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Sample records for alkali halide photocathodes

  1. Fabrication of alkali halide UV photocathodes by pulsed laser deposition

    SciTech Connect

    Brendel', V M; Bukin, V V; Garnov, Sergei V; Bagdasarov, V Kh; Denisov, N N; Garanin, Sergey G; Terekhin, V A; Trutnev, Yurii A

    2012-12-31

    A technique has been proposed for the fabrication of atmospheric corrosion resistant alkali halide UV photocathodes by pulsed laser deposition. We produced photocathodes with a highly homogeneous photoemissive layer well-adherent to the substrate. The photocathodes were mounted in a vacuum photodiode, and a tungsten grid was used as an anode. Using pulsed UV lasers, we carried out experiments aimed at evaluating the quantum efficiency of the photocathodes. With a dc voltage applied between the photocathode and anode grid, we measured a shunt signal proportional to the total charge emitted by the cathode exposed to UV laser light. The proposed deposition technique enables one to produce photocathodes with photoemissive layers highly uniform in quantum efficiency, which is its main advantage over thin film growth by resistive evaporation. (laser technologies)

  2. Aging of alkali halide windows

    NASA Astrophysics Data System (ADS)

    Kennedy, Michael; Trung, D.; Meyer, Franz; Buth, T.; Ristau, Detlev; Schmidt, Holger; Korth, Joerg U.; Hamburg, K.

    1995-07-01

    The environmental effect on the aging behavior of NaCl and KCl windows was studied. Laser windows were aged at different relative humidities in a controlled climate-chamber. Degradation is monitored with a microscope inspection system equipped with a computer controlled image processing board. The temporal development of surface defect density under different atmospheric conditions was investigated with respect to optical absorption and damage thresholds of the windows at 10.6 micrometers . Laser windows coated with single layers of NaF deposited by an adapted IAD-technique were analyzed. The performance of the coated and uncoated laser windows is discussed under consideration of typical applications. In comparison to the bare samples, the coated windows show an improved resistivity against environmental influences. Accelerated testing theory is employed to model the aging behavior of the samples. An approach to deduce a qualified acceleration factor is made in order to extrapolate the lifetime of alkali halide laser window under normal conditions.

  3. The Additive Coloration of Alkali Halides

    ERIC Educational Resources Information Center

    Jirgal, G. H.; and others

    1969-01-01

    Describes the construction and use of an inexpensive, vacuum furnace designed to produce F-centers in alkali halide crystals by additive coloration. The method described avoids corrosion or contamination during the coloration process. Examination of the resultant crystals is discussed and several experiments using additively colored crystals are

  4. The Additive Coloration of Alkali Halides

    ERIC Educational Resources Information Center

    Jirgal, G. H.; and others

    1969-01-01

    Describes the construction and use of an inexpensive, vacuum furnace designed to produce F-centers in alkali halide crystals by additive coloration. The method described avoids corrosion or contamination during the coloration process. Examination of the resultant crystals is discussed and several experiments using additively colored crystals are…

  5. Solvation at nanoscale: Alkali-halides in water clusters

    SciTech Connect

    Partanen, Leena; Mikkelae, Mikko-Heikki; Huttula, Marko; Tchaplyguine, Maxim; Zhang Chaofan; Andersson, Tomas; Bjoerneholm, Olle

    2013-01-28

    The solvation of alkali-halides in water clusters at nanoscale is studied by photoelectron spectroscopy using synchrotron radiation. The Na 2p, K 3p, Cl 2p, Br 3d, and I 4d core level binding energies have been measured for salt-containing water clusters. The results have been compared to those of alkali halide clusters and the dilute aqueous salt solutions. It is found that the alkali halides dissolve in small water clusters as ions.

  6. Ionic alkali halide XUV laser feasibility study

    SciTech Connect

    Yang, T.T.; Gylys, V.T.; Bower, R.D.; Harris, D.G.; Blauer, J.A.; Turner, C.E.; Hindy, R.N.

    1989-11-10

    The objective of this work is to assess the feasibility of a select set of ionic alkali halide XUV laser concepts by obtaining the relevant kinetic and spectroscopic parameters required for a proof-of-principle and conceptual design. The proposed lasers operate in the 80--200 nm spectral region and do not require input from outside radiation sources for their operation. Frequency up-conversion and frequency mixing techniques and therefore not considered in the work to be described. An experimental and theoretical study of a new type of laser operating in the extreme ultraviolet wavelength region has been conducted. The lasing species are singly ionized alkali halide molecules such as Rb{sup 2+}F{sub {minus}}, Rb{sup 2+}Br{sup {minus}} and Cs{sup 2+}F{sup {minus}}. These species are similar in electronic structure to the rare gas halide excimers, such as XeF and Krf, except that the ionic molecules emit at wavelengths of 80--200 nm, much shorter than the conventional rare-gas halide excimer laser. The radiative lifetime of these molecules are typically near 1 ns, which is about an order of magnitude shorter than that for rare-gas halide systems. The values of the cross section for stimulated emission are on the order of 1 {times} 10{sup {minus}16}cm{sup 2}. Because of the fundamental similarity to existing UV lasers, these systems show promise as a high power, efficient XUV lasers. 55 refs., 50 figs., 5 tabs.

  7. Enhanced Quantum Efficiency From Hybrid Cesium Halide/Copper Photocathode

    SciTech Connect

    Kong, Lingmei; Joly, Alan G.; Droubay, Timothy C.; Gong, Yu; Hess, Wayne P.

    2014-04-28

    The quantum efficiency of Cu is found to increase dramatically when coated by a CsI film and then irradiated by a UV laser. Over three orders of magnitude quantum efficiency enhancement at 266 nm is observed in CsI/Cu(100), indicating potential application in future photocathode devices. Upon laser irradiation, a large work function reduction to a value less than 2 eV is also observed, significantly greater than for similarly treated CsBr/Cu(100). The initial QE enhancement, prior to laser irradiation, is attributed to interface interaction, surface cleanliness and the intrinsic properties of the Cs halide film. Further QE enhancement following activation is attributed to formation of inter-band states and Cs metal accumulation at the interface induced by laser irradiation.

  8. Relation between the electroforming voltage in alkali halide-polymer diodes and the bandgap of the alkali halide

    SciTech Connect

    Bory, Benjamin F.; Wang, Jingxin; Janssen, René A. J.; Meskers, Stefan C. J.; Gomes, Henrique L.; De Leeuw, Dago M.

    2014-12-08

    Electroforming of indium-tin-oxide/alkali halide/poly(spirofluorene)/Ba/Al diodes has been investigated by bias dependent reflectivity measurements. The threshold voltages for electrocoloration and electroforming are independent of layer thickness and correlate with the bandgap of the alkali halide. We argue that the origin is voltage induced defect formation. Frenkel defect pairs are formed by electron–hole recombination in the alkali halide. This self-accelerating process mitigates injection barriers. The dynamic junction formation is compared to that of a light emitting electrochemical cell. A critical defect density for electroforming is 10{sup 25}/m{sup 3}. The electroformed alkali halide layer can be considered as a highly doped semiconductor with metallic transport characteristics.

