Solar cells in bulk InP using an open tube diffusion process

A simple open tube diffusion technique for the fabrication of n+p junction solar cells is described. Large area (greater than 0.25 square cm) solar cells have been made by this process with a photovoltaic conversion efficiency of 15.2 percent under simulated AMO illumination. An ideality factor is 1.04 and a saturation current density of 9.6 times 10 to the minus 16th power A/square cm have been observed for these cells. These are the lowest (best) values reported to date for diffused structures in bulk InP

Encapsulated diffusion of sulphur into InP

This talk outlines a simple process for the fabrication of n(+)-p solar cells in indium phosphide. Large area cells (greater than 0.25 sq cm) have been made by this process, with a photovoltaic conversion efficiency of 15.21 percent under AM0 conditions of illumination. An ideality factor of 1.1 and a saturation current density of 8 x 10 to the minus 15th power A/sq cm have been observed for these cells. The technique for cell fabrication involves the diffusion of sulfur into InP by an open tube process, and gives highly reproducible results from run to run. A vacuum-deposited layer of gallium sulphide (Ga2S3) was used as the source for sulfur diffusion, with a chemically vapor deposited SiO2 cap layer to prevent decomposition of the InP surface during heat treatment. Diffusions were carried out in a flowing nitrogen ambient at 585 to 708 C, and characterized by their surface carrier concentration and the diffusion constant. The diffusion profile for sulfur in InP is estimated to be of the complementary error function type. The activation energy of the diffusion was estimated to be 1.94 eV. The technique described here is ideally suited for the fabrication of shallow n(+)-p junctions in InP, and has been used for space-borne solar cells

Le CROS : mise en place d'un organe de concertation entre les acteurs du développement dans le Sud Ouest malgache

Le Sud Ouest de Madagascar est resté pendant longtemps une région isolée. Les producteurs (analphabètes à 80%) ont particulièrement souffert du manque de formation et de difficultés de communication avec les autres acteurs du développement. Dans ce contexte, avec une offre atomisée, ne comptant pas leurs coûts de production, les agriculteurs sont souvent amenés à vendre à perte pour le plus grand profit des acteurs de l'aval des filières. Depuis 1994, au sein du CROS (Comité Régional d'Orientation du Sud Ouest), les producteurs s'assoient à la même table que les pouvoirs publics (administration et recherche), les opérateurs économiques (agro-industries, établissement financier, exportateurs), les collectivités décentralisées et les bailleurs de fonds organisés en cinq collèges. Le CROS est présidé par un producteur. Des contrats ou des conventions entre membres du CROS ou avec des partenaires extérieurs sont négociés pendant ou à la suite des sessions du CROS qui ont lieu deux fois par an. Cela peut aller des conditions de location vente de matériel agricole à la résolution des problèmes hydrauliques d'un périmètre ou au paiement à la qualité des exportations de pois du Cap. Cette communication voudrait faire le point sur les atouts et les contraintes d'une démarche originale dans laquelle la recherche ne peut être absente

Comparative performance of diffused junction indium phosphide solar cells

A comparison is made between indium phosphide solar cells whose p-n junctions were processed by open tube capped diffusion, and closed tube uncapped diffusion, of sulfur into Czochralski grown p-type substrates. Air mass zero, total area, efficiencies ranged from 10 to 14.2 percent, the latter value attributed to cells processed by capped diffusion. The radiation resistance of these latter cells was slightly better, under 1 MeV electron irradiation. However, rather than being process dependent, the difference in radiation resistance could be attributed to the effects of increased base dopant concentration. In agreement with previous results, both cells exhibited radiation resistance superior to that of gallium arsenide. The lowest temperature dependency of maximum power was exhibited by the cells prepared by open tube capped diffusion. Contrary to previous results, no correlation was found between open circuit voltage and the temperature dependency of Pmax. It was concluded that additional process optimization was necessary before concluding that one process was better than another

Contemporaneous Trachyandesitic and Calc-alkaline Volcanism of the Huerto Andesite, San Juan Volcanic Field, Colorado, USA

