RESUMEN
A single crystal of the ternary uranium silicide UIr[Formula: see text]Si[Formula: see text] was studied by means of of X-ray diffraction, magnetization, heat capacity and electrical transport measurements. The studied compound orders antiferromagnetically at the Néel temperature of 5.5 K and undergoes a metamagnetic transition at 1.8 K in a field of 1.52 T. The metamagnetic transition has a spin-flop character.
RESUMEN
Using inelastic X-ray scattering beyond the dipole limit and hard X-ray photoelectron spectroscopy we establish the dual nature of the U [Formula: see text] electrons in U[Formula: see text] (M = Pd, Ni, Ru, Fe), regardless of their degree of delocalization. We have observed that the compounds have in common a local atomic-like state that is well described by the U [Formula: see text] configuration with the [Formula: see text] and [Formula: see text] quasi-doublet symmetry. The amount of the U 5[Formula: see text] configuration, however, varies considerably across the U[Formula: see text] series, indicating an increase of U 5f itineracy in going from M = Pd to Ni to Ru and to the Fe compound. The identified electronic states explain the formation of the very large ordered magnetic moments in [Formula: see text] and [Formula: see text], the availability of orbital degrees of freedom needed for the hidden order in [Formula: see text] to occur, as well as the appearance of Pauli paramagnetism in [Formula: see text] A unified and systematic picture of the U[Formula: see text] compounds may now be drawn, thereby providing suggestions for additional experiments to induce hidden order and/or superconductivity in U compounds with the tetragonal body-centered [Formula: see text] structure.
RESUMEN
Single crystals of the ternary cerium arsenide CeAgAs2 were grown by chemical vapor transport. They were studied by means of x-ray diffraction, magnetization, heat capacity and electrical transport measurements. The experimental research was supplemented with electronic band structure calculations. The compound was confirmed to order antiferromagnetically at the Néel temperature of 4.9 K and to undergo metamagnetic transition in a field of 0.5 T at 1.72 K. The electrical resistivity shows distinct increase at low temperatures, which origin is discussed in terms of pseudo-gap formation in the density of states at the Fermi level and quantum corrections to the resistivity in the presence of atom disorder due to crystal structure imperfections.
RESUMEN
A polycrystalline sample of La2NiSi3 was investigated by means of heat capacity, magnetic susceptibility, magnetization, electrical resistivity and magnetoresistivity measurements. The compound was basically characterized as a Pauli paramagnet with metallic-like electrical conductivity, notably reduced in magnitude and weakly temperature dependent, as is usually observed for atomically disordered systems. Furthermore, the experimental data revealed the presence of a small amount of paramagnetic impurities. As a result, the low-temperature electrical resistivity in La2NiSi3 was found to be governed by both quantum corrections due to electron-electron interactions ([Formula: see text] contribution) and spin-flip Kondo scattering ([Formula: see text] contribution). The presence of paramagnetic impurities led to an increase in s-electron spin splitting due to the s-d interactions, manifested by a B (1/2) dependence of the magnetoresistivity, anomalously observed in the present study for thermal energy being larger than the Zeeman splitting energy [Formula: see text].
