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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 289 records · Page 16
All sourcesNASA NTRSDOE OSTI
NASA NTRS1974

Electron-impact excitation of the low-lying electronic states of formaldehyde

Electron-impact excitation has been observed at incident electron energies of 10.1 and 20.1 eV to the first five excited electronic states of formaldehyde lying at and below the 1B2 state at 7.10 eV. These excitations include two new transitions in the energy-loss range 5.6-6.2 eV and 6.7-7.0 eV which have been detected for the first time, either through electron-impact excitation or photon absorption. The differential cross sections of these new excitations are given at scattering angles between 15 and 135 deg. These cross-section ratios peak at large scattering angles - a characteristic of triplet - singlet excitations. The design and performance of the electron-impact spectrometer used in the above observations is outlined and discussed.

Chutjian, A.↗
NASA NTRS2019

Cyclotron Lines in Highly Magnetized Neutron Stars

Cyclotron lines, also called cyclotron resonant scattering features are spectral features, generally appearing in absorption, in the X-ray spectra of objects containing highly magnetized neutron stars, allowing the direct measurement of the magnetic field strength in these objects. Cyclotron features are thought to be due to resonant scattering of photons by electrons in the strong magnetic fields. The main content of this contribution focusses on electron cyclotron lines as found in accreting X-ray binary pulsars (XRBP) with magnetic fields on the order of several 1012 Gauss. Also, possible proton cyclotron lines from single neutron stars with even stronger magnetic fields are briefly discussed. With regard to electron cyclotron lines, we present an updated list of XRBPs that show evidence of such absorption lines. The first such line was discovered in a 1976 balloon observation of the accreting binary pulsar Hercules X-1, it is considered to be the first direct measurement of the magnetic field of a neutron star. As of today (end 2018), we list 35 XRBPs showing evidence of one ore more electron cyclotron absorption line(s). A few have been measured only once and must be confirmed (several more objects are listed as candidates). In addition to the Tables of objects, we summarize the evidence of variability of the cyclotron line as a function of various parameters (especially pulse phase, luminosity and time), and add a discussion of the different observed phenomena and associated attempts of theoretical modeling. We also discuss our understanding of the underlying physics of accretion onto highly magnetized neutron stars. For proton cyclotron lines, we present tables with seven neutron stars and discuss their nature and the physics in these objects.

Staubert, R.↗
NASA NTRS1994

Energetic electrons in the magnetophere of Saturn

The energy spectra and angular distributions of electrons observed by Pioneer 11 as a function of radial distance in the inner magnetosphere of Saturn are reanalyzed and phase space densities are then calculated. The radial dependence of phase space density requires a distributed loss process. The loss is greatest in the region of the E ring (5.5 less than L less than 8.5) and is attributed to collisions with the ring particles in agreement with earlier work by Van Allen et al. (1980b). Quantitative analysis yields the following properties of the E ring: the particle radii are in the range of 4 x 10(exp -5) to 3.2 x 10(exp -4) cm and the thickness of the ring is approximately 3 R(sub s). Between the inner edge of the E ring (5.5 R(sub s)) and the outer edge of the A ring (2.3 R(sub s)) there are more energetic electrons than can be supplied by radial diffusion from an external source. Detailed calculations show that a cosmic ray albedo neutron decay (CRAND) source in the A and B rings is a plausible source for this excess. The radial diffusion coefficient required to explain the E ring absorption and CRAND source for electrons is 1 x 10(exp -12) greater than D(sub 0) greater than 3 x 10(exp -12) R(sub s)(exp 2)/s, assuming that D(sub LL) = D(sub 0)L(exp 3). As part of the reanalysis program, a method for the deconvolution of pitch angle distributions observed by simple detectors on a rotating spacecraft is developed. This process removes the instrumental response and rotational smear due to finite sampling periods and yields true angular distributions.

