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Register a new userMagnetic studies of the lightly Ru doped perovskite rhodates Sr(Ru,Rh)O$_3$
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K. Yamaura
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The solid solution between the ferromagnetic metal SrRuO$_3$ and the enhanced paramagnetic metal SrRhO$_3$ was recently reported [K. Yamaura et al., Phys. Rev. B 69 (2004) 024410], and an unexpected feature was found in the specific heat data at $x$=0.9 of SrRu$_{1-x}$Rh$_x$O$_3$. The feature was reinvestigated further by characterizing additional samples with various Ru concentrations in the vicinity of $x$=0.9. Specific heat and magnetic susceptibility data indicate that the feature reflects a peculiar magnetism of the doped perovskite, which appears only in the very narrow composition range 0.85$<$$x$$le$0.95.
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We investigated Sr$_3$Ru$_2$O$_7$, a quantum critical metal that shows a metamagnetic quantum phase transition and electronic nematicity, through density functional calculations. These predict a ferromagnetic ground state in contrast to the experimentally observed paramagnetism, raising the question of competing magnetic states and associated fluctuations that may suppress magnetic order. We did a search to identify such low energy antiferromagnetically ordered metastable states. We find that the lowest energy antiferromagnetic state has a striped order. This corresponds to the E-type order that has been shown to be induced by Mn alloying. We also note significant transport anisotropy in this E-type ordered state. These results are discussed in relation to experimental observations.
We report the magnetic and electronic properties of the bilayer ruthenate Sr$_3$Ru$_2$O$_7$ upon Fe substitution for Ru. We find that Sr$_3$(Ru$_{1-x}$Fe$_x$)$_2$O$_7$ shows a spin-glass-like phase below 4 K for $x$ = 0.01 and commensurate E-type antiferromagnetically ordered insulating ground state characterized by the propagation vector $q_c$ = (0.25 0.25 0) for $x$ $geq$ 0.03, respectively, in contrast to the paramagnetic metallic state in the parent compound with strong spin fluctuations occurring at wave vectors $q$ = (0.09 0 0) and (0.25 0 0). The observed antiferromagnetic ordering is quasi-two-dimensional with very short correlation length along the $c$ axis, a feature similar to the Mn-doped Sr$_3$Ru$_2$O$_7$. Our results suggest that this ordered ground state is associated with the intrinsic magnetic instability in the pristine compound, which can be readily tipped by the local magnetic coupling between the 3$d$ orbitals of the magnetic dopants and Ru 4$d$ orbitals.
We investigated the electronic structures of the two-dimensional layered perovskite Sr$_{2}$textit{M}O$_{4}$ (textit{M}=4textit{d} Ru, 4textit{d} Rh, and 5textit{d} Ir) using optical spectroscopy and polarization-dependent O 1textit{s} x-ray absorption spectroscopy. While the ground states of the series of compounds are rather different, their optical conductivity spectra $sigma(omega)$ exhibit similar interband transitions, indicative of the common electronic structures of the 4textit{d} and 5textit{d} layered oxides. The energy splittings between the two $e_{g}$ orbitals, $i.e.$, $d_{3z^{2}-r^{2}}$ and $d_{x^{2}-y^{2}}$, are about 2 eV, which is much larger than those in the pseudocubic and 3textit{d} layered perovskite oxides. The electronic properties of the Sr$_{2}$textit{M}O$_{4}$ compounds are discussed in terms of the crystal structure and the extended character of the 4textit{d} and 5textit{d} orbitals.
One way to induce insulator to metal transitions in the spin-orbit Mott insulator Sr2IrO4 is to substitute iridium with transition metals (Ru, Rh). However, this creates intriguing inhomogeneous metallic states, which cannot be described by a simple doping effect. We detail the electronic structure of the Ru-doped case with angle-resolved photoemission and show that, contrary to Rh, it cannot be connected to the undoped case by a rigid shift. We further identify bands below $E_F$ coexisting with the metallic ones that we assign to non-bonding Ir sites. We rationalize the differences between Rh and Ru by a different hybridization with oxygen, which mediates the coupling to Ir and sensitively affects the effective doping. We argue that the spin-orbit coupling does not control neither the charge transfer nor the transition threshold.
Triple-layered ruthenate Sr$_4$Ru$_3$O$_{10}$ shows a first-order itinerant metamagnetic transition for in-plane magnetic fields. Our experiments revealed rather surprising behavior in the low-temperature transport properties near this transition. The in-plane magnetoresistivity $rho$$_{ab}$(H) exhibits ultrasharp steps as the magnetic field sweeps down through the transition. Temperature sweeps of $rho$$_{ab}$ for fields within the transition regime show non-metallic behavior in the up-sweep cycle of magnetic field, but show a significant drop in the down-sweep cycle. These observations indicate that the transition occurs via a new electronic phase separation process; a lowly polarized state is mixed with a ferromagnetic state within the transition regime.
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