  9. Photocathode transfer and storage techniques using alkali vapor feedback control

    SciTech Connect

    Springer, R.W.; Cameron, B.J.

    1991-12-20

    Photocathodes of quantum efficiency above 1% at the doubled YAG frequency of 532 nM are very sensitive to the local vacuum environment. These cathodes must have a band gap of less than 2.3 eV, and a work function that is also on the order of {approximately}2 volts or less. As such, these surfaces are very reactive as they provide many surface states for the residual gases that have positive electron affinities such as oxygen and omnipotent water. Attendant to this problem is that the optimal operating point for some of these cesium based cathodes is unstable. Three of the cesium series were tried, the Cs-Ag-Bi-O, the Cs{sub 3}Sb and the K{sub 2}CsSb. The most stable material found is the K{sub 2}CsSb. The vacuum conditions can be met by a variety of pumping schemes. The vacuum is achieved by using sputter ion diode pumps, and baking at 250{degrees}C or less for whatever time is required to reduce the pump currents to below 1 uA at room temperature. To obtain the required partial pressure of cesium, a simple very sensitive diagnostic gauge has been developed that can discriminate between free alkali and other gases present. This Pressure Alkali Monitor (PAM) can be used cesium sources to provide a low partial pressure using standard feedback techniques. Photocathodes of arbitrary composition have been transferred to a separate vacuum system and preserved for over 10 days with less than a 25% loss to the QE at 543.5 nM.

  10. Cohesive Energy-Lattice Constant and Bulk Modulus-Lattice Constant Relationships: Alkali Halides, Ag Halides, Tl Halides

    NASA Technical Reports Server (NTRS)

    Schlosser, Herbert

    1992-01-01

    In this note we present two expressions relating the cohesive energy, E(sub coh), and the zero pressure isothermal bulk modulus, B(sub 0), of the alkali halides. Ag halides and TI halides, with the nearest neighbor distances, d(sub nn). First, we show that the product E(sub coh)d(sub 0) within families of halide crystals with common crystal structure is to a good approximation constant, with maximum rms deviation of plus or minus 2%. Secondly, we demonstrate that within families of halide crystals with a common cation and common crystal structure the product B(sub 0)d(sup 3.5)(sub nn) is a good approximation constant, with maximum rms deviation of plus or minus 1.36%.

  11. Alkali halide microstructured optical fiber for X-ray detection

    NASA Astrophysics Data System (ADS)

    DeHaven, S. L.; Wincheski, R. A.; Albin, S.

    2015-03-01

    Microstructured optical fibers containing alkali halide scintillation materials of CsI(Na), CsI(Tl), and NaI(Tl) are presented. The scintillation materials are grown inside the microstructured fibers using a modified Bridgman-Stockbarger technique. The x-ray photon counts of these fibers, with and without an aluminum film coating are compared to the output of a collimated CdTe solid state detector over an energy range from 10 to 40 keV. The photon count results show significant variations in the fiber output based on the materials. The alkali halide fiber output can exceed that of the CdTe detector, dependent upon photon counter efficiency and fiber configuration. The results and associated materials difference are discussed.

  12. Morphology of alkali halide thin films studied by AFM

    NASA Astrophysics Data System (ADS)

    Golek, F.; Mazur, P.; Ryszka, Z.; Zuber, S.

    2006-04-01

    Thin layers of alkali halides were investigated by atomic force microscope (AFM). The studied systems were: LiBr/KBr(0 0 1) with -16.7% misfit, LiF/Si(0 0 1) with +4.4% misfit, LiBr/LiF(0 0 1) with +36.8% misfit and NaCl/Si(0 0 1) with +46.5% misfit. The results show that the surface morphology strongly depends on the temperature of layer formation. The alkali halides deposited on the foreign substrate at elevated temperatures or at room temperature and subsequently annealed form preferentially 3D islands leaving uncovered substrate areas between them. It is suggested that Ostwald ripening takes place at elevated temperatures.

  13. Alkali halide microstructured optical fiber for X-ray detection

    SciTech Connect

    DeHaven, S. L. E-mail: russel.a.wincheski@nasa.gov; Wincheski, R. A. E-mail: russel.a.wincheski@nasa.gov; Albin, S.

    2015-03-31

    Microstructured optical fibers containing alkali halide scintillation materials of CsI(Na), CsI(Tl), and NaI(Tl) are presented. The scintillation materials are grown inside the microstructured fibers using a modified Bridgman-Stockbarger technique. The x-ray photon counts of these fibers, with and without an aluminum film coating are compared to the output of a collimated CdTe solid state detector over an energy range from 10 to 40 keV. The photon count results show significant variations in the fiber output based on the materials. The alkali halide fiber output can exceed that of the CdTe detector, dependent upon photon counter efficiency and fiber configuration. The results and associated materials difference are discussed.

  14. Volcanic Origin of Alkali Halides on Io

    NASA Technical Reports Server (NTRS)

    Schaefer, L.; Fegley, B., Jr.

    2003-01-01

    The recent observation of NaCl (gas) on Io confirms our earlier prediction that NaCl is produced volcanically. Here we extend our calculations by modeling thermochemical equilibrium of O, S, Li, Na, K, Rb, Cs, F, Cl, Br, and I as a function of temperature and pressure in a Pele-like volcanic gas with O/S/Na/Cl/K = 1.518/1/0.05/0.04/0.005 and CI chondritic ratios of the other (as yet unobserved) alkalis and halogens. For reference, the nominal temperature and pressure for Pele is 1760 plus or minus 210 K and 0.01 bars based on Galileo data and modeling.

  15. A new polarizable force field for alkali and halide ions

    SciTech Connect

    Kiss, Pter T.; Baranyai, Andrs

    2014-09-21

    We developed transferable potentials for alkali and halide ions which are consistent with our recent model of water [P. T. Kiss and A. Baranyai, J. Chem. Phys. 138, 204507 (2013)]. Following the approach used for the water potential, we applied Gaussian charge distributions, exponential repulsion, and r{sup ?6} attraction. One of the two charges of the ions is fixed to the center of the particle, while the other is connected to this charge by a harmonic spring to express polarization. Polarizability is taken from quantum chemical calculations. The repulsion between different species is expressed by the combining rule of Kong [J. Chem. Phys. 59, 2464 (1972)]. Our primary target was the hydration free energy of ions which is correct within the error of calculations. We calculated water-ion clusters up to 6 water molecules, and, as a crosscheck, we determined the density and internal energy of alkali-halide crystals at ambient conditions with acceptable accuracy. The structure of hydrated ions was also discussed.

