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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 1,747 records · Page 97

Comparative study of flux pinning, creep and critical currents between YBaCuO crystals with and without Y2BaCuO5 inclusions

In the Y-Ba-Cu-O system, YBa2Cu3O(x) phase is produced by the following peritectic reaction: Y2BaCuO5 + liquid yields 2YBa2Cu3O(x). Through the control of processing conditions and starting compositions, it becomes possible to fabricate large crystals containing fine Y2BaCuO5(211) inclusions. Such crystals exhibit Jc values exceeding 10000 A/sq cm at 77 K and 1T. Recently, researchers developed a novel process which can control the volume fraction of 211 inclusions. Elimination of 211 inclusions is also possible. In this study, researchers prepared YBaCuO crystals with and without 211 inclusions using the novel process, and compared flux pinning, flux creep and critical currents. Magnetic field dependence of Jc for YBaCuO crystals with and with 211 inclusions is shown. It is clear that fine 211 inclusions can contribute to flux pinning. It was also found that flux creep rate could be reduced by increasing flux pinning force. Critical current density estimates based on the conventional flux pinning theory were in good agreement with experimental results.

Murakami, Masato↗

Eliminating Voltage Decay of Lithium-Rich Li 1.14 Mn 0.54 Ni 0.14 Co 0.14 O 2 Cathodes by Controlling the Electrochemical Process

Lithium-rich material owns a particularly high capacity owing to the activation of electrochemical inactive Li 2 MnO 3 phase. But at the same time, MnO 2 phase formed after Li 2 MnO 3 activation confronts a severe problem of converting to spinel phase, and resulting in voltage decay. To our knowledge, this phenomenon is inherent property of layered manganese oxide materials and can hardly be overcome. Based on this, unlike previous reports, herein we design a method for the first time to accelerate the phase transformation by tuning the charge upper-limit voltage at a high value, so the phase transformation process can be finished in a few cycles. Then material structure remains stable while cycling at a low upper-limit voltage. By this novel method voltage decay is eliminated significantly.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Generation of one-way Einstein–Podolsky–Rosen steering using interference-controlled asymmetric dissipation process

We show that one-way Einstein–Podolsky–Rosen (EPR) steering effects can be generated via the asymmetric dissipation scheme induced by the spontaneously generated coherence (SGC) in a resonantly driven V-type atomic system. According to the dressed atomic states and Bogoliubov transformation, we find that there exist two identical dissipation channels being responsible for the appearance of entanglement and symmetric two-way steering effects in the absence of SGC effect. More interestingly, the one-way EPR steering effect occurs when the population differences between the dressed states are prominently modified by the SGC effect. As a consequence, the symmetry of the two dissipation channels is broken by the quantum interference, leading to the generation of one-way EPR steering effect.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Potential-Dynamic Surface Chemistry Controls the Electrocatalytic Processes of Ethanol Oxidation on Gold Surfaces

Electro-catalysis has various important applications especially fuel cells. As a key element in electro-catalysis, the surface chemistry of electro-catalysts may strongly influence the catalytic activity and reaction mechanism, the fundamental understanding of which would provide guidance for designing high-efficiency catalysts. Herein, we utilized our recently developed in situ liquid SIMS approach to investigate the electro-catalytic oxidation of ethanol on gold surfaces in alkaline environments involved in direct alcohol fuel cells. Formation of adsorbed hydroxide intermediates on the gold surfaces upon electro-oxidation was molecularly witnessed under operando conditions, the evolution of which was revealed to govern the electro-catalytic processes. Moreover, the hydroxide intermediates as active sites participated in the reaction through transferring nucleophilic hydroxyl groups into the adjacent ethanol molecules. This work brings new light into electro-catalytic research and will facilitate the improvement of catalytic systems on the basis of surface chemistry-catalytic performance relationship.

Zhang, Yanyan↗

High Performance Platinum Group Metal Free Membrane Electrode Assemblies through Control of Interfacial Processes

The quantitative goal of this project was to produce a high-performance anion exchange membrane water electrolyzer (AEM-WE) completely free of platinum group metals (PGMs), which could operate for at least 500 hours with less than 50 microV/hour degradation, at 500 mA/cm 2 . To achieve this goal, work focused on the optimization of electrocatalyst conductivity, with dispersion and utilization in the membrane electrode assembly (MEA) improved through refinement of deposition techniques. Critical factors were also explored with significant work undertaken by Northeastern University to further understand catalyst-membrane-ionomer interfaces and how they differ from liquid electrolyte. Water management and optimal cell operational parameters were established through the design, fabrication, and test of a new test station at Proton specific for AEM evaluation. Additionally, AEM material stability and robustness at high potentials and gas evolution conditions were advanced at Penn State.

08 HYDROGEN↗