Transition from antiferromagnetic ordering to cluster-glass behaviour in the solid solution Gd4NiMg1−xAlx (0 ≤ x ≤ 0.9)

Various samples of the solid solution Gd4NiMg1−xAlx were synthesized from the elements in sealed tantalum ampoules in an induction furnace. These gadolinium-rich compounds crystallize with the cubic Gd4RhIn type structure, space group F 4 ¯ 3 m . All samples were characterized on the basis of Guinier powder patterns. The lattice parameter decreases with increasing aluminium content in a Vegard-like manner. The structures of two crystals were refined on the basis of diffractometer data: a = 1359.3(1), wR2 = 0.0711, 481 F2 values, 20 variables for Gd4NiMg0.52(1)Al0.48(1) and a = 1351.40(6), wR2 = 0.0665, 478 F2 values, 21 variables for Gd4NiMg0.10(1)Al0.90(1). The main structural motif is a rigid three-dimensional network of edge- and corner-sharing Gd6Ni trigonal prisms and isolated (Mg/Al)4 tetrahedra in fcc packing. The edge length of the tetrahedra drastically decreases from Gd4NiMg (309 pm) to Gd4NiMg0.10(1)Al0.90(1) (294 pm). The Gd4NiMg1−xAlx samples show Curie–Weiss behaviour with slightly higher magnetic moment values than the theoretical one for a free Gd3+ ion. By substitution of Gd4NiMg with aluminium the cell volume decreases and the atomic disorder (Mg/Al) induces a random distribution of the magnetic interactions. This leads to a shift of the Néel temperatures to lower values when increasing the aluminium content. Already for Gd4NiMg0.4Al0.6 the long-range antiferromagnetic ordering no longer exists and the system comes into a cluster-glass state.