Raman selection rules in uniaxial media: The nonpolar modes of Mn Ga2 Se4

Under the terms of the Creative Commons Attribution License 3.0 (CC-BY).It is known that optically anisotropic media can change the polarization of light propagating inside them. As regards Raman spectroscopy, this affects the light intensity measured in different geometrical configurations and results in an apparent unfulfillment of selection rules. We present an experimental and theoretical study of such effects in the defect chalcopyrite semiconductor MnGa2Se4. Optical anisotropy is taken into account by including in the calculation of Raman intensities the phase difference appearing between ordinary and extraordinary waves as they propagate, in uniaxial media, with different velocities. Birefringence can be obtained from Raman measurements provided that the distance run by the light is known.We acknowledge financial support from research project MAT2001-3713-C04.Peer Reviewe

Apatite germanates doped with tungsten: Synthesis, structure, and conductivity

et al.High oxygen content apatite germanates, La10Ge 6-xWxO27+x, have been prepared by doping on the Ge site with W. In addition to increasing the oxygen content, this doping strategy is shown to result in stabilisation of the hexagonal lattice, and yield high conductivities. Structural studies of La10Ge 5.5W0.5O27.5 show that the interstitial oxygen sites are associated to a different degree with the Ge/WO4 tetrahedra, leading to five coordinate Ge/W and significant disorder for the oxygen sites associated with these units. Raman spectroscopy studies suggest that in the case of the WO5 units, the interstitial oxygen is more tightly bonded and therefore not as mobile as in the case of the GeO5 units, thus not contributing significantly to the conduction process. © 2011 The Royal Society of Chemistry.Financial support from Spanish project MAT2007-64486-C07-02 is acknowledged.Peer Reviewe

New objects in old structures: The Iron Age hoard of the Palacio III megalithic funerary complex (Almadén de la Plata, Seville, Spain)

Cultural contact, exchange and interaction feature high in the list of challenging topics of current research on European Prehistory. Not far off is the issue of the changing role of monuments in the making and maintaining of key cultural devices such as memory and identity. Addressing both these highly-debated issues from a science-based perspective, in this paper we look at an unusual case study set in southern Iberia and illustrate how these archaeological questions can benefit from robust materials-science approaches.We present the contextual, morphological and analytical study of an exceptional Early Iron Age hoard composed of a number of different (and mostly exotic) materials such as amber, quartz, silver and ceramic. This hoard, found under the fallen orthostat of a megalithic structure built at least 2000 years earlier, throws new light on long-distance exchange networks and the effect they could have had on the cultural identities and social relations of local Iberian Early Iron Age communities. Moreover, the archaeometric study reveals how diverse and distant the sources of these item are (Northern Europe to Eastern and Western Mediterranean raw materials, as well as local and eastern technologies), therefore raising questions concerning the social mechanisms used to establish change and resistance in contexts of colonial encounter

The interplay of university and industry through the FP5 network

To improve the quality of life in a modern society it is essential to reduce the distance between basic research and applications, whose crucial roles in shaping today's society prompt us to seek their understanding. Existing studies on this subject, however, have neglected the network character of the interaction between university and industry. Here we use state-of-the-art network theory methods to analyze this interplay in the so-called Framework Programme--an initiative which sets out the priorities for the European Union's research and technological development. In particular we study in the 5th Framework Programme (FP5) the role played by companies and scientific institutions and how they contribute to enhance the relationship between research and industry. Our approach provides quantitative evidence that while firms are size hierarchically organized, universities and research organizations keep the network from falling into pieces, paving the way for an effective knowledge transfer.Comment: 21 pages (including Appendix), 8 figures. Published online at http://stacks.iop.org/1367-2630/9/18

Synthesis and characterization of NaNiF3·3H2O: An unusual ordered variant of the ReO3 type

