Structure evolution upon chemical and physical pressure in (Sr1-xBax)2FeSbO6

Here we demonstrate the gradual structural transformation from the monoclinic I2/m to tetragonal I4/m, cubic Fm-3m and hexagonal P6(3)/mmc structure upon the isovalent larger-for-smaller A-site cation substitution in the B-site ordered double-perovskite system (Sr1-xBax)(2)FeSbO6. This is the same transformation sequencepreviously observed up to Fm-3m upon heating the parent Sr2FeSbO6 phase to high temperatures. High-pressure treatment, on the other hand, transforms the hexagonal P6(3)/mmc structure of the other end member Ba2FeSbO6 back to the cubic Fm-3m structure. Hence we may conclude that chemical pressure, physical pressure and decreasing temperature all work towards the same direction in the (Sr1-xBax)(2)FeSbO6 system. Also shown is that with increasing Ba-for-Sr substitution level, i.e. with decreasing chemical pressure effect, the degree-of-order among the B-site cations, Fe and Sb, decreases.