Influence of processing additives to nano-morphology and efficiency of bulk-heterojunction solar cells: A comparative review

Research and development towards high efficiency plastic solar cells have been accelerating in recent years. Polymer-based bulk heterojunction solar cells are offering an attractive and inexpensive concept for large scale production by solution processing as well as advantageous flexible and aesthetic form factors. The thin film nano-morphology of bulk-heterojunction solar cells has been shown to dramatically influence the photovoltaic performance of the devices. This article reviews the different methods used to control the film nano-morphology of bulk-heterojunction solar cells focussing on the chemical additives during solution processing. All power conversion efficiency limiting mechanisms of bulk-heterojunction solar cells are discussed in detail. It is shown, how the formation of optimal percolation pathways between donor and acceptor influences the photovoltaic device performance. It is explained how the film nano-morphology relates to light absorption, free charge carrier generation as well as charge transport to the electrodes.     

Assignment of raw material and authentication of spirits by gas chromatography, hydrogen- and carbon-isotope ratio measurements I. Analytical methods and results of a study of commercial products

Gas chromatography and the determination of natural isotope ratios are powerful analytical methods which can be used to check the authenticity of alcoholic beverages and to detect any adulteration. To check the origin and the authenticity of commercial fruit spirits, whiskies, etc., 197 samples were analysed by gas chromatography, ²H-NMR and ¹³C isotope mass spectrometry. The discrimination between different varieties was demonstrated by bivariate and multivariate discriminant analysis using different concentrations of volatile compounds such as methanol, butan-1-ol, 2- and 3-methyl-butanol, benzaldehyde and hexanol as well as isotopic data like (D/H)_I, (D/H)_II and ¹³C/¹²C isotopomers of ethanol. The results show that by using multivariate discriminant analysis it is possible to distinguish not only between different groups of spirits, e.g. those made of stone-fruit, malaceous fruit, grain and corn, but also between individual varieties, such as cherry, plum, mirabelle and apple. If the detection of highly rectified ethyl alcohol of agricultural origin and the identification of its raw materials are required, then natural isotope ratios are the only discriminant analytical parameters available.     

Gemeinsame österreichisch-ungarische Sedimentforschung im Rahmen des EFRE-Projektes SEDDON

The multiple uses of the Danube River for navigation, hydropower production and as a drinking water supply influence its ecological quality. Flow restrictions due to regulation as well as impacts on the sediment regime such as retention in the catchment area and interruption of the sediment continuum result in changes of the hydromorphological structures and can produce major problems in the context of sediment management. In light of these facts, cross-border investigations of sediment transport at the Danube River are called for. As there are no uniform research approaches shared by Austria and Hungary, the EU-funded project SEDDON (Sediment Research and Management at the Danube River) aims to compare different monitoring and modeling techniques used to determine sediment transport, and to develop mutual solutions. Further, the laboratory equipment currently used for hydraulic model experiments is evaluated and a research channel with a free flowing discharge of up to 10 m³/s without pumping will be constructed, allowing large-scale joint laboratory tests concerning sediment to be performed.     

Photoprocesses of chlorin e6 bound to lysozyme or bovin serum albumin

The ground and excited state processes of chlorin e6 in aqueous solution were studied in the presence of lysozyme and also bovine serum albumin. Non-covalent binding to proteins was analyzed using fluorescence, UV–visible and circular dichroism absorption spectroscopy. The number of binding sites, n, was 1.5–2.4 and the apparent macroscopic dissociation constant, K_d was 0.2–2.5 μM. The binding of chlorin e6 to lysozyme, in contrast to that of bovine serum albumin, imparted fluorescence quenching; circular dichroism spectra revealed a chiral environment upon binding to β-sheets of bovine serum albumin. Time-resolved photolysis showed a longer triplet lifetime upon interaction with the proteins owing to shielding of the dye. The quantum yields for both damage to chlorin e6 (Φ_d) and for protein oxidation (Φ_ox) were determined under oxygen-free conditions; Φ_d was smaller because of shielding by the protein with respect to the self-quenching of the free dye. The major effects concerning photooxidation in the absence and presence of oxygen are discussed.     

Determination of thermal radiative properties of packed-bed media containing a mixture of polydispersed particles

Thermal radiative characteristics of packed beds containing a mixture of polydispersed SiO₂, ZnO, and C particles are determined numerically by employing the Monte Carlo technique, which is validated with the experimentally measured overall transmittance. A radiative heat transfer model is formulated for a pseudo-continuum multi-component medium of Mie-scattering particles. Good agreement is achieved by incorporating approximate phase functions that reproduce the experimentally observed preference for forward scattering.     

Performance of a solid oxide fuel cell couple operated via in situ catalytic partial oxidation of n-butane

The operation of a pair of anode-to-anode-facing solid oxide fuel cells (SOFCs) via in situ catalytic partial oxidation (CPO) of n-butane was investigated. In this simple “no-chamber” setup, butane is partially oxidized by heterogeneous reactions inside the porous anodes, providing processed fuel and the heat required for SOFC operation. The cell couple yielded a power density of up to 270 mW cm⁻², and the maximum total power obtained was 1.2 W with cell sizes of 13 mm × 23 mm. The maximum electrical efficiency was 1.3%. High CO concentrations of up to 1000 ppm were detected in the exhaust gas, indicating that the cell couple could not efficiently consume the complete provided fuel. A flame, lit at the exhaust, minimized the carbon monoxide level while having insignificant influence on the cell performance. Thermal insulation of the cell couple improved the output remarkably, showing the strong influence of temperature on cell performance. The two cells had a distance of only 2 mm, suggesting a potential for high volumetric power densities in multi-cell configurations for a self-sustained combined heat and power system.     

Biotransformation of alkylglycerols in plant cell cultures: Production of platelet activating factor and other biologically active ether lipids

Plant cells in culture are capable of incorporating exogenous 1-O-alkyl-sn-glycerols into various neutral and ionic ether lipids. 1-O-Alkyl-2-acyl-sn-glycerol-3-phosphocholines, the major class of compounds thus formed, are used for the preparation of platelet activating factor (PAF) in high yields. Similarly, the prochiral 2-O-alkyl-sn-glycerols are transformed to chiral 2-O-alkyl glycerophospholipids from which compounds can be obtained that exhibit antiviral activity in plant and animal cells. Reaction of 1-O-alkyl-2-acyl-sn-glycerol-3-phosphocholines with phospholipase D in the presence of ethanolamine leads to 1-O-alkyl-2-acyl-sn-glycerol-3-phosphoethanolamines, which serve as starting material, for the preparation of 1-O-alkyl-2-acyl-sn-glycero-3-phospho-(N-acyl)ethanolamines, compounds known to have antitumor activity. Based on a paper presented at the Third International Conference on Platelet-Activating Factor and Structurally Related Alkyl Ether Lipids, Tokyo, Japan, May 1989. Dedicated to Professor Morris Kates, Ottawa, on the occasion of his retirement.     

Occurrence of Ti3+ and Fe2+ in Mullite

Electron paramagnetic studies showed that Ti³⁺ and Fe²⁺ occur in mullites taken from a refractory material which was fused-cast under a reducing atmosphere. Exposure of the mullite samples to temperatures >1600°C caused oxidation of Ti³⁺ and Fe²⁺ to Ti⁴⁺ and Fe³⁺, respectively.