Abstract
Investigation of the quaternary system, Ca⁻Eu⁻Cd⁻Sb, led to a discovery of the new solid solutions, Ca(1-x)Eu(x)Cd₂Sb₂, with the CaAl₂Si₂ structure type (x ≈ 0.3⁻0.9, hP5, P 3 ¯ m1, a = 4.6632(5)⁻4.6934(3) Å, c = 7.630(1)⁻7.7062(7) Å), Ca(2-x)Eu(x)CdSb₂ with the Yb₂CdSb₂ type (x ≈ 0.6, oS20, Cmc2₁, a = 4.646(2) Å, b = 17.733(7) Å, c = 7.283(3) Å), and Eu(11-x)Ca(x)Cd₆Sb(12) with the Sr(11)Cd₆Sb(12) type (x ≈ 1, mS58, C2/m, a = 32.407(4) Å, b = 4.7248(5) Å, c = 12.377(1) Å, β = 109.96(1)°). Systematic crystallographic studies of the Ca(1-x)Eu(x)Cd₂Sb₂ series indicated expansion of the unit cell upon an increase in the Eu content, in accordance with a larger ionic radius of Eu(2+) vs. Ca(2+). The Ca(2-x)Eu(x)CdSb₂ composition with x ≈ 0.6 adopts the non-centrosymmetric space group, Cmc2₁, although the parent ternary phase, Ca₂CdSb₂, crystallizes in the centrosymmetric space group, Pnma. Two non-equivalent Ca sites in the layered crystal structure of Ca(2-x)Eu(x)CdSb₂ get unevenly occupied by Eu, with a preference for the interlayer position, which offers a larger available volume. Similar size-driven preferred occupation is observed in the Eu(11-x)Ca(x)Cd₆Sb(12) solid solution with x ≈ 1.