Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userCrystal, local atomic and electronic structures of YbFe$_2$Zn$_{20-x}$Cd$_x$ ($0 leq x leq 1.4$): a multi-band system with possible coexistence of light and heavy fermions
65
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
The partial (up to 7 %) substitution of Cd for Zn in the Yb-based heavy-fermion material YbFe$_2$Zn$_{20}$ is known to induce a slight ($sim 20$ %) reduction of the Sommerfeld specific heat coefficient $gamma$ and a huge (up to two orders of magnitude) reduction of the $T^2$ resistivity coefficient $A$, corresponding to a drastic and unexpected reduction of the Kadowaki-Woods ratio $A/gamma ^2$. Here, Yb $L_{3}$-edge X-ray absorption spectroscopy shows that the Yb valence state is close to $3+$ for all $x$, whereas X-ray diffraction reveals that Cd replace the Zn ions only at the $16c$ site of the $Fdbar{3}m$ cubic structure, leaving the $48f$ and $96g$ sites with full Zn occupation. Ab-initio electronic structure calculations in pure and Cd-doped materials, carried out without considering correlations, show multiple conduction bands with only minor modifications of the band dispersions near the Fermi level and therefore do not explain the resistivity drop introduced by Cd substitution. We propose that the site-selective Cd substitution introduces light conduction bands with substantial contribution of Cd($16c$) $5p$ levels that have weak coupling to the Yb$^{3+}$ $4f$ moments. These light fermions coexist with heavy fermions originated from other conduction bands with larger participation of Zn($48f$ and $96g$) $4p$ levels that remain strongly coupled with the Yb$^{3+}$ local moments.
rate research
Read More
Remarkably, doping isovalent $d^{10}$ and $d^0$ cations onto the $B$ site in $A_2B$$B$O$_6$ double perovskites has the power to direct the magnetic interactions between magnetic $B$ cations. This is due to changes in orbital hybridization, which favors different superexchange pathways, and leads to the formation of alternative magnetic structures depending on whether $B$ is $d^{10}$ or $d^0$. Furthermore, the competition generated by introducing mixtures of $d^{10}$ and $d^0$ cations can drive the material into the realms of exotic quantum magnetism. Here, a W$^{6+}$ $d^0$ dopant was introduced to a $d^{10}$ hexagonal perovskite Ba$_2$CuTeO$_6$, which possesses a spin ladder geometry of Cu$^{2+}$ cations, creating a Ba$_2$CuTe$_{1-x}$W$_x$O$_6$ solid solution ($x$ = 0 - 0.3). Neutron and synchrotron X-ray diffraction show that W$^{6+}$ is almost exclusively substituted for Te$^{6+}$ on the corner-sharing site within the spin ladder, in preference to the face-sharing site between ladders. This means the intra-ladder interactions are selectively tuned by the $d^0$ cations. Bulk magnetic measurements suggest this suppresses magnetic ordering in a similar manner to that observed for the spin-liquid like material Sr$_2$CuTe$_{1-x}$W$_x$O$_6$. This further demonstrates the utility of $d^{10}$ and $d^0$ dopants as a tool for tuning magnetic ground states in a wide range of perovskites and perovskite-derived structures.
Electron-electron (e-e) and electron-hole (e-h) interactions are often associated with many exotic phenomena in correlated electron systems. Here, we report an observation of anomalous excitons at 3.75 , 4.67 and 6.11 eV at 4.2 K in bulk-SrTiO$_3$. Fully supported by ab initio GW Bethe-Salpeter equation calculations, these excitons are due to surprisingly strong e-h and e-e interactions with different characters: 4.67 and 6.11 eV are resonant excitons and 3.75 eV is a bound Wannier-like exciton with an unexpectedly higher level of delocalization. Measurements and calculations on SrTi$_{1-x}$Nb$_x$O$_3$ for 0.0001$leq$x$leq$0.005 further show that energy and spectral-weight of the excitonic peaks vary as a function of electron doping (x) and temperature, which are attributed to screening effects. Our results show the importance of e-h and e-e interactions yielding to anomalous excitons and thus bring out a new fundamental perspective in SrTiO$_3$.
We report the temperature and magnetic field dependence of transport properties in epitaxial films of the manganite La$_{1-x}$Ca$_{x}$MnO$_{3}$ in the overdoped region of the phase diagram for $x > 0.5$, where a charge--ordered (CO) and an antiferromagnetic (AF) phase are present. Resistivity, magnetoresistance and angular dependence of magnetoresistance were measured in the temperature interval $4.2 ~mathrm{K} < T < 300 ~mathrm{K}$, for three concentrations $x = 0.52, 0.58$ and $0.75$ and in magnetic fields up to 5 T. The semiconductor/insulator--like behavior in zero field was observed in the entire temperature range for all three concentrations textit{x} and the electric conduction, at lower temperatures, in the CO state obeys 3D Motts variable--range hopping model. A huge negative magnetoresistance for $x = 0.52$ and $x = 0.58$, a metal--insulator transition for $B > 3 ~mathrm{T}$ for $x = 0.52$ and the presence of anisotropy in magnetoresistance for $x = 0.52$ and $x = 0.58$ show the fingerprints of colossal magnetoresistance (CMR) behavior implying the existence of ferromagnetic (FM) clusters. The declining influence of the FM clusters in the CO/AF part of the phase diagram with increasing $x$ contributes to a possible explanation that a phase coexistence is the origin of the CMR phenomenon.
Here we report the observation of Fermi surface (FS) pockets via the Shubnikov de Haas effect in Na$_x$CoO$_2$ for $x = 0.71$ and 0.84, respectively. Our observations indicate that the FS expected for each compound intersects their corresponding Brillouin zones, as defined by the previously reported superlattice structures, leading to small reconstructed FS pockets, but only if a precise number of holes per unit cell is emph{localized}. For $0.71 leq x < 0.75$ the coexistence of itinerant carriers and localized $S =1/2$ spins on a paramagnetic triangular superlattice leads at low temperatures to the observation of a deviation from standard Fermi-liquid behavior in the electrical transport and heat capacity properties, suggesting the formation of some kind of quantum spin-liquid ground state.
We report the successful synthesis of FeSe$_{1-x}$S$_{x}$ single crystals with $x$ ranging from 0 to 1 via a hydrothermal method. A complete phase diagram of FeSe$_{1-x}$S$_{x}$ has been obtained based on resistivity and magnetization measurements. The nematicity is suppressed with increasing $x$, and a small superconducting dome appears within the nematic phase. Outside the nematic phase, the superconductivity is continuously suppressed and reaches a minimum $T_c$ at $x$ = 0.45; beyond this point, $T_c$ slowly increases until $x$ = 1. Intriguingly, an anomalous resistivity upturn with a characteristic temperature $T^*$ in the intermediate region of $0.31 leq x leq 0.71$ is observed. $T^{*}$ shows a dome-like behavior with a maximum value at $x$ = 0.45, which is opposite the evolution of $T_c$, indicating competition between $T^*$ and superconductivity. The origin of $T^*$ is discussed in detail. Furthermore, the normal state resistivity evolves from non-Fermi-liquid to Fermi-liquid behavior with S doping at low temperatures, accompanied by a reduction in electronic correlations. Our study addresses the lack of single crystals in the high-S doping region and provides a complete phase diagram, which will promote the study of relations among nematicity, superconductivity, and magnetism.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
