1,894 research outputs found

    The NASA/IPAC Infrared Science Archive (IRSA): The Demo

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    This paper describes the services available at the NASA/IPAC Infrared Science Archive (IRSA). Currently there are nearly 250,000 data requests a month, taking advantage of IRSA's data repository which includes 660 million sources (60 catalogs), 10 million images (22 image sets; 10.4 TB) and over 30,000 spectra (7 spectroscopic datasets). These data are the science products of: The Two Micron All Sky Survey (2MASS), The Infrared Astronomical Satellite (IRAS), The Midcourse Space Experiment (MSX), The Submillimeter Wave Astronomy Satellite (SWAS), The Infrared Space Observatory (ISO), The Infrared Telescope in Space (IRTS), The Spitzer First Look Survey (FLS), Spitzer Legacy & Ancillary data, Spitzer Reserved Observations (ROC) and the Spitzer Space Telescope data. IRSA is also seamlessly interoperable with ten remote archives and services: GOODS, ISO, MAST, VizieR, DSS, NVSS, FIRST, HEASARC, NED and JPL, which help expand the available dataset wavelength range from X-ray to radio. The majority of IRSA's image collections are Simple Image Access (SIA) compliant and are available through the Virtual Observatory (VO) data mining tools. The IRSA demo includes IRSA's ¯ve main services: inventory service RADAR, catalog query service Gator, data fusion service OASIS, general search service for complex data collections Atlas, and IRSA's 2MASS Image data access services. IRSA's website is http://irsa.ipac.caltech.edu

    The emission of volatile halocarbons by seaweeds and their response towards environmental changes

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    Volatile halocarbons can deplete the protective stratospheric ozone layer contributing to global climate change and may even affect local climate through aerosol production. These compounds are produced through anthropogenic and biogenic processes. Biogenic halocarbons may be produced as defence compounds, anti-oxidants or by-products of metabolic processes. These compounds include very short-lived halocarbons (VSLH), e.g. bromoform (CHBr3), dibromomethane (CH2Br2), methyl iodide (CH3I), diiodomethane (CH2I2). Efforts to quantify the biogenic sources of these compounds, especially those of marine origin, e.g. seaweeds, phytoplankton and seagrass meadows, are often complicated by inherent biological variability as well as spatial and temporal changes in emissions. The contribution of the coastal region and the oceans to the stratospheric load of halocarbons has been widely debated. This highlights the need to understand the factors affecting the release of these compounds from marine sources for which data for modelling purposes are generally lacking. Seaweeds are important sources of biogenic halocarbons subjected to changing environmental conditions. Huge uncertainties in the prediction of current and future global halocarbon pool exist due to the lack of spatial and temporal data input from coastal and oceanic sources. Therefore, investigating the effect of changing environmental conditions on the emission of VSLH by the seaweeds could help towards better estimations of halocarbon emissions. This is especially important in light of global changes in both climate and the environment, the expansion of seaweed cultivation industry and the interactions between halocarbon emission and their environment. In this paper, we review current knowledge of seaweed halocarbon emissions, how environmental factors affect these emissions and identify gaps in understanding. Our aim is to direct much needed research to improve understanding of the contribution of marine biogenic sources of halocarbons and their impact on the environment

    Associations of problematic internet use, weight-related self-stigma, and nomophobia with physical activity: findings from mainland China, Taiwan, and Malaysia

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    Insufficient physical activity is a common problem for university students because they may engage in sedentary lifestyle owing to excessive time spent on their smartphones and social media use. This may result in problematic internet use (PIU) and nomophobia (fear of not having a mobile phone). Moreover, prior evidence shows that weight-related self-stigma is an important factor contributing to low physical activity. Therefore, the present study examined the associations between PIU, nomophobia, and physical activity among university students across mainland China, Taiwan, and Malaysia. Participants (3135 mainland Chinese, 600 Taiwanese, and 622 Malaysian) completed the Bergen Social Media Addiction Scale (BSMAS), Smartphone Application-Based Addiction Scale (SABAS), Nomophobia Questionnaire (NMPQ), Weight Self-Stigma Questionnaire (WSSQ), and International Physical Activity Questionnaire Short Form (IPAQ-SF). The measurement invariance of the assessed questionnaires was supported across the three regions. The present findings analyzed using partial least squares structural equation modeling showed that (i) greater nomophobia was associated with higher levels of physical activity, (ii) greater weight-related self-stigma was associated with higher levels of physical activity, and (iii) greater nomophobia was associated with greater weight-related self-stigma. Although the present findings suggest the possibility that experiencing some level of nomophobia or weight-related self-stigma appears to help improve physical activity, it is not recommended that these be encouraged, but reducing PIU should be targeted as a means to improve physical activity

