9 research outputs found

    Coadsorption of sodium and elemental sulfur on nickel (100) surfaces, 1996

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    This study examined the structural and electronic growth properties of the coadsorption of Sodium and elemental Sulfur on Nickel (100) surfaces at room temperature. The investigation was conducted in an ultra high vacuum system using low energy electron diffraction, Auger electron spectroscopy, and work function measurements. The main objective of the study was to create a low work function substrate that would be useful for low work function devices. The research occurred in four stages: (1) adsorption of S on clean Ni(100), (2) adsorption of Na on clean Ni(100), (3) coadsorption of Na on S covered Ni(100), and (4) coadsorption of S on Na covered Ni(100). The measurements obtained suggest that S grows on Ni(100) in a layer by layer mode, forming a p(2x2) initially and a c(2x2) at the completion of the first layer. The second layer of S is disordered. The measurements also indicate that deposition of Na at room temperature forms a single c(2x2) layer. The coadsorption studies showed that the presence of S on the surface of Ni(100) increased the amount of Na that can be deposited on the substrate. A low work function of 0.8eV was obtained during the study. Furthermore, the presence of Na on Ni(100) was found not to affect the deposition of S, however the S was found to destroy the metallic character of the underlying Na

    Hydrogen and Fuel Cell Technology: Progress, Challenges, and Future Directions

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    AbstractThe Department of Energy's (DOE) hydrogen and fuel cell activities are presented, focussing on key targets and progress. Recent results on the cost, durability, and performance of fuel cells are discussed, along with the status of hydrogen-related technologies and cross-cutting activities. DOE has deployed fuel cells in key early markets, including backup power and forklifts. Recent analyses show that fuel cell electric vehicles (FCEVs) are among the most promising options to reduce greenhouse gas emissions and petroleum use. Preliminary analysis also indicates that the total cost of ownership of FCEVs will be comparable to other advanced vehicle and fuel options

    State-resolved gas-surface reactivity of methane in the symmetric C-H stretch vibration on Ni(100)

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    The state-resolved reactivity of CH4 in its totally symmetric C-H stretch vibration (�1) has been measured on a Ni(100) surface. Methane molecules were accelerated to kinetic energies of 49 and 63:5 kJ=mol in a molecular beam and vibrationally excited to �1 by stimulated Raman pumping before surface impact at normal incidence. The reactivity of the symmetric-stretch excited CH4 is about an order of magnitude higher than that of methane excited to the antisymmetric stretch (�3) reported by Juurlink et al. [Phys. Rev. Lett. 83, 868 (1999)] and is similar to that we have previously observed for the excitation of the first overtone (2�3). The difference between the state-resolved reactivity for �1 and �3 is consistent with predictions of a vibrationally adiabatic model of the methane reaction dynamics and indicates that statistical models cannot correctly describe the chemisorption of CH4 on nickel

    Efficient Stimulated Raman Pumping for Quantum-State Resolved Surface Reactivity Measurements

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    We describe the use of stimulated Raman pumping in a molecular beam to perform quantum state resolved gas-surface reactivity measurements for molecules prepared in totally symmetric vibrational states. Vibrational states of homonuclear diatomics as well as totally symmetric vibrations of polyatomic molecules cannot be prepared by direct infrared excitation but are accessible through stimulated Raman pumping by two laser fields when the difference between the incident laser frequencies matches the vibration. We generate a suitable resonant pair of high-energy pump and Stokes laser beams in an injection seeded Raman amplifier filled with the sample gas and equipped with internal gas recirculation. The ability to partially saturate the Raman pumping process in the molecular beam is used to quantify the fraction of vibrationally excited molecules in the irradiated volume, which is needed for quantitative reactivity measurements. We illustrate the method with state resolved reactivity measurements for CH4, prepared in its symmetric C-H stretch vibration on a Ni(100) single crystal surface.LCP

    U.S. DOE Progress Towards Developing Low-Cost, High Performance, Durable Polymer Electrolyte Membranes for Fuel Cell Applications

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    Low cost, durable, and selective membranes with high ionic conductivity are a priority need for wide-spread adoption of polymer electrolyte membrane fuel cells (PEMFCs) and direct methanol fuel cells (DMFCs). Electrolyte membranes are a major cost component of PEMFC stacks at low production volumes. PEMFC membranes also impose limitations on fuel cell system operating conditions that add system complexity and cost. Reactant gas and fuel permeation through the membrane leads to decreased fuel cell performance, loss of efficiency, and reduced durability in both PEMFCs and DMFCs. To address these challenges, the U.S. Department of Energy (DOE) Fuel Cell Technologies Program, in the Office of Energy Efficiency and Renewable Energy, supports research and development aimed at improving ion exchange membranes for fuel cells. For PEMFCs, efforts are primarily focused on developing materials for higher temperature operation (up to 120 °C) in automotive applications. For DMFCs, efforts are focused on developing membranes with reduced methanol permeability. In this paper, the recently revised DOE membrane targets, strategies, and highlights of DOE-funded projects to develop new, inexpensive membranes that have good performance in hot and dry conditions (PEMFC) and that reduce methanol crossover (DMFC) will be discussed
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