High-resolution Mn K-edge x-ray emission and absorption spectroscopy study of the electronic and local structure of the three different phases in Nd0.5Sr0.5MnO3

Nd0.5Sr0.5MnO3 is particularly representative of mixed-valent manganites since their three characteristic macroscopic phases (charge-ordered insulator, ferromagnetic-metallic, and paramagnetic insulator) appear at different temperatures.We here report a complete x-ray emission and absorption spectroscopy (XES-XAS) study of Nd0.5Sr0.5MnO3 as a function of temperature to investigate the electronic and local structure changes of the Mn atom in these three phases. Compared with the differences in the XES-XAS spectra between Nd0.5Sr0.5MnO3 and the single-valent reference compounds NdMnO3 (Mn3+) and Sr/CaMnO3 (Mn4+), only modest changes have been obtained across the magnetoelectrical transitions. The XES spectra, including both the Mn Kα and Kβ emission lines, have mainly shown a subtle decrease in the local spin density accompanying the passage to the ferromagnetic-metallic phase. For the same phase, the small intensity variations in the pre-edge region of the high-resolution XAS spectra reflect an increase of the p-d mixing. The analysis of these XAS spectra imply a charge segregation between the two different Mn sites far from one electron, being in intermediate valences Mn+3.5±δ/2(δ < 0.2 e−) for all the phases. Our results indicate that the spin, charge, and geometrical structure of the Mn atom hardly change among the three macroscopic phases demonstrating the strong competition between the ferromagnetic conductor and the charge-0rdered insulator behaviors in the manganites

Electronic states of R F e2 O4(R=Lu, Yb, Tm, Y) mixed-valence compounds determined by soft x-ray absorption spectroscopy and x-ray magnetic circular dichroism

We here report an investigation of the electronic states in the RFe2O4(R=Lu,Yb,Tm,Y) mixed-valence ferrites by means of soft x-ray absorption spectroscopy (XAS) and x-ray magnetic circular dichroism (XMCD) measurements together with ab initio theoretical calculations. The presence of Fe+2 and Fe+3 pure ionic species is discarded in the XAS spectra at the OK edge in both experimental data and simulations based on the multiple scattering theory. Similarly, no trace of Fe+2/Fe+3 contributions is detected in the XMCD spectra at the FeK edge. On the other hand, the XAS and XMCD spectra at the FeL2,3 edges can be well described in terms of Fe+2/Fe+3 contributions, and are also supported by multiplet calculations. This finding can be interpreted as the existence of a mixture of 3d5/3d6 configurations at the Fe atoms. Alternative ferrimagnetic spin orderings based on a trimodal Fe valence distribution are also proposed and discussed. Finally, a possible explanation for the strong dependence of the FeL2,3 edges XMCD signal magnitude on both the sample surface preparation and detection method is presented

Intrinsic electrical properties of LuFe2O4

We here revisit the electrical properties of LuFe2O4, compound candidate for exhibiting multiferroicity. Measurements of dc electrical resistivity as a function of temperature, electric-field polarization measurements at low temperatures with and without magnetic field, and complex impedance as a function of both frequency and temperature were carried out in a LuFe2O4 single crystal, perpendicular and parallel to the hexagonal c axis, and in several ceramic polycrystalline samples. Resistivity measurements reveal that this material is a highly anisotropic semiconductor, being about two orders of magnitude more resistive along the c axis. The temperature dependence of the resistivity indicates a change in the conduction mechanism at TCO ˜ 320 K from thermal activation above TCO to variable range hopping below TCO. The resistivity values at room temperature are relatively small and are below 5000 O¿cm for all samples but we carried out polarization measurements at sufficiently low temperatures, showing that electric-field polarization curves are a straight line as expected for a paraelectric or antiferroelectric material. Furthermore, no differences are found in the polarization curves when a magnetic field is applied either parallel or perpendicular to the electric field. The analysis of the complex impedance data corroborates that the claimed colossal dielectric constant is a spurious effect mainly derived from the capacitance of the electrical contacts. Therefore, our data unequivocally evidence that LuFe2O4 is not ferroelectric

X-ray absorption and emission spectroscopy study of Mn and Co valence and spin states in TbM n1-x C ox O3