Randall, B. A.↗
NASA NTRS1994

Energetic electrons in the magnetosphere of Saturn

The energy spectra and angular distributions of electrons observed by Pioneer 11 as a function of radial distance in the inner magnetosphere of Saturn are reanalyzed and phase space densities are then calculated. The radial dependence of phase space density requires a distributed loss process. The loss is greatest in the region of the E ring (5.5 less than L less than 8.5) and is attributed to collisions with the ring particles in agreement with earlier work by Van Allen et al. (1980). Quantitative analysis yields the following properties of the E ring: the particle radii are in the range of 4 x 10(exp -5) to 3.2 x 10(exp -4) cm and the thickness of the ring is approximately 3 R(sub s). Between the inner edge of the E ring (5.5 R(sub s)) and the outer edge of the A ring (2.3 R(sub s)) there are more energetic electrons than can be supplied by radial diffusion from an external source. Detailed calculations show that a cosmic ray albedo neutron decay (CRAND) source in the A and B rings is a plausible source for this excess. The radial diffusion coefficient required to explain the E ring absorption and CRAND source for electrons is 1 x 10(exp -12) greater than D(sub 0) greater than 3 x 10(exp -12) R(exp 2, sub s)/s, assuming that D(sub LL) = D(sub 0)L(exp 3). As part of the reanalysis program, a method for the deconvolution of pitch angle distributions observed by simple detectors on a rotating spacecraft is developed. This process removes the instrumental response and rotational smear due to finite sampling periods and yields true angular distributions.

Randall, B. A.↗
NASA NTRS1972

A study of the unidentified interstellar diffuse features.

The interstellar diffuse lines at 5780 and 5797 A have been observed in 66 stars using the Washburn Observatory echelle spectrograph coupled with an image tube. At a resolution of 0.17 A, the profiles of these diffuse lines are asymmetric and steeper to the blue. There is also a broad, shallow feature shortward of 5780 A. The FWHM of 5780 and 5797 are respectively 2.7 A and 1.1 A. Equivalent widths of 5780, 5797 have been measured at a resolution of 0.26 A, and they present a very tight correlation. It is very likely that these two diffuse lines are carried by the same agent. This investigation proposes that the two lines are produced by the pure electronic transitions of the impurity centers in solid grains, with the broad, shallow absorption feature shortward of 5780 A as the absorption sideband associated with the parent pure electronic line.

Wu, C.-C.↗
NASA NTRS1978

Shortcomings in our understanding of the lower ionosphere as revealed by an analysis of radiowave absorption measurements

The present knowledge of ion production and loss processes in the D- and lower E-regions is evaluated with reference to a series of equatorial ground-based radiowave absorption measurements. An equatorial noontime reference electron density profile, corresponding to a nonflaring sun at solar cycle maximum, is derived on the basis of multifrequency absorption and virtual height measurements and data from a rocket-borne investigation. It is found that the Meira (1971) nitric oxide profile does not agree with the Gnanalingan (1974) empirical expression relating absorption to solar flux. Meira's densities below 90 km must be reduced by a factor of about 5 in order to correspond. A wide disparity is observed between the effective recombination coefficient and the average dissociative recombination coefficient for the known ion composition in the lower ionosphere. A study of diurnal variations of radiowave absorption and virtual height shows a great disagreement between calculated and measured values.

Gnanalingam, S.↗
NASA NTRS1974

Measurement of plasma temperature and density using radiation absorption

A light beam of predetermined wavelength, preferably monochromatic, is directed through a plasma to be measured. The absorption of the light by the plasma is detected for deriving an absorption coefficient of the plasma. Knowing the absorption coefficient of the plasma and independently measuring either the electron density or temperature of the plasma allows solution of an equation to derive the other unknown quantity, i.e. either electron density or temperature. In a preferred method, the absorption coefficient of the plasma is derived simultaneously for two probing light beams of substantially different predetermined wave-lengths. Knowing these two coefficients allows solution of two simultaneous equations to derive the electron density and temperature of the plasma.

Kenneth W Billman↗
DOE OSTI2025

Strain Effects in SrHfO 3 Films Grown by Hybrid Molecular Beam Epitaxy

Perovskite oxide heterostructures host a large number of interesting phenomena such as ferroelectricity, which are often driven by octahedral distortions in the crystal that may induce polarization. SrHfO 3 (SHO) is a perovskite oxide with a pseudocubic lattice parameter of 4.08 Å that previous density functional theory (DFT) calculations suggest can be stabilized in a ferroelectric P4mm phase when stabilized with sufficient compressive strain. Additionally, it is insulating and possesses a large band gap and a high dielectric constant, making it an ideal candidate for oxide electronic devices. Here, to test the viability of epitaxial strain as a driver of ferroic phase transitions, SHO films were grown by hybrid molecular beam epitaxy (hMBE) with a tetrakis(ethylmethylamino)hafnium(IV) source on GdScO 3 and TbScO 3 substrates. Strained SHO phases were characterized using X-ray diffraction, X-ray absorption spectroscopy, and scanning transmission electron microscopy to determine the space group of the strained films, with the results compared to those of DFT-optimized models of phase stability versus strain. Contrary to past reports, we find that compressively strained SrHfO 3 undergoes octahedral tilt distortions without associated ferroelectric polarization and most likely takes on the I4/mcm phase with the a 0 a 0 c – tilt pattern.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2025

