RESUMO
Geometric magnetic frustration arises when the geometry of a structure prevents the simultaneous fulfillment of nearest-neighbor antiferromagnetic interactions and is commonly observed in lattices that exhibit a triangular topology, such as those found in the pyrochlore structure. Via a mild hydrothermal route, we have synthesized seven quaternary ß-pyrochlore-related fluorides AxM2+xM3+(2-x)F6 (A = Cs and Rb; M2+ = Co2+, Ni2+, and Zn2+; and M3+ = V3+ and Fe3+). Crystal structures and compositions were determined using a combination of single-crystal X-ray diffraction and energy-dispersive spectroscopy. After adjusting the reaction conditions, phase-pure products of AxM2+xM3+(2-x)F6 were obtained. The magnetic susceptibility and isothermal magnetization data for all seven compounds were collected to interpret the magnetic behavior, which ranged from paramagnetic to antiferromagnetic with and without a ferromagnetic component. We found that the magnetic behavior of the AxM2+xV3+(2-x)F6 pyrochlore structures strongly depends on the presence or absence of unpaired electrons on the M2+ position. The titled pyrochlore compounds, with the exception of the Zn-analogue, can be considered frustrated materials, with frustration indices in the range of 6-13.
RESUMO
Mild hydrothermal synthesis was employed to grow high-quality single crystals of ternary fluoridohafnates at low temperatures. The series of new materials was characterized using single-crystal X-ray diffraction, and the crystal structures of AHfF6 (A = Mg and Sr), A2HfF8 (A = Ba and Pb), Ca5Hf3F22, and Cd2HfF8(H2O)6 are discussed herein. Although some material compositions have similar stoichiometries, all of the compositions adopt different structural motifs. A comparison of the crystal structures and synthesis techniques of ternary fluoridohafnates and ternary fluoridozirconates is also reported, and the impact of the subtle changes of synthesis conditions on overall structures is discussed.
RESUMO
The solvothermal synthesis, structure determination and optical characterization of five new metastable halometallate compounds, [1,10-phenH][Pb3.5I8] (1), [1,10-phenH2][Pb5I12]·(H2O) (2), [1,10-phen][Pb2I4] (3), [1,10-phen]2[Pb5Br10] (4) and [1,10-phenH][SbI4]·(H2O) (5), are reported. The materials exhibit rich structural diversity and exhibit structural dimensionalities that include 1D chains, 2D sheets and 3D frameworks. The optical spectra of these materials are consistent with bandgaps ranging from 2.70 to 3.44 eV. We show that the optical behavior depends on the structural dimensionality of the reported materials, which are potential candidates for semiconductor applications.
RESUMO
Inverse weberites are of interest as geometrically frustrated magnetic materials due to their unique cation arrangement. We have synthesized nine isostructural materials that adopt the inverse weberite crystal structure, which consists of cross-linked kagome layers. These materials, having the general formula MIIMIIIF5(H2O)2 (MII = Co, Mn, Ni, Zn; MIII = Ga, Cr, Fe, V), were synthesized using mild hydrothermal conditions, which yielded phase-pure samples after optimization of the reaction conditions. Their crystal structures and optical, thermal, and magnetic behavior were characterized using single-crystal X-ray diffraction, UV-vis spectroscopy, thermogravimetric analysis, and measurement of the magnetic susceptibility and isothermal magnetization data, respectively. Three distinct types of magnetism were observed, including simple paramagnetism, antiferromagnetism, and canted antiferromagnetism; the last type is accompanied by a high frustration index fin the range 4.16-8.09. We demonstrated that the magnetic behavior of inverse weberites depends on the presence or absence of unpaired-electron-containing cations on the two distinct crystallographic sites, which can be employed for the prediction of the magnetic properties of other compounds in this rich and diverse family.