  16. Alkali halide clusters produced by fast ion impact

    PubMed Central

    Fernandez-Lima, Francisco Alberto; Nascimento, Marco Antonio Chaer; da Silveira, Enio Frota

    2011-01-01

    The most abundant geometries and relative stabilities of alkali halide clusters with a (XY)no configuration (e.g., LiF, NaCl, KBr) are described. Five main series were obtained: linear, cyclic, cubic, arc strips and nanotubes. The stability analysis shows that higher members are likely to be formed from the lower member of the same series and/or from two building blocks (n = 1, 2). The energy analysis (D-plot) indicates that the most compact ones (e.g., cubic and nanotubes) present higher stability when compared to the linear, cyclic and arc strip structures; moreover, relative stability between the cubic and nanotube series varies with the cluster size. PMID:22389542

  17. Electronic States of F-Centers in Alkali Halide Crystals

    NASA Astrophysics Data System (ADS)

    Matsunaga, Katsuyuki; Narita, Nobutaka; Tanaka, Isao; Adachi, Hirohiko

    1996-08-01

    The electronic states of F-centers in alkali halides with NaCl-type structure have been investigated using the discrete variational (DV) Xα cluster method. The electronic transition accompanied by optical absorption is examined on the basis of Slater's transition state concept. The photo-absorption energies of F-centers computed for the compounds with relatively small anions agree well with experimental data, but those for iodides and bromides exhibit much lower values than the observed values. We have also investigated the change in the absorption energy by the atom displacement. By the inward displacement of 1st neighbor cations, the absorption energies are decreased to approach the experimental values. The relaxation of the 1st neighbors estimated from the computation exhibits fairly small values in fluorides, while large values in iodides and bromides. The effect of lattice relaxation around an F-center is discussed in connection with the bonding nature of the F-center level.

  18. Model polarizabilities and multipoles for ionic compounds. Alkali halides

    NASA Astrophysics Data System (ADS)

    Davis, Stephen L.

    1988-01-01

    Various dipole interaction models were compared with one another and with literature values for dissociation energies, multipole moments (u, Q, and ?), and polarizabilities ? for the alkali halide molecules. A displaced-shell (D-shell) model, which takes account of the overlap repulsion as in the shell model but also uses the effective electron shell displacements in calculating the electrostatic interactions, gives slightly better dissociation energies and as good or better dipole and quadrupole moments than the other models. All of the models considered here give mean polarizabilities in fairly good agreement with published SCF values; however, none gives consistently good polarizability anisotropies. It is found that both the overlap repulsion (as treated in the shell model) and the effective displacements of the electron shells (as treated in the D-shell model) have large effects on the calculated polarizability anisotropies relative to the DID model.

  19. Laser Control of Product Electronic State: Desorption from Alkali Halides

    SciTech Connect

    Beck, Kenneth M.); Joly, Alan G.); Dupuis, Nicholas F.; Perozzo, Peggy; Hess, Wayne P.); Sushko, P V.; Shluger, Alexander L.

    2004-02-01

    We demonstrate laser control of the electronic product state distribution of photodesorbed halogen atoms from alkali halide crystals. Our general model of surface exciton desorption dynamics is developed into a simple method for laser control of the relative halogen atom spin orbit laser desorption yield. By tuning the excitation laser photon energy in a narrow region of the absorption threshold, the relative Cl(2P1/2) yield can be made to vary from near 0 to 80% from KCI and from near 0 to 60% for NaCl. We described the physical properties necessary to obtain a high degree of product state control and the limitation induced when these requirements are not met. These results demonstrate that laser control can be applied to solid state surface reactions and provide strong support for surface exciton-based desorption models.

  20. The entropies of the hard sphere alkali halide crystals

    NASA Astrophysics Data System (ADS)

    Cox, John W.; Beyerlein, Adolph L.

    1982-08-01

    An asymptotic expansion for the entropy of hard-sphere alkali halide crystals with N small and large particle pairs is obtained: SN/NkB ???13 ln(?ls2e)/(?l?s) +3 ln(?1/3-1)+3 ln ?-C-D?-E?2+???, where kB is the Boltzman constant, e is the natural number, ? is the ratio of the system volume to its high compression limiting volume, ?l and ?s are the mean thermal de Broglie wavelengths [?=(h2/2?mkBT)1/2, m being the mass] of the large and small particles, respectively, ?ls is the hard-sphere collision diameter of nearest neighbor large and small particles; C, D, E, etc. are well-defined parameters dependent on the small to large particle radius ratio and the lattice structure, and ?=[(?1/3-1)+(1-?ls/?ls')], where ?ls' is the average distance between nearest neighbor large and small particles in the high compression limit. If the small to large particle radius ratio is less than ?2-1 for the ''NaCl'' lattice and less than ?3-1 for the ''CsCl'' lattice ?lsalkali metal fluoride salts approach the experimental values at temperatures approaching the melting point which is consistent with the contention that the hard sphere contribution to the entropy dominates other contributions at high temperatures. The predicted difference between the entropies of the two alkali halide lattices is also consistent with the experimental data at higher temperatures.

  1. Efficient destruction of CF4 through in situ generation of alkali metals from heated alkali halide reducing mixtures.

    PubMed

    Lee, Myung Churl; Choi, Wonyong

    2002-03-15

    Perfluorocarbons (PFCs) are the most potent green house gases that are very recalcitrant at destruction. An effective way of converting PFCs using hot solid reagents into safe products has been recently introduced. By investigating the thermal reductive destruction of tetrafluoromethane (CF4) we provided new insight and more physicochemical consideration on this novel process. The complete destruction of CF4was successfully achieved by flowing the gas through a heated reagent bed (400-950 degrees C) that contained powder mixtures of alkali halides, CaO, and Si. The silicon acted as a reducing agent of alkali halides for the in-situ production of alkali metals, and the calcium oxide played the role of a halide ion acceptor. The absence of any single component in this ternary mixture drastically reduced the destruction efficiency of CF4. The CF4 destruction efficiencies with the solid reagent containing the alkali halide, MX, increased in the order of Li approximately Na < K < Cs for alkali cations and I < Br < Cl < F for halide anions. This trend agreed with the endothermicity of the alkali metal generation reaction: the higher the endothermicity, the lower the destruction efficiency. Alkali metal generation was indirectly detected by monitoring H2 production from its reaction with water. The production of alkali metals increased with NaF, KF, and CsF in this order. The CsF/CaO/Si system exhibited the complete destruction of CF4 at as low as 600 degrees C. The solid product analysis by X-ray diffraction (XRD) showed the formation of CaF2 and the depletion of Si with black carbon particles formed in the solid reagent residue. No CO/CO2 and toxic HF and SiF4 formation were detected in the exhaust gas. PMID:11944694

  2. Investigating Metallization in Shock-Compressed Alkali Halides

    NASA Astrophysics Data System (ADS)

