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TT: Fachverband Tiefe Temperaturen
TT 30: Superconductivity: Cuprate High-Temperature Superconductors 2
TT 30.5: Vortrag
Mittwoch, 25. März 2009, 15:00–15:15, HSZ 304
Doping by metal-oxygen complexes and phase separation in the superconducting solid solution Bi2+ySr2−xLaxCuO6+δ — •Jürgen Röhler1, Christoph Trabant1, Sebastian Standop1, Helmut Dwelk2, and Alica Krapf2 — 1Universität zu Köln, 50937 Köln — 2Humboldt Universität zu Berlin, 12489 Berlin
Hole doping, nh (x), of the single-layer superconductor
Bi2+ySr2−xLax
CuO6+δ (BLSCO) is shown from systematic x-ray absorption measurements at the Cu-, La- and Bi-sites to be
controlled by formation of the metal-oxygen complexes
[La3+–O2−], or/and [Bi3+–O2−]. It is not, as
generally assumed, controlled simply by cationic La3+/Sr2+ mixed valency.
Interstitial excess oxygen atoms, taken up together with the
substitution of Sr2+ by La3+ and partially also by excess
Bi3+, reside at two different sites in two different complex ion formations :
[La–O] and/or [Bi–O] close
to the faces of the CuO6 octahedra, and [La2–O] in between the
Sr–O and Bi–O layers. The former dope holes into the
CuO2 planes. The latter do not, but break the van der Waals bonds
in the Bi-O double layers allowing for the stabilization of
co-existing monoclinic and orthorhombic superstructures. The intricate
competition between these three different
complex formations is connected with the electronic inhomogeneities in the
underdoped, and the macroscopic decomposition in the overdoped regimes.
It may be also at the origin of the singular stability of BLSC around its optimum
doped composition xLa≃ 0.35, and of the hole saturation in the overdoped
regime at nh≃ 0.2.
Supported by the ESRF through projects HE2644 and HE2955.