Browsing by Author "Suard, E"

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    High/low-moment phase transition in hexagonal Mn-Fe-P-Si compounds
    (American Physical Society, 2012-07-30) Dung, NH; Zhang, L; Ou, ZQ; Zhao, L; van Eijck, L; Mulders, AM; Avdeev, M; Suard, E; van Dijk, NH; Brück, E
    Using high-resolution neutron diffraction measurements for Mn-rich hexagonal Mn-Fe-P-Si compounds, we show that the substitution of Mn for Fe on the 3f sites results in a linear decrease of the Fe/Mn(3f) magnetic moments, while the Mn(3g) magnetic moments remain constant. With increasing temperature, the Mn(3g) magnetic moments show almost no change, while the Fe/Mn(3f) moments decrease quickly when the transition temperature is approached. The reduction of the magnetic moments at the transition temperature and in the high-temperature range is discussed based on changes in interatomic distances and lattice parameters and high-temperature magnetic-susceptibility measurement. © 2012, American Physical Society.
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    Magnetic structure of the quasi-two-dimensional antiferromagnet NiPS 3
    (American Physical Society, 2015-12-07) Wildes, AR; Simonet, V; Ressouche, E; McIntyre, GJ; Avdeev, M; Suard, E; Kimber, SAJ; Lançon, D; Pepe, G; Moubaraki, B; Hicks, TJ
    The magnetic structure of the quasi-two-dimensional antiferromagnet NiPS3 has been determined by magnetometry and a variety of neutron diffraction techniques. The experiments show that the samples must be carefully handled, as gluing influences the magnetometry measurements while preferred orientation complicates the interpretation of powder diffraction measurements. Our global set of consistent measurements show numerous departures from previously published results. We show that the compound adopts a k = [010] antiferromagnetic structure with the moment directions mostly along the a axis, and that the paramagnetic susceptibility is isotropic. The critical behavior was also investigated through the temperature dependence of the magnetic Bragg peaks below the Néel temperature. ©2015 American Physical Society
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    Solid-state chemistry shuffling of alkali ions toward new layered oxide materials
    (American Chemical Society, 2024-01-09) Mpanga, EM; Wernert, R; Fauth, F; Suard, E; Avdeev, M; Fraisse, B; Camacho, PS; Carlier, D; Lebedev, O; Cassidy, SJ; Rousse, G; Berthelot, R
    Alkali transition-metal layered compounds usually contain only one type of alkali cation between the edge-shared octahedra layers. Herein, the ternary phase diagram A2Ni2TeO6 (A = Li, Na, K) was explored through solid-state synthesis and new alkali-mixed compositions showing alternation of distinct alkali layers are obtained. Such intergrowth structures are synthesized either by a single high-temperature treatment from raw chemicals or through reaction between layered precursors, the latter involving a solid-state process triggered at moderate temperatures. The in-depth characterization of the multiple cationic orderings is performed by combining powder diffraction techniques (X-rays and neutrons), high-resolution transmission electron microscopy, and solid-state NMR spectroscopy. In addition to the Ni/Te honeycomb ordering, alternation of lithium layers with sodium or potassium layers is observed for compositions (Li/Na)2Ni2TeO6 or (Li/K)2Ni2TeO6, respectively. Crystal structure solving was achieved by stacking building blocks of the respective single alkali layered oxides and unveiled a complex out-of-plane ordering of honeycomb layers. Moreover, a solid-state reaction between Li2Ni2TeO6 and NaKNi2TeO6 enables preparation of the new phase Li∼1Na∼0.5K∼0.5Ni2TeO6, a unique example containing up to three alkali cations and exhibiting a more complex stacking with sodium and potassium cations occupying the same layer. This investigation confirms that the chemical versatility of layered alkali transition-metal compounds could also occur on the alkali layer. Following the research methodology described here, we revisit the crystal chemistry of alkali transition-metal layered materials by exploring alkali ion substitutions previously thought infeasible, in order to find new alkali-mixed compositions. © 2024 American Chemical Society.