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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 127 records · Page 7
All sourcesNASA NTRSDOE OSTI
DOE OSTI2012

Liquid crystalline phase synthesis of nanoporous MnO{sub 2} thin film arrays as an electrode material for electrochemical capacitors

Graphical abstract: Three-dimensional (3D) MnO{sub 2} thin film arrays with nanoporous structure is electrodeposited on Ti foil from hexagonal lyotropic liquid crystalline phase. Low-angle X-ray diffraction (XRD), wide-angle XRD, field emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM) are employed to study the morphology and the structure of the as-synthesized MnO{sub 2} materials. Galvanostatic charge/discharge measurements show the nanoporous, 3D electrode material exhibits excellent capacitive performance between the potential range of −0.1 to 0.9 V, and a maximum specific capacitance as high as 462 F g{sup −1} are achieved in 0.5 M Na{sub 2}SO{sub 4} solution at a charge/discharge current density of 4 A g{sup −1}. Highlights: ► 3D MnO{sub 2} thin film arrays with nanoporous structure is fabricated for the first time. ► A maximum specific capacitance as high as 462 F g{sup −1} is obtained. ► The 3D and nanoporous superarchitecture facilitate electrolyte penetration. -- Abstract: Three-dimensional (3D) MnO{sub 2} thin film arrays with nanoporous structure is electrodeposited on Ti foil from hexagonal lyotropic liquid crystalline phase. Low-angle X-ray diffraction (XRD), wide-angle XRD, field emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM) are employed to study the morphology and the structure of the as-synthesized MnO{sub 2} materials. Galvanostatic charge/discharge measurements show the nanoporous, 3D electrode material exhibits excellent capacitive performance between the potential range of −0.1 to 0.9 V, and a maximum specific capacitance as high as 462 F g{sup −1} are achieved in 0.5 M Na{sub 2}SO{sub 4} solution at a charge/discharge current density of 4 A g{sup −1}.

36 MATERIALS SCIENCE↗
DOE OSTI2020

Frequency modulated radio frequency electric field for ion manipulation

A method of manipulating ions comprises injecting ions between a first surface and a second surface positioned parallel to and spaced apart from each other and defining a central axis therebetween, wherein the first surface comprises first outer electrodes coupled to the first surface and a first inner array of electrodes coupled to the first surface and positioned between the first outer electrodes, wherein the second surface comprises second outer electrodes coupled to the second surface and a second inner array of electrodes coupled to the second surface and positioned between the second outer electrodes, and applying a frequency modulated RF voltage to at least one electrode of the first inner array of electrodes or the second inner array of electrodes to confine ions between the first surface and the second surface and to guide ions between the first surface and the second surface along the central axis.

42 ENGINEERING↗
DOE OSTI2013

Electrodeposition of gold nanoparticle arrays on ITO glass as electrode with high electrocatalytic activity

Highlights: ► Electrodeposition of gold nanoparticle arrays on ITO glass as catalytic-electrodes. ► The sizes and densities of the gold nanoparticles can be easily controlled. ► Such arrays on ITO glass shows high electrocatalytic activity and good stability. - Abstract: Herein, we reported a templateless, surfactantless, and simple electrochemical method to directly fabricate gold nanoparticle (AuNP) arrays on indium tin oxide (ITO) glass substrates as effective electrocatalytic electrodes. The as-prepared AuNP arrays have been characterized by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), etc. AuNPs with small sizes (<20 nm) were uniformly deposited on the ITO glass under constant current densities, and particle densities can be adjusted by varying the applied charges. The resultant AuNP array electrode showed higher catalytic activity and good stability toward electro-oxidation of ascorbic acid compared with other electrodes, such as bare ITO electrode, bare glassy carbon electrode and bulk gold film electrode.

36 MATERIALS SCIENCE↗
DOE OSTI2015

Improving in vitro to in vivo extrapolation by incorporating toxicokinetic measurements: A case study of lindane-induced neurotoxicity