The valence and spin state evolution of Mn and Co on TbMn1-xCoxO3 series is precisely determined by means of soft and hard x-ray absorption spectroscopy (XAS) and Kß x-ray emission spectroscopy (XES). Our results show the change from Mn3+ to Mn4+ both high-spin (HS) together with the evolution from Co2+ HS to Co3+ low-spin (LS) with increasing x. In addition, high energy resolution XAS spectra on the K pre-edge region are interpreted in terms of the strong charge transfer and hybridization effects along the series. These results correlate well with the spin values of Mn and Co atoms obtained from the Kß XES data. In this paper, we determine that Co enters into the transition metal sublattice of TbMnO3 as a divalent ion in HS state, destabilizing the Mn long-range magnetic order since very low doping compositions (x=0.1). Samples in the intermediate composition range (0.4=x=0.6) adopt the crystal structure of a double perovskite with long-range ferromagnetic ordering which is due to Mn4+-O-Co2+ superexchange interactions with both cations in HS configuration. Ferromagnetism vanishes for x=0.7 due to the structural disorder that collapses the double perovskite structure. The spectroscopic techniques reveal the occurrence of Mn4+ HS and a fluctuating valence state Co2+ HS/Co3+ LS in this composition range. Disorder and competitive interactions lead to a magnetic glassy behavior in these samples

Valence change of praseodymium in Pr0.5Ca0.5CoO3 investigated by x-ray absorption spectroscopy

X-ray absorption spectroscopy measurements in Pr0.5Ca0.5CoO3 were performed at the Pr M4,5, Pr L3, and Ca L2,3 absorption edges as a function of temperature below 300 K. Ca spectra show no changes down to 10 K while a noticeable thermally dependent evolution takes place at the Pr edges across the metal-insulator transition. Spectral changes are analyzed by different methods, including multiple scattering simulations, which provide quantitative details on an electron loss at Pr 4f orbitals. We conclude that in the insulating phase a fraction [15(+5)%] of Pr3+ undergoes a further oxidation to adopt a hybridized configuration composed of an admixture of atomic-like 4f1 states (Pr4+) and f- symmetry states on the O 2p valence band (Pr3+L states) indicative of a strong 4f- 2p interaction.Comment: 19 pages (.doc), 4 figures, Phys. Rev. B, in pres

Effects of A -site ordering on the Mn local structure and polar phases of R Ba Mn 2 O 6 ( R = La , Nd, Sm, and Y)

We have investigated the temperature dependence of the Mn local structure in A-site ordered RBaMn2O6 (R = La, Nd, Sm, and Y) perovskites, in parallel with their disordered counterparts, R0.5Ba0.5MnO3, by means of x-ray emission (XES) and x-ray absorption spectroscopy (XAS) The end member LaBaMn2O6 shows a nearly regular MnO6 octahedron independent of temperature. With decreasing the R ionic radius in the ordered samples, the XAS results indicate that a local distortion develops in the MnO6 octahedron at the low-temperature charge-localized and polar phases. For NdBaMn2O6, this local distortion is tiny, indicating the absence of charge segregation at the Mn site. This is followed by a bigger local distortion anticipated for SmBaMn2O6 in its respective charge-localized and polar phase and finally, the biggest local distortion for the smallest A-site cation ordered compound, YBaMn2O6, for which it even persists above the polar charge-localization transition temperatures. The high-resolution XAS spectra confirm the presence of charge segregation between two nonequivalent Mn sites in the low-temperature polar phase of Sm and Y ordered samples. Thus, our XAS study suggests a displacive mechanism for the charge-localization and polar transitions in the Nd and Sm ordered samples while a combination of displacive and order-disorder contributions is revealed for YBaMn2O6. Besides, calorimetric measurements confirm the combination of the two mechanisms, order-disorder and displacive, for the ordered Sm and Y compounds. On the other hand, the A-site disordered R0.5Ba0.5MnO3 samples with R cations smaller than Nd present a significant static (temperature-independent) local disorder, which explains why polar charge-localization transitions are not developed in these samples. Finally, we correlate our results about the Mn local structure and character of the transitions with the macroscopic magnetic and electric behavior of both A-site ordered and disordered compounds