Locally, voluminous andesitic volcanism both preceded and followed large eruptions of silicic ash-flow tuff from many calderas in the San Juan volcanic field. The most voluminous post-collapse lava suite of the central San Juan caldera cluster is the 28 Ma Huerto Andesite, a diverse assemblage erupted from at least 5-6 volcanic centres that were active around the southern margins of the La Garita caldera shortly after eruption of the Fish Canyon Tuff. These andesitic centres are inferred, in part, to represent eruptions of magma that ponded and differentiated within the crust below the La Garita caldera, thereby providing the thermal energy necessary for rejuvenation and remobilization of the Fish Canyon magma body. The multiple Huerto eruptive centres produced two magmatic series that differ in phenocryst mineralogy (hydrous vs anhydrous assemblages), whole-rock major and trace element chemistry and isotopic compositions. Hornblende-bearing lavas from three volcanic centres located close to the southeastern margin of the La Garita caldera (Eagle Mountain-Fourmile Creek, West Fork of the San Juan River, Table Mountain) define a high-K calc-alkaline series (57-65 wt % SiO2) that is oxidized, hydrous and sulphur rich. Trachyandesitic lavas from widely separated centres at Baldy Mountain-Red Lake (western margin), Sugarloaf Mountain (southern margin) and Ribbon Mesa (20 km east of the La Garita caldera) are mutually indistinguishable (55-61 wt % SiO2); they are characterized by higher and more variable concentrations of alkalis and many incompatible trace elements (e.g. Zr, Nb, heavy rare earth elements), and they contain anhydrous phenocryst assemblages (including olivine). These mildly alkaline magmas were less water rich and oxidized than the hornblende-bearing calc-alkaline suite. The same distinctions characterize the voluminous precaldera andesitic lavas of the Conejos Formation, indicating that these contrasting suites are long-term manifestations of San Juan volcanism. The favoured model for their origin involves contrasting ascent paths and differentiation histories through crustal columns with different thermal and density gradients. Magmas ascending into the main focus of the La Garita caldera were impeded, and they evolved at greater depths, retaining more of their primary volatile load. This model is supported by systematic differences in isotopic compositions suggestive of crust-magma interactions with contrasting lithologie

Non-purged voltammetry explored with AGNES

The reduction of oxygen increases pH in the surroundings of an electrode. A theoretical model estimates the steady-state pH profile from the surface of the electrode up to the bulk solution. A very simple formula predicts that, in non-deareated solutions, for bulk pH-values between 4.0 and 10.0, the corresponding surface pH could be as high as 10.3, regardless of the thickness of the diffusion layer and composition of the sample (except if it has a buffering capacity). For bulk pH lower than 3.0 or higher than 10, pH increases are negligible. Less steep pH-profiles are obtained with buffers (such as MOPS 0.01 M or MES 0.01 M). The change in surface pH modifies the local speciation and hinders the standard interpretation of voltammetric responses. The electroanalytical technique Absence of Gradients and Nernstian Equilibrium Stripping (AGNES), implemented with Screen Printed Electrodes (SPE), provides experimental insights into this phenomenon. AGNES probes the free metal concentration at the electrode surface, from which the surface pH can be estimated for systems of known composition. These estimations agree with the theoretical model for the assayed systems. Additionally, the quantification of the bulk free Zn2+ and Cd2+ concentrations with specific modifications of AGNES for non-purged synthetic solutions is discussed. In general, more accurate determinations of the bulk free metal concentrations in non-purged solutions are expected: i) when the calibration is performed in a medium where the pH increase induces similar changes in the surface free metal concentration and in the sample solution and ii) when the system is more buffered.This work was financially supported by the Spanish Ministry of Education and Science (Projects CTQ2009-07831, CTM2009-14612 and CTM2012-39183), from the “Comissionat per a Universitats i Recerca del Departament d'Innovació, Universitats i Empresa de la Generalitat de Catalunya”

Free Zn2+ determination in natural freshwater of the Pyrenees: towards on-site measurements with AGNES

