RESUMEN

The magnetoelectric effect in the RX3(BO3)4 system (R = Ho, Eu, Sm, Nd, Gd; X = Fe, Al) varies significantly with the cation R despite very similar structural arrangements. Our structural studies reveal a symmetry reducing tilting of the BO3 planes and of the FeO6 polyhedra in the systems exhibiting low magnetic field induced electric polarization. Neutron scattering measurements reveal a lack of magnetic ordering indicating the primary importance of the atomic structure in the multiferroic behavior of this system.

RESUMEN

Solar cells based on hybrid perovskites have shown high efficiency while possessing simple processing methods. To gain a fundamental understanding of their properties on an atomic level, we investigate single crystals of CH3NH3PbI3 with a narrow transition (~5 K) near 327 K. Temperature dependent structural measurements reveal a persistent tetragonal structure with smooth changes in the atomic displacement parameters (ADPs) on crossing T*. We show that the ADPs for I ions yield extended flat regions in the potential wells consistent with the measured large thermal expansion parameter. Molecular dynamics simulations reveal that this material exhibits significant asymmetries in the Pb-I pair distribution functions. We also show that the intrinsically enhanced freedom of motion of the iodine atoms enables large deformations. This flexibility (softness) of the atomic structure results in highly localized atomic relaxation about defects and hence accounts for both the high carrier mobility as well as the structural instability.

RESUMEN

High pressure x-ray diffraction measurements on perovskite RMnO3 (R = Dy, Ho and Lu) reveal that varying structural changes occur for different R ions. Large lattice changes (orthorhombic strain) occur in DyMnO3 and HoMnO3 while the Jahn-Teller (JT) distortion remains stable. Conversely, in the small R-ion system LuMnO3, Mn-O bond distortions are observed between 4 and 8 GPa with a broad minimum in the JT distortion. High pressure infrared measurements indicate that a phonon near 390 cm(-1) corresponding to the complex motion of the Mn and O ions changes anomalously for LuMnO3. It softens in the 4-8 GPa region, which is consistent with the structural change in Mn-O bonds and then hardens at higher pressures. By contrast, the phonons continuously harden with increasing pressure for DyMnO3 and HoMnO3. Density functional theory methods show that E-phase LuMnO3 is the most stable phase up to the 10 GPa pressure examined. Simulations indicate that the distinct structural change under pressure in LuMnO3 can possibly be used to optimize the electric polarization by pressure/strain.

RESUMEN

Detailed structural measurements on multiple length scales were conducted on a new perovskite phase of ScMnO3, and on orthorhombic LuMnO3 as a benchmark. Complementary density functional theory (DFT) calculations were carried out, and predict that ScMnO3 possesses E-phase magnetic order at low temperature with displacements of the Mn sites (relative to the high temperature state) of ∼0.07 Å, compared to ∼0.04 Å predicted for LuMnO3. However, detailed local, intermediate and long-range structural measurements by x-ray pair distribution function analysis, single crystal x-ray diffraction and x-ray absorption spectroscopy, find no local or long-range distortions on crossing into the low temperature E-phase of the magnetically ordered state. The measurements place upper limits on any structural changes to be at most one order of magnitude lower than DFT predictions and suggest that this theoretical approach does not properly account for the spin-lattice coupling in these oxides and may possibly predict the incorrect magnetic order at low temperatures. The results suggest that the electronic contribution to the electrical polarization dominates and should be more accurately treated in theoretical models.

RESUMEN

Adsorption mechanisms of Zn2+ and Ni2+ on hydrous manganese oxide (HMO) were investigated using XAS. Analyses reveal that both metal ions retain their primary hydration shell when sorbed to HMO, which is consistent with physical sorption. These local structures are invariant of pH (3.0-7.0) and adsorbate loading (10(-4) - 10(-2) mol (g of HMO)-1), suggesting one average type of adsorption mechanism. In addition to the first shell, a second shell was observed with 6-8 O atoms at 3.34 A for Ni and 8-10 O atoms at 3.49 A for Zn. The lack of Ni or Zn contributions in the second shell eliminates the possibility of surface precipitation or polymerization. Likewise, the absence of Mn atoms in the second shell suggests outer-sphere adsorption. Interestingly, the local structure of Ni and Zn sorbed to HMO did not change with reaction time when as much as 90% of the sorbed contribution was due to the slow sorption process, thus supporting intraparticle diffusion as the rate-limiting mechanism. This result demonstrates that adsorption sites located along the micropore walls of HMO are similar to ones located on the external surface. Overall, metals from the same group in the Periodic Table appear to form similar adsorption complexes with HMO.

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RESUMEN

The study of sulfur within the plasma cells of Ascidia ceratodes [Carlson, R. M. K. (1975) Proc. Natl. Acad. Sci. U.S.A. 72, 2217-2221; Frank, P., Carlson, R. M. K., & Hodgson, K. O. (1986) Inorg. Chem. 25, 470-478; Hedman, B., Frank, P., Penner-Hahn, J. E., Roe, A. L., Hodgson, K. O., Carlson, R. M. K., Brown, G., Cerino, J., Hettel, R., Troxel, T., Winick, H., & Yang, J. (1986) Nucl. Instrum. Methods Phys. Res., Sect. A 246, 797-800] has been extended with X-ray absorption near-edge structure (XANES) spectroscopy. An intense absorption feature at 2482.4 eV and a second feature at 2473.7 eV indicate a large endogenous sulfate concentration, as well as smaller though significant amounts of thiol or thioether sulfur, respectively. A strong shoulder was observed at 2481.7 eV on the low-energy side of the sulfate absorption edge, deriving from a novel type of sulfur having a slightly lower oxidation state than sulfate sulfur. The line width of the primary transition on the sulfur edge of a vanadium (III) sulfate solution was found to be broadened relative to that of sodium sulfate, possibly deriving from the formation of the VSO4+ complex ion [Britton, H. T. S., & Welford, G. (1940) J. Chem. Soc., 761-764; Duffy, J. A., & Macdonald, W. J. D. (1970) J. Chem. Soc., 977-980; Kimura, T., Morinaga, M., & Nakano, J. (1972) Nippon Kagaku Zaishi, 664-667]. Similar broadening appears to characterize the oxidized sulfur types in vanadocytes. A very good linear correlation between oxidation state and peak position (in electronvolts) was found for a series of related sulfur compounds. This correlation was used to determine a 5+ oxidation state for the additional sulfur type at 2481.7 eV. (ABSTRACT TRUNCATED AT 250 WORDS)

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