    Diamond, Matthew

    2015-06-01

    Laser-shock compression on four alkali halides has been used to probe the transition from insulating to metallic states, a high-pressure transition in chemical bonding that has fundamental implications for planetary formation and structure. Collectively, pressures up to 450 GPa were explored across a total of fourteen single-crystal samples of CsI, CsBr, KBr and NaCl. Velocity interferometry was used to record shock velocities and reflectivities at 532 nm during decaying shock compression. The data show up to three-fold increases in density as well as significant increases in optical reflectivity in response to high pressures and temperatures. Ionic salts are simple model systems amenable to first-principles theory and serve as analog materials for predicting whether specific chemical constituents can reside in the rocky mantles or metallic cores of planets. A key objective is to disentangle the complementary roles of temperature and compression in transforming ionic into metallic bonding. Furthermore, at high pressures CsI becomes analogous to Xe: they are isoelectronic and follow matching equations of state. Therefore, studies on CsI can inform understanding of noble-gas geochemistry at conditions deep inside planets.

  3. Strong Turbulence in Alkali Halide Negative Ion Plasmas

    NASA Astrophysics Data System (ADS)

    Sheehan, Daniel

    1999-11-01

    Negative ion plasmas (NIPs) are charge-neutral plasmas in which the negative charge is dominated by negative ions rather than electrons. They are found in laser discharges, combustion products, semiconductor manufacturing processes, stellar atmospheres, pulsar magnetospheres, and the Earth's ionosphere, both naturally and man-made. They often display signatures of strong turbulence^1. Development of a novel, compact, unmagnetized alkali halide (MX) NIP source will be discussed, it incorporating a ohmically-heated incandescent (2500K) tantulum solenoid (3cm dia, 15 cm long) with heat shields. The solenoid ionizes the MX vapor and confines contaminant electrons, allowing a very dry (electron-free) source. Plasma densities of 10^10 cm-3 and positive to negative ion mass ratios of 1 <= fracm_+m- <= 20 are achievable. The source will allow tests of strong turbulence theory^2. 1 Sheehan, D.P., et al., Phys. Fluids B5, 1593 (1993). 2 Tsytovich, V. and Wharton, C.W., Comm. Plasma Phys. Cont. Fusion 4, 91 (1978).

  4. Model of self-trapped excitons in alkali halides

    NASA Astrophysics Data System (ADS)

    Puchin, V. E.; Shluger, A. L.; Tanimura, K.; Itoh, N.

    1993-03-01

    We have carried out an ab initio many-electron variational calculation of the adiabatic potential-energy surface (APES) for the lowest triplet state of the self-trapped exciton (STE) in LiCl, NaCl, and KCl. Calculations of the H center in these crystals show that the <111> orientation is favored, in agreement with experimental results for NaCl but not for KCl, in which it is oriented along a <110> direction (no measurement exists for LiCl), and hence most detailed calculations for STE's are carried out for NaCl. It is found that the APES minimum for each crystal occurs when the Cl-2 molecular ion is displaced along its molecular axis from its symmetrical position (D2h) nearly halfway to the nearest halogen lattice point. The calculated transition energies for the optical absorption and luminescence at this configuration agree with the experimental values for the triplet STE, although the calculated stretching vibration frequency of the Cl-2 molecular ion in NaCl is much smaller than that for the H center, contradictory to recent resonant Raman studies. Other minima are found at the nearest F-H pair configuration, in which the Cl-2 molecular ion is reoriented by 90° from the initial orientation and next-nearest F-H pair. Extremely small luminescence energy at these configurations excludes the possibility that they are the candidates for the luminescent state of the STE. It is found that, after the displacement of the Cl-2 molecular ion beyond the first minimum of the APES towards the nearest F-H pair configuration, the total energy is lowered by reorientation, inducing an anomaly on the APES. The results of a recent experimental investigation, including existence of several types of relaxed configuration of the STE in alkali halides, the stretching vibration frequency, and the femtosecond oscillation on APES, are discussed on the basis of the results of the calculation.

  5. Comparison of CsBr and KBr coated Cu photocathodes. Effects of laser irradiation and work function changes

    SciTech Connect

    He, Weidong; VilayurGanapathy, Subramanian; Joly, Alan G.; Droubay, Timothy C.; Chambers, Scott A.; Maldonado, Juan R.; Hess, Wayne P.

    2013-02-20

    Thin films (7 nm layers) of CsBr and KBr were deposited on Cu(100) to investigate photoemission properties of these potential photocathode materials. After thin film deposition and prolonged laser ultraviolet (UV) irradiation (266 nm picosecond laser) photoemission quantum efficiency increases by factors of 26 and 77 for KBr/Cu(100) and CsBr/Cu(100) photocathodes, respectively. Immediately following thin film deposition, a decrease in work function is observed, compared to bare Cu, in both cases. Quantum efficiency enhancements are attributed to the decrease in photocathode work function, due to the deposition of alkali halide thin films, and photo-induced processes, that introduce defect states into the alkali halide bandgap, induced by UV laser irradiation. It is possible that alkali metal formation occurs during UV irradiation and that this further contributes to photoemission enhancement. Our results suggest that KBr, a relatively stable alkali-halide, has potential for photocathode applications.

  6. Direct observation of bi-alkali antimonide photocathodes growth via in operando x-ray diffraction studies

    SciTech Connect

    Ruiz-Osés, M.; Ben-Zvi, I.; Liang, X.; Muller, E.; Schubert, S.; Attenkofer, K.; Rao, T.; Smedley, J.; Padmore, H.; Vecchione, T.; Wong, J.; Xie, J.

    2014-12-01

    Alkali antimonides have a long history as visible-light-sensitive photocathodes. This work focuses on the process of fabrication of the bi-alkali photocathodes, K{sub 2}CsSb. In-situ synchrotron x-ray diffraction and photoresponse measurements were used to monitor phase evolution during sequential photocathode growth mode on Si(100) substrates. The amorphous-to-crystalline transition for the initial antimony layer was observed at a film thickness of 40 Å . The antimony crystalline structure dissolved upon potassium deposition, eventually recrystallizing upon further deposition into K-Sb crystalline modifications. This transition, as well as the conversion of potassium antimonide to K{sub 2}CsSb upon cesium deposition, is correlated with changes in the quantum efficiency.

  7. High temperature corrosion of silicon based ceramics in environments containing halogens and alkali halides

    SciTech Connect

    McNallan, M.

