No Arabic abstract
Helical magnetic structures and its responses to external magnetic fields in Yb(Ni$_x$Cu$_{1-x}$)$_3$Al$_9$, with a chiral crystal structure of the space group $R32$, have been investigated by resonant X-ray diffraction. It is shown that the crystal chirality is reflected to the helicity of the magnetic structure by a one to one relationship, indicating that there exists an antisymmetric exchange interaction mediated via the conduction electrons. When a magnetic field is applied perpendicular to the helical axis ($c$ axis), the second harmonic peak of $(0, 0, 2q)$ develops with increasing the field. The third harmonic peak of $(0, 0, 3q)$ has also been observed for the $x$=0.06 sample. This result provides a strong evidence for the formation of a chiral magnetic soliton lattice state, a periodic array of the chiral twist of spins, which has been suggested by the characteristic magnetization curve. The helical ordering of magnetic octupole moments, accompanying with the magnetic dipole order, has also been detected.
We report measurements and analyses of resistivity, thermopower, and thermal conductivity of polycrystalline samples of perovskite LaRh$_{1-x}$Ni$_x$O$_3$. The thermopower is found to be large at 800 K (185 $mu$V/K for $x=$0.3), which is ascribed to the high-temperature stability of the low-spin state of Rh$^{3+}$/Rh$^{4+}$ ions. This clearly contrasts with the thermopower of the isostructural oxide LaCoO$_3$, which rapidly decreases above 500 K owing to the spin-state transition. The spin state of the transition-metal ions is one of the most important parameters in oxide thermoelectrics.
We report on a single-crystal neutron diffraction study of the evolution of the antiferromagnetic order in the heavy-fermion compound CePd$_{1-x}$Ni$_x$Al which exhibits partial geometric frustration due to its distorted Kagome structure. The magnetic structure is found to be unchanged with a propagation vector $Q_mathrm{AF} approx (0.5~0~0.35)$ for all Ni concentrations $x$ up to $x_c approx 0.14$. Upon approaching the quantum critical concentration $x_c$, the ordered moment vanishes linearly with Neel temperature $T_{rm N}$, in good agreement with CePdAl under hydrostatic pressure. For all Ni concentrations, substantial short-range magnetic correlations are observed above $T_{rm N}$ as a result of frustration.
We present a comprehensive study of the magnetization dynamics and phase evolution in Cr$_{1/3}$NbS$_{2}$, which realizes a chiral soliton lattice (CSL). The magnetic field dependence of the ac magnetic response is analyzed for five harmonic components, $M_{nomega}(H)$ $(n =1-5)$, using a phase sensitive measurement over a frequency range, $f = 11 - 10,000$ Hz. At a critical field, the modulated CSL continuously evolves from a helicity-rich to a ferromagnetic domain-rich structure, where the crossover is revealed by the onset of an anomalous nonlinear magnetic response that coincides with extremely slow dynamics. The behavior is indicative of the formation of a spatially coherent array of large ferromagnetic domains which relax on macroscopic time-scales. The frequency dependence of the ac magnetic loss displays an asymmetric distribution of relaxation times across the highly nonlinear CSL regime, which shift to shorter time-scales with increasing temperature. We experimentally resolve the tricritical point at $T_{TCP}$ in a temperature regime above the ferromagnetic Curie temperature which separates the linear and nonlinear regimes of the CSL at the phase transition. A comprehensive phase diagram is constructed which summarized the features of the field and temperature dependence of the magnetic crossovers and phase transitions in Cr$_{1/3}$NbS$_{2}$.
Magnetic susceptibility of the isostructural Ce(Ni{1-x}Cu{x})5 alloys (0< x <0.9) was studied as a function of the hydrostatic pressure up to 2 kbar at fixed temperatures 77.3 and 300 K, using a pendulum-type magnetometer. A pronounced magnitude of the pressure effect is found to be negative in sign and to depend strongly and non-monotonously on the Cu content, showing a sharp maximum in vicinity of x = 0.4. The experimental results are discussed in terms of the Ce valence change under pressure. It has been concluded that the fractional occupation of the f-states, which corresponds to the half-integer valence of Ce ion (3.5), is favorable for the valence instability in alloys studied. For the reference CeNi5 compound the main contributions to magnetic susceptibility and their volume dependence are calculated ab initio within the local spin density approximation (LSDA), and appeared to be in close agreement with experimental data.
We report the results of ac and dc magnetization (M) and heat-capacity (C) measurements on the solid solution, Sr$_3$Cu$_{1-x}$Zn$_x$IrO$_6$. While the Zn end member is known to form in a rhombohedral pseudo one-dimensional K$_4$CdCl$_6$ structure with an antiferromagnetic ordering temperature of (T$_N$ =) 19 K, the Cu end member has been reported to form in a monoclinically distorted form with a Curie temperature of (T$_C$ =) 19 K. The magnetism of the Zn compound is found to be robust to synthetic conditions and is broadly consistent with the behavior known in the literature. However, we find a lower magnetic ordering temperature (T$_o$) for our Cu compound (~ 13 K), thereby suggesting that T$_o$ is sensitive to synthetic conditions. The Cu sample appears to be in a spin-glass-like state at low temperatures, judged by a frequency dependence of ac magnetic susceptibility and a broadening of the C anomaly at the onset of magnetic ordering, in sharp contrast to earlier proposals. Small applications of magnetic field, however, drive this system to ferromagnetism as inferred from the M data. Small substitutions for Cu/Zn (x = 0.75 or 0.25) significantly depress magnetic ordering; in other words, T$_o$ varies non-monotonically with x (T$_o$ ~ 6, 3 and 4 K for x = 0.25, 0.5, and 0.67 respectively). The plot of inverse susceptibility versus temperature is non-linear in the paramagnetic state as if correlations within (or among) the magnetic chains continuously vary with temperature. The results establish