Samarium Magnetism Studied on SmPd2Al3 Single Crystal

In this paper, specific features of Sm magnetism in an intermetallic compound have been studied. For this purpose, a high-quality single crystal of SmPd2Al3 was grown and subjected to detailed measurements of specific heat, magnetization, ac susceptibility, and electrical resistivity with respect to temperature and a magnetic field applied along the principal crystallographic directions. SmPd2Al3 magnetism was found to be strongly anisotropic with the easy-magnetization direction along the c axis where the main magnetic features are concentrated. The a-axis response remains weak, paramagneticlike, even in the magnetically ordered state. Ferromagnetism with TC=12.4 K has been indicated by all the measured physical properties. At lower temperatures, three successive order-order phase transitions have been observed on the temperature dependence of the specific heat as three anomalies: at 3.4, 3.9, and 4.4 K, respectively. The low-temperature magnetization data can be understood within a scenario that considers the antiferromagnetic ground state as being gradually destroyed through a series of four metamagnetic transitions at 0.03, 0.35, 0.5, and 0.75 T, as detected in the 1.8 K magnetization data. The experimental data are discussed together with the results of electronic-structure and crystal-field calculations from first principles, which were performed as an important part of the study for comprehension and explanation of the observed behavior of the SmPd2Al3 compound

Pressure Evolution of Magnetism in URhGa

In this paper, we report the results of an ambient and high pressure study of a 5f-electron ferromagnet URhGa. The work is focused on measurements of magnetic and thermodynamic properties of a single crystal sample and on the construction of the p-T phase diagram. Diamond anvil cells were employed to measure the magnetization and electrical resistivity pressures up to ~ 9 GPa. At ambient pressure, URhGa exhibits collinear ferromagnetic ordering of uranium magnetic moments {\mu}U ~ 1.1 {\mu}B (at 2 K) aligned along the c-axis of the hexagonal crystal structure below the Curie temperature TC = 41K. With the application of pressure up to 5GPa the ordering temperature TC initially increases whereas the saturated moment slightly decreases. The rather unexpected evolution is put in the context of the UTX family of compounds.Comment: arXiv admin note: text overlap with arXiv:1611.0327

Colloquium: Hidden Order, Superconductivity, and Magnetism -- The Unsolved Case of URu2Si2

This Colloquium reviews the 25 year quest for understanding the continuous (second-order) mean-field-like phase transition occurring at 17.5 K in URu2Si2. About ten years ago, the term hidden order (HO) was coined and has since been utilized to describe the unknown ordered state, whose origin cannot be disclosed by conventional solid-state probes, such as x rays, neutrons, or muons. HO is able to support superconductivity at lower temperatures (Tc ~ 1.5 K), and when magnetism is developed with increasing pressure both the HO and the superconductivity are destroyed. Other ways of probing the HO are via Rh-doping and very large magnetic fields. During the last few years a variety of advanced techniques have been tested to probe the HO state and their attempts will be summarized. A digest of recent theoretical developments is also included. It is the objective of this Colloquium to shed additional light on the HO state and its associated phases in other materials.Comment: 25 pages, 16 figures, published in Reviews of Modern Physic

Physics of Polymorphic Transitions in CeRuSn

We report a detailed study of the polymorphic transitions in ternary stannide CeRuSn on high quality single crystals through a combination of X-ray diffraction experiments conducted at 300, 275 and 120 K, and measurements of the thermal expansion, magnetization, and resistivity, along main crystallographic axes. In addition, the transition was followed as a function of pressure up to 0.8 GPa. The present X-ray diffraction data show that the room temperature polymorph consists of the lattice doubled along the c axis with respect to the CeCoAl-type structure consistent with previous reports. Upon cooling, the compound undergoes two successive transitions, first to a quintuple (290 K) and than to a triple CeCoAl superstructure at 225 K. The transitions are accompanied by a tremendous volume change due to a strong shrinking of the lattice along the c axis, which is clearly observed in thermal expansion. We advance arguments that the volume collapse originates from an increasing number of crystallographically inequivalent Ce sites and the change of ratio between the short and long Ce-Ru bonds. The observed properties of the polymorphic transition in CeRuSn are reminiscent of the transition in elementary Cerium, suggesting that similar physics, i.e., a Kondo influenced transition and strong lattice vibrations might be the driving forces