Approaches for extrapolating in vitro toxicity testing results for prediction of human in vivo outcomes are needed. The purpose of this case study was to employ in vitro toxicokinetics and PBPK modeling to perform in vitro to in vivo extrapolation (IVIVE) of lindane neurotoxicity. Lindane cell and media concentrations in vitro, together with in vitro concentration-response data for lindane effects on neuronal network firing rates, were compared to in vivo data and model simulations as an exercise in extrapolation for chemical-induced neurotoxicity in rodents and humans. Time- and concentration-dependent lindane dosimetry was determined in primary cultures of rat cortical neurons in vitro using “faux” (without electrodes) microelectrode arrays (MEAs). In vivo data were derived from literature values, and physiologically based pharmacokinetic (PBPK) modeling was used to extrapolate from rat to human. The previously determined EC{sub 50} for increased firing rates in primary cultures of cortical neurons was 0.6 μg/ml. Media and cell lindane concentrations at the EC{sub 50} were 0.4 μg/ml and 7.1 μg/ml, respectively, and cellular lindane accumulation was time- and concentration-dependent. Rat blood and brain lindane levels during seizures were 1.7–1.9 μg/ml and 5–11 μg/ml, respectively. Brain lindane levels associated with seizures in rats and those predicted for humans (average = 7 μg/ml) by PBPK modeling were very similar to in vitro concentrations detected in cortical cells at the EC{sub 50} dose. PBPK model predictions matched literature data and timing. These findings indicate that in vitro MEA results are predictive of in vivo responses to lindane and demonstrate a successful modeling approach for IVIVE of rat and human neurotoxicity. - Highlights: • In vitro to in vivo extrapolation for lindane neurotoxicity was performed. • Dosimetry of lindane in a micro-electrode array (MEA) test system was assessed. • Cell concentrations at the MEA EC{sub 50} equaled rat brain levels associated with seizure. • PBPK-predicted human brain levels at seizure also equaled EC{sub 50} cell concentrations. • In vitro MEA results are predictive of lindane in vivo dose–response in rats/humans.

60 APPLIED LIFE SCIENCES↗
DOE OSTI2014

Ion manipulation device

An ion manipulation method and device is disclosed. The device includes a pair of substantially parallel surfaces. An array of inner electrodes is contained within, and extends substantially along the length of, each parallel surface. The device includes a first outer array of electrodes and a second outer array of electrodes. Each outer array of electrodes is positioned on either side of the inner electrodes, and is contained within and extends substantially along the length of each parallel surface. A DC voltage is applied to the first and second outer array of electrodes. A RF voltage, with a superimposed electric field, is applied to the inner electrodes by applying the DC voltages to each electrode. Ions either move between the parallel surfaces within an ion confinement area or along paths in the direction of the electric field, or can be trapped in the ion confinement area.

42 ENGINEERING↗
DOE OSTI2014

Ion manipulation device with electrical breakdown protection

An ion manipulation method and device is disclosed. The device includes a pair of substantially parallel surfaces. An array of inner electrodes is contained within, and extends substantially along the length of, each parallel surface. The device includes a first outer array of electrodes and a second outer array of electrodes. Each outer array of electrodes is positioned on either side of the inner electrodes, and is contained within and extends substantially along the length of each parallel surface. A DC voltage is applied to the first and second outer array of electrodes. A RF voltage, with a superimposed electric field, is applied to the inner electrodes by applying the DC voltages to each electrode. Ions either move between the parallel surfaces within an ion confinement area or along paths in the direction of the electric field, or can be trapped in the ion confinement area. The surfaces are housed in a chamber, and at least one electrically insulative shield is coupled to an inner surface of the chamber for increasing a mean-free-path between two adjacent electrodes in the chamber.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2014

Vacuum chamber for ion manipulation device

An ion manipulation method and device is disclosed. The device includes a pair of substantially parallel surfaces. An array of inner electrodes is contained within, and extends substantially along the length of, each parallel surface. The device includes a first outer array of electrodes and a second outer array of electrodes. Each outer array of electrodes is positioned on either side of the inner electrodes, and is contained within and extends substantially along the length of each parallel surface. A DC voltage is applied to the first and second outer array of electrodes. A RF voltage, with a superimposed electric field, is applied to the inner electrodes by applying the DC voltages to each electrode. Ions either move between the parallel surfaces within an ion confinement area or along paths in the direction of the electric field, or can be trapped in the ion confinement area. A predetermined number of pairs of surfaces are disposed in one or more chambers, forming a multiple-layer ion mobility cyclotron device.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Ion manipulation method and device

An ion manipulation method and device is disclosed. The device includes a pair of substantially parallel surfaces. An array of inner electrodes is contained within, and extends substantially along the length of, each parallel surface. The device includes a first outer array of electrodes and a second outer array of electrodes. Each outer array of electrodes is positioned on either side of the inner electrodes, and is contained within and extends substantially along the length of each parallel surface. A DC voltage is applied to the first and second outer array of electrodes. A RF voltage, with a superimposed electric field, is applied to the inner electrodes by applying the DC voltages to each electrode. Ions either move between the parallel surfaces within an ion confinement area or along paths in the direction of the electric field, or can be trapped in the ion confinement area.

