Browsing by Author "Valldor, Martin"

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Canted Antiferromagnetism on Rectangular Layers of Fe2+ in Polymorphic CaFeSeO
(2017-04-17)
Lai, Kwing To
;
Komarek, Alexander Christoph
;
Fernandez-Diaz, Maria Teresa
;
Chang, Pi-Shan
;
Huh, Sungjoon
From stoichiometric amounts of CaO, Fe, and Se, pure powders and single crystals of quaternary Ca-infinity(2)[FeSe2/2O2/2] can be obtained by solid-state reaction and self-flux growth, respectively. The as-synthesized compound exhibits a polymorphic crystal structure, where the two modifications have different stacking sequences of (2)(infinity)[FeSe2/2O2/2](2-) layers. The two polymorphs have similar unit cells but different crystal symmetries (Cmc2(1), and Pnma), of which the former is non-centrosymmetric. Fe is divalent (d(6)) and high-spin, as proven by X-ray spectroscopy, Mossbauer spectroscopy, and powder neutron diffraction data. The latter two, in combination with magnetic susceptibility and specific heat data, reveal a long-range antiferromagnetic spin order (T-N = 160 K) with a minor spin canting. CaFeSeO is an electronic insulator, as confirmed by resistivity measurements and density functional theory calculations. The latter also suggest a relatively small energy difference between the two polymorphs, explaining their intimate intergrowth.
Synthesis and Characterization of Ba[CoSO]: Magnetic Complexity in the Presence of Chalcogen Ordering
(2015-07-20)
Valldor, Martin
;
Roessler, Ulrich K.
;
Prots, Yurii
;
Kuo, Chang-Yang
;
Chiang, Jen-Che
Barium thio-oxocobaltate(II), Ba[CoS2/2O2/2], was synthesized by the reaction of equimolar amounts of BaO, Co, and S in closed silica ampoules. The title compound (Cmcm, a=3.98808(3), b=12.75518(9), c=6.10697(4)angstrom) is isostructural to Ba[ZnSO]. The use of soft X-ray absorption spectroscopy confirmed that cobalt is in the oxidation state +2 and tetrahedrally coordinated. Its coordination consists of two sulfur and two oxygen atoms in an ordered fashion. High-temperature magnetic susceptibility data indicate strong low-dimensional spin-spin interactions, which are suggested to be closely related to the layer-type crystal structure and perhaps the ordered distribution of sulfur and oxygen. Antiferromagnetic ordering below T-N=222K is observed as an anomaly in the specific heat, coinciding with a significant lowering of the magnetic susceptibility. Density functional theory calculations within a generalized-gradient approximation (GGA)+U approach identify an antiferromagnetic ground state within the square-like two-dimensional layers of Co, and antiferromagnetic correlations for nearest and next nearest neighbors along bonds mediated by oxygen or sulfur. However, this magnetic state is subject to frustration by relatively strong interlayer couplings.