Abstract
The crystal structures of the rhombohedral compounds ACrX 2 (A = Na, Ag, Cu; X = S, Se) at 300 and 4 K have been refined from neutron-diffraction powder data. The structures are based on cubic close-packings of the anions with Cr in half of the octahedral holes, so that CrX2 sandwiches are formed. Na occupies the octahedral holes between these sandwiches, Ag and Cu half of the tetrahedral holes; Ag and Cu have anomalously large (and anisotropic) thermal parameters, probably indicating a statistical distribution of these atoms around their average positions. The Ag and Cu compounds undergo reversible phase transitions at 397°C (AgCrS 2 ), 402°C (CuCrS 2 ), or 202°C (AgCrSe 2 ); in the high-temperature forms the Ag and Cu atoms are randomly distributed over all tetrahedral holes between the CrX 2 sandwiches. The magnetic structures of NaCrS 2 , NaCrSe 2 , and AgCrSe 2 at 4.2 K have been determined by neutron diffraction. The magnetic moments of Cr 3+ (about 15 % less than the spin-only value) are perpendicular to the c axis. The moments in pseudohexagonal (110) planes are collinear, spins at a distance (−⅓,⅓,⅓) being antiparallel, spins at a distance (⅓, −⅓,⅔) parallel. The spins in adjacent (110) planes make angles , where , = 0° for NaCrSe 2 , = 14° for AgCrSe 2 , = 33° for NaCrS 2 . Thus, NaCrSe 2 2 consists of ferromagnetic layers perpendicular to c, the spins in adjacent layers being antiparallel. In NaCrS 2 and AgCrSe 2 the layers are helimagnetic. These magnetic structures and those of KCrS 2 and LiCrS 2 are discussed in terms of antiferromagnetic direct Cr-Cr interactions and ferromagnetic Cr-X-Cr interactions between Cr neighbors in the layers; the former interaction predominates for small, the latter for large Cr-Cr distances.
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