The present work reports new features of an X-ray diffraction pattern from Bi-Sr-Ca-Cu-0 (2212). The crystal had the orthorhombic cell with the lattice parameters: a= 5.407 A, b= 5.410 i\, ~~30.762 A, wave vectors of modulation q'= +S b\*+c\*, where 6~0.2 1, A new observation is diffuse spots locate
High resolution synchrotron X-ray powder diffraction study of the structure of Tℓ2Ba2CaCu2O8
✍ Scribed by M. Eibschutz; L.G. Van Uitert; W.H. Grodkiewicz; D.E. Cox
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 139 KB
- Volume
- 162-164
- Category
- Article
- ISSN
- 0921-4534
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✦ Synopsis
Polycrystalline material of approximate composition Te2Ba 2 Ca Cu2Os was synthesized by melting oxides together, pressing pellets and heating in sealed quartz tubes. High resolution synchrotron X-ray powder data obtained at beam-lineoXTA at the National Synchrotron Light Source revealed a tetragonal phase with a = 3.8545, c ----29.322A, and a few weak impurity peaks. Rietveld refinement based on space group I4/mmm gave results in essential agreement with those obtained in previous x-ray single crystal and neutron powder determinations, including appreciable positional disorder of the thallium and oxygen atoms in the Tt~-O planes. The refined site occupancies were found to be high for Ca and low for T~, consistent with partial substitution of the type (T~l.65Ca035)Ba2(Ca0 ssT~0 15)Cu208. However, the possibility that there is some Cu on the T~ sites cannot be excluded.
Recently there has been much interest in superconductors with superconducting transition temperatures (To) above 77K; these conductors do not contain rare earth elements. One such family of these high Tc superconductors consists of the T~-Ba-Ca-Cu-O compounds. 1 The superconducting compounds in the system T£-Ba-Ca-Cu-O have the general formula T£2Ba2 Can-1Cun 04n + 2, where n is the number of Cu-O layers stacked consecutively.
📜 SIMILAR VOLUMES
Single-crystal, stage-1 IBi2Sr2CaCu2Os+ x was synthes~zext. X-ray diffraction patterns indicate that upon intercalation, the c-axis correlation length decrea.,,,s substantially, but the in-plane host layer structure appears to remain unchanged. The compounds exhibit resonance Raman scattering. Raman