291 research outputs found

    High-frequency electron paramagnetic resonance investigation of the Fe3+ impurity center in polycrystalline PbTiO3 in its ferroelectric phase

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    The intrinsic iron(III) impurity center in polycrystalline lead titanate was investigated by means of high-frequency electron paramagnetic resonance (EPR) spectroscopy in order to determine the local-environment sensitive fine structure parameter D. At a spectrometer frequency of 190 GHz, spectral analysis of a powder sample was unambiguously possible. The observed mean value D = +35.28 GHz can be rationalized if Fe3+ ions substitute for Ti4+ at the B-site of the perovskite ABO3 lattice forming a directly coordinated iron - oxygen vacancy defect associate. A consistent fit of the multi-frequency data necessitated use of a distribution of D values with a variance of about 1 GHz. This statistical distribution of values is probably related to more distant defects and vacancies.Comment: 6 pages, 3 figures, 1 table, to appear in J. App. Phys, 96 (2004

    Exploring the role of structure in a time constrained decision task

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    The structure of the basal ganglia is remarkably similar across a number of species (often described in terms of direct, indirect and hyperdirect pathways) and is deeply involved in decision making and action selection. In this article, we are interested in exploring the role of structure when solving a decision task while avoiding to make any strong assumption regarding the actual structure. To do so, we exploit the echo state network paradigm that allows to solve complex task based on a random architecture. Considering a temporal decision task, the question is whether a specific structure allows for better performance and if so, whether this structure shares some similarity with the basal ganglia. Our results highlight the advantage of having a slow (direct) and a fast (hyperdirect) pathway that allows to deal with late information during a decision making task

    Experimental evidence for the relaxation coupling of all longitudinal 7Li magnetization orders in the superionic conductor Li10GeP2S12

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    This contribution addresses the experimental proof of the relaxation coupling of the 7Li (I = 3/2) longitudinal magnetization orders in the solid-state electrolyte Li10GeP2S12 (LGPS). This effect was theoretically described by Korb and Petit in 1988 but has not yet been shown experimentally. In a 2D-T1/spin-alignment echo (SAE) experiment, the inverse Laplace transformation of the spectral component over two time dimensions revealed the asymmetric course of the spin-lattice relaxation following from the coupling of all longitudinal orders. These observations were supported by Multi-quantum-filter experiments and by simulations of the 2D-T1/SAE experiment with a lithium spin system. Since the asymmetric relaxation effects are directly dependent on the velocities and degrees of freedom of ion motion they could be used especially in fast Li-ion conductors as a separation tool for environments with different mobility processes

    Application of pixel segmentation to the low rate compression of complex SAR imagery

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    This paper describes a technique to identify pixels within a subregion (chip) of a complex or detected SAR image which are to be losslessly compressed while the remainder of the image is subjected to a high compression ratio. This multi-modal compression is required for the intelligent low rate compression of SAR imagery, which addresses the problem of transmitting massive amounts of high resolution complex SAR data from a remote airborne sensor to a ground station for exploitation by an automatic target recognition (ATR) system, in a real time environment, over a narrow bandwidth. The ATR system results might then be presented to an image analyst who, using the contextual information from the SAR image, makes final target determination

    Insights on Water Interaction at the Interface of Nitrogen Functionalized Hydrothermal Carbons

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    Hydrothermal carbon (HTC) derived from biomass is a class of cost-efficient, eco-friendly functional carbon materials with various potential applications. In this work, solid-state nuclear magnetic resonance (NMR), longitudinal (T1) relaxation time and diffusion NMR were employed to investigate the structure and water dynamics for HTC and nitrogen-functionalized hydrothermal carbon (N-HTC) samples ((N)-HTC). Results showed that the presence of N-functional groups influences the water interaction with (N)-HTC more strongly than surface area, pore size distribution or oxygenated functional groups. Furthermore, the degree of water interaction can be tuned by adjusting the synthesis temperature and the precursor ratio. Water motion was more strongly inhibited in N-HTC than in N-free HTC, thereby suggesting the existence of a differently structured hydration shell around N-HTC particles. In addition, the diffusion data of water in the N-HTC material shows two components that do not exchange on the time scale of the experiment (tens of milliseconds), indicating a significant fraction of slow mobile water that exists inside the structure of N-HTC. 1H–2H isotope exchange and cross-polarization NMR results show this internal water only in a near-surface layer of the N-HTC particles. Based on these findings, a model for water interaction with (N)-HTC particles is proposed

    The nature of iron-oxygen vacancy defect centers in PbTiO3

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    The iron(III) center in ferroelectric PbTiO3 together with an oxygen vacancy forms a charged defect associate, oriented along the crystallographic c-axis. Its microscopic structure has been analyzed in detail comparing results from a semi-empirical Newman superposition model analysis based on finestructure data and from calculations using density functional theory. Both methods give evidence for a substitution of Fe3+ for Ti4+ as an acceptor center. The position of the iron ion in the ferroelectric phase is found to be similar to the B-site in the paraelectric phase. Partial charge compensation is locally provided by a directly coordinated oxygen vacancy. Using high-resolution synchrotron powder diffraction, it was verified that lead titanate remains tetragonal down to 12 K, exhibiting a c/a-ratio of 1.0721.Comment: 11 pages, 5 figures, accepted in Phys. Rev.
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