Nitrate-To-Ammonia Electroconversion at Neutral pH on Polycrystalline Vanadium Sulfide Derived from Vanadium Disulfide

The electrochemical nitrate reduction reaction (NO3RR) offers a pathway to produce NH3 for fuel and fertilizer from waste NO3-. In this work, a polycrystalline vanadium sulfide (VSx), which is derived from solvothermally grown and annealed VS2, is shown to exhibit excellent NO3RR activity (2.3 +- 0.6 mg.cm-2 geo..h-1 @ -0.92 VRHE) and Faradaic efficiency to NH4+ (69 +- 6% at -0.69 VRHE) in buffered neutral pH electrolyte containing 0.1 M NO3-. A variety of characterization techniques are leveraged to support the VSx assignment, including X-ray photoelectron spectroscopy, near-edge X-ray absorption fine structure spectroscopy, selected area electron diffraction, and X-ray diffraction measurements. The VS2 annealing step reduces the oxide character and generates VSx, which, based on the improved NO3RR activity, results in the creation of active sites for NO3- binding. To help shed light on NO3RR on VSx, VS2 is used as a model system, and a grand-canonical density functional theory (GC-DFT) investigation of VS2 shows strong evidence that S vacancies are active sites for NO3RR, where NO3- outcompetes H+ for adsorption at the S-vacancy sites. Moreover, GC-DFT results highlight a thermodynamically favorable reaction to generate NH4+ in an aqueous electrolyte at relevant cathodic potentials. As an annealed material, VSx may contain undersaturated V sites, which show an electronic structure similar to the theoretically calculated S-vacancy site of VS2, and these sites may contribute to the observed increase in NO3RR activity and selectivity for NH4+ on VSx versus unannealed VS2. Finally, kinetic isotope effect measurements suggest that the kinetic rate-limiting step of the NO3RR on VSx is not proton-coupled, indicating it may be the first electron transfer to adsorbed NO3*.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2025

Photocatalytic Semiconductor–Metal Hybrid Nanoparticles: Single-Atom Catalyst Regime Surpasses Metal Tips

Semiconductor–metal hybrid nanoparticles (HNPs) are promising materials for photocatalytic applications, such as water splitting for green hydrogen generation. While most studies have focused on Cd containing HNPs, the realization of actual applications will require environmentally compatible systems. Using heavy-metal free ZnSe-Au HNPs as a model, we investigate the dependence of their functionality and efficiency on the cocatalyst metal domain characteristics ranging from the single-atom catalyst (SAC) regime to metal-tipped systems. The SAC regime was achieved via the deposition of individual atomic cocatalysts on the semiconductor nanocrystals in solution. Utilizing a combination of electron microscopy, X-ray absorption spectroscopy, and X-ray photoelectron spectroscopy, we established the presence of single Au atoms on the ZnSe nanorod surface. Upon increased Au concentration, this transitions to metal tip growth. Photocatalytic hydrogen generation measurements reveal a strong dependence on the cocatalyst loading with a sharp response maximum in the SAC regime. Ultrafast dynamics studies show similar electron decay kinetics for the pristine ZnSe nanorods and the ZnSe-Au HNPs in either SAC or tipped systems. This indicates that electron transfer is not the rate-limiting step for the photocatalytic process. Combined with the structural-chemical characterization, we conclude that the enhanced photocatalytic activity is due to the higher reactivity of the single-atom sites. This holistic view establishes the significance of SAC-HNPs, setting the stage for designing efficient and sustainable heavy-metal-free photocatalyst nanoparticles for numerous applications.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
NASA NTRS1981

X-ray line emission from the Puppis A supernova remnant - Oxygen lines

Six prominent X-ray emission lines of O VII and O VIII have been detected from a portion of the Puppis A supernova remnant in observations with the Einstein Observatory Focal Plane Crystal Spectrometer. The lines are sufficiently well resolved to serve as diagnostics of the emitting plasma. From the relative intensities of the lines, it is inferred that the population of O VIII is about 1.5 times that of O VII, and that electron collisions are the dominant excitation mechanism in the plasma. A locus of allowed electron temperatures and interstellar-absorption column densities is derived: 1.5 x 10 to the 6th K, and (2-6) x 10 to the 21st per sq cm. The data are consistent with either a thin plasma source in equilibrium at a temperature of 2.2 x 10 to the 6th K with a column density of 4 x 10 to the 21st per sq cm, or with a nonequilibrium source in which the electrons have been shock-heated to a higher temperature and oxygen is underionized.

