No Arabic abstract
It is generally difficult to quantify the amounts of light elements in materials because of their low X-ray-scattering power, as this means that they cannot be easily estimated via X-ray analyses. Meanwhile, the recently reported layered superconductor, Sc$_{20}$C$_{8-x}$B$_x$C$_{20}$, requires a small amount of boron, which is a light element, for its structural stability. In this context, here, we quantitatively evaluate the optimal $x$ value using both the experimental and computational approaches. Using the high-pressure synthesis approach that can maintain the starting composition even after sintering, we obtain the Sc$_{20}$(C,B)$_{8}$C$_{20}$ phase by the reaction of the previously reported Sc$_{15}$C$_{19}$ and B (Sc$_{15}$B$_y$C$_{19}$). Our experiments demonstrate that an increase in $y$ values promotes the phase formation of the Sc$_{20}$(C,B)$_{8}$C$_{20}$ structure; however, there appears to be an upper limit to the nominal $y$ value to form this phase. The maximum $T_mathrm{c}$ $(=7.6text{ K})$ is found to correspond with the actual $x$ value of $x sim 5$ under the assumption that the sample with the same $T_mathrm{c}$ as the reported value $(=7.7text{ K})$ possesses the optimal $x$ amount. Moreover, we construct the energy convex hull diagram by calculating the formation enthalpy based on first principles. Our computational results indicate that the composition of Sc$_{20}$C$_4$B$_4$C$_{20}$ $(x=4)$ is the most thermodynamically stable, which is reasonably consistent with the experimentally obtained value.
We have investigated the in-plane anisotropy of the c-axis magnetoresistance (MR) in both superconducting and normal states of single crystals of NdO0.7F0.3BiS2 under in-plane magnetic fields. In the superconducting states of NdO0.7F0.3BiS2, four-fold-symmetric in-plane anisotropy of the c-axis MR was observed below the superconducting transition temperature. Since the crystal structure of NdO0.7F0.3BiS2 is tetragonal, the rotational symmetry in the superconducting state is preserved in the present compound. This result is clearly different from the previous report observed in LaO0.5F0.5BiSSe single crystals, where the in-plane MR in the superconducting state shows two-fold symmetry. On the other hand, in the normal states of NdO0.7F0.3BiS2, two-fold symmetric MR with a small amplitude was observed. The possible origin of the two-fold-symmetric behavior was discussed with the presence of local structural disorder in the conducting plane of BiCh2-based compounds.
We have synthesized bulk Mg(B$_{1-x}$C$_x$)$_2$ from a mixture of elemental Mg, B, and the binary compound B$_4$C. Carbon incorporation was dramatically improved by a two step reaction process at an elevated temperature of 1200 $^o$C. This reaction process results in a solubility limit near x$sim$0.07. We found that impurities in the starting B cause an additive suppression of T$_c$. We combine these data with T$_c$ and H$_{c2}$(T=0) data from CVD wires as well as plasma spray synthesized powders and present a unifying H$_{c2}$ and T$_c$ versus x plot.
X-ray diffraction indicates that the structure of the recently discovered room temperature carbonaceous sulfur hydride (C-S-H) superconductor is derived from previously established van der Waals compounds found in the H$_2$S-H$_2$ and CH$_4$-H$_2$ systems. Crystals of the superconducting phase were produced by a photochemical synthesis technique leading to the superconducting critical temperature $T_c$ of 288 K at 267 GPa. Single-crystal x-ray diffraction patterns measured from 124 to 178 GPa, within the pressure range of the superconducting phase, give an orthorhombic structure derived from the Al$_2$Cu-type determined for (H$_2$S)$_2$H$_2$ and (CH$_4$)$_2$H$_2$ that differs from those predicted and observed for the S-H system to these pressures. The formation and stability of the C-S-H compound can be understood in terms of the close similarity in effective volumes of the H$_2$S and CH$_4$ components over a broad range of pressures. The relative amounts of carbon and sulfur in the structure is not determined, and denser carbon-bearing S-H structures may form at higher pressures. The results are consistent with hole-doping enhancement of $T_c$ by carbon proposed for the room-temperature superconductivity in this system.
The B-T phase diagram for thin film YBa_2Cu_3O_7-d with B parallel to the superconducting layers has been constructed from GHz transport measurements to 150T. Evidence for a transition from a high T regime dominated by orbital effects, to a low T regime where paramagnetic limiting drives the quenching of superconductivity, is seen. Up to 110T the upper critical field is found to be linear in T and in remarkable agreement with extrapolation of the longstanding result of Welp et al arising from magnetisation measurements to 6T. Beyond this a departure from linear behaviour occurs at T=74K, where a 3D-2D crossover is expected to occur.
Superconductors with topological surface or edge states have been intensively explored for the prospect of realizing Majorana bound states, which obey non-Abelian statistics and are crucial for topological quantum computation. The traditional routes for making topological insulator/superconductor and semiconductor/superconductor heterostructures suffer fabrication difficulties and can only work at low temperature. Here, we use angle-resolved photoemission spectroscopy to directly observe the evolution of a topological transition of band structure nearby the Fermi level in two-dimensional high-T$_{c}$ superconductor FeTe$_{1-x}$Se$_{x}$/SrTiO$_{3}$(001) monolayers, fully consistent with our theoretical calculations. Furthermore, evidence of edge states is revealed by scanning tunneling spectroscopy with assistance of theoretical calculations. Our study provides a simple and tunable platform for realizing and manipulating Majorana states at high temperature.