Oxide electronics

Abstract:

The superconducting oxide BaPb(1-x)Bi(x)O3, discovered in 1975 (ref. 1), is an exotic system having an unusually high transition temperature (T(c)) of ~12K, despite a relatively low density of states at the Fermi level. The subsequent prediction that doping the electronically inactive barium donor sites, instead of the bismuth sites, might induce superconductivity with a higher T(c) led to the discovery in 1988 of superconductivity in the Ba(1-x)K(x)BiO3 system (T(c) ~30 K for x = 0.4). But it remains an open question why many of the superconducting properties of these materials are similar to those of the well-known copper oxide superconductors, despite their pronounced structural differences: the former have a three-dimensional bismuth-oxygen framework, whereas the structures of the latter are predominantly two-dimensional, consisting of copper-oxygen planes. Understanding of the copper oxide superconductors has gained immensely from the study of many different superconducting systems, and so it might be expected that the identification of bismuth oxide superconductors beyond the substituted BaBiO3 compounds will prove to be similarly fruitful. Here we report the synthesis of a second family of superconducting bismuth oxides, based on SrBiO3. We show that partial substitution of potassium or rubidium for strontium induces superconductivity with: T(c) values of ~12 K for Sr(1-x)K(x)BiO3 (x= 0.45-0.6) and ~13K for Sr(1-x)Rb(x)BiO3 (x = 0.5).

Abstract:

We report the first experimental observation of a pressure-induced structural phase transition in the RNiO3 series. At ≈ 40 kbar, the space group of NdNiO3 changes from Pbnm (orthorhombic) to the more symmetrical R3̄c (rhombohedral). This experiment confirms our previous results on PrNiO3 indicating that the symmetry of the structure increases with pressure.

Abstract:

It is shown that the superconducting and structural properties of Tl2Ba2CuO6+δ depend on at least two defects. The Tl/Cu ratio used during synthesis determines the concentration of a defect that is likely to be Cu substitution on the Tl site, based on previously published work that proves the existence of such a defect. The structure exhibits a smaller orthorhombic strain, or tetragonal symmetry, for high concentrations of this defect. Tc tends to be lowered by this defect. An oxygen interstitial defect in the Tl-O double layer has a more pronounced effect on Tc, allowing the compound to be overdoped as the concentration of this defect increases. Features in the diffraction data also suggest the existence of a third defect which may involve the filling of oxygen vacancies at an oxygen site in the structure during early stages of oxygenation.