Winkler, P. F.↗
DOE OSTI2025

Charge Transfer and Recombination Pathways through Fullerene Guests in Porphyrin-Based MOFs

Porphyrin-based metal–organic frameworks (MOFs) offer a unique platform for building porous donor–acceptor networks that exhibit long-lived charge separation and transport upon incorporation of electron acceptor guest species. Here, in this work, porphyrin-based MOFs, PCN-222(H 2 ) and PCN-222(Zn), synthesized as nanoparticle suspensions, are successfully infiltrated with fullerene acceptor molecules, C 60 or PC 61 BM, in both polar and nonpolar solvent environments. The location and relative binding strength of these guest species are evaluated through a combination of N 2 physisorption measurements, photoluminescence quenching, and UV–vis absorption titration experiments. Semiempirical tight binding calculations are used to screen potential locations of the fullerene guest within the MOF pores, and hybrid density functional theory (DFT)-computed interaction energies confirm the energetically favorable positions. The fundamental photophysics of these donor–acceptor host–guest combinations are probed using ultrafast transient absorption spectroscopy. Sub-picosecond electron transfer involving initial exciplex population is observed, with slow charge recombination lifetimes on the order of τ ~1 ns for all systems in both dimethylformamide and 1,4-dioxane. Charge recombination occurs through population of fullerene and/or framework porphyrin triplet states depending on the porphyrin metalation status. The photophysics of the fullerene-loaded MOFs are discussed in the context of relevant porphyrin–fullerene donor–acceptor molecules to highlight the unique role of the framework environment in dictating photoinduced electron transfer and decay pathways.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2026

Synthesis of epitaxial TaO$_2$ thin films on Al$_2$O$_3$ by suboxide molecular-beam epitaxy and thermal laser epitaxy

Tantalum dioxide (TaO2) is a metastable tantalum compound. Here, we report the epitaxial stabilization of TaO2 on Al2O3 (1-102) (r-plane sapphire) substrates using suboxide molecular-beam epitaxy (MBE) and thermal laser epitaxy (TLE), demonstrating single-oriented, monodomain growth of anisotropically strained thin films. Microstructural investigation is performed using synchrotron X-ray diffraction and scanning transmission electron microscopy. The tetravalent oxidation state of tantalum is confirmed using X-ray absorption and photoemission spectroscopy as well as electron energy-loss spectroscopy. Optical properties are investigated via spectroscopic ellipsometry and reveal a 0.3 eV Mott gap of the tantalum 5d electrons. Density-functional theory and group theoretical arguments are used to evaluate the limited stability of the rutile phase and reveal the potential to unlock a hidden metal-insulator transition concomitant with a structural phase transition to a distorted rutile phase, akin to NbO2. Our work expands the understanding of tantalum oxides and paves the way for their integration into next-generation electronic and photonic devices.

FOS: Physical sciences↗
NASA NTRS1986

Real-time atmospheric absorption spectra for in-flight tuning of an airborne dial system

Real-time measurements of atmospheric absorption spectra are displayed and used to precisely calibrate and fix the frequency of an Alexandrite laser to specific oxygen absorption features for airborne Differential Absorption Lidar (DIAL) measurements of atmospheric pressure and temperature. The DIAL system used contains two narrowband tunable Alexandrite lasers: one is electronically scanned to tune to oxygen absorption features for on-line signals while the second is used to obtain off-line (nonabsorbed) atmospheric return signals. The lidar operator may select the number of shots to be averaged, the altitude, and altitude interval over which the signals are averaged using single key stroke commands. The operator also determines exactly which oxygen absorption lines are scanned by comparing the line spacings and relative strengths with known line parameters, thus calibrating the laser wavelength readout. The system was used successfully to measure the atmospheric pressure profile on the first flights of this lidar, November 20, and December 9, 1985, aboard the NASA Wallops Electra aircraft.

Dombrowski, M.↗
NASA NTRS1994

Energy deposition and K-shell ionization of supernovae

We present explicit evaluation of K-shell ionization caused by photoelectric absorption, by Compton scattering, and by electron collisions in supernovae envelopes. Each process derives from the radioactivity that dominates the bolometric luminosity of the model supernovae. We include the ionization by bremsstrahlung. We find that electron-collision ionization with decelerating Compton electrons is the dominant process of K-shell ionization for light elements (lighter than Si) whereas photoelectric K-shell absorption of Comptonized gammas is the dominant process of K-shell ionization for heavy elements (like Fe). The relative importance of the ionization processes also depends upon composition and upon time, as well as upon supernova type. For Type Ia all four ionization sources are of importance. We present fitting formulas for the deposition of radioactive power in each class of models studied. The energy deposition of all mechanisms decreases with time, including the rate of K-shell ionizations of all elements throughout the supernovae model evaluated herein. We compare the relative contributions to the energy deposition and confirm with greater numerical detail results already established.

