Context modelling and a context-aware framework for pervasive service creation: A model-driven approach

Pervasive service creation entails a complex process that involves a diversity of development aspects. Context-awareness is an important facet of pervasive service creation, which deals with the acquisition, rendering, representation and utilisation of context information. In this paper we tackle context-awareness at the application level dealing with the representation and utilisation of context by services. We propose a model-driven approach that facilitates the creation of a context modelling framework and simplifies the design and implementation of pervasive services. To conclude, we demonstrate the benefits of our model-driven approach via the creation of a pervasive museum service and its evaluation using selected software metrics.     

Quecksilber in Fischen

European Food Research and Technology - Der Quecksilbergehalt von Fischen wurde bestimmt. Der Mittelwert von 1400 Bestimmungen zeigte, daß das Gesamtquecksilber der frischen Fischmuskulatur...     

Role of the Anion on the Transport and Structure of Organic Mixed Conductors

Organic mixed conductors are increasingly employed in electrochemical devices operating in aqueous solutions that leverage simultaneous transport of ions and electrons. Indeed, their mode of operation relies on changing their doping (oxidation) state by the migration of ions to compensate for electronic charges. Nevertheless, the structural and morphological changes that organic mixed conductors experience when ions and water penetrate the material are not fully understood. Through a combination of electrochemical, gravimetric, and structural characterization, the effects of water and anions with a hydrophilic conjugated polymer are elucidated. Using a series of sodium‐ion aqueous salts of varying anion size, hydration shells, and acidity, the links between the nature of the anion and the transport and structural properties of the polymer are systematically studied. Upon doping, ions intercalate in the crystallites, permanently modifying the lattice spacings, and residual water swells the film. The polymer, however, maintains electrochemical reversibility. The performance of electrochemical transistors reveals that doping with larger, less hydrated, anions increases their transconductance but decreases switching speed. This study highlights the complexity of electrolyte‐mixed conductor interactions and advances materials design, emphasizing the coupled role of polymer and electrolyte (solvent and ion) in device performance.     

On the Role of Contact Resistance and Electrode Modification in Organic Electrochemical Transistors

Contact resistance is renowned for its unfavorable impact on transistor performance. Despite its notoriety, the nature of contact resistance in organic electrochemical transistors (OECTs) remains unclear. Here, by investigating the role of contact resistance in n‐type OECTs, the first demonstration of source/drain‐electrode surface modification for achieving state‐of‐the‐art n‐type OECTs is reported. Specifically, thiol‐based self‐assembled monolayers (SAMs), 4‐methylbenzenethiol (MBT) and pentafluorobenzenethiol (PFBT), are used to investigate contact resistance in n‐type accumulation‐mode OECTs made from the hydrophilic copolymer P‐90, where the deliberate functionalization of the gold source/drain electrodes decreases and increases the energetic mismatch at the electrode/semiconductor interface, respectively. Although MBT treatment is found to increase the transconductance three‐fold, contact resistance is not found to be the dominant factor governing OECT performance. Additional morphology and surface energy investigations show that increased performance comes from SAM‐enhanced source/drain electrode surface energy, which improves wetting, semiconductor/metal interface quality, and semiconductor morphology at the electrode and channel. Overall, contact resistance in n‐type OECTs is investigated, whilst identifying source/drain electrode treatment as a useful device engineering strategy for achieving state of the art n‐type OECTs.     

The Effect of Alkyl Spacers on the Mixed Ionic-Electronic Conduction Properties of N-Type Polymers

Conjugated polymers with mixed ionic and electronic transport are essential for developing the complexity and function of electrochemical devices. Current n-type materials have a narrow scope and low performance compared with their p-type counterparts, requiring new molecular design strategies. This work presents two naphthalene diimide-bithiophene (NDI-T2) copolymers functionalized with hybrid alkyl-glycol side chains, where the naphthalene diimide unit is segregated from the ethylene glycol (EG) units within the side chain by an alkyl spacer. Introduction of hydrophobic propyl and hexyl spacers is investigated as a strategy to minimize detrimental swelling close to the conjugated backbone and balance the mixed conduction properties of n-type materials in aqueous electrolytes. It is found that both polymers functionalized with alkyl spacers outperform their analogue bearing EG-only side chains in organic electrochemical transistors (OECTs). The presence of the alkyl spacers also leads to remarkable stability in OECTs, with no decrease in the ON current after 2 h of operation. Through this versatile side chain modification, this work provides a greater understanding of the structure-property relationships required for n-type OECT materials operating in aqueous media.     