    1999-07-01

    Silicon carbide and other silicon-based ceramics obtain their oxidation resistance by the formation of protective silica films in oxygen containing environments. In the presence of chlorine or alkali chlorides, this film may not form, or may be unprotective, so that accelerated oxidation occurs. Chlorine and alkali halides may contribute to accelerated oxidation via three possible mechanisms. Active oxidation occurs at relatively low temperatures and high ratios of chlorine to oxygen, and is characterized by simultaneous formation of silicon chlorides and non-protective oxides. Silica film disruption occurs at higher temperatures when volatile chlorides format the interface between SiC and the Si0{sub 2} scale, and cause bubbles to form in the film. Alkali fluxing occurs in the presence of alkali chloride vapors. In alkali fluxing, a low melting glass is formed by the reaction between the alkali vapor species and silica rather than by reactions with chlorine itself.

  8. Refined potentials for rare gas atom adsorption on rare gas and alkali-halide surfaces

    NASA Technical Reports Server (NTRS)

    Wilson, J. W.; Heinbockel, J. H.; Outlaw, R. A.

    1985-01-01

    The utilization of models of interatomic potential for physical interaction to estimate the long range attractive potential for rare gases and ions is discussed. The long range attractive force is calculated in terms of the atomic dispersion properties. A data base of atomic dispersion parameters for rare gas atoms, alkali ion, and halogen ions is applied to the study of the repulsive core; the procedure for evaluating the repulsive core of ion interactions is described. The interaction of rare gas atoms on ideal rare gas solid and alkali-halide surfaces is analyzed; zero coverage absorption potentials are derived.

  9. CO/sub 2/ laser absorption and saturation studies of molecular impurities in alkali halide crystals

    SciTech Connect

    Sievers, A.J.

    1980-12-01

    The objective of this research program has been to explore the equilibrium and non-equilibrium dynamical properties of ReO/sub 4//sup -/ molecules embedded in alkali halide lattices using electromagnetic radiation. Both incoherent sources and CO/sub 2/ laser radiation have been used to explore the full dynamic range of the molecular vibrational modes. To achieve this objective stable molecular dopant - alkali halide combinations have been fabricated which have vibrational modes near the CO/sub 2/ laser frequencies. In order to uncouple the molecular modes from the lattice modes, to simplify the analysis as much as possible, low temperature spectroscopic measurements were required. In general, it was found that the molecular vibrational modes in the low temperature quiescent lattice had extremely narrow linewidths (less than 0.1 cm/sup -1/) so that most of the coincidences with the CO/sub 2/ laser lines were eliminated.

  10. Reactions between cold methyl halide molecules and alkali-metal atoms

    SciTech Connect

    Lutz, Jesse J.; Hutson, Jeremy M.

    2014-01-07

    We investigate the potential energy surfaces and activation energies for reactions between methyl halide molecules CH{sub 3}X (X = F, Cl, Br, I) and alkali-metal atoms A (A = Li, Na, K, Rb) using high-level ab initio calculations. We examine the anisotropy of each intermolecular potential energy surface (PES) and the mechanism and energetics of the only available exothermic reaction pathway, CH{sub 3}X + A ? CH{sub 3} + AX. The region of the transition state is explored using two-dimensional PES cuts and estimates of the activation energies are inferred. Nearly all combinations of methyl halide and alkali-metal atom have positive barrier heights, indicating that reactions at low temperatures will be slow.

  11. Development of processes for the production of solar grade silicon from halides and alkali metals

    NASA Technical Reports Server (NTRS)

    Dickson, C. R.; Gould, R. K.

    1980-01-01

    High temperature reactions of silicon halides with alkali metals for the production of solar grade silicon in volume at low cost were studied. Experiments were performed to evaluate product separation and collection processes, measure heat release parameters for scaling purposes, determine the effects of reactants and/or products on materials of reactor construction, and make preliminary engineering and economic analyses of a scaled-up process.

  12. Alkali metal/halide thermal energy storage systems performance evaluation

    NASA Astrophysics Data System (ADS)

    Phillips, W. M.; Stearns, J. W.

    A pseudoheat-pipe heat transfer mechanism has been demonstrated effective in terms of both total heat removal efficiency and rate, on the one hand, and system isothermal characteristics, on the other, for solar thermal energy storage systems of the kind being contemplated for spacecraft. The selection of appropriate salt and alkali metal substances for the system renders it applicable to a wide temperature range. The rapid heat transfer rate obtainable makes possible the placing of the thermal energy storage system around the solar receiver canister, and the immersing of heat transfer fluid tubes in the phase change salt to obtain an isothermal heat source.

  13. Alkali metal/halide thermal energy storage systems performance evaluation

    NASA Technical Reports Server (NTRS)

    Phillips, W. M.; Stearns, J. W.

    1986-01-01

    A pseudoheat-pipe heat transfer mechanism has been demonstrated effective in terms of both total heat removal efficiency and rate, on the one hand, and system isothermal characteristics, on the other, for solar thermal energy storage systems of the kind being contemplated for spacecraft. The selection of appropriate salt and alkali metal substances for the system renders it applicable to a wide temperature range. The rapid heat transfer rate obtainable makes possible the placing of the thermal energy storage system around the solar receiver canister, and the immersing of heat transfer fluid tubes in the phase change salt to obtain an isothermal heat source.

  14. Demulsifying petroleum emulsions with aryl sulfonates-oxyalkylated phenolformaldehyde resins and alkali metal halides

    SciTech Connect

    Allan, B.W.

    1981-11-10

    A process for recovering oil from oil-in-water petroleum emulsions stabilized with clay and/or other solids by subjecting them to the action of an optimum amount of non-ionic, water soluble, aryl sulfonates-oxyalkylated phenol formaldehyde resins at a ph of 7.0 to 8.0 and then adding a saturated aqueous alkali metal halide solution to the resulting mixture. The process is carried out at between about 200/sup 0/F and 240/sup 0/F. And the mixture is allowed to stand in the quiescent state for a period of about 1 to about 10 hours to allow the halide solution to increase th specific gravity of the resulting aqueous phase by at least 0.02 thereby causing the bitumen to float and facilitating recovery of the oil.

  15. Local structure and lattice dynamics of alkali halide crystals with an anion vacancy

    NASA Astrophysics Data System (ADS)

    Larin, A. V.; Kislov, A. N.; Nikiforov, A. E.; Popov, S. .

    2008-09-01

    The local structure and vibrations in the region of an anion vacancy are studied using the pair interionic potentials within the shell model for crystals Me +Cl- ( Me + = Rb+, K+, Na+). The pair potentials are derived from first-principles calculations of different clusters by the Hartree-Fock-Roothaan method with the one-electron states constructed in the form of molecular orbitals as linear combinations of atomic orbitals (MO LCAO). The calculations are performed with the GAMESS program package (US). The correlation corrections are included in the calculations. The validity of the model parameters is verified by comparing the calculated with experimental structural and dynamic properties of ideal alkali halide crystals.

  16. Response of alkali halide scintillators to neutrons from 5 to 100 MeV

    SciTech Connect

    Bartle, C.M.; Haight, R.C.

