Author/Authors :
Wu، نويسنده , , M.M. and Cheng، نويسنده , , Y.Z. and Peng، نويسنده , , J. and Xiao، نويسنده , , X.L. and Chen، نويسنده , , D.F. and Kiyanagi، نويسنده , , R. and Fieramosca، نويسنده , , J.S. and Short، نويسنده , , S. E. Jorgensen, I. Johnsen، نويسنده , , J. and Hu، نويسنده , , Z.B.، نويسنده ,
Abstract :
The syntheses and structures of Er2−xCexW3O12 were studied. It was found that pure phases could form only for 0.0 ≦ x ≦ 0.4 and 1.5 ≦ x ≦ 2.0. Compounds with 0 ≦ x ≦ 0.4 have the hydrated orthorhombic structure at room temperature and transform to unhydrated orthorhombic one above 135 °C whereas samples with 1.5 ≦ x ≦ 2.0 crystallize in monoclinic structure. Thermal expansion properties of Er2−xCexW3O12 were studied with high temperature X-ray powder diffraction. Samples with 0 ≦ x ≦ 0.4 exhibit negative thermal expansion in temperature range of 200–800 °C and higher cerium content leads to more negative thermal expansion coefficient. However, compounds with 1.5 ≦ x ≦ 2.0 show positive thermal expansion owing to the edge-sharing polyhedra.
Keywords :
D. Thermal expansion , C. Thermogravimetric analysis , D. Crystal structure , C. X-ray diffraction