posted on 2007-02-06, 00:00authored byGeng Bang Jin, Eun Sang Choi, Robert P. Guertin, James S. Brooks, Travis H. Bray, Corwin H. Booth, Thomas E. Albrecht-Schmitt
γ-LnLn‘S3 (Ln = La, Ce; Ln‘ = Er, Tm, Yb) have been prepared as dark red to black single crystals
by the reaction of the respective lanthanides with sulfur in a Sb2S3 flux at 1000 °C. This isotypic series
of compounds adopts a layered structure that consists of the smaller lanthanides (Er, Tm, and Yb) bound
by sulfide in six- and seven-coordinate environments that are connected together by the larger lanthanides
(La and Ce) in eight- and nine-coordinate environments. The layers can be broken down into three distinct
one-dimensional substructures containing three crystallographically unique Ln‘ centers. The first of these
is constructed from one-dimensional chains of edge-sharing [Ln‘S7] monocapped trigonal prisms that are
joined to equivalent chains via edge sharing to yield ribbons. There are parallel chains of [Ln‘S6] distorted
octahedra that are linked to the first ribbons through corner sharing. These latter units also share corners
with a one-dimensional ribbon composed of parallel chains of [Ln‘S6] polyhedra that edge-share both in
the direction of chain propagation and with adjacent identical chains. Magnetic susceptibility measurements
show Curie−Weiss behavior from 2 to 300 K with antiferromagnetic coupling and no evidence for
magnetic ordering. The θp values range from −0.4 to −37.5 K, and spin-frustration may be indicated for
the Yb-containing compounds. All compounds show magnetic moments substantially reduced from those
calculated for the free ions. The optical band gaps for γ-LaLn‘S3 (Ln‘ = Er, Tm, Yb) are approximately
1.6 eV, whereas γ-CeLn‘S3 (Ln‘ = Er, Tm, Yb) are approximately 1.3 eV.