The electronic structures of the ferromagnetic superconductors $mathrm{UGe}_2$ and $mathrm{UCoGe}$ in the paramagnetic phase were studied by angle-resolved photoelectron spectroscopy using soft X-rays ($h u =400-500$). The quasi-particle bands with l
arge contributions from $mathrm{U}~5f$ states were observed in the vicinity of $E_mathrm{F}$, suggesting that the $mathrm{U}~5f$ electrons of these compounds have an itinerant character. Their overall band structures were explained by the band-structure calculations treating all the $mathrm{U}~5f$ electrons as being itinerant. Meanwhile, the states in the vicinity of $E_mathrm{F}$ show considerable deviations from the results of band-structure calculations, suggesting that the shapes of Fermi surface of these compounds are qualitatively different from the calculations, possibly caused by electron correlation effect in the complicated band structures of the low-symmetry crystals. Strong hybridization between $mathrm{U}~5f$ and $mathrm{Co}~3d$ states in $mathrm{UCoGe}$ were found by the $mathrm{Co}~2p-3d$ resonant photoemission experiment, suggesting that $mathrm{Co}~3d$ states have finite contributions to the magnetic, transport, and superconducting properties.
The electronic structure of the ferromagnetic superconductor URhGe in the paramagnetic phase has been studied by angle-resolved photoelectron spectroscopy using soft x rays (hn=595-700 eV). Dispersive bands with large contributions from U 5f states w
ere observed in the ARPES spectra, and form Fermi surfaces. The band structure in the paramagnetic phase is partly explained by the band-structure calculation treating all U 5f electrons as being itinerant, suggesting that an itinerant description of U 5f states is a good starting point for this compound. On the other hand, there are qualitative disagreements especially in the band structure near the Fermi level (E_B < 0.5 eV). The experimentally observed bands are less dispersive than the calculation, and the shape of the Fermi surface is different from the calculation. The changes in spectral functions due to the ferromagnetic transition were observed in bands near the Fermi level, suggesting that the ferromagnetism in this compound has an itinerant origin.
The magnetic and electronic properties of Sr1-xLaxRuO3 were studied by means of dc-magnetization, ac-susceptibility, specific heat, and electrical resistivity measurements. The dc-magnetization and ac-susceptibility measurements have revealed that th
e transition temperature and the ordered moment of the ferromagnetic order are strongly suppressed as La is substituted for Sr. The ac-susceptibility exhibits a peak at T* due to the occurrence of spontaneous spin polarization. Furthermore, we observed that T* shows clear frequency variations for x>= 0.3. The magnitude of the frequency shifts of T* is comparable to that of cluster-glass systems, and the frequency dependence is well described in terms of the Vogel-Fulcher law. On the other hand, it is found that the linear specific heat coefficient gamma enhances with the suppression of the ferromagnetic order. The relatively large gamma values reflect the presence of the Ru 4d state at Fermi level, and hence, the magnetism of this system is considered to be tightly coupled with the itinerant characteristics of the Ru 4d electrons. The present experimental results and analyses suggest that the intrinsic coexistence of the spatially inhomogeneous magnetic state and the itinerant nature of the Ru 4d electrons is realized in this system, and such a feature may be commonly involved in La- and Ca-doped SrRuO3.
High-energy-resolution core-level and valence-band photoelectron spectroscopic studies were performed for the heavy Fermion uranium compounds UGe2, UCoGe, URhGe, URu2Si2, UNi2Al3, UPd2Al3, and UPt3 as well as typical localized and itinerant uranium c
ompounds to understand the relationship between the uranium valence state and their core-level spectral line shapes. In addition to the main line and high-binding energy satellite structure recognized in the core-level spectra of uranium compounds, a shoulder structure on the lower binding energy side of the main lines of localized and nearly localized uranium compounds was also found. The spectral line shapes show a systematic variation depending on the U 5f electronic structure. The core-level spectra of UGe2, UCoGe, URhGe, URu2Si2, and UNi2Al3 are rather similar to those of itinerant compounds, suggesting that U 5f electrons in these compounds are well hybridized with ligand states. On the other hand, the core-level spectra of UPd2Al3 and UPt3 show considerably different spectral line shapes from those of the itinerant compounds, suggesting that U 5f electrons in UPd2Al3 and UPt3 are less hybridized with ligand states, leading to the correlated nature of U 5f electrons in these compounds. The dominant final state characters in their core-level spectra suggest that the numbers of 5f electrons in UGe2, UCoGe, URhGe, URu2Si2, UNi2Al3, and UPd2Al3 are close to but less than three, while that of UPt3 is close to two rather than to three.
