4, with a fixed diameter of the core (~ 4.1 and ~ 6.3 nm for the former and latter sets, respectively) and thickness of shells up to 2.5 nm were synthesized from metal chlorides in a diethylene glycol solution. The nanoparticles were characterized by X-ray diffraction, transmission electron microscopy, and magnetic measurements. The analysis of the results of magnetic measurements shows that coating of magnetic nanoparticles with the shells results in two simultaneous effects: first, it modifies the parameters of the core-shell interface, and second, it makes the particles acquire combined features of the core and the shell. The first effect becomes especially prominent when the parameters of core and shell strongly differ from each other. The results obtained are useful for optimizing and tailoring the parameters of core/shell spinel ferrite magnetic nanoparticles for their use in various technological and biomedical applications.