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Li photoionization cross sections determined from spectral intensity measurements as function of threshold wavelength, discussing radiative electron-ion recombination into first excited state
The interaction of thermal oxygen or helium ions and ring current protons may produce a wide variety of phenomena in the magnetosphere. These include the production of energetic oxygen ions or energetic helium ions, modification of the bulge region in the afternoon plasmasphere, heating of electrons in the upper ionosphere and production of stable auroral red arcs, precipitation of energetic protons, and precipitation of energetic alpha particles. Large-amplitude waves generated in the interaction may also lead to wave-wave coupling. The theory developed also suggests that heavier ions such as lithium artificially injected into the ring current to remove ring current protons may be heated substantially in the process. Computations of wave growth have been made for the first time by using measured ring current flux and anisotropies.
Our breakthrough propulsion architecture is an innovative way to take advantage of kilometer-scale, multi-hundred megawatt, space-based, phased-array lasers to enable rapid transportation throughout the solar system. In this architecture, the laser would beam power over distances of up to 40 AU increasing the available power density relative to solar insolation by two orders of magnitude. The receiving vehicle would have a photovoltaic array with cells tuned to the laser frequency that outputs a voltage of 6 kV to directly-drive a lithium-fueled gridded ion thruster system at an ultra-high specific impulse of 40,000 s. Such a system could enable final spacecraft speeds of greater than 40 AU/year, potentially enabling missions to the solar gravity lens focus at 550 AU in less than 15 years. This is the propulsion architecture of the 22nd century.
The process by which the solar wind assimilates newly ionized atoms is important for understanding the presence of planetary or interstellar helium in the solar wind, the dynamics of the Active Magnetospheric Particle Tracer Explorers (AMPTE) lithium releases in front of the earth's bow shock, and the formation of cometary tails. In this paper is examined how newborn ions can be coupled to the solar wind in the direction parallel to the magnetic field by means of electromagnetic instabilities driven by the distribution of newborn ions. The linear properties of three instabilities are analyzed and compared with numerical solutions of the linear dispersion equation, while their nonlinear behavior is followed by means of computer simulation to obtain the characteristic time for the pickup process. With a primary emphasis on the AMPTE lithiuim releases, various degrees of realism are introduced into the calculations to model the upstream conditions and the intersection of the lithium with the bow shock. It is shown that a time-dependent shock model is needed to correctly reproduce the amount of lithium which is transmitted through the shock and that the resulting lithium ion distribution is still likely to be subject to the same type of instabilities in the magnetosheath. Applications of these results to comets, in particular the artificial comet expected to be generated by the AMPTE barium release in the magnetosheath, is also briefly discussed.
Demonstrated improved performance with wide operating temperature electrolytes containing ester co - solvents (i.e., methyl propionate and ethyl butyrate) in a number of prototype cells: center dot Successfully scaled up low temperature technology to 12 Ah size prismatic Li - ion cells (Quallion, LCC), and demonstrated good performance down to - 60 o C. center dot Demonstrated wide operating temperature range performance ( - 60 o to +60 o C) in A123 Systems LiFePO 4 - based lithium - ion cells containing methyl butyrate - based low temperature electrolytes. These systems were also demonstrated to have excellent cycle life performance at ambient temperatures, as well as the ability to be cycled up to high temperatures.
The total elastic and positronium formation cross sections of the inelastic collisions between positrons and various one-valence-electron atoms, (namely hydrogen, lithium, sodium, potassium and rubidium), and one-valence-electron ions, (namely hydrogen-like, lithium-like and alkaline-earth positive ions) are determined using an elaborate modified coupled-static approximation. Special attention is devoted to the behavior of the Ps cross sections at the energy regions lying above the Ps formation thresholds.
