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At least 1,567 records · Page 87

A Nanoscale Vacuum Field Emission Gated Diode with an Umbrella Cathode

A nanoscale field emission vacuum channel gated diode structure is proposed and a tungsten cathode with an umbrella-like geometry and sharp vertical edge is fabricated. The edge of the suspended cathode becomes the field emission surface. Unlike in the traditional transistor with the gate typically located between the source and the drain, the bottom silicon plate becomes the gate here and the anode terminal is located between the umbrella cathode and the gate. The fabricated devices show excellent diode characteristics and the gated diode structure is attractive for extremely low gate leakage.

Vacuum field emission diode↗

Molten carbonate fuel cell cathode with mixed oxide coating

A molten carbonate fuel cell cathode having a cathode body and a coating of a mixed oxygen ion conductor materials. The mixed oxygen ion conductor materials are formed from ceria or doped ceria, such as gadolinium doped ceria or yttrium doped ceria. The coating is deposited on the cathode body using a sol-gel process, which utilizes as precursors organometallic compounds, organic and inorganic salts, hydroxides or alkoxides and which uses as the solvent water, organic solvent or a mixture of same.

30 DIRECT ENERGY CONVERSION↗

Cathode material for lithium batteries

A method of manufacture an article of a cathode (positive electrode) material for lithium batteries. The cathode material is a lithium molybdenum composite transition metal oxide material and is prepared by mixing in a solid state an intermediate molybdenum composite transition metal oxide and a lithium source. The mixture is thermally treated to obtain the lithium molybdenum composite transition metal oxide cathode material.

25 ENERGY STORAGE↗

Cation-substituted spinel oxide and oxyfluoride cathodes for lithium ion batteries

The present invention includes compositions and methods of making cation-substituted and fluorine-substituted spinel cathode compositions by firing a LiMn.sub.2-y-zLi.sub.yM.sub.zO.sub.4 oxide with NH.sub.4HF.sub.2 at low temperatures of between about 300 and 700.degree. C. for 2 to 8 hours and a .eta. of more than 0 and less than about 0.50, mixed two-phase compositions consisting of a spinel cathode and a layered oxide cathode, and coupling them with unmodified or surface modified graphite anodes in lithium ion cells.

25 ENERGY STORAGE↗

Cathode material for lithium batteries

A method of manufacture an article of a cathode (positive electrode) material for lithium batteries. The cathode material is a lithium molybdenum composite transition metal oxide material and is prepared by mixing in a solid state an intermediate molybdenum composite transition metal oxide and a lithium source. The mixture is thermally treated to obtain the lithium molybdenum composite transition metal oxide cathode material.

25 ENERGY STORAGE↗

Solid oxide fuel cell power plant having a fixed contact oxidation catalyzed section of a multi-section cathode air heat exchanger

The multi-section cathode air heat exchanger (102) includes at least a first heat exchanger section (104), and a fixed contact oxidation catalyzed section (126) secured adjacent each other in a stack association. Cool cathode inlet air flows through cool air channels (110) of the at least first (104) and oxidation catalyzed sections (126). Hot anode exhaust flows through hot air channels (124) of the oxidation catalyzed section (126) and is combusted therein. The combusted anode exhaust then flows through hot air channels (112) of the first section (104) of the cathode air heat exchanger (102). The cool and hot air channels (110, 112) are secured in direct heat exchange relationship with each other so that temperatures of the heat exchanger (102) do not exceed 800.degree. C. to minimize requirements for using expensive, high-temperature alloys.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Simulations of Field-Emission Electron Beams from CNT Cathodes in RF Photoinjectors

Average field emission currents of up to 700 mA were produced by Carbon Nano Tube (CNT) cathodes in a 1.3 GHz RF gun at Fermilab High Brightness Electron Source Lab. (HBESL). The CNT cathodes were manufactured at Xintek and tested under DC conditions at RadiaBeam. The electron beam intensity as well as the other beam properties are directly related to the time-dependent electric field at the cathode and the geometry of the RF gun. This report focuses on simulations of the electron beam generated through field-emission and the results are compared with experimental measurements. These simulations were performed with the time-dependent Particle In Cell (PIC) code WARP.