An on-site methodology has been developed for the direct determination of free Zn2+ with AGNES (Absence of Gradients and Nernstian Equilibrium Stripping) in freshwaters. This implementation includes: i) the use of screen printed electrodes, which provide good limits of detection and easy transportation and deployment; ii) no need for sample purging; iii) a calibration in a synthetic river solution that reproduces well the speciation changes of the natural samples and allows the oxygen interferences to be minimised; iv) the addition of a background electrolyte up to 0.01 mol L-1 in both the calibration and freshwater samples; v) chemical stripping chronopotentiometry as the quantification stage of AGNES. This procedure minimizes the effects of working at low ionic strength and in the presence of dissolved oxygen. In the laboratory, the methodology was checked with different natural samples taken from rivers Garonne, Gave de Cauterets and Gave de Pau in the Pyrenees. Results appeared in good agreement with theoretical estimations computed from Visual Minteq. On-site measurements were performed for the first time with AGNES in the Gave de Cauterets in Soulom (France) and the results were corroborated with purged measurements performed in the laboratory.English language editing by Holly Pearson is acknowledged. The authors acknowledge support for this research from the Communaut e d’Agglom eration de Pau Pyr en ees (CDAPP), from the Spanish Ministerio de Ciencia e Innovacio´n (project numbers CTM2012–39183 and CTM2013– 48967), from the European Community EFA15/08 (PyrMet) and from the Comissionat d’Universitats i Recerca de la Generalitat de Catalunya (project number 2014SGR1132)

Direct determination of free metal concentration by implementing stripping chronopotentiometry as second stage of AGNES

The electroanalytical technique Absence of Gradients and Nernstian Equilibrium Stripping (AGNES) has been extended by applying stripping chronopotentiometry (SCP) as the re-oxidation stage in the determination of the free concentration of Zn2+, Cd2+ and Pb2+. This new approach, called AGNES-SCP, has been implemented with screen-printed electrodes (SPE) and the standard Hanging Mercury Drop Electrode (HMDE). Clear advantages of this variant have been shown: (i) the easy resolution of the peaks of different metals present in mixtures and (ii) the sparing of blanks. A rigorous computation of the faradaic charge along the SCP stage takes into account the contribution of other oxidants, which can be efficiently measured at the end of the deposition stage of AGNES. The free Cd concentration determined in an oxalate solution at pH 6 with an HMDE as the working electrode agreed well with values obtained with a Cd Ion Selective Electrode. The free metal concentration measured using an SPE for the system Cd and nitrilotriacetic acid (NTA) at pH = 4.8 also conformed well with Visual MINTEQ results

Determination of free metal ion concentrations with AGNES in low ionic strength media

The determination of free metal ion concentrations of heavy metals, like Zn2+ or Cd2+, with AGNES (Absence of Gradients and Nernstian Equilibrium Stripping) requires an adequate selection of parameters such as deposition potential (linked to the gain, [M-0]/[M2+]) and deposition time. In systems with low ionic strength, the peak potential of the Differential Pulse Polarogram (DPP) measured with low supporting electrolyte is not always suitable for the computation of the gain with existing expressions. The application of AGNES with a constant potential (regardless of the ionic strength) provides a direct measurement of the metal ion activity. When working with low ionic strength solutions, the selection of appropriate instrumentation is important to avoid changes in liquid junction potentials or leakages from the employed electrodes. The deposition times (for a given gain) have not been found to be greatly affected by the probed ionic strengths when working with just metal. A new strategy for the practical implementation of AGNES to measure free metal ion concentrations in samples with low KNO3 or Ca(NO3)(2) concentrations consists in the computation of the deposition potential (to reach a certain gain) from the DPP peak potential at a sufficiently high ionic strength using a new expression. A speciation experiment with Zn2+ and glycine at pHs between 4 and 7.5, where [KNO3] = 0.001 M, shows that this methodology works well and also proves that it is possible to perform AGNES in systems with very low ionic strength. (C) 2012 Elsevier B.V. All rights reserved

INFLUENCE OF PIEZOELECTRIC ANISOTROPY ON ELECTROMECHANICAL PERFORMANCE OF ULTRASOUND NDT PROBES AT ELEVATED TEMPERATURES

When designing an ultrasound non-destructive (NDT) probe for high temperature applications, one has to take into account a multitude of temperature induced effects, such as the temperature dependence of key physical properties of probe materials. In this paper, the significant influence of temperature change on piezoelectric properties and piezoelectric anisotropy, and thus on the ultrasound properties of the whole probe, is discussed theoretically. This is demonstrated within the thermodynamic Landau-Ginzburg-Devonshire (LGD) framework and the KLM model of equivalent circuits for two different piezoelectric, acoustically active probe materials from the same family - barium titanate and lead titanate. These two materials are model materials for the whole family of piezoelectric perovskites, including the commercially widely used PZT and relaxor ferroelectrics PMN-PT and PZN-PT