24 POWER TRANSMISSION AND DISTRIBUTION↗
DOE OSTI2018

Ion manipulation device

An ion manipulation method and device is disclosed. The device includes a pair of substantially parallel surfaces. An array of inner electrodes is contained within, and extends substantially along the length of, each parallel surface. The device includes a first outer array of electrodes and a second outer array of electrodes. Each outer array of electrodes is positioned on either side of the inner electrodes, and is contained within and extends substantially along the length of each parallel surface. A DC voltage is applied to the first and second outer array of electrodes. A RF voltage, with a superimposed electric field, is applied to the inner electrodes by applying the DC voltages to each electrode. Ions either move between the parallel surfaces within an ion confinement area or along paths in the direction of the electric field, or can be trapped in the ion confinement area.

47 OTHER INSTRUMENTATION↗
DOE OSTI2017

A facile one-step synthesis of Mn{sub 3}O{sub 4} nanoparticles-decorated TiO{sub 2} nanotube arrays as high performance electrode for supercapacitors

Via a facile one-step chemical bath deposition route, homogeneously dispersed Mn{sub 3}O{sub 4} nanoparticles have been successfully deposited onto the inner surface of TiO{sub 2} nanotube arrays (TNAs). The content and size of Mn{sub 3}O{sub 4} can be controlled by changing the deposition time. Field emission scanning electron microscopy and transmission electron microscopy analysis reveal the morphologies structures of Mn{sub 3}O{sub 4}/TNAs composites. The crystal-line structures are characterized by the X-ray diffraction patterns and Raman spectra. X-ray photoelectron spectroscopy further confirms the valence states of the sample elements. The electrochemical properties of Mn{sub 3}O{sub 4}/TNAs electrodes are systematically investigated by the combine use of cyclic voltammetry, galvanostatic charge-discharge and electrochemical impedance spectroscopy. The resulting Mn{sub 3}O{sub 4}/TNAs electrode prepared by deposition time of 3 h shows the highest specific capacitance of 570 F g{sup −1} at a current density of 1 A g{sup −1}. And it also shows an excellent long-term cycling stability at a current density of 5 A g{sup −1}, which remaining 91.8% of the initial capacitance after 2000 cycles. Thus this kind of Mn{sub 3}O{sub 4} nanoparticles decorated TNAs may be considered as an alternative promising candidate for high performance supercapacitor electrodes. - Graphical abstract: Mn{sub 3}O{sub 4} nanoparticles have been uniformly deposited onto the inner surfaces of TiO{sub 2} nanotube arrays through a facile one-step chemical bath deposition method. As electrodes for supercapacitors, they exhibit a relatively high specific capacity and excellent cycling stability. - Highlights: • Mn{sub 3}O{sub 4} nanoparticles have been deposited onto TiO{sub 2} nanotube arrays by chemical bath deposition. • The Mn{sub 3}O{sub 4}/TNAs exhibits a highest specific capacitance of 570 F g{sup –1} at a current density of 1 A g{sup –1}. • The Mn{sub 3}O{sub 4}/TNAs electrode shows an excellent cycling stability of 91.8% after 2000 cycles.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2018

Characterization of applied fields for ion mobility separations in traveling wave based structures for lossless ion manipulations (SLIM)

Ion mobility (IM) is rapidly gaining attention for the analysis of biomolecules due to the ability to distinguish the shapes of ions. However, conventional constant electric field drift tube IM has limited resolving power, constrained by practical limitations on the path length and maximum applied voltage. The implementation of traveling waves (TW) in IM removes the latter limitation, allowing higher resolution to be achieved using extended path lengths. These can be readily obtainable in structures for lossless ion manipulations (SLIM), which are fabricated from electric fields that are generated by appropriate potentials applied to arrays of electrodes patterned on two parallel surfaces. In this work we have investigated the relationship between the various SLIM variables, such as electrode dimensions, inter-surface gap, and the TW applied voltages, that directly impact the fields experienced by ions. Ion simulation and theoretical calculations have been utilized to understand the dependence of SLIM geometry and effective electric field. The variables explored impact both ion confinement and the observed IM resolution in Structures for Lossless Ion Manipulations (SLIM) modules.

Hamid, Ahmed M.↗
DOE OSTI2014

High optical and switching performance electrochromic devices based on a zinc oxide nanowire with poly(methyl methacrylate) gel electrolytes

High performance electrochromic devices have been fabricated and demonstrated utilizing a solid polymer electrolyte and zinc oxide (ZnO) nanowire (NW) array counter electrode. The poly(methyl methacrylate) based polymer electrolyte was spin coated upon hydrothermally grown ZnO NW array counter electrodes, while electron beam evaporated NiO{sub x} thin films formed the working electrodes. Excellent optical contrast and switching speeds were observed in the fabricated devices with active areas of 2 cm{sup 2}, exhibiting an optical contrast of 73.11% at the wavelength of 470 nm, combined with a fast switching time of 0.2 s and 0.4 s for bleaching and coloration, respectively.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2017

Method and device for ion mobility separations

Methods and devices for ion separations or manipulations in gas phase are disclosed. The device includes a single non-planar surface. Arrays of electrodes are coupled to the surface. A combination of RF and DC voltages are applied to the arrays of electrodes to create confining and driving fields that move ions through the device. The DC voltages are static DC voltages or time-dependent DC potentials or waveforms.