43 PARTICLE ACCELERATORS↗

Compatibility of a Conventional Non-aqueous Magnesium Electrolyte with a High Voltage V 2 O 5 Cathode and Mg Anode

A major roadblock for magnesium ion battery development is the availability of an electrolyte that can deposit Mg reversibly and at the same time is compatible with a high voltage cathode. We report a prospective full magnesium cell utilizing a simple, non-aqueous electrolyte composed of high concentration magnesium bis(trifluoromethane sulfonyl)imide in diglyme, which is compatible with a high voltage vanadium pentoxide (V 2 O 5 ) cathode and a Mg metal anode. For this system, plating and stripping of Mg metal can be achieved with magnesium bis(trifluoromethane sulfonyl)imide in diglyme electrolyte over a wide concentration range, however, reversible insertion of Mg into V 2 O 5 cathode can only be attained at high electrolyte concentrations. Reversible intercalation of Mg into V 2 O 5 is characterized and confirmed by X-ray diffraction, X-ray absorption near edge spectroscopy and energy dispersive spectroscopy.

Sa, Niya↗

"Ion" B-Dot and Faraday Cup Results Located Inside The Cathode Knob Of The Self Magnetic Pinch (Smp) Diode (A New Diagnostic For Diode Behavior?)

This paper describes our effort to measure the back-streaming ions emitted from the target x-ray convertor and thus estimate the ion contribution to the A-K gap bipolar current flow. Knowing the ion contribution is quite important in order to calculate the expected x-ray dose and compare it with the actual measurements. Our plans were first to measure the total ion current using B-dot monitors, Rogowski coils, and Faraday cups and then to utilize filtered Faraday cups and time of flight techniques to identify and measure the various ionic species. The kinetic energy (velocities) of the ions should help evaluate the actual voltage applied at the anode-cathode (A-K) gap. LSP simulations found that the most prominent ions are protons and carbon single plus (C+). For an 8-MV A-K voltage, the estimated proton current back-streaming through an 1 cm in diameter hollow cathode tip was on the average 3 kA and the carbon current 0.7 kA. Since only a small fraction of the ions will make it through the cylindrical aperture, the corresponding total currents were calculated to be respectively 25kA for proton and 7 kA for carbon ions, a quite substantial contribution to the total bipolar beam current. Hence, approximately only 10% of the total back-streaming ionic currents could make it through the hollow cathode tip aperture. Unfortunately the diagnostic cables connecting the Faraday cup and the B-dot monitors to the screen room scopes experienced a large amount of charge pick-up that obliterated our effort to directly measure those relatively small currents. However, we succeeded in measuring those currents indirectly with activation techniques [Contribution of the back-streaming ions to the self-magnetic pinch (SMP) diode Current., M. G. Mazarakis, M. G. Mazarakis, M. E. Cuneo, S. D. Fournier, M. D. Johnston, M. L. Kiefer, J. J. Leckbee, D. S. Nielsen, B.V.Oliver, M. E. Sceiford, S. C. Simpson, T. J. Renk, C. L. Ruiz, T. J. Webb, and D. Ziska. Subitted for publication.]. In the following sections we present some typical cable pick-up results and also our efforts to verify that the observed “current” scope traces were indeed not ion currents but instead cable charge pic-up. Interestingly enough we also discovered that the appearance of those “currents” are in synchronism with the A-K gap impedance variation (decrease) and the MITL sheath current re-trapping. Hence those B-dots or Faraday cups could be utilized as diode behavior diagnostics.

Mazarakis, Michael G.↗

High voltage cathode material for Li-ion batteries

A cathode electrode material for use in rechargeable Li-ion batteries, based on the integration of two Li-based materials of NASICON- and Spinel-type structures, is described in the present invention. The structure and composition of the cathode can be described by a core material and a surface coating surrounding the core material, wherein the core of the cathode particle is of the formula LiMn2-xNixO4−δ (0.5≦x≦0 & 0≦δ≦1) and having a spinel crystal structure, the surface coating is of the formula Li1+xMxTi2-x(PO4)3 (M: is a trivalent cation, 0.5≧x≧0) having a NASICON-type crystal structure.

Hagh, Nader Marandian↗

Polyanthraquinone-based organic cathode for high-performance rechargeable magnesium-ion batteries

A rechargeable magnesium ion electrochemical cell comprising an anode, a cathode, and a non-aqueous magnesium electrolyte disposed between the anode and the cathode is described herein. The cathode comprises a redox-active anthraquinone-based polymer comprising one or more of 1,4-polyanthraquinone or 2,6-polyanthraquinone. Both 2,6-polyanthraquinone and 1,4-polyanthraquinone can operate with 1.5-2.0 V with above 100 mAh/g capacities at a reasonable rate, higher than the state-of-the-art Mg—Mg6S8 battery. More than 1000 cycles with very small capacity loss can be realized.

