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We report a near-broken-gap alignment between p-type FeWO4 and n-type Fe2WO6, a model pair for the realization of Ohmic direct junction thermoelectrics. Both undoped materials have a large Seebeck coefficient and high electrical conductivity at elevated temperatures, due to inherent electronic defects. see more A band-alignment diagram is proposed based on X-ray photoelectron and ultraviolet-visible light reflectance spectroscopy. Experimentally acquired nonrectifying I-V characteristics and the constructed band-alignment diagram support the proposed formation of a near-broken-gap junction. We have additionally performed computational modeling based on density functional theory (DFT) on bulk models of the individual compounds to rationalize the experimental band-alignment diagram and to provide deeper insight into the relevant band characteristics. The DFT calculations confirm an Fe-3d character of the involved band edges, which we suggest is a decisive feature for the unusual band overlap.Humidity- and temperature-dependent errors in concentrations reported by electrochemical sensors for atmospheric nitrogen dioxide significantly limit the reliability of the data. A basic understanding of the source of these errors has been missing. Empirical, software-based corrections are of limited reliability. The sensors feature a 40 wt % (≈4 molal) sulfuric acid electrolyte, and carbon working and quasi-reference (QRE) electrodes. We show that the sensor behaves as a truncated transmission line with resistance and capacitance elements varying with humidity. High-amplitude current fluctuations are due to humidity fluctuations, and are charging currents in response to fluctuations in interfacial capacitance. Baseline currents are due to very small differences in the open-circuit electrode potential between working and reference electrodes. We deduce that acid concentration changes in the meniscus within the porous electrode structure, in response to changes in the ambient temperature and humidity, cause both the capacitance fluctuations and the baseline changes. The open-circuit potential differences driving the baseline current variations are in part due to a difference in the liquid junction potential between the QRE and working electrode, dependent on humidity and temperature and caused by a gradient of acid concentration, and in part due to temperature- and acid-concentration-dependent variations in the rate of the potential-determining reactions. Based on the understanding obtained, we demonstrate a simple hardware change that corrects these unwanted errors.Mounting evidence indicates that climate tipping points can have large, potentially irreversible, impacts on the earth system and human societies. Yet, climate change metrics applied in current sustainability assessment methods generally do not consider these tipping points, with the use of arbitrarily determined time horizons and assumptions that the climate impact of a product or service is independent of emission timing. Here, we propose a new method for calculating climate tipping characterization factors for greenhouse gases (carbon dioxide, methane, and nitrous oxide) at midpoint. It covers 13 projected tipping points, incorporates the effect that the crossing of a given tipping point has on accelerating the crossing of other tipping points, and addresses uncertainties in the temperature thresholds that trigger the tipping points. To demonstrate the added value of the new metric, we apply it to emissions stemming from end-of-life of plastic polymers and compare them with commonly used metrics. This highlights the need to consider climate tipping in sustainability assessment of products and services.The Mobile ObserVations of Ultrafine Particles study was a two-year project to analyze potential air quality impacts of ultrafine particles (UFPs) from aircraft traffic for communities near an international airport. The study assessed UFP concentrations within 10 miles of the airport in the directions of aircraft flight. Over the course of four seasons, this study conducted a mobile sampling scheme to collect time-resolved measures of UFP, CO2, and black carbon (BC) concentrations, as well as UFP size distributions. Primary findings were that UFPs were associated with both roadway traffic and aircraft sources, with the highest UFP counts found on the major roadway (I-5). Total concentrations of UFPs alone (10-1000 nm) did not distinguish roadway and aircraft features. However, key differences existed in the particle size distribution and the black carbon concentration for roadway and aircraft features. These differences can help distinguish between the spatial impact of roadway traffic and aircraft UFP emissions using a combination of mobile monitoring and standard statistical methods.Isopropylbenzene (IPB) and α-methylstyrene (AMS), two members of C9 aromatics, are important in both industrial production and laboratory research, but the separation of IPB/AMS mixtures is still a big challenge. Here, we provide a new strategy to separate IPB and AMS using nonporous adaptive crystals of four pillararenes, perethylated pillar[5]arene, perethylated pillar[6]arene, perbromoethylated pillar[5]arene, and perbromoethylated pillar[6]arene (BrP6). Among them, BrP6 selectively adsorbs IPB from an equal volume mixture of IPB and AMS with >95% purity for solid-vapor phase adsorption and >94% purity for solid-liquid phase adsorption, while the selectivities for the other three pillararenes are unsatisfactory. Single-crystal structural analyses combined with powder X-ray diffraction and differential scanning calorimetry experiments demonstrate that the selectivity arises from the different stabilities of guest-loaded BrP6 crystals. Moreover, the reversible transitions between guest-free and IPB-loaded structures indicate the preeminent recycling performance of BrP6 crystals.A light addressable potentiometric sensor (LAPS) is a versatile sensing platform for bioassay. However, the lack of carbon-based LAPS (C-LAPS) is a bottleneck for its sustainable development in a carbon electronic era. Herein, a study of C-LAPS based on the combinations of carbon dots (CDs) and liquid exfoliated graphene (LEG) is presented. Devices of C-LAPS are first fabricated by self-assembling the hydrothermally synthesized CDs and the cosolvent ultrasonic delaminated LEG on poly(diallyldimethylammonium chloride) (PDDA)-modified indium tin oxide (ITO) glasses. According to the stacking orders of CDs and LEG, C-LAPS are named as CDs/LEG@PDDA/ITO and LEG/CDs@PDDA/ITO. Then, their electronic and photoelectronic features are measured and compared with the pure CD- and pure LEG-decorated ITO electrodes. Furthermore, working mechanisms are proposed by means of the classical theories of energy band bending and built-in electric field at the heterojunction of CDs and LEG. The resemblances of CDs/LEG@PDDA/ITO-based C-LAPS with Si-based LAPS (Si-LAPS) are confirmed from the points of view of production and separation of the photogenerated carriers, the formation of photocurrent, and the distinction with LEG/CDs@PDDA/ITO.
Homepage: https://www.selleckchem.com/products/gcn2-in-1.html
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