Low-energy Hydrogen Research Articles

Mechanism of soft x-ray continuum radiation from low-energy pinch discharges of hydrogen and ultra-low field ignition of solid fuels

EUV continuum radiation (10–30 nm) arising only from very low energy pulsed pinch gas discharges comprising some hydrogen was first observed at BlackLight Power, Inc. and reproduced at the Harvard Center for Astrophysics (CfA). The source was determined to be due to the transition of H to the lower-energy hydrogen or hydrino state H(1/4) whose emission matches that observed wherein alternative sources were eliminated. The identity of the catalyst that accepts 3 · 27.2 eV from the H to cause the H to H(1/4) transition was determined to HOH versus 3H. The mechanism was elucidated using different oxide-coated electrodes that were selective in forming HOH versus plasma forming metal atoms as well as from the intensity profile that was a mismatch for the multi-body reaction required during 3H catalysis. The HOH catalyst was further shown to give EUV radiation of the same nature by igniting a solid fuel comprising a source of H and HOH catalyst by passing a low voltage, high current through the fuel to produce explosive plasma. No chemical reaction can release such high-energy light. No high field existed to form highly ionized ions that could give radiation in this EUV region that persisted even without power input. This plasma source serves as strong evidence for the existence of the transition of H to hydrino H(1/4) by HOH as the catalyst and a corresponding new power source wherein initial extraordinarily brilliant light-emitting prototypes are already producing photovoltaic generated electrical power. The hydrino product of a catalyst reaction of atomic hydrogen was analyzed by multiple spectroscopic techniques. Moreover, the mH catalyst was identified to be active in astronomical sources such as the Sun, stars and interstellar medium wherein the characteristics of hydrino match those of the dark matter of the Universe.

Current mapping of low-energy (120 eV) helium and hydrogen irradiated tungsten by conductive atomic force microscopy

Both conductive atomic force microscopy (CAFM) and transmission electron microscopy have been used to characterize the defects or He bubbles in low-energy (120 eV) H and He irradiated tungsten (W). By a comparative study, we find that the current mapping from CAFM is very sensitive in the detection of nanometer-sized defects in low-energy H and He irradiated W. Our calculation confirms that the resistance change in H and He irradiated W is strongly affected by the distance between atomic force microscopy tip and defects/He bubbles. CAFM can accurately detect defects/He bubbles in the W surface layer, however, it is infeasible to measure them in the deep layer (>20 nm), especially due to the existence of defects in the surface layer.

Altering the Wettability and Dyeability Properties of Cotton Fabric using Low Energy Hydrogen Ion Showers

Altering the Wettability and Dyeability Properties of Cotton Fabric using Low Energy Hydrogen Ion Showers

Sputtering of carbon using hydrogen ion beams with energies of 60–800 eV

This article presents the result of a study on the sputtering of carbon films by low-energy hydrogen ions. In particular, the etching rate and surface roughness were measured. The range of energies where the sputtering switches from pure chemical to a combination of chemical and physical mechanisms was determined. It is shown that Sigmund’s theory for ion etching does not work well for fields of energy less than 150eV and that it accurately describes the dependence of a sputtering coefficient on ion energy for energies greater than 300eV. A strong smoothing effect for the surface of carbon film was also found. This result is interesting in itself and for its significance for the manufacture of super-smooth surfaces for X-ray applications.