    1994-12-31

    The response of three alkali halide scintillators to neutrons in the range 5 to 100 MeV was investigated with the spallation neutron source at LAMPF/WNR. Scintillating crystals were NaI(Tl), KI(Tl) and CsI(Tl), each 2.5 cm in diameter and 1.2 cm thick. Pulse shapes that depend on particle type were observed for NaI(Tl) and CsI(Tl) but not for KI(Tl). Pulse height spectra for are reported as a function of neutron energy, and, where pulse shape discrimination was observed, for individual charged-particle groups.

  17. Application of secondary ion mass spectrometer for measuring the diffusion profiles in alkali-halide crystals

    NASA Astrophysics Data System (ADS)

    Chernyavskii, A. V.; Kaz, M. S.

    2015-04-01

    Depth profiles of magnesium, fluorine and oxygen impurities was examined in the surface layers of alkali-halide KBr crystals using method of secondary ion mass spectrometry. Samples of potassium bromide, coated with a surface film of magnesium fluoride were subjected to isothermal diffusion annealing in air at various times. It is shown that the diffusion of O ions occurs from the ambient atmosphere besides the diffusion of Mg and F ions during annealing of KBr crystals. Accurate estimation of the diffusion coefficients of cationic impurity Mg requires taking into account the possible interaction of this impurity and oxygen.

  18. MULTI-ALKALI PHOTOCATHODE DEVELOPMENT AT BROOKHAVEN NATIONAL LAB FOR APPLICATION IN SUPERCONDUCTING PHOTOINJECTORS. KICKERS.

    SciTech Connect

    BURRILL, A.; BEN-ZVI, I.; RAO, T.; PATE, D.; SEGALOV, Z.

    2005-05-16

    The development of a suitable photocathode for use in a high average current photoinjector at temperatures ranging from 273 K down to 2 K is a subject of considerable interest, and active research. The choice of photocathode material is often a trade-off made based on the quantum efficiency of the cathode material, the tolerance to adverse vacuum conditions, and the laser wavelength needed to produce photoelectrons. In this paper an overview of the BNL work to date on CsK{sub 2}Sb photocathodes on a variety of substrates, irradiated at multiple wavelengths, and at temperatures down to 170 K will be discussed. The application of this photocathode material into a SRF photoinjector will also be discussed.

  19. Multi-Alkali Photocathode Development at Brookhaven National Lab for Application in Superconducting Photoinjectors

    SciTech Connect

    Burrill, A.; Ben-Zvi, I.; Pate, D.; Rao, T.; Segalov, Z.; Dowell, D.; /SLAC

    2006-02-15

    The development of a suitable photocathode for use in a high average current photoinjector at temperatures ranging from 273 K down to 2 K is a subject of considerable interest, and active research. The choice of photocathode material is often a trade-off made based on the quantum efficiency of the cathode material, the tolerance to adverse vacuum conditions, and the laser wavelength needed to produce photoelectrons. In this paper an overview of the BNL work to date on CsK{sub 2}Sb photocathodes on a variety of substrates, irradiated at multiple wavelengths, and at temperatures down to 170 K will be discussed. The application of this photocathode material into a SRF photoinjector will also be discussed.

  20. Anharmonic vibrational relaxation dynamics for a molecular impurity mode in alkali halide crystals

    NASA Astrophysics Data System (ADS)

    Moerner, W. E.; Chraplyvy, A. R.; Sievers, A. J.

    1984-06-01

    High-resolution diode-laser spectroscopy and the nonequilibrium techniques of incoherent laser saturation and transient hole-burning spectroscopy have been used to measure the relaxation dynamics (specifically T1 and T2) of the ?3 internal vibrational mode of ReO4- molecules as functions of temperature and host alkali halide lattice. Inhomogeneously broadened linewidths less than 0.02 cm-1 were observed in annealed crystals at low temperatures. To retrieve the homogeneous linewidths from the inhomogeneously broadened lines, hole-burning measurements of T2 were performed with the use of a CO2 laser as a saturating pump and either a Pb-salt diode laser or another CO2 laser as a tunable probe. Holes as narrow as 10 MHz (full width at half maximum) were observed in inhomogeneously broadened lines several cm-1 wide. Excited-state lifetimes T1 were measured by CO2-laser saturation measurements, which provide values for the saturation intensity Is and hence the product T1T2. Above 10 K the dominant dephasing (T2) mechanism is acousticphonon scattering, whereas below 10 K T2 achieves the fundamental upper limit of 2T1, signifying that dephasing is lifetime limited. The results of a systematic study of the alkali halide host lattice dependence of the excited-state decay rate at low temperatures show that the decay channel consists of multistep emission of lower-energy internal modes, localized phonon modes, and band phonons.

  1. Microscopic model for the two-phonon Raman spectra of alkali halides

    NASA Astrophysics Data System (ADS)

    Gallo, P.; Mazzacurati, V.; Ruocco, G.; Signorelli, G.

    1993-05-01

    The second-order Raman-scattering (SORS) cross section of alkali halides has been evaluated by using the Buckingham expansion for the induced polarizability. This ab initio approach leads to a microscopic expression of the SORS cross section without free parameters. The first two nonzero contributions of the expansion, namely, the dipole-induced dipole (DID) coming from the first-order dressed polarizability and the BTQ (second-dipole hyperpolarizability dipole propagator effective charge) coming from the second-dipole-quadrupole polarizability, have been considered. The short-range contribution to the induced polarizability coming from the electronic overlap has not been included in the present work. The SORS spectra are expressed in terms of the dynamical quantities of the crystal (eigenvectors and eigenfrequencies) and in terms of some bare ionic susceptibilities, namely, the ions' bare polarizabilities ?+ and ?- and the second-dipole-quadrupole bare polarizabilities B+ and B-. As an example the results are shown in the case of KBr. Considerations on the long-range nature of the DID spectrum and on the short-range nature of the BTQ spectrum are made. The relative weights of the two contributions to the SORS in the whole class of alkali halides are also discussed.

  2. Molecular dispersion energy parameters for alkali and halide ions in aqueous solution

    SciTech Connect

    Reiser, S.; Deublein, S.; Hasse, H.; Vrabec, J.

    2014-01-28

    Thermodynamic properties of aqueous solutions containing alkali and halide ions are determined by molecular simulation. The following ions are studied: Li{sup +}, Na{sup +}, K{sup +}, Rb{sup +}, Cs{sup +}, F{sup −}, Cl{sup −}, Br{sup −}, and I{sup −}. The employed ion force fields consist of one Lennard-Jones (LJ) site and one concentric point charge with a magnitude of ±1 e. The SPC/E model is used for water. The LJ size parameter of the ion models is taken from Deublein et al. [J. Chem. Phys. 136, 084501 (2012)], while the LJ energy parameter is determined in the present study based on experimental self-diffusion coefficient data of the alkali cations and the halide anions in aqueous solutions as well as the position of the first maximum of the radial distribution function of water around the ions. On the basis of these force field parameters, the electric conductivity, the hydration dynamics of water molecules around the ions, and the enthalpy of hydration is predicted. Considering a wide range of salinity, this study is conducted at temperatures of 293.15 and 298.15 K and a pressure of 1 bar.

