摘要

A new method for the synthesis of Ce0.80Sm0.20O1.90 is presented. A drying of a solution of ethylene glycol and stoichiometric amounts of the acetates Ce(C2H3O2)(3)center dot xH(2)O and Sm(C2H3O2)(3)center dot xH(2)O resulted in a highly crystalline product of [Ce0.80Sm0.20(G(2)H(3)O(2))(3)(C2H6O2)](n), a new chained polymeric coordination compound. With the calcination of this precursor at 900 degrees C and sintering at 1150 degrees C, pure Ce0.80Sm0.20O1.90, was obtained with the desired homogeneity and density. This paper reports elemental (CHN and ICP-MS) and single crystal X-ray structure analyses of the precursor [Ce0.80Sm0.20(C2H3O2)(3)(C2H6O2)](n). Its thermal decomposition to Ce0.80Sm0.20O1.90 has been studied via HT-XRD and TG-DTA analysis. The structure and composition of Ce0.80Sm0.20O1.90 was also confirmed by powder XRD (Rietveld refinement).

  • 出版日期2012-8