Bubble growth from clustered hydrogen and helium atoms in tungsten under a fusion environment

Bubbles seriously degrade the mechanical properties of tungsten and thus threaten the safety of nuclear fusion devices, however, the underlying atomic mechanism of bubble growth from clustered hydrogen and helium atoms is still mysterious. In this work, first-principles calculations are therefore carried out to assess the stability of tungsten atoms around both hydrogen and helium clusters. We find that the closest vacancy-formation energies of interstitial hydrogen and helium clusters are substantially decreased. The first-nearest and second-nearest vacancy-formation energies close to vacancy–hydrogen clusters decrease in a step-like way to ∼0, while those close to vacancy–helium clusters are reduced almost linearly to ∼−5.46 eV when atom number reaches 10. The vacancy-formation energies closest to helium clusters are more significantly reduced than those nearest to hydrogen clusters, whatever the clusters are embedded at interstitial sites or vacancies. The reduction of vacancy-formation energies results in instability and thus emission of tungsten atoms close to interstitial helium and vacancy–helium clusters, which illustrates the experimental results, that the tungsten atoms can be emitted from the vicinity of vacancy–helium clusters. In addition, the emission of unstable tungsten atoms close to hydrogen clusters may become possible once they are disturbed by the environment. The emission of tungsten atoms facilitates the growth and evolution of hydrogen and helium clusters and ultimately the bubble formation. The results also explain the bubble formation even if no displacement damage is produced in tungsten exposed to low-energy hydrogen and helium plasma.

Microsolvation of Fluoromethane.

Fluorinated organic compounds are ubiquitous in the pharmaceutical and agricultural industries. To better discern the mode of action of these compounds, it is critical to understand the potential for and strength of hydrogen bonds involving fluorine. It is known that CH3F forms a hydrogen bond with H2O in the gas phase but does not dissolve in bulk water. This paper examines CH3F surrounded by one to six water molecules. For systems of similar topologies, CH3F formed hydrogen bonds of nearly the same strength as water. Although CH3F can bind to a second water cluster with only a modest loss in binding energy, it must bind to these clusters as a double hydrogen bond acceptor. This means that CH3F cannot form a low-energy cyclic 2D hydrogen bonding network with water molecules, which limits its solubility in bulk water. However, CH3F should be able to bind to the periphery of small hydrogen bonding networks. These conclusions were not appreciably altered by SMD calculations. A more complete consideration of solvation, especially entropic effects, was not undertaken. Data for geometries, population changes, and vibrational frequency shifts were also analyzed and compared to binding energies.

Enhancement in multicolor photoresponse for quaternary capped In0.5Ga0.5As/GaAs quantum dot infrared photodetectors implanted with hydrogen ions

In(Ga)As/GaAs-based quantum dot infrared photodetectors (QDIPs) are among the most efficient devices in the mid-wavelength infrared and long-wavelength infrared regions for various defense and space application purposes. Considering the importance of the results reported so far on In(Ga)As/GaAs QDIPs, here we had tried to develop a post-growth method for enhancing QDIP characteristics using both low energy and high energy light ion (hydrogen) implantations. The field-assisted tunneling process of dark current generation was suppressed due to the hydrogen ion implantation, even at a very high operational bias. A stronger multicolor photo-response was obtained for devices implanted with low energy hydrogen ions. From experimental results, we proposed a device model which explains the improved QDIPs performance caused by hydrogen ion implantation.

A novel kerf‐free wafering process combining stress‐induced spalling and low energy hydrogen implantation

AbstractIn this work, we studied the potential use of low‐energy hydrogen implantation as a guide for the stress‐induced cleavage. Low‐energy, high fluence hydrogen implantation in silicon leads, in the right stiffening conditions, to the detachment of a thin layer, around a few hundreds nm thick, of monocrystalline silicon. We implanted monocrystalline silicon wafers with low‐energy hydrogen, and then glued them on a cheap metal layer. Upon cooling down, the stress induced by the stressor layers (hardened glue and metal) leads to the detachment of a thin silicon layer, which thickness is determined by the implantation energy. We were then able to clearly demonstrate that, as expected, hydrogen oversaturation layer is very efficient to guide the stress. Using such process, thin silicon layers of around 710 nm‐thick were successfully detached from low‐energy implanted silicon wafers. Such layers can be used for the growth of very good quality monocrystalline silicon of around 50 µm‐thick or less. (© 2016 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)