    Atomically dispersed nickel-nitrogen-sulfur species anchored on porous carbon nanosheets for efficient water oxidation

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    Developing low-cost electrocatalysts to replace precious Ir-based materials is key for oxygen evolution reaction (OER). Here, we report atomically dispersed nickel coordinated with nitrogen and sulfur species in porous carbon nanosheets as an electrocatalyst exhibiting excellent activity and durability for OER with a low overpotential of 1.51 V at 10 mA cm(-2) and a small Tafel slope of 45 mV dec(-1) in alkaline media. Such electrocatalyst represents the best among all reported transition metal- and/or heteroatom-doped carbon electrocatalysts and is even superior to benchmark Ir/C. Theoretical and experimental results demonstrate that the well-dispersed molecular S vertical bar NiNx species act as active sites for catalyzing OER. The atomic structure of S vertical bar NiNx centers in the carbon matrix is clearly disclosed by aberration-corrected scanning transmission electron microscopy and synchrotron radiation X-ray absorption spectroscopy together with computational simulations. An integrated photoanode of nanocarbon on a Fe2O3 nanosheet array enables highly active solar-driven oxygen production

    Unusual synergistic effect in layered Ruddlesden-Popper oxide enables ultrafast hydrogen evolution

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    Efficient electrocatalysts for hydrogen evolution reaction are key to realize clean hydrogen production through water splitting. As an important family of functional materials, transition metal oxides are generally believed inactive towards hydrogen evolution reaction, although many of them show high activity for oxygen evolution reaction. Here we report the remarkable electrocatalytic activity for hydrogen evolution reaction of a layered metal oxide, Ruddlesden-Popper-type Sr2RuO4 with alternative perovskite layer and rock-salt SrO layer, in an alkaline solution, which is comparable to those of the best electrocatalysts ever reported. By theoretical calculations, such excellent activity is attributed mainly to an unusual synergistic effect in the layered structure, whereby the (001) SrO-terminated surface cleaved in rock-salt layer facilitates a barrier-free water dissociation while the active apical oxygen site in perovskite layer promotes favorable hydrogen adsorption and evolution. Moreover, the activity of such layered oxide can be further improved by electrochemistry-induced activation

    Engineering grain boundaries at the 2D limit for the hydrogen evolution reaction

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    Atom-thin transition metal dichalcogenides (TMDs) have emerged as fascinating materials and key structures for electrocatalysis. So far, their edges, dopant heteroatoms and defects have been intensively explored as active sites for the hydrogen evolution reaction (HER) to split water. However, grain boundaries (GBs), a key type of defects in TMDs, have been overlooked due to their low density and large structural variations. Here, we demonstrate the synthesis of wafer-size atom-thin TMD films with an ultra-high-density of GBs, up to ~1012 cm−2. We propose a climb and drive 0D/2D interaction to explain the underlying growth mechanism. The electrocatalytic activity of the nanograin film is comprehensively examined by micro-electrochemical measurements, showing an excellent hydrogen-evolution performance (onset potential: −25 mV and Tafel slope: 54 mV dec−1), thus indicating an intrinsically high activation of the TMD GBs

    Determination of Specific Electrocatalytic Sites in the Oxidation of Small Molecules on Crystalline Metal Surfaces

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    The identification of active sites in electrocatalytic reactions is part of the elucidation of mechanisms of catalyzed reactions on solid surfaces. However, this is not an easy task, even for apparently simple reactions, as we sometimes think the oxidation of adsorbed CO is. For surfaces consisting of non-equivalent sites, the recognition of specific active sites must consider the influence that facets, as is the steps/defect on the surface of the catalyst, cause in its neighbors; one has to consider the electrochemical environment under which the “active sites” lie on the surface, meaning that defects/steps on the surface do not partake in chemistry by themselves. In this paper, we outline the recent efforts in understanding the close relationships between site-specific and the overall rate and/or selectivity of electrocatalytic reactions. We analyze hydrogen adsorption/desorption, and electro-oxidation of CO, methanol, and ammonia. The classical topic of asymmetric electrocatalysis on kinked surfaces is also addressed for glucose electro-oxidation. The article takes into account selected existing data combined with our original works.M.J.S.F. is grateful to PNPD/CAPES (Brazil). J.M.F. thanks the MCINN (FEDER, Spain) project-CTQ-2016-76221-P
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