  3. Alkali Halide Interfacial Behavior in a Sequence of Charged Slit Pores

    SciTech Connect

    Wander, Matthew C; Shuford, Kevin L

    2011-01-01

    In this paper, a variety of alkali halide, aqueous electrolyte solutions in contact with charged, planar-graphite slit-pores are simulated using classical molecular dynamics. Size trends in structure and transport properties are examined by varying the choice of ions among the alkali metal and halide series. As with the uncharged pores, system dynamics are driven by changes in water hydration behavior and specifically by variations in the number of hydrogen bonds per water molecule. Overall, the larger ions diffuse more rapidly under high surface charge conditions than the smaller ions. In particular, for the 1 nmslit, ion diffusivity increased by a factor of 4 compared to the uncharged case. Finally, a quantitative fit to the interfacial charge structure is presented, which confirms the presence of two distinct types of layers in an aqueous interface. This model indicates that the chemistry of the interface is able to create a small interfacial potential, and it shows how water molecules can rotate to increase charge separation in response to a surface potential.

  4. Ab initio perspective on the Mollwo-Ivey relation for F centers in alkali halides

    NASA Astrophysics Data System (ADS)

    Tiwald, Paul; Karsai, Ferenc; Laskowski, Robert; Grfe, Stefanie; Blaha, Peter; Burgdrfer, Joachim; Wirtz, Ludger

    2015-10-01

    We revisit the well-known Mollwo-Ivey relation that describes the "universal" dependence of the absorption energies of F-type color centers on the lattice constant a of alkali-halide crystals, Eabs?a-n. We perform both state-of-the-art ab initio quantum chemistry and post-DFT calculations of F-center absorption spectra. By "tuning" independently the lattice constant and the atomic species we show that the scaling with the lattice constant alone (keeping the elements fixed) would yield n =2 in agreement with the "particle-in-the-box" model. Keeping the lattice constant fixed and changing the atomic species enables us to quantify the ion-size effects which are shown to be responsible for the exponent n ?1.8 .

  5. Silicon Halide-alkali Metal Flames as a Source of Solar Grade Silicon

    NASA Technical Reports Server (NTRS)

    Olson, D. B.; Gould, R. K.

    1979-01-01

    A program is presented which was aimed at determining the feasibility of using high temperature reactions of alkali metals and silicon halides to produce low cost solar-grade silicon. Experiments are being conducted to evaluate product separation and collection processes, measure heat release parameters for scaling purposes, and determine the effects of the reactants and/or products on materials of reactor construction. During the current reporting period, the results of heat release experiments were used to design and construct a new type of thick-wall graphite reactor to produce larger quantities of silicon. A reactor test facility was constructed. Material compatibility tests were performed for Na in contact with graphite and several coated graphites. All samples were rapidly degraded at T = 1200K, while samples retained structural strength at 1700K. Pyrolytic graphite coatings cracked and separated from substances in all cases.

  6. Studies of Non-Proportionality in Alkali Halide and Strontium Iodide Scintillators Using SLYNCI

    SciTech Connect

    Ahle, L; Bizarri, G; Boatner, L; Cherepy, N J; Choong, W; Moses, W W; Payne, S A; Shah, K; Sheets, S; Sturm, B W

    2009-05-05

    Recently a collaboration of LLNL and LBNL has constructed a second generation Compton coincidence instrument to study the non-proportionality of scintillators [1-3]. This device, known as SLYNCI (Scintillator Light-Yield Non-proportionality Characterization Instrument), has can completely characterize a sample with less than 24 hours of running time. Thus, SLYNCI enables a number of systematic studies of scintillators since many samples can be processed in a reasonable length of time. These studies include differences in nonproportionality between different types of scintillators, different members of the same family of scintillators, and impact of different doping levels. The results of such recent studies are presented here, including a study of various alkali halides, and the impact of europium doping level in strontium iodide. Directions of future work area also discussed.

  7. Studies of non-proportionality in alkali halide and strontium iodide scintillators using SLYNCI

    SciTech Connect

    Ahle, Larry; Bizarri, Gregory; Boatner, Lynn; Cherepy, Nerine J.; Choong, Woon-Seng; Moses, William W.; Payne, Stephen A.; Shah, Kanai; Sheets, Steven; Sturm, Benjamin, W.

    2010-10-14

    Recently a collaboration of LLNL and LBNL has constructed a second generation Compton coincidence instrument to study the non-proportionality of scintillators. This device, known as SLYNCI (Scintillator Light-Yield Non-proportionality Characterization Instrument), has can completely characterize a sample with less than 24 hours of running time. Thus, SLYNCI enables a number of systematic studies of scintillators since many samples can be processed in a reasonable length of time. These studies include differences in nonproportionality between different types of scintillators, different members of the same family of scintillators, and impact of different doping levels. The results of such recent studies are presented here, including a study of various alkali halides, and the impact of europium doping level in strontium iodide. Directions of future work area also discussed.

  8. Ion Segregation and Deliquescence of Alkali Halide Nanocrystals on SiO2

    SciTech Connect

    Arima, Kenta; Jiang, Peng; Lin, Deng-Sung; Verdaguer, Albert; Salmeron, Miquel

    2009-08-11

    The adsorption of water on alkali halide (KBr, KCl, KF, NaCl) nanocrystals on SiO{sub 2} and their deliquescence was investigated as a function of relative humidity (RH) from 8% to near saturation by scanning polarization force microscopy. At low humidity, water adsorption solvates ions at the surface of the crystals and increases their mobility. This results in a large increase in the dielectric constant, which is manifested in an increase in the electrostatic force and in an increase in the apparent height of the nanocrystals. Above 58% RH, the diffusion of ions leads to Ostwald ripening, where larger nanocrystals grow at the expense of the smaller ones. At the deliquescence point, droplets were formed. For KBr, KCl, and NaCl, the droplets exhibit a negative surface potential relative to the surrounding region, which is indicative of the preferential segregation of anions to the air/solution interface.

  9. MD Study on the Thermal Conductivity of Molten Alkali Halides: Effect of Ionic Mass Difference

    NASA Astrophysics Data System (ADS)

    Ishii, Yoshiki; Oono, Takuya; Takase, Keiichi; Ohtori, Norikazu

    2014-02-01

    A definition suitable for the average ionic mass used for two kinds of expressions of the thermal conductivity for molten alkali halides has been explored from the viewpoint of the difference in anion and cation masses. One is the scaling equation, , where is the average ionic mass between the anion and cation and is the number density, which was previously obtained from molecular dynamics (MD) simulation. The other is the equation used in the corresponding-states (CS) analysis which has been applied to the thermal conductivities calculated by the MD simulation. Among some representative definitions, it turned out that a simple arithmetic average is best for the equation. As an estimation method of the thermal conductivity, it was shown that both equations have comparable precision. It was indicated that considering the difference in ionic masses between the anion and cation is important for building a more precise correlation in the CS analysis.