Nanostructured LaNiO3 Perovskite Electrocatalyst for Enhanced Urea Oxidation

Urea electrooxidation has attracted considerable interest as an alternative anodic reaction in the electrochemical generation of hydrogen due to both the lower electrochemical potential required to drive the reaction and also the possibility of eliminating a potentially harmful substance from wastewater during hydrogen fuel production. Nickel and nickel-containing oxides have shown activities comparable to those of precious-metal catalysts for the electrooxidation of urea in alkaline conditions. Herein, we investigate the use of nanostructured LaNiO3 perovskite supported on Vulcan carbon XC-72 as an electrocatalyst. This catalyst exhibits an exceptionally high mass activity of ca. 371 mA mgox–1 and specific activity of 2.25 A mg–1 cmox–2 for the electrooxidation of urea in 1 M KOH, demonstrating the potential applications of Ni-based perovskites for direct urea fuel cells and low-energy hydrogen production. While LaNiO3 is shown to be stable at low overpotentials, through in-depth mechanistic studies the ...

Excitation and charge transfer in low-energy hydrogen-atom collisions with neutral atoms: Theory, comparisons, and application to Ca

A theoretical method for the estimation of cross sections and rates for excitation and charge transfer processes in low-energy hydrogen atom collisions with neutral atoms, based on an asymptotic two-electron model of ionic-covalent interactions in the neutral atom-hydrogen atom system, is presented. The calculation of potentials and non-adiabatic radial couplings using the method is demonstrated. The potentials are used together with the multi-channel Landau-Zener model to calculate cross sections and rate coefficients. The main feature of the method is that it employs asymptotically exact atomic wavefunctions, which can be determined from known atomic parameters. The method is applied to Li+H, Na+H, and Mg+H collisions, and the results compare well with existing detailed full-quantum calculations. The method is applied to the astrophysically important problem of Ca+H collisions, and rate coefficients are calculated for temperatures in the range 1000-20000 K.

Surface degeneration of W crystal irradiated with low-energy hydrogen ions.

The damage layer of a W (100) crystal irradiated with 120 eV hydrogen ions at a fluence of up to 1.5 × 1025/m2 was investigated by scanning electron microscopy and conductive atomic force microscopy (CAFM). The periodic surface degeneration of the W crystal at a surface temperature of 373 K was formed at increasing hydrogen fluence. Observations by CCD camera and CAFM indicate the existence of ultrathin surface layers due to low-energy H irradiation. The W surface layer can contain a high density of nanometer-sized defects, resulting in the thermal instability of W atoms in the surface layer. Our findings suggest that the periodic surface degeneration of the W crystal can be ascribed to the lateral erosion of W surface layers falling off during the low-energy hydrogen irradiation. Our density functional theory calculations confirm the thermal instability of W atoms in the top layer, especially if H atoms are adsorbed on the surface.

Hydrogen Attachment/Abstraction Dissociation (HAD) of Gas-Phase Peptide Ions for Tandem Mass Spectrometry.

Dissociation of gas-phase peptide ions through interaction with low-energy hydrogen (H) radical (∼0.15 eV) was observed with a quadrupole ion trap mass spectrometry. The H radical generated by thermal dissociation of H2 molecules passing through a heated tungsten capillary (∼2000 °C) was injected into the ion trap containing target peptide ions. The fragmentation spectrum showed abundant c-/z- and a-/x-type ions, attributable to H attachment/abstraction to/from peptide ion. Because the low-energy neutral H radical initiated the fragmentation, the charge state of the precursor ion was maintained during the dissociation. As a result, precursor ions of any charge state, including singly charged positive and negative ions, could be analyzed for amino acid sequence. The sequence coverage exceeding 90% was obtained for both singly protonated and singly deprotonated substance P peptide. This mass spectrometry also preserved labile post-translational modification bonds. The modification sites of triply phosphorylated peptide (kinase domain of insulin receptor) were identified with the sequence coverage exceeding 80%.

