25,120 research outputs found

    Logarithmic behavior of degradation dynamics in metal--oxide semiconductor devices

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    In this paper the authors describe a theoretical simple statistical modelling of relaxation process in metal-oxide semiconductor devices that governs its degradation. Basically, starting from an initial state where a given number of traps are occupied, the dynamics of the relaxation process is measured calculating the density of occupied traps and its fluctuations (second moment) as function of time. Our theoretical results show a universal logarithmic law for the density of occupied traps ˉϕ(T,EF)(A+Blnt)\bar{} \sim \phi (T,E_{F}) (A+B \ln t), i.e., the degradation is logarithmic and its amplitude depends on the temperature and Fermi Level of device. Our approach reduces the work to the averages determined by simple binomial sums that are corroborated by our Monte Carlo simulations and by experimental results from literature, which bear in mind enlightening elucidations about the physics of degradation of semiconductor devices of our modern life

    Black string corrections in variable tension braneworld scenarios

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    Braneworld models with variable tension are investigated, and the corrections on the black string horizon along the extra dimension are provided. Such corrections are encrypted in additional terms involving the covariant derivatives of the variable tension on the brane, providing profound consequences concerning the black string horizon variation along the extra dimension, near the brane. The black string horizon behavior is shown to be drastically modified by the terms corrected by the brane variable tension. In particular, a model motivated by the phenomenological interesting case regarding Eotvos branes is investigated. It forthwith provides further physical features regarding variable tension braneworld scenarios, heretofore concealed in all previous analysis in the literature. All precedent analysis considered uniquely the expansion of the metric up to the second order along the extra dimension, what is able to evince solely the brane variable tension absolute value. Notwithstanding, the expansion terms aftermath, further accomplished in this paper from the third order on, elicits the successive covariant derivatives of the brane variable tension, and their respective coupling with the extrinsic curvature, the Weyl tensor, and the Riemann and Ricci tensors, as well as the scalar curvature. Such additional terms are shown to provide sudden modifications in the black string horizon in a variable tension braneworld scenarioComment: 12 pages, 5 figures, accepted in PR

    Palinología, Estratigrafía y Geometría de la cuenca continental pensIlvaniense de Santa Susana (Suroeste de Portugal)

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    The continental Pennsylvanian Santa Susana Basin (SSB) is located along an important N-S strike shear zone (Santa Susana Shear Zone - SSSZ) that separates the Ossa-Morena and South Portuguese Zones (SW Portugal). This shear zone controlled the sedimentation of the basin and probably its post-sedimentary evolution. The lower (basal) unit is mostly conglomeratic and is known essentially from drill-hole data while the upper unit, that covers most of the current surface area, is composed by sandstones, shales and some coal beds. Fluvial sedimentary rocks seem to prevail, but evidences of lacustrine sedimentation can be found in restricted areas within the upper unit. Palynological data indicate that at least part of the sedimentation took place during the Early Kasimovian (Cantabrian) but the sporomorph content of different localities suggest that significantly older sediments (Late Moscovian -Early Bashkirian) may be present. Geometrical, structural, and cartographical evidences indicate that the SSB formed as a pull-apart basin along the SSSZ and was later partially uplifted during latest Varsican and Alpine orogenies.>La cuenca continental Pensilvaniense de Santa Susana (SSB) está localizada a lo largo de una importante zona de cizalla con dirección aproximada N-S (Zona de Cizalla de Santa Susana - SSSZ) que separa las Zonas de Ossa-Morena y Sur-Portuguesa (Suroeste de Portugal). La zona de cizalla ha controlado la sedimentación en la cuenca y posiblemente su evolución post-sedimentaria. La unidad inferior (basal), estudiada fundamentalmente mediante datos de sondeos, es mayormente conglomerática, mientras que su unidad superior, que cubre actualmente una gran parte de la superficie expuesta, está compuesta por areniscas, pizarras y niveles de carbón. Las rocas de origen fluvial son las más abundantes, sin embargo existen evidencias de sedimentación lacustre en áreas muy limitadas de la unidad superior. Los datos palinológicos indican que al menos parte de la sedimentación tuvo lugar durante el Kasimoviense temprano (Cantabriense) aunque el contenido en esporomorfos de diferentes localidades sugieren la existencia de sedimentos significativamente más antiguos (Moscoviense tardio/Bashkiriense temprano). Evidencias geométricas, estructurales y cartográficas sugieren la creación de una cuenca en pull-apart a lo largo de la ZCSS

    Modified poly(heptazine imides) : minimizing H<sub>2</sub>O<sub>2</sub> decomposition to maximize oxygen reduction

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    Photocatalysis provides a sustainable pathway to produce the consumer chemical H2O2 from atmospheric O2 via an oxygen reduction reaction (ORR). Such an alternative is attractive to replace the cumbersome traditional anthraquinone method for H2O2 synthesis on a large scale. Carbon nitrides have shown very interesting results as heterogeneous photocatalysts in ORR because their covalent two-dimensional (2D) structure is believed to increase selectivity toward the two-electron process. However, an efficient and scalable application of carbon nitrides for this reaction is far from being achieved. Poly(heptazine imides) (PHIs) are a more powerful subgroup of carbon nitrides whose structure provides high crystallinity and a scaffold to host transition-metal single atoms. Herein, we show that PHIs functionalized with sodium and the recently reported fully protonated PHI exhibit high activity in two-electron ORR under visible light. The latter converted O2 to up to 1556 mmol L–1 h–1 g–1 H2O2 under 410 nm irradiation using inexpensive but otherwise chemically demanding glycerin as a sacrificial electron donor. We also prove that functionalization with transition metals is not beneficial for H2O2 synthesis, as the metal also catalyzes its decomposition. Transient photoluminescence spectroscopy suggests that H-PHIs exhibit higher activity due to their longer excited-state lifetime. Overall, this work highlights the high photocatalytic activity of the rarely examined fully protonated PHI and represents a step forward in the application of inexpensive covalent materials for photocatalytic H2O2 synthesis
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