Magnetically Frustrated Quaternary Chalcogenides with Interpenetrating Diamond Lattices
Abstract
A series of quaternary sulfides of the composition Na3MGaS4 (M = Mn (1), Fe (2), and Co (3)) have been synthesized in sealed quartz ampules. In these compounds, divalent transition metal and Ga occupy the same crystallographic site in the Ga-S network, forming a supertetrahedral, T2 (adamantane) unit, through the corner-sharing of four M/GaS4 tetrahedra. The corner sulfur atoms of the T2 clusters are further connected to similar T2 units to form an open continuous three-dimensional (3D) anionic framework of composition {[Ga2M2S8]n}6-. The framework resembles a zinc blende structure type if each T2 cluster is considered as a single tetrahedron and two such frameworks are intertwined to generate channels wherein reside the extra-framework Na+ ions. Placement of transition metals (Mn or Fe or Co) in the corner of a perfect supertetrahedron, adamantane building unit, generates an ideal lattice for geometrical magnetic frustration, which, on dilution with nonmagnetic metal (Ga), creates an ideal case for random frustration. Preliminary magnetic measurements indicate high negative values of the Weiss constant (-200 to -400 K) and the absence of any magnetic ordering, reinforcing the presence of magnetic frustration in all of these compounds.
Recommended Citation
S. Mohapatra et al., "Magnetically Frustrated Quaternary Chalcogenides with Interpenetrating Diamond Lattices," Inorganic Chemistry, vol. 56, no. 14, pp. 7650 - 7656, American Chemical Society (ACS), Jul 2017.
The definitive version is available at https://doi.org/10.1021/acs.inorgchem.7b00121
Department(s)
Chemistry
Keywords and Phrases
Ladders; Selenides; Magnetic Susceptibility
International Standard Serial Number (ISSN)
0020-1669; 1520-510X
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2017 American Chemical Society (ACS), All rights reserved.
Publication Date
01 Jul 2017
Comments
The authors acknowledge the funding from ERDC (Missouri S&T) and University of Missouri Research Board (UMRB).