Substituent interference on supramolecular assembly in urea gelators: synthesis, structure prediction and NMR.

Eighteen N-aryl-N'-alkyl urea gelators were synthesised in order to understand the effect of head substituents on gelation performance. Minimum gelation concentration values obtained from gel formation studies were used to rank the compounds and revealed the remarkable performance of 4-methoxyphenyl urea gelator 15 in comparison to 4-nitrophenyl analogue 14, which could not be simply ascribed to substituent effects on the hydrogen bonding capabilities of the urea protons. Crystal structure prediction calculations indicated alternative low energy hydrogen bonding arrangements between the nitro group and urea protons in gelator 14, which were supported experimentally by NMR spectroscopy. As a consequence, it was possible to relate the observed differences to interference of the head substituents with the urea tape motif, disrupting the order of supramolecular packing. The combination of unbiased structure prediction calculations with NMR is proposed as a powerful approach to investigate the supramolecular arrangement in gel fibres and help understand the relationships between molecular structure and gel formation.

Acceptorless dehydrogenation of small molecules through cooperative base metal catalysis.

The dehydrogenation of unactivated alkanes is an important transformation both in industrial and biological systems. Recent efforts towards this reaction have revolved around high temperature, organometallic C–H activation by noble metal catalysts that produce alkenes and hydrogen gas as the sole products. Conversely, natural desaturase systems proceed through stepwise hydrogen atom transfer at physiological temperature; however, these transformations require a terminal oxidant. Here we show combining tetra-n-butylammonium decatungstate (TBADT) and cobaloxime pyridine chloride (COPC) can catalytically dehydrogenate unactivated alkanes and alcohols under near-UV irradiation at room temperature with hydrogen as the sole by-product. This noble metal-free process follows a nature-inspired pathway of high- and low-energy hydrogen atom abstractions. The hydrogen evolution ability of cobaloximes is leveraged to render the system catalytic, with cooperative turnover numbers up to 48 and yields up to 83%. Our results demonstrate how cooperative base metal catalysis can achieve transformations previously restricted to precious metal catalysts.

Effects of a dielectric material in an ion source on the ion beam current density and ion beam energy.

To understand a strong focusing phenomenon that occurs in a low-energy hydrogen ion beam, the electron temperature, the electron density, and the space potential in an ion source with cusped magnetic fields are measured before and after the transition to the focusing state using an electrostatic probe. The experimental results show that no significant changes are observed before or after the transition. However, we found unique phenomena that are characterized by the position of the electrostatic probe in the ion source chamber. Specifically, the extracted ion beam current density and energy are obviously enhanced in the case where the electrostatic probe, which is covered by a dielectric material, is placed close to an acceleration electrode.

Hydrogen passivation effect on the conversion efficiency of Si solar cells by low-energy proton implantation

We investigated the hydrogen passivation effect on the conversion efficiency of Si solar cells by including low-energy hydrogen ion implantation in the cell fabrication process. The solar cells were implanted with various proton energies and doses just before the co-firing process. The quantum efficiency specifically in the blue wavelengths of the solar cells increased with a low implantation dose and energy indicating improvement of surface passivation. However, quantum efficiency decreased when the implantation dose and energy were increased, indicating a high defect-assisted surface recombination of minority carriers. The cells implanted with a low dose and energy in the presence of SiNx showed interfacial passivation with enhanced photocurrent, minority carrier lifetime and short-circuit current density for improved conversion efficiency.

