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New clathrate type phases where Li atoms fill vacancies in the Ge-framework have been identified.

The influence of structural disorder on superconductivity is not yet fully understood. A concurrent examination of crystallographic and physical properties of LaHg

The new phase Be

In an attempt to incorporate tin (Sn) into high-entropy alloys composed of refractory metals Hf, Nb, Ti and Zr with the addition of 3d transition metals Cu, Fe, and Ni, we synthesized a series of alloys in the system HfTiZrSnM (M = Cu, Fe, Nb, Ni). The alloys were characterized crystallographically, microstructurally, and compositionally, and their physical properties were determined, with the emphasis on superconductivity. All Sn-containing alloys are multi-phase mixtures of intermetallic compounds (in most cases four). A common feature of the alloys is a microstructure of large crystalline grains of a hexagonal (Hf, Ti, Zr)5Sn3 partially ordered phase embedded in a matrix that also contains many small inclusions. In the HfTiZrSnCu alloy, some Cu is also incorporated into the grains. Based on the electrical resistivity, specific heat, and magnetization measurements, a superconducting (SC) state was observed in the HfTiZr, HfTiZrSn, HfTiZrSnNi, and HfTiZrSnNb alloys. The HfTiZrSnFe alloy shows a partial SC transition, whereas the HfTiZrSnCu alloy is non-superconducting. All SC alloys are type II superconductors and belong to the Anderson class of “dirty” superconductors.

High-entropy alloys (HEAs) are characterized by a simultaneous presence of a crystal lattice and an amorphous-type chemical (substitutional) disorder. In order to unravel the effect of crystal-glass duality on the electronic transport properties of HEAs, we performed a comparative study of the electronic transport coefficients of a 6-component alloy Al

In a search for unconventional heavy-Fermion compounds with the localized 4f moments distributed quasiperiodically instead of a conventional distribution on a regular, translationally periodic lattice, we have successfully synthesized a stable Ce

International audience; In a search for unconventional heavy-Fermion compounds with the localized 4f moments distributed quasiperiodically instead of a conventional distribution on a regular, translationally periodic lattice, we have successfully synthesized a stable Ce3Au13Ge4 Tsai-type 1/1 quasicrystalline approximant of the off-stoichiometric composition Ce3+xAu13+yGe4+z (x = 0.17, y = 0.49, z = 1.08) and determined its structural model. The structure is body-centered-cubic (bcc), with space group Im3̅, unit cell parameter a = 14.874(3) Å, and Pearson symbol cI174, and can be described as a bcc packing of partially interpenetrating multishell rhombic triacontahedral clusters. The cerium sublattice, corresponding to the magnetic sublattice, consists of a bcc packing of Ce icosahedra with an additional Ce atom in a partially occupied site (occupation 0.7) at the center of each icosahedron. The measurements of its magnetic properties and the specific heat have demonstrated that it is a regular intermetallic compound with no resemblance to heavy-Fermion systems. The partially occupied Ce2 site in the center of each Ce1 icosahedron, the mixed-occupied Au/Ge ligand sites between the Ce2 and Ce1 atoms, and the random compositional fluctuations due to nonstoichiometry of the investigated Ce3+xAu13+yGe4+z alloy introduce randomness into the Ce magnetic sublattice, which causes a distribution of the indirect-exchange antiferromagnetic interactions between the spins. Together with the geometric frustration of the triangularly distributed Ce moments, this leads to a spin-glass phase below the spin freezing temperature Tf ≈ 0.28 K.

The CoCrFeMnNi high-entropy alloy (HEA) is a magnetically concentrated crystalline system with all lattice sites magnetic, containing randomness (five different types of spins are randomly positioned on the lattice) and frustration (a consequence of mixed ferromagnetic and antiferromagnetic interactions). The sample material was prepared as a non-equiatomic, fully random solid solution of the five magnetic elements and we have studied experimentally the nature of the magnetic state. Upon cooling, no long-range magnetic ordering takes place, but the spin system undergoes a kinetic freezing transition to a spin glass phase, where below the spin freezing temperature T f ≈ 20 K, ergodicity of the system is broken. The observed broken-ergodicity phenomena include zero-field-cooled – field-cooled magnetization splitting in low magnetic fields, a frequency-dependent cusp in the ac susceptibility, an ultraslow time-decay of the thermoremanent magnetization and the memory effect, where the state of the spin system reached upon isothermal aging at a certain temperature can be retrieved after a reverse temperature cycle. All these phenomena are associated with the out-of-equilibrium dynamics of a nonergodic, frustrated system of coupled spins that approach thermal equilibrium, but can never reach it on a finite experimental time scale, so that we are observing only transient effects of partial equilibration within localized spin domains.