et al.A new hydrated sodium nickel fluoride with nominal composition NaNiF3·3H2O was synthesized using an aqueous solution route. Its structure was solved by means of ab initio methods from powder X-ray diffraction and neutron diffraction data. NaNiF3·3H2O crystallizes in the cubic crystal system, space group Pn3̅ with a = 7.91968(4) Å. The framework, derived from the ReO3 structure type, is built from NaX6 and NiX6 (X = O, F) corner-shared octahedra, in which F and O atoms are randomly distributed on a single anion site. The 2a × 2a × 2a superstructure arises from the strict alternate three-dimensional linking of NaX6 and NiX6 octahedra together with the simultaneous tilts of the octahedra from the cube axis (φ = 31.1°), with a significant participation of hydrogen bonding. NaNiF3·3H2O corresponds to a fully cation-ordered variant of the In(OH)3 structure, easily recognizable when formulated as NaNi(XH)6 (X = O, F). It constitutes one of the rare examples for the a+a+a+ tilting scheme with 1:1 cation ordering in perovskite-related compounds. The Curie-like magnetic behavior well-reflects the isolated paramagnetic Ni2+ centers without worth mentioning interactions. While X-ray and neutron diffraction data evidence Na/Ni order in combination with O/F disorder as a main feature of this fluoride, results from Raman and magic-angle spinning NMR spectroscopies support the existence of specific anion arrangements in isolated square windows identified in structural refinements. In particular, formation of water molecules derives from unfavorable FH bond formation.We thank Ministerio de Ciencia e Innovación and Comunidad de Madrid for funding Project Nos. MAT2010-19837-C06 and P2009/PPQ-1626, respectively. Financial support from Universidad CEU San Pablo is also acknowledged.Peer reviewe

Caracterización estructural y espectroscópica de fibras cristalinas de Ce0.4Zr0.6O2 crecidas mediante el método de fusión zonal asistida por láser

[EN] A structural and spectroscopic characterization of crystalline rods of Ce0.4Zr0.6O2 grown by the laser floating zone (LFZ) method is presented. A precursor rod of Ce0.4Zr0.6O2 composition was sintered at 1500 ºC in air atmosphere and then processed by the LFZ technique with a CO2 laser. The processed material was characterized by XRD, SEM and Raman spectroscopy. In the as-grown, dark-color processed rod, the Raman spectrum evolves radially from a t’-like one, corresponding to Ce0.37Zr0.63O2 composition, at the edge of the rod, to a very broad and weak, cubic-like one, at the center. The degree of cerium reduction and oxygen non-stoichiometry were determined through measurements of the electronic Raman spectrum of Ce3+. A strong Ce3+ signal was found at the core of the rod, indicating strong reduction, whereas no Ce3+ signal was detected at the edge. To restore oxygen and Ce4+ content a section of the fiber was reoxidized at 620 ºC for 24 h. A very homogeneous spectrum was found in the reoxidized sample, that was assigned to a t’-phase of composition Ce0.42Zr0.58O2.[ES] Presentamos una caracterización estructural y espectroscópica de fibras cristalinas de Ce0.4Zr0.6O2 crecidas mediante fusión zonal asistida por láser (LFZ). Una barra del material precursor, de composición Ce0.4Zr0.6O2, fue sinterizada a 1500 ºC en atmósfera de aire y después procesada por LFZ con un láser de CO2. El material procesado fue caracterizado por difracción de rayos X, microscopía electrónica de barrido y espectroscopía Raman. En la fibra recién procesada, de color gris oscuro, el espectro Raman varía radialmente desde un espectro de tipo t’, correspondiente a una composición Ce0.37Zr0.63O2, en el borde de la fibra, hasta un espectro muy ensanchado y débil, de aspecto cúbico, en el centro. El grado de reducción del cerio y la no estequiometría del oxígeno se determinaron a través de las medidas del Raman electrónico del Ce3+. La señal de Ce3+ era muy intensa en el centro de la fibra, lo que indica una fuerte reducción, mientras que no se detectó en el borde. Para restablecer el contenido de oxígeno y de Ce4+ una parte de la fibra fue reoxidada a 620 ºC durante 24 h. El espectro de la muestra reoxidada, de color amarillo pálido y muy homogénea, fue asignado a una fase t’ de composición Ce0.42Zr0.58O2.Financial support from Spanish project MAT2004-03070-C05-03 is acknowledged.Peer reviewe

Temperature-dependent studies of the geometrically frustrated pyrochlores Ho2Ti2O7 and Dy2Ti2O7

A temperature-dependent Raman study of Ho2Ti2O7 and Dy2Ti2O7 single crystals was performed in the 5–873 K temperature range. Polarized spectra allowed us to establish the symmetries of the observed bands and revise the mode assignment made in previous works. Our studies revealed also two additional bands near 287 and 300 cm−1 for Dy2Ti2O7, which can be assigned to crystal field transitions in Dy3+ ions. Temperature dependent Raman studies showed large increase of linewidths. These changes have been analyzed in terms of strong third-order phonon-phonon anharmonic interactions. The Raman spectra also showed anomalous softening of the majority of phonon modes upon cooling in the whole temperature range studied. In contrast to this behavior, the F2g 310 cm−1 and Eg 330 cm−1 phonon modes showed hardening upon cooling down to about 100–120 K and then anomalous softening below this temperature. This anomalous behavior of phonon wave numbers has been attributed to the increase in octahedral distortion upon cooling