In the present work, a number of additives have been investigated for their effect on the charge characteristics of cells containing low temperature, high ester content electrolytes (1.0 M LiPF6 in ethylene carbonate (EC) + ethyl methyl carbonate (EMC) + methyl propionate (MP) 20:20:60 vol % + X additive). These experimental three-electrode cells are composed of graphite anodes, LiNiCoAlO2 cathodes, and a lithium metal reference electrode. Cells were first subjected to electrochemical characterization at various temperatures, consisting of performing Electrochemical Impedance Spectroscopy (EIS), linear micropolarization and Tafel polarization measurement to determine the kinetic parameters for both the anodes and cathodes. Following electrochemical characterization, the cells were subjected to charging at decreasing temperatures using C/5 rates to 4.10V, with a constant potential C/50 current taper. Analysis of the C/20 discharge following the charge at low temperature revealed either the presence or absence of a high voltage plateau during the initial stages of the discharge. This plateau has been linked to the presence of lithium metal on the anode previously and was used as a measure for the extent of lithium plating in the cell. Differential analysis (dV/dQ) was applied as well to more clearly visualize the position of the high voltage plateau and use the peak position (x-axis) in the dV/dQ plot as a gauge for the amount of plating which took place in the cell on the prior charge. Most additives investigated increased the resistance of the anode and decreased the resistance of the cathode, thereby leading to an overall increase in plating observed at low temperature. One additive, LiFSI, was found to be beneficial during low temperature charging, however studies of electrode kinetics from the cell containing LiFSI did not reveal significant improvements compared to the baseline.
NASA Glenn Research Center (GRC) is currently working on polymers for fuel cell and lithium battery applications. The desire for more efficient, higher power density, and a lower environmental impact power sources has led to interest in proton exchanges membrane fuels cells (PEMFC) and lithium batteries. A PEMFC has many advantages as a power source. The fuel cell uses oxygen and hydrogen as reactants. The resulting products are electricity, heat, and water. The PEMFC consists of electrodes with a catalyst, and an electrolyte. The electrolyte is an ion-conducting polymer that transports protons from the anode to the cathode. Typically, a PEMFC is operated at a temperature of about 80 C. There is intense interest in developing a fuel cell membrane that can operate at higher temperatures in the range of 80 C- 120 C. Operating the he1 cell at higher temperatures increases the kinetics of the fuel cell reaction as well as decreasing the susceptibility of the catalyst to be poisoned by impurities. Currently, Nafion made by Dupont is the most widely used polymer membrane in PEMFC. Nafion does not function well above 80 C due to a significant decrease in the conductivity of the membrane from a loss of hydration. In addition to the loss of conductivity at high temperatures, the long term stability and relatively high cost of Nafion have stimulated many researches to find a substitute for Nafion. Lithium ion batteries are popular for use in portable electronic devices, such as laptop computers and mobile phones. The high power density of lithium batteries makes them ideal for the high power demand of today s advanced electronics. NASA is developing a solid polymer electrolyte that can be used for lithium batteries. Solid polymer electrolytes have many advantages over the current gel or liquid based systems that are used currently. Among these advantages are the potential for increased power density and design flexibility. Automobiles, computers, and cell phones require highly efficient power density for lowering emissions and meeting increasing consumer demands. Many of the solutions can be provided by proton exchange membrane fuel cells and lithium batteries. NASA Glenn Research Center has recognized this need, and is presently engaged in a solution. The goals for the summer include mastering synthesis techniques, understanding the reactions occurring during the synthesis, and characterizing the resulting polymer membranes using NMR, DSC, and TGA for the PEMFC and lithium batteries.
In order to study the access of solar wind ions to the magnetosphere, together with the processes that transport and accelerate magnetospheric particles, the Active Magnetospheric Particle Tracer Explorers (AMPTE) mission will release and monitor lithium and barium tracer ions in both the solar wind and the magnetosphere. A single, massive release of barium in the dawn magnetosheath will in addition create a visible artificial comet in the flowing solar wind plasma, within which studies of a range of different plasma effects will be undertaken. The AMPTE will obtain comprehensive measurements of natural magnetospheric particle populations' elemental composition and dynamics. AMPTE comprises three spacecraft: the Ion Release Module, the Charge Composition Explorer, and the United Kingdom Subsatellite.