On the evaluation and improvement of arabic wordnet coverage and usability

The final publication is available at Springer via http://dx.doi.org/10.1007/s10579-013-9237-0[EN] Built on the basis of the methods developed for Princeton WordNet and EuroWordNet, Arabic WordNet (AWN) has been an interesting project which combines WordNet structure compliance with Arabic particularities. In this paper, some AWN shortcomings related to coverage and usability are addressed. The use of AWN in question/answering (Q/A) helped us to deeply evaluate the resource from an experience-based perspective. Accordingly, an enrichment of AWN was built by semi-automatically extending its content. Indeed, existing approaches and/or resources developed for other languages were adapted and used for AWN. The experiments conducted in Arabic Q/A have shown an improvement of both AWN coverage as well as usability. Concerning coverage, a great amount of named entities extracted from YAGO were connected with corresponding AWN synsets. Also, a significant number of new verbs and nouns (including Broken Plural forms) were added. In terms of usability, thanks to the use of AWN, the performance for the AWN-based Q/A application registered an overall improvement with respect to the following three measures: accuracy (+9.27 % improvement), mean reciprocal rank (+3.6 improvement) and number of answered questions (+12.79 % improvement).The work presented in Sect. 2.2 was done in the framework of the bilateral Spain-Morocco AECID-PCI C/026728/09 research project. The research of the two first authors is done in the framework of the PROGRAMME D'URGENCE project (grant no. 03/2010). The research of the third author is done in the framework of WIQEI IRSES project (grant no. 269180) within the FP 7 Marie Curie People, DIANA-APPLICATIONS-Finding Hidden Knowledge in Texts: Applications (TIN2012-38603-C02-01) research project and VLC/CAMPUS Microcluster on Multimodal Interaction in Intelligent Systems. 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Comment on "X-ray resonant scattering studies of orbital and charge ordering in Pr1-xCaxMnO3"

In a recent published paper [Phys. Rev. B 64, 195133 (2001)], Zimmermann et al. present a systematic x-ray scattering study of charge and orbital ordering phenomena in the Pr1-xCaxMnO3 series with x= 0.25, 0.4 and 0.5. They propose that for Ca concentrations x=0.4 and 0.5, the appearance of (0, k+1/2, 0) reflections are originated by the orbital ordering of the eg electrons in the a-b plane while the (0, 2k+1, 0) reflections are due to the charge ordering among the Mn3+ and Mn4+ ions. Moreover, for small Ca concentrations (x<0.3), the orbital ordering is only considered and it occurs at (0, k, 0) reflections. A rigorous analysis of all these resonance reflections will show the inadequacy of the charge-orbital model proposed to explain the experimental results. In addition, this charge-orbital model is highly inconsistent with the electronic balance. On the contrary, these reflections can be easily understood as arising from the anisotropy of charge distribution induced by the presence of local distortions, i.e. due to a structural phase transition.Comment: 10 pages, 2 figures.To be published Phys. Rev.

Use of hyperspectral transmittance imaging to evaluate the internal quality of nectarines

[EN] The internal quality of nectarines (Prunus persica L. Batsch var. nucipersica) cv. 'Big Top' (yellow flesh) and 'Magique' (white flesh) has been inspected using hyperspectral transmittance imaging. Hyperspectral images of intact fruits were acquired in the spectral range of 630-900 nm using transmittance mode during their ripening under controlled conditions. The detection of split pit disorder and classification according to an established firmness threshold were performed using PLS-DA. The prediction of the Internal Quality Index (IQI) related to ripeness was performed using PLS-R. The most important variables were selected using interval-PLS. As a result, an accuracy of 94.7% was obtained in the detection of fruits with split pit of the 'Big Top' cultivar. Accuracies of 95.7% and 94.6% were achieved in the classification of the 'Big Top' and 'Magique' cultivars, respectively, according to the firmness threshold. The internal quality was predicted through the IQI with R-2 values of 0.88 and 0.86 for the two cultivars. The results obtained indicate the great potential of hyperspectral transmittance imaging for the assessment of the internal quality of intact nectarines.This work was partially funded by INIA and FEDER funds through project RTA2015-00078-00-00. Sandra Munera thanks INIA for the FPI-INIA grant num. 43 (CPR2014-0082), partially supported by European Union FSE funds.Munera, S.; Blasco Ivars, J.; Amigo, J.; Cubero-García, S.; Talens Oliag, P.; Aleixos Borrás, MN. (2019). Use of hyperspectral transmittance imaging to evaluate the internal quality of nectarines. Biosystems Engineering. 182:54-64. https://doi.org/10.1016/j.biosystemseng.2019.04.001S546418

Calidad de la espirometría en un laboratorio de función pulmonar

Introduction: Spirometry is a principal test to study the pulmonar pathology and phisiology. Our aim is to test our spi- rometry quality. Material and methods: Cross-sectional descriptive study of 103 patients. Spirometries were classified on grades from A to F. Results: 66% of our spirometries have a good quality (A or B grades) and 76,7 % an aceptable quality (C grade). Conclusion: Our quality results are good, but we must improve them