کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1333274 | 979072 | 2007 | 9 صفحه PDF | دانلود رایگان |

New oxides of general formula Sr2Ru2−xCoxO6−δ (0.5⩽x⩽1.5) have been synthesized as polycrystalline materials and characterized structurally by X-ray diffraction. For 0.5⩽x<0.67 the orthorhombic, Pnma, perovskite structure of the end member, SrRuO3, is found. At x=0.67 a phase separation into an Ru-rich Pnma phase and a Co-rich I2/c phase occurs. The I2/c form is also found for x=1.0 but another orthorhombic phase, Imma, obtains for x=1.33 and 1.5. Reductive weight losses indicate negligible oxygen non-stoichiometry, i.e., δ∼0, for all compositions even those rich in Co. High-resolution electron energy loss spectroscopy (EELS) indicates that cobalt is high-spin Co3+ or high-spin Co4+ for all x. Appropriate combinations of Ru4+, Ru5+, HS Co3+ and HS Co4+ are proposed for each x which are consistent with the observed Ru(Co)–O distances. Significant amounts of Co4+ must be present for large x values to explain the short observed distances. Broad maxima in the d.c. susceptibilities are found between 78 and 97 K with increasing x, along with zero-field-cooled (ZFC) and field-cooled (FC) divergences suggesting glassy magnetic freezing. A feature near 155 K for all samples indicates a residual amount of ferromagnetic SrRuO3 not detected by X-ray diffraction.
Correlation between the average B-site radius, the Goldschmidt tolerance factor and the sequence of space groups and Glazer tilt systems found for the perovskite solid solution Sr2Ru2−xCoxO6.Figure optionsDownload as PowerPoint slide
Journal: Journal of Solid State Chemistry - Volume 180, Issue 4, April 2007, Pages 1209–1217