With the need for long periods of extravehicular activities (EVAs) on the Moon or Mars or a near-asteroid, the need for long-performance batteries has increased significantly. The energy requirements for the EVA suit, as well as surface systems such as rovers, have increased significantly due to the number of applications they need to power at the same time. However, even with the best state-of-the-art Li-ion batteries, it is not possible to power the suit or the rovers for the extended period of performance. Carrying a charging system along with the batteries makes it cumbersome and requires a self-contained power source for the charging system that is usually not possible. An innovative method to charge and use the Li-ion batteries for long periods seems to be necessary and hence, with the advent of the Li-ion supercapacitors, a method has been developed to extend the performance period of the Li-ion power system for future exploration applications. The Li-ion supercapacitors have a working voltage range of 3.8 to 2.5 V, and are different from a traditional supercapacitor that typically has a working voltage of 1 V. The innovation is to use this Li-ion supercapacitor to charge Liion battery systems on an as-needed basis. The supercapacitors are charged using solar arrays and have battery systems of low capacity in parallel to be able to charge any one battery system while they provide power to the application. Supercapacitors can safely take up fast charge since the electrochemical process involved is still based on charge separation rather than the intercalation process seen in Li-ion batteries, thus preventing lithium metal deposition on the anodes. The lack of intercalation and eliminating wear of the supercapacitors allows for them to be charged and discharged safely for a few tens of thousands of cycles. The Li-ion supercapacitors can be charged from the solar cells during the day during an extended EVA. The Liion battery used can be half the capacity required for a nominal EVA. The small Li-ion battery can be divided into two parallel modules with independent charging ports that would allow the supercapacitors to charge one battery while the other is providing power to the rover or suit.
Properties of simple atoms and ions - atomic helium, rubidium, lithium, barium, and potassium transitions
We have demonstrated a route to reversibly intercalate fluoride-anion receptor complexes in graphite via a nonaqueous electrochemical process. This approach may find application for a rechargeable lithium-fluoride dual-ion intercalating battery with high specific energy. The cell chemistry presented here uses graphite cathodes with LiF dissolved in a nonaqueous solvent through the aid of anion receptors. Cells have been demonstrated with reversible cathode specific capacity of approximately 80 mAh/g at discharge plateaus of upward of 4.8 V, with graphite staging of the intercalant observed via in situ synchrotron X-ray diffraction during charging. Electrochemical impedance spectroscopy and B-11 nuclear magnetic resonance studies suggest that cointercalation of the anion receptor with the fluoride occurs during charging, which likely limits the cathode specific capacity. The anion receptor type dictates the extent of graphite fluorination, and must be further optimized to realize high theoretical fluorination levels. To find these optimal anion receptors, we have designed an ab initio calculations-based scheme aimed at identifying receptors with favorable fluoride binding and release properties.
The present invention includes compositions, surface and bulk modifications, and methods of making of (1-x)Li[Li.sub.1/3Mn.sub.2/3]O.sub.2.xLi[Mn.sub.0.5-yNi.sub.0.5-yCo.sub.2- y]O.sub.2 cathode materials having an O3 crystal structure with a x value between 0 and 1 and y value between 0 and 0.5, reducing the irreversible capacity loss in the first cycle by surface modification with oxides and bulk modification with cationic and anionic substitutions, and increasing the reversible capacity to close to the theoretical value of insertion/extraction of one lithium per transition metal ion (250-300 mAh/g).
Topics addressed include: ion-cyclotron waves; plasma waves; solar wind lithium releases; bow shock; Pi2 wave bursts; auroral kilometric radiation; ion energization; magnetic field corrections; electric fields; magnetospheric processes; electron acceleration; inner heliosphere; nightside auroral zone; computerized simulation; plasma wave turbulence; and magnetohydrodynamic waves in plasma sheets.