  10. Quantum Efficiency Enhancement in CsI/Metal Photocathodes

    SciTech Connect

    Kong, Lingmei; Joly, Alan G.; Droubay, Timothy C.; Hess, Wayne P.

    2015-02-01

    High quantum efficiency enhancement is found for hybrid metal-insulator photocathodes consisting of thin films of CsI deposited on Cu(100), Ag(100), Au(111) and Au films irradiated by 266 nm laser pulses. Low work functions (near or below 2 eV) are observed following ultraviolet laser activation. Work functions are reduced by roughly 3 eV from that of clean metal surfaces. We discuss various mechanisms of quantum efficiency enhancement for alkali halide/metal photocathode systems and conclude that the large change in work function, due to Cs accumulation of Cs metal at the metal-alkali halide interface, is the dominant mechanism for quantum efficiency enhancement

  11. Silicon halide-alkali metal flames as a source of solar grade silicon

    NASA Technical Reports Server (NTRS)

    Olsen, D. B.; Miller, W. J.

    1979-01-01

    The feasibility of using alkali metal-silicon halide diffusion flames to produce solar-grade silicon in large quantities and at low cost is demonstrated. Prior work shows that these flames are stable and that relatively high purity silicon can be produced using Na + SiCl4 flames. Silicon of similar purity is obtained from Na + SiF4 flames although yields are lower and product separation and collection are less thermochemically favored. Continuous separation of silicon from the byproduct alkali salt was demonstrated in a heated graphite reactor. The process was scaled up to reduce heat losses and to produce larger samples of silicon. Reagent delivery systems, scaled by a factor of 25, were built and operated at a production rate of 0.5 kg Si/h. Very rapid reactor heating rates are observed with wall temperatures reaching greater than 2000 K. Heat release parameters were measured using a cooled stainless steel reactor tube. A new reactor was designed.

  12. Chemistry of alkali cation exchanged faujasite and mesoporous NaX using alkyl halides and phosphates

    NASA Astrophysics Data System (ADS)

    Lee, Min-Hong

    The purpose of this work was to increase the reactivity of Faujasite X (NaX) zeolite toward the reactive decontamination of materials subject to nucleophilic attack by means of zeolite cation optimization and by means of the synthesis of mesoporous Faujasite X. Primary alkyl halides and trialkyl phosphates have been the test materials on which the cation-optimized and mesoporous zeolites have been tested. In the alkali cation optimization work, reactions of methyl iodide and 1-chloropropane with alkali metal cation exchanged Faujasite zeolite X were investigated at room temperature. The reactivity of the framework and the product formation were shown to depend on zeolite framework counter-cation. A quantitative study of zeolite product formation has been carried out, primarily using solid-state NMR spectroscopy. Large alkali cations showed preference toward substitution chemistry. In contrast, alkyl halide exposed LiX and NaX zeolites underwent both substitution and elimination. Subsequently introduced water molecules led to hydrolysis of framework species that was sensitive to framework counter-cation. The mesoporous NaX zeolites work undertakes to test whether an improvement in surface chemical reactivity can be achieved by introducing mesopores into the already reactive nucleophilic microporous NaX zeolite. Incorporation of the polydiallyl dimethyl ammonium chloride (PDADMAC) template and the formation of mesopores in Faujasite X zeolite (NaX) were successful and well-characterized. The mesopores are proposed to have occurred from incorporation of the cationic PDADMAC polymer into the zeolite by compensating zeolite framework charge. Subsequent sodium cation exchange of calcined mesoporous NaX was shown to restore the chemical reactivity characteristic of as-synthesized NaX. Trialkyl organophosphorous compounds underwent substitution reactions. The reactivity of both microporous and mesoporous Faujasite zeolite X and the product formation was shown to depend on the length of the alkyl chain. Although introduced mesopores alleviated the limited reagent diffusion to reactive sites due to the microporosity of the NaX zeolites, no marked improvement in the product yields was achieved with either the 1-chloroalkanes or the trialkyl phosphates test compounds, regardless of alkyl chain length. The disappointing results have been attributed to lack of substantial net increase in the numbers of zeolite nucleophilic sites accompanying mesopore introduction.

  13. Aggregation kinetics of Eu2+-cation vacancy dipoles in the alkali halides: Dimer versus trimer formation

    NASA Astrophysics Data System (ADS)

    Muoz F., A.; Cabrera B., E.; Riveros R., H.; Patrn, Marco; Rubio O., J.

    1985-06-01

    The aggregation of Eu2+-cation vacancy dipoles in Eu-doped NaCl, KCl, KBr, and RbBr single crystals has been carefully studied by measuring the evolution of dipole concentration as a function of the annealing time at 333, 343, 348, 353, 363, and 373 K using the electron-paramagnetic-resonance technique. The experimentally determined data were analyzed in terms of both pure second- and third-order kinetics equations with back reaction. In order to make the former, the formalism developed by Unger and Perlman was followed. In the other case, the data were analyzed in terms of an analytical solution to the pure third-order kinetics equation with back reaction which is presented in this paper for the first time. It is clearly shown that the experimental data can be fitted with the same accuracy to both the dimerization and trimerization models. In order to get additional information which could help to make a decision between the dimerization and trimerization models, a calculation of the activation energies for both processes was also performed in each of the systems investigated. The values obtained for both processes are quite similar and in the range expected for impurity diffusion in the alkali halides. This result indicates that, even with this knowledge, it is not possible to take any decision about the nature of the complex formed during the initial stage of dipole aggregation. Taking into account all these results, we have also analyzed the only possibility left to determine the order of the reaction involved, i.e., the concentration dependence of the rate constant in the kinetics equation at the very initial stage of aggregation. To do that, a large number of dipole-decay data points were measured at short annealing times after the quenching treatment in order to get a good knowledge of the dipole-decay curve when only a small amount of dipoles had been clustered to form aggregates into the alkali halide matrix. The analysis of the data taken at the earlier stage of aggregation, without assuming any reaction order a priori, indicates unambiguously that this dependence is the one expected for a pure second-order kinetics equation. This result indicates conclusively that dimers are really the complexes which are formed during the very initial stage of the clustering process. With all the experimental evidence presented in this paper, it appears that the long-existing controversy of dimer versus trimer formation in the aggregation kinetics of doubly valent impurity ions in the alkali halides may be definitively solved. It is also inferred that considerable caution must be exercised in using previous works in which dimers have been claimed to be the complexes formed during the initial stage of the aggregation process just by fitting the experimentