Synthesis, crystal structure and low-temperature X-ray investigations of K 3Cu 8Se 6

Abstract

The new ternary mixed-valent copper selenide K 3Cu 8Se 6 has been prepared by the reaction of elemental copper with K 2Se 3 and additional selenium (molar ratio 1: 3: 1) at 623 K. The compound crystallizes in the monoclinic space group C2/m and is isotypic to K 3Cu 8S 6, RbCu 8S 6, Rb 3Cu 8Se 6 and Cs 3Cu 8Se 6. The structure consists of 1 ∞ [Cu 8Se 6] layers which are separated by the potassium cations. The copper atoms are either tetrahedrally distorted or trigonal planar coordinated by the selenium atoms. In the crystal structure the trigonal planar coordinated Cu atoms form double chains which are running parallel to the b-axis. These double chains are connected into layers via the distorted CuSe 4 tetrahedra which share edges and corners with the Se 3 triangles around Cu. In this part of the structure a very short Cu-Cu distances of only 2.497 (2) Å appears which is shorter than the Cu-Cu distance in elemental copper. Because the tetrahedrally coordinated copper ions exhibit unusual large anisotropic displacement parameters at room temperature, a low-temperature structure determination was performed. At low temperatures the anisotropic displacement coefficients are significantly smaller for all atoms, but even at 150 K some coefficients for the tetrahedrally coordinated Cu atoms are twice as large as for the trigonal planar coordinated Cu centers. However, the experiment shows that the nature of the disorder seems to be predominantly due to an enlarged mobility of the copper ions at room-temperature which is freezed on cooling. Our give no hints for the formation of a superstructure like in K 3Cu 8S 6.