47 OTHER INSTRUMENTATION↗
DOE OSTI2018

High-Performance Flexible All-Solid-State Asymmetric Supercapacitors Based on Vertically Aligned CuSe@Co(OH) 2 Nanosheet Arrays

The developments of electrode active materials provide the opportunities for next-generation energy storage devices. The arrangement of electrode materials on the substrate has recently emerged as a promising strategy for preparing high-performance supercapacitors. In this paper, we demonstrate a novel vertically aligned CuSe@Co(OH) 2 nanosheet arrays electrode for supercapacitor application. The materials are thoroughly characterized by structural and spectroscopic techniques. Electrochemical performance of CuSe@Co(OH) 2 nanosheet arrays are investigated in detail, which exhibit a specific capacitance as much as 1180 F g -1 at a current density of 1 A g -1 . A flexible asymmetric all-solid-state supercapacitor is fabricated using CuSe@Co(OH) 2 nanosheet arrays as the positive electrode and activated carbon as the negative electrode. The device delivers a volumetric capacitance of 441.4 mF cm -3 with maximum energy density and maximum power density is 0.17 and 62.1 mW cm -3 , as well as robust cycling stability (~80.4% capacitance retention after 10 000 cycles), excellent flexibility, and mechanical stability. Finally, the excellent electrochemical performance can be attributed to its unique vertically aligned configuration.

25 ENERGY STORAGE↗
DOE OSTI2015

Ion manipulation device to prevent loss of ions

An ion manipulation method and device to prevent loss of ions is disclosed. The device includes a pair of surfaces. An inner array of electrodes is coupled to the surfaces. A RF voltage and a DC voltage are alternately applied to the inner array of electrodes. The applied RF voltage is alternately positive and negative so that immediately adjacent or nearest neighbor RF applied electrodes are supplied with RF signals that are approximately 180 degrees out of phase.

47 OTHER INSTRUMENTATION↗
DOE OSTI2015

Characterization of Traveling Wave Ion Mobility Separations in Structures for Lossless Ion Manipulations

We report on the development and characterization of a new traveling wave-based Structure for Lossless Ion Manipulations (TW-SLIM) for ion mobility separations (IMS). The TW-SLIM module uses parallel arrays of rf electrodes on two closely spaced surfaces for ion confinement, where the rf electrodes are separated by arrays of short electrodes, and using these TWs can be created to drive ion motion. In this initial work, TWs are created by the dynamic application of dc potentials. The capabilities of the TW-SLIM module for efficient ion confinement, lossless ion transport, and ion mobility separations at different rf and TW parameters are reported. The TW-SLIM module is shown to transmit a wide mass range of ions (m/z 200–2500) utilizing a confining rf waveform (~1 MHz and ~300 V p-p ) and low TW amplitudes (<20 V). Additionally, the short TW-SLIM module achieved resolutions comparable to existing commercially available low pressure IMS platforms and an ion mobility peak capacity of ~32 for TW speeds of <210 m/s. TW-SLIM performance was characterized over a wide range of rf and TW parameters and demonstrated robust performance. In conclusion, the combined attributes of the flexible design and low voltage requirements for the TW-SLIM module provide a basis for devices capable of much higher resolution and more complex ion manipulations.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2016

Self-supported porous CoO semisphere arrays as binder-free electrodes for high-performance lithium ion batteries

Highlights: • CoO semisphere arrays are prepared by a template-assisted electrodeposition method. • Interconnected semisphere arrays are favorable for fast ion/electron transfer. • CoO semisphere arrays show excellent Li ion storage performance. - Abstract: Construction of hierarchical porous metal oxides arrays is critical for the development of high-performance electrochemical energy storage devices. Herein we report porous CoO semisphere arrays using an electrodeposited polystyrene template method. Interestingly, the as-prepared porous CoO semisphere arrays consist of bowl-like semispheres with diameters of ∼500 nm and show highly porous structure. As a preliminary test as anode for lithium ion batteries (LIBs), the porous CoO semispheres arrays exhibit superior electrochemical performances with good cyclability (695.5 mAh g{sup −1} after 150 cycles at 0.5 A g{sup −1}) and high-rate capability. The porous semispherical architecture provides positive roles in the enhancement of electrochemical properties, including fast electronic transportation path, short diffusion of Li ion and high sufficient interfacial contact area between the active material and the electrolyte. The developed methodology enables a new fabrication of porous metal oxides with applications in electro-catalysis, optical and electrochemical devices.

36 MATERIALS SCIENCE↗