Catalytic Conversions in Aqueous Media. Part 2. A Novel and Highly Efficient Biphasic Hydrogenation of Renewable Methyl Esters of Linseed and Sunflower Oils to High Quality Biodiesel Employing Rh/TPPTS Complexes

An unusual high catalytic activity (TOF = 117,000 h⁻¹) and high catalyst productivity (TON = 9,700) have been achieved in the first example of partial hydrogenation of renewable polyunsaturated crude methyl esters of linseed and sunflower oils catalyzed by water soluble Rh/TPPTS complexes [TPPTS = P(C₆H₄-m-SO₃Na)₃] in aqueous/organic two-phase systems to afford monounsaturated fatty esters which is biodiesel first generation of improved oxidative stability, energy and environmental performance at a low pour point. This exceptionally high catalytic activity contrast with the general perception that industrially applied water soluble Rh/TPPTS catalysts normally exhibit very low rates in the conversions of higher molecular weight starting materials in aqueous/organic two-phase systems. For part 1 of this series see Ref. [14].     

CO2 capture using membrane contactors: a systematic literature review

With fossil fuel being the major source of energy, CO₂ emission levels need to be reduced to a minimal amount namely from anthropogenic sources. Energy consumption is expected to rise by 48% in the next 30 years, and global warming is becoming an alarming issue which needs to be addressed on a thorough technical basis. Nonetheless, exploring CO₂ capture using membrane contactor technology has shown great potential to be applied and utilised by industry to deal with post- and pre-combustion of CO₂. A systematic review of the literature has been conducted to analyse and assess CO₂ removal using membrane contactors for capturing techniques in industrial processes. The review began with a total of 2650 papers, which were obtained from three major databases, and then were excluded down to a final number of 525 papers following a defined set of criteria. The results showed that the use of hollow fibre membranes have demonstrated popularity, as well as the use of amine solvents for CO₂ removal. This current systematic review in CO₂ removal and capture is an important milestone in the synthesis of up to date research with the potential to serve as a benchmark databank for further research in similar areas of work. This study provides the first systematic enquiry in the evidence to research further sustainable methods to capture and separate CO₂.     

Synergistic effects of buffer layer processing additives for enhanced hole carrier selectivity in inverted Organic Photovoltaics

Solution based inverted Organic Photovoltaic (OPVs) usually use Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) derivatives combined with pristine processing additives as hole selective contact on top of the hydrophobic conjugated polymer:fullerene active layer. In this study, PEDOT:PSS based hole selective contact is treated with two different boiling point additives, 2,5,8,11-tetramethyl-6-dodecyn-5,8-diol ethoxylate (Dynol) and Zonyl FS-300 fluorosurfactant (Zonyl). Although corresponding inverted OPVs using the above PEDOT:PSS:Additives show similar power conversion efficiency (PCE) values, the mechanisms of their implementation on inverted OPV operation are not identical. By understanding the synergistic effects of PEDOT:PSS processing additives on the hole selectivity of inverted OPVs we demonstrate a novel combination of PEDOT:PSS additives mixture as an effective route to further increase the hole selectivity, reliability andpower conversion efficiency of inverted OPVs.     

Distinguishing the causes of firing with the membrane potential slope

In this letter, we aim to measure the relative contribution of coincidence detection and temporal integration to the firing of spikes of a simple neuron model. To this end, we develop a method to infer the degree of synchrony in an ensemble of neurons whose firing drives a single postsynaptic cell. This is accomplished by studying the effects of synchronous inputs on the membrane potential slope of the neuron and estimating the degree of response-relevant input synchrony, which determines the neuron's operational mode. The measure is calculated using the normalized slope of the membrane potential prior to the spikes fired by a neuron, and we demonstrate that it is able to distinguish between the two operational modes. By applying this measure to the membrane potential time course of a leaky integrate-and-fire neuron with the partial somatic reset mechanism, which has been shown to be the most likely candidate to reflect the mechanism used in the brain for reproducing the highly irregular firing at high rates, we show that the partial reset model operates as a temporal integrator of incoming excitatory postsynaptic potentials and that coincidence detection is not necessary for producing such high irregular firing.