Liao, Chen↗

Ultrastable cathodes for lithium sulfur batteries

A cathode for a lithium-sulfur battery includes a copper-containing current collector, over which an active material layer is disposed. A method of producing the cathode is provided. A lithium-sulfur battery including the cathode provides improved capacity and cycleability.

Elam, Jeffrey W.↗

Dual conductor surface modified SOFC cathode particles and methods of making same

A novel method to produce ALD films disposed on powders is disclosed. Examples include the formation of a cobalt doped zirconia (CDZ), hafnia, and cobalt doped hafnia (CDH) films on lanthanum strontium cobalt iron oxide (LSCF) powder for solid oxide fuel cell cathodes. The coated powders are sintered into porous cathodes that have utility for preventing the migration of cations in the powder to the surface of the sintered cathode and/or other performance enhancing attributes.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Li-substituted layered spinel cathode materials for sodium ion batteries

Systems, methods, and compositions are disclosed for a Li-substituted layered-tunneled O3/spinel Na(NixFeyMnz)O2 cathode material, Na0.87Li0.25Ni0.4Fe0.2Mn0.4O2+∂ (LS-NFM) for enhanced sodium ion storage and cycling stability. The LS-NFM electrode is prepared by adjusting the stoichiometric ratio of the Na ion over the sum of Li and transition metal ions below 1. The Rietveld refinement of XRD data indicates that the cathode is composed of 94% layered and 6% spinel components. When cycled at a high current density of 100 mA g−1, LS-NFM cathode exhibited a first-cycle Coulombic efficiency of 88% and reversible discharge capacity of 107 mAh g−1 after 50 cycles with the capacity retention of 95%.

Xiong, Hui↗

Next-Generation Cobalt-Free Cathodes – A Prospective Solution to the Battery Industry's Cobalt Problem*

Lithium-ion batteries are over-reliant on cobalt-containing cathodes. Current projections estimate hundreds of millions of electric vehicles (EVs) will be on the road by 2050, and this ever-growing demand threatens to deplete global cobalt reserves at an alarming rate. Moreover, cobalt supply-chain issues have significantly increased cobalt prices throughout the last decade. As such, energy storage research and development need to reduce reliance on cobalt to meet ever-growing demands for lithium-ion batteries. This chapter summarizes the science/technology gaps and potential of numerous cobalt-free Li-ion cathodes, including layered, spinel, olivine, and disordered rocksalt systems. Despite the promising performance of these Co-free cathodes, scale-up and manufacturing bottlenecks associated with these materials must also be addressed to enable widespread adoption in commercial batteries. Overall, this review broadly highlights the enormous promise of “zero-cobalt” Li-ion batteries to enable sustainable production of EVs in the coming decades.

Muralidharan, Nitin↗

Stabilized birnessite cathode for high power and high energy density applications

A battery comprises a housing, an electrolyte disposed in the housing, an anode disposed in the housing, a stabilized cathode disposed in the housing and comprising a cathode material. The cathode material comprises a composition selected from birnessite or layered-polymorph of manganese dioxide (δ-MnO2), the composition being stabilized by bismuth and copper ions, a conductive carbon, and a binder. The anode can be at least 50% (m/m) lithium, magnesium, aluminum, or zinc.

Yadav, Gautam G.↗

Carbon dioxide treatment of cathodes

A method for producing water resistant cathodes is discussed. The method uses mixing cathode powder with solid carbon dioxide to create a mixture and heating the mixture to a temperature. The heating occurs for a time sufficient to cause lithium carbonate coatings to form on the powder. A method for coating lithium-containing cathode surfaces is also discussed. This method uses simultaneously sublimating solid CO 2 and condensing atmospheric water vapor onto surfaces. Afterwards allowing the lithium to react with the sublimated CO 2 for a time sufficient to create a lithium carbonate film on the surface.

Kahvecioglu, Ozgenur↗

Coatings for cathode active materials

A cathode active material includes a plurality of cathode active compound particles and a coating disposed over each of the cathode active compound particles. The coating includes a lithium (Li)-ion conducting oxide containing lanthanum (La) and titanium (Ti).

Wu, Huiming↗