A new scheme for mode locking a free-electron laser amplifier is proposed based on electron beam current modulation. It is found that certain properties of the original concept, based on the energy modulation of electrons, are improved including the spectral brightness of the source and the purity of the series of short pulses. Numerical comparisons are made between the new and old schemes and between a mode-locked free-electron laser and self-amplified spontaneous emission free-electron laser. Illustrative examples using a hypothetical mode-locked free-electron laser amplifier are provided. The ability to generate intense coherent radiation with a large bandwidth is demonstrated.

Until recently, the use of oxalic acid for chemically cleaning the Savannah River Site (SRS) radioactive waste tanks focused on using concentrated 4 and 8-wt% solutions. Recent testing and research on applicable dissolution mechanisms have concluded that under appropriate conditions, dilute solutions of oxalic acid (i.e., 1-wt%) may be more effective. Based on the need to maximize cleaning effectiveness, coupled with the need to minimize downstream impacts, SRS is now developing plans for using a 1-wt% oxalic acid solution. A technology gap associated with using a 1-wt% oxalic acid solution was a dearth of suitable corrosion data. Assuming oxalic acid's passivation of carbon steel was proportional to the free oxalate concentration, the general corrosion rate (CR) from a 1-wt% solution may not be bound by those from 8-wt%. Therefore, after developing the test strategy and plan, the corrosion testing was performed. Starting with the envisioned process specific baseline solvent, a 1-wt% oxalic acid solution, with sludge (limited to Purex type sludge-simulant for this initial effort) at 75 C and agitated, the corrosion rate (CR) was determined from the measured weight loss of the exposed coupon. Environmental variations tested were: (a) Inclusion of sludge in the test vessel or assuming a …

OPV cell efficiencies have increased significantly over the last decade and verified champion efficiencies are currently at 8.3% for both single and multi-junction device types. These increases in efficiency have been driven through the development and optimization of the donor and acceptor materials in bulk heterojunction active layers. Plextronics and Solarmer Energy Inc. are two of the world leading developers of these donor and acceptor materials. Solarmer Energy has reported NREL certified 6.77% efficiencies using optimized low band gap donor materials in combination with PC61BM and PC71BM acceptors and recently reported a champion NREL certified efficiency of 8.1%. Plextronics has reported Newport certified efficiencies of 6.7% using PC71BM acceptors with low band gap materials. In addition, Plextronics has also demonstrated that OPV efficiency of P3HT based materials can be improved by 50% by improving the Voc using alternative acceptors (indene substituted C60 and C70) to PC61BM and PC71BM. However, performance of these alternative acceptors in combination with low band gap materials has not been investigated and the potential for efficiency improvement is evident. In this collaboration, four low band gap donor materials from Solarmer Energy Inc were combined with Plextronics’ indene-class acceptors Plextronics’ indene substituted C60 and C70 acceptors to …

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We have developed an automated data analysis method for atmospheric particles using scanning transmission X-ray microscopy coupled with near edge X-ray fine structure spectroscopy (STXM/NEXAFS). This method is applied to complex internally mixed submicrometer particles containing organic and inorganic material. Several algorithms were developed to exploit NEXAFS spectral features in the energy range from 278 to 320 eV for quantitative mapping of the spatial distribution of elemental carbon, organic carbon, potassium, and noncarbonaceous elements in particles of mixed composition. This energy range encompasses the carbon K-edge and potassium L2 and L3 edges. STXM/NEXAFS maps of different chemical components were complemented with a subsequent analysis using elemental maps obtained by scanning electron microscopy coupled with energy dispersive X-ray analysis (SEM/EDX). We demonstrate the application of the automated mapping algorithms for data analysis and the statistical classification of particles.

The cathode catalyst layer within a proton-exchange-membrane fuel cell is the most complex and critical, yet least understood, layer within the cell. The exact method and equations for modeling this layer are still being revised and will be discussed in this paper, including a 0.8 reaction order, existence of Pt oxides, possible non-isopotential agglomerates, and the impact of a film resistance towards oxygen transport. While the former assumptions are relatively straightforward to understand and implement, the latter film resistance is shown to be critically important in explaining increased mass-transport limitations with low Pt-loading catalyst layers. Model results demonstrate agreement with experimental data that the increased oxygen flux and/or diffusion pathway through the film can substantially decrease performance. Also, some scale-up concepts from the agglomerate scale to the more macroscopic porous-electrode scale are discussed and the resulting optimization scenarios investigated.