During the AMPTE (Active Magnetospheric Particle Tracer Explorers) solar wind lithium release on September 11, and again on September 20, 1984, an intense burst of electrostatic noise was observed near the upstream edge of the ion cloud. Comparisons with measurements by the IMP-6 and ISEE-1 spacecraft show that the spectrum and overall features of this noise are very similar to electrostatic noise observed at the Earth's bow shock. A stability analysis using realistic parameters shows that the electrostatic noise can be accounted for by an ion beam-plasma instability caused by the solar wind proton beam streaming through the nearly stationary lithium cloud. The growth rate of this instability is largest when the ion density and solar wind proton density are similar, which explains why the noise only occurs near the outer edge of the ion cloud. The similarity to the noise in the Earth's bow shock suggest that a shock may exist in the solar wind plasma flow upstream of the ion cloud. If the noise is associated with a shock, then it must be an electrostatic shock, since the ion cyclotron radii are too small for the existence of a MHD shock. Since the electrostatic instability occurs at phase velocities near the lithium thermal velocity, the electrostatic turbulence may play a role in heating the lithium ions and transferring momentum from the solar wind to the ion cloud.
Norbornene-based polymers have shown promise as solid electrolytes for lithium-based rechargeable electrochemical cells. These polymers are characterized as single-ion conductors. Single-ion-conducting polymers that can be used in lithium cells have long been sought. Single-ion conductors are preferred to multiple-ion conductors as solid electrolytes because concentration gradients associated with multiple-ion conduction lead to concentration polarization. By minimizing concentration polarization, one can enhance charge and discharge rates. Norbornene sulfonic acid esters have been synthesized by a ring-opening metathesis polymerization technique, using ruthenium-based catalysts. The resulting polymer structures (see figure) include sulfonate ionomers attached to the backbones of the polymer molecules. These molecules are single-ion conductors in that they conduct mobile Li+ ions only; the SO3 anions in these polymers, being tethered to the backbones, do not contribute to ionic conduction. This molecular system is especially attractive in that it is highly amenable to modification through functionalization of the backbone or copolymerization with various monomers. Polymers of this type have been blended with poly(ethylene oxide) to lend mechanical integrity to free-standing films, and the films have been fabricated into solid polymer electrolytes. These electrolytes have been demonstrated to exhibit conductivity of 2 10(exp -5)S/cm (which is high, relative to the conductivities of other solid electrolytes) at ambient temperature, plus acceptably high stability. This type of norbornene-based polymeric solid electrolyte is in the early stages of development. Inasmuch as the method of synthesis of these polymers is inherently flexible and techniques for the fabrication of the polymers into solid electrolytes are amenable to optimization, there is reason to anticipate further improvements.
The influence of OH ion impurities on thermoluminescent sensitivity and supralinearity in LiF:Mg, Ti is analyzed. Available evidence is shown to be consistant with the presence of Ti-OH and Mg-OH complexes. The track interaction model is used to explain the data, with competing centers decreasing sensitivity and supralinearity at high concentrations.
In a previous publication [Can. J. Phys. 75, 11 (1997)] we calculated the generalized polarizabilities up to multipole order 3 as well as certain higher-order hyperpolarizabilities for two-electron atoms and ions of Z=2-6 and 10. In this paper we apply some of these results to calculate excited-state energies in three times ionized (lithium-like) carbon. For states with angular momentum L greater than or equal to 3 accurate results are obtained using an asymptotic polarizability expansion that includes nonadiabatic effects. Comparison is made with recent optical measurements, and a critical discussion of the correct form of the expansion is given. In addition, the possibility of very accurate measurements of the fine-structure splitting encourages us to present a table of such splittings to very high accuracy. An appendix contains similar results for lithium-like oxygen and neon ions.