The, Lih-Sin↗
DOE OSTI2024

In situ detection of ferric reductase activity in the intestinal lumen of an insect

The rise of atmospheric oxygen as a result of photosynthesis in cyanobacteria and chloroplasts has transformed most environmental iron into the ferric state. In contrast, cells within organisms maintain a reducing internal milieu and utilize predominantly ferrous iron. Ferric reductases are enzymes that transfer electrons to ferric ions, either extracellularly or within endocytic vesicles, enabling cellular ferrous iron uptake through Divalent Metal Transporter 1. In mammals, duodenal cytochrome b is a ferric reductase of the intestinal epithelium, but how insects reduce and absorb dietary iron remains unknown. Here we provide indirect evidence of extracellular ferric reductase activity in a small subset of Drosophila melanogaster intestinal epithelial cells, positioned at the neck of the midgut’s anterior region. Dietary-supplemented bathophenanthroline sulphate (BPS) captures locally generated ferrous iron and precipitates into pink granules, whose chemical identity was probed combining in situ X-ray absorption near edge structure and electron paramagnetic resonance spectroscopies. An increased presence of manganese ions upon BPS feeding was also found. Control animals were fed with ferric ammonium citrate, which is accumulated into ferritin iron in distinct intestinal subregions suggesting iron trafficking between different cells inside the animal. Spectroscopic signals from the biological samples were compared to purified Drosophila and horse spleen ferritin and to chemically synthesized BPS-iron and BPS-manganese complexes. The results corroborated the presence of BPS-iron in a newly identified ferric iron reductase region of the intestine, which we propose constitutes the major site of iron absorption in this organism.

EPR↗
NASA NTRS1981

On the theory of Gamma Ray Amplification through Stimulated Annihilation Radiation (GRASAR)

The theory of photon emission, absorption, and scattering in a relativistic plasma of positrons, electrons, and photon was studied. Expressions for the emissivities and absorption coefficients of pair annihilation, pair production, and Compton scattering are given and evaluated numerically. The conditions for negative absorption were investigated. In a system of photons and e(+) - e(-) pairs, an emission line at at approximately 0.43 MeV can be produced by grasar action provided that the pair chemical potential exceeds approximately 1 MeV. At a temperature of approximately 10 to the 9th power. This requires a pair density approximately 10 to the 30th power cm to the (-3) power a value much larger than the thermodynamic equilbrium pair density at this temperature. This emission line could account without a gravitational redshift for the observed lines at this energy from gamma ray bursts.

Ramaty, R.↗
NASA NTRS2008

Molecules for Fluorescence Detection of Specific Chemicals

A family of fluorescent dye molecules has been developed for use in on-off fluorescence detection of specific chemicals. By themselves, these molecules do not fluoresce. However, when exposed to certain chemical analytes in liquid or vapor forms, they do fluoresce (see figure). These compounds are amenable to fixation on or in a variety of substrates for use in fluorescence-based detection devices: they can be chemically modified to anchor them to porous or non-porous solid supports or can be incorporated into polymer films. Potential applications for these compounds include detection of chemical warfare agents, sensing of acidity or alkalinity, and fluorescent tagging of proteins in pharmaceutical research and development. These molecules could also be exploited for use as two-photon materials for photodynamic therapy in the treatment of certain cancers and other diseases. A molecule in this family consists of a fluorescent core (such as an anthracene or pyrene) attached to two end groups that, when the dye is excited by absorption of light, transfer an electron to the core, thereby quenching the fluorescence. The end groups can be engineered so that they react chemically with certain analytes. Upon reaction, electrons on the end groups are no longer available for transfer to the core and, consequently, the fluorescence from the core is no longer quenched. The chemoselectivity of these molecules can be changed by changing the end groups. For example, aniline end groups afford a capability for sensing acids or acid halides (including those contained in chemical warfare agents). Pyridine or bipyridyl end groups would enable sensing of metal ions. Other chemicals that can be selectively detected through suitable choice of end groups include glucose and proteins. Moreover, the fluorescent cores can be changed to alter light-absorption and -emission characteristics: anthracene cores fluoresce at wavelengths around 500 nm, whereas perylene cores absorb and emit at wavelengths of about 600 nm.

Fedor, Steve↗