Here we describe the gold-indium reaction along gold wires soldered at both ends. It begins with the combined radial/axial reaction in the vicinity of the solder mound as seen in metallurgical sections along the axis of the wire. We show that this combined radial/axial reaction has no effect on the resistance of the system, even though it shortens the length of the gold wire while converting it to gold indide. After this radial/axial reaction is complete, a purely axial reaction begins. For thin gold wires (i.e. 38.1 {micro}m diameter) the onset of that reaction is strongly correlated with the time at which the linear reaction model predicts the complete consumption of the gold wire inside the solder mounds. This purely axial reaction converts the whole wire rapidly to gold indide, and leads to substantial resistance changes and complete distortion of the wire between the solder mounds. The reaction product is AuIn{sub 2} everywhere, but both Sn and Pb also are identified everywhere on the surface by Electron Dispersive Spectroscopy.

Large-scale EE programs would modestly increase tariffs but reduce consumers' electricity bills significantly. However, the primary benefit of EE programs is a significant reduction in power shortages, which might make these programs politically acceptable even if tariffs increase. To increase political support, utilities could pursue programs that would result in minimal tariff increases. This can be achieved in four ways: (a) focus only on low-cost programs (such as replacing electric water heaters with gas water heaters); (b) sell power conserved through the EE program to the market at a price higher than the cost of peak power purchase; (c) focus on programs where a partial utility subsidy of incremental capital cost might work and (d) increase the number of participant consumers by offering a basket of EE programs to fit all consumer subcategories and tariff tiers. Large scale EE programs can result in consistently negative cash flows and significantly erode the utility's overall profitability. In case the utility is facing shortages, the cash flow is very sensitive to the marginal tariff of the unmet demand. This will have an important bearing on the choice of EE programs in Indian states where low-paying rural and agricultural consumers form the majority of …

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Absorption isotherm data exists for a wide variety of hydrogen-metal systems. When working with high purity gases, appropriately sized equipment, and hydrides with equilibrium pressures above several hundred Pa, data collection is relatively straightforward. Special consideration must be given to experiments involving low equilibrium pressure hydrides, as even sub-ppm levels of gas impurities can generate partial pressures many times greater than the equilibrium pressures to be measured. Tritium absorption experiments are further complicated by the continuous generation of helium-3. The time required to transfer and absorb a known quantity of tritium onto a sample ultimately limits the minimum pressure range that can be studied using the standard technique. Equations are presented which show the pressure of helium-3 in a sample cell based on the amount of tritium to be absorbed, the sample cell volume and temperature, and the decay time of tritium. Sample calculations for zirconium show that at 300 C, the estimated helium-3 pressure in the cell will be equal to the hydrogen absorption pressure after only milliseconds of tritium decay. An alternate method is presented that permits the collection of equilibrium data at pressures orders of magnitude lower than possible using a direct approach.

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Scanning transmission x-ray microscopy (STXM) combines x-ray microscopy and near edge x-ray absorption fine structure spectroscopy (NEXAFS). This combination provides spatially resolved bonding and oxidation state information. While there are reviews relevant to STXM/NEXAFS applications in other environmental fields (and magnetic materials) this chapter focuses on atmospheric aerosols. It provides an introduction to this technique in a manner approachable to non-experts. It begins with relevant background information on synchrotron radiation sources and a description of NEXAFS spectroscopy. The bulk of the chapter provides a survey of STXM/NEXAFS aerosol studies and is organized according to the type of aerosol investigated. The purpose is to illustrate the current range and recent growth of scientific investigations employing STXM-NEXAFS to probe atmospheric aerosol morphology, surface coatings, mixing states, and atmospheric processing.

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The ability to manage inventories of carbon, tritium, and high-Z elements in fusion plasmas depends on means for effective dust removal. A dust conveyor, based on a moving electrostatic potential well, was tested with particles of tungsten, carbon, glass and sand. A digital microscope imaged a representative portion of the conveyor, and dust particle size and volume distributions were derived before and after operation. About 10 mm3 volume of carbon and tungsten particles were moved in under 5 seconds. The highest driving amplitude tested of 3 kV was the most effective. The optimal driving frequency was 210 Hz (maximum tested) for tungsten particles, decreasing to below 60 Hz for the larger sand particles. Measurements of particle size and volume distributions after 10 and 100 cycles show the breaking apart of agglomerated carbon, and the change in particle distribution over short timescales (<1 s).