Impact of extrusion parameters on the properties of rice products: A physicochemical and X-ray tomography study

Abstract Rice pellets were produced by extrusion according to an experimental design varying temperature (120–135–150 °C), moisture content (17–20–23%) and screw speed (300–400–500 rpm). The internal expanded structure of the pellets was assessed by X-ray tomography and texture with a texture analyser. The extent of starch depolymerisation and the types of protein depolymerisation/interactions were studied in complement to the starch–proteins morphology assessed by microscopy. The physico-chemical properties of the pellets were mainly affected by moisture and temperature, with moisture having the highest impact. High moisture content (23%) resulted in higher mean walls thickness of the extruded pellet, less starch depolymerisation, more protein aggregation through disulfide bonds and harder pellets. The internal expanded structure and texture of the rice pellets were mainly explained by protein changes and less by the extent of starch depolymerisation in this study. When proteins mainly interacted through medium energy interactions (disulfide bonds), protein aggregates were larger, cells walls thicker and pellets were less porous and harder with more fracture events. On the contrary, when proteins interacted through low energy (hydrogen and hydrophobic bonds) and high energy bonds (unextractable proteins), proteins were more depolymerised and aggregates were smaller and finely distributed, cells walls thinner and pellets were less hard with less fracture events.

Ordered arrangement of irradiation-induced defects of polycrystalline tungsten irradiated with low-energy hydrogen ions

Low-energy (20–520eV) hydrogen ion irradiations were performed at W surface temperature of 373–1073K and a fluence ranging from 5.0×1023 to 1.0×1025/m2. Conductive atomic force microscopy (CAFM) as a nondestructive analytical technique was successfully used to detect irradiation-induced defects in polycrystalline W. The size and density of these nanometer-sized defects were strongly dependent on the fluence of hydrogen ions. Both ion energy (E) and temperature (T) play a crucial role in determining the ordering of nanometer-sized defects. Ordered arrangements were formed at relatively high E and T. This can be attributed to the stress-driven ripple effect of defect growth at crystal grains, resulting in the movement of W lattice along one certain crystal planes.

Formation of multilayered magnetic nanotracks with perpendicular anisotropy via deoxidization using ion irradiation on ultraviolet-imprinted intaglio nanostructures

We proposed a method to fabricate perpendicular magnetic nanotracks in the cobalt oxide/palladium multilayer films using UV-nanoimprinting lithography and low-energy hydrogen-ion irradiation. This is a method to magnetize UV-imprinted intaglio nanotracks via low-energy hydrogen ion irradiation, resulting the irradiated region are magnetically separated from the non-irradiated region. Multilayered magnetic nanotracks with a line width of 140 nm, which were fabricated by this parallel process without additional dry etching process, exhibited a saturation magnetization of 290 emu cm−3 and a coercivity of 2 kOe. This study demonstrates a cost-effective mass production of multilayered perpendicular magnetic nanotracks and offers the possibility to achieve high density storage and memory devices.

Spatially dependent cluster dynamics model of He plasma surface interaction in tungsten for fusion relevant conditions

In fusion reactors, plasma facing components (PFC) and, in particular, the divertor will be irradiated with high fluxes of low-energy (∼100 eV) helium and hydrogen ions. Tungsten is one of the leading candidate divertor materials for ITER and DEMO fusion reactors. However, the behaviour of tungsten under high dose, coupled helium/hydrogen exposure remains to be fully understood. The PFC response and performance changes are intimately related to microstructural changes, such as the formation of point defect clusters, helium and hydrogen bubbles or dislocation loops. Computational materials' modelling results are described here that investigate the mechanisms controlling microstructural evolution in tungsten. The aim of this study is to understand and predict sub-surface helium bubble growth under high flux helium ion implantation (∼1022 m−2 s−1) at high temperatures (>1000 K). We report results from a spatially dependent cluster dynamics model based on reaction–diffusion rate theory to describe the evolution of the microstructure under these conditions. The key input parameters to the model (diffusion coefficients, migration and binding energies, initial defect production) are determined from a combination of atomistic modelling and available experimental data. The results are in good agreement with results of an analytical model that is presented in a separate paper. In particular, it is found that the sub-surface evolution with respect to bubble size and concentration of the helium bubbles strongly depends on the flux and temperature.