We have investigated the nature of the magnetic state of a single-crystalline FeCoCrMnAl nanocomposite high-entropy alloy (HEA), composed of crystallographically oriented magnetic nanoplatelets embedded in a magnetic matrix of different magnetic order. The two-phase nanocomposite was formed by a bcc-B2 spinodal decomposition. Due to the single-crystalline nature of the material, there is no symmetry breaking of the surface atomic monolayer at the borders between the two phases and there are no interface regions between the nanoplatelets and the matrix. The material also does not exhibit grain structure, allowing for the observation of the true intrinsic magnetism of a nanocomposite HEA. Upon cooling, the predominantly Fe‒Cr‒Mn chemically disordered bcc matrix orders first at T C 1 ≈ 425 K in an asperomagnetic-type magnetic state. Below T C 2 ≈ 370 K, the B2 nanoplatelets that are predominantly an Al30(Co,Mn)70 pseudo-binary intermetallic compound, start to order in a ferromagnetic (FM)-type manner. We have focused to the question whether the magnetic state of the nanocomposite below T C 2 is a collective state of the interacting nanoplatelets and the matrix or their coupling is weak enough that the magnetic ordering of each of them can be treated independently. Experimental results support the development of a single collective, disordered FM-type magnetic state upon cooling due to the exchange coupling between the nanoplatelets and the matrix. The nanocomposite is magnetically soft and the strong variation of the magnetization with the temperature in a large interval Δ T ≈ 125 K just above room temperature due to two successive magnetic phase transitions make this material promising for the application in magnetocaloric refrigeration.

A magnetic field driven quantum critical point (QCP) is studied experimentally in the Ce3Al magnetically anisotropic intermetallic compound, which shows both antiferromagnetic (AFM) ordering and heavy–fermion behavior. Measurements of the magnetic susceptibility, the magnetoresistance and the specific heat on a Ce3Al monocrystalline sample performed down to 0.35 K in magnetic fields up to 9 T demonstrate that the QCP is anisotropic regarding the orientation of the magnetic field relative to the magnetically easy direction. External magnetic field drives the AFM transition continuously toward zero temperature when applied in the (a, b) easy plane, reaching the QCP at the critical field B c a , b = 4.6 ± 0.4 T, where a quantum phase transition from the AFM to the paramagnetic state takes place. The magnetoresistance experiments below 1 K indicate that intermediate magnetic states may have formed near the QCP. For the field applied along the c hard direction, the QCP has not been observed within our experimental range of the magnetic field. The anisotropic, magnetic field driven QCP in the Ce3Al results from competition of the exchange interaction with the Zeeman interaction in the presence of a large magnetocrystalline anisotropy. The anisotropy of the QCP is a consequence of the fact that the magnetic anisotropy locks the magnetization into the easy plane and cannot be pulled out of the plane by the available laboratory field. Consequently, only the component of the magnetic field vector that lies in the easy plane participates in the QCP formation. In AFM systems with a large magnetic anisotropy, the magnetic field driven QCP is a continuous variable of the magnetic field vector orientation relative to the easy direction.

We address the nature of the collective magnetic state in an ideal high-entropy alloy (HEA), representing a magnetically concentrated system with all lattice sites occupied by localized magnetic moments and containing randomness and frustration due to chemical disorder. Being a “metallic glass on a topologically ordered lattice”, HEAs possess simultaneously the properties of an ordered crystal and an amorphous glass. The influence of this crystal-glass duality on the collective magnetic state was studied experimentally on a hexagonal Tb-Dy-Ho-Er-Tm (TDHET) HEA, composed of rare-earth (RE) elements with zero pair mixing enthalpies that assure completely random mixing of the elements and very similar atomic radii that minimize lattice distortions, representing a prototype of an ideal HEA. The TDHET HEA is characterized by probability distributions of the atomic moments P ( μ ) , the exchange interactions P ( J ) , the magnetocrystalline anisotropy P ( D ) , and the dipolar interactions P ( H d ) . Based on the measurements of the static and dynamic magnetization, the magnetization M ( H ) curves, the thermoremanent magnetization, the specific heat and the magnetoresistance, we found that the collective magnetic state of the TDHET is temperature-dependent, forming a speromagnetic (SPM) state in the temperature range between about 140 and 30 K and an asperomagnetic (ASPM) state below 20 K. In the intermediate temperature range between 30 and 20 K, a spin glass (SG) state is formed, representing a transition state between the speromagnetic and asperomagnetic states. The observed temperature evolution of the magnetic ground state in the TDHET HEA upon cooling in the sequence SPM→SG→ASPM is a result of temperature-dependent, competing magnetic interactions. The distribution of the exchange interactions P ( J ) shifts continuously on the J axis from the high-temperature SPM-type with the average interaction biased towards a net negative value, J ‾ 0 , through the SG-type with J ‾ = 0 , to the low-temperature ASPM-type with J ‾ > 0 . This shift is a band-structure effect, closely linked with the crystallinity of the spin system, which the TDHET HEA shares with the topologically ordered crystals. The probability distributions P ( μ ) , P ( J ) , P ( D ) and P ( H d ) are, on the other hand, a consequence of chemical disorder, a property that the TDHET HEA shares with the amorphous magnets. Both features, the topologically ordered lattice and the amorphous-type chemical disorder essentially determine the magnetic state of an ideal, RE-based HEA.

We investigated molecular dynamics in two ammonium borane systems from the group of promising ion conductors. The investigation was performed by means of H-1 and B-11 NMR spectroscopy and spin-lattice relaxation techniques. We identified two reorientational processes, the rotations of NH4 units that are present already at low temperatures and rotations of large boron cages, B10H10 or B12H12, which are thermally activated and become prominent above 250 K. Activation energies for these processes were determined. In addition, solid-state ion conductivity measurements were conducted to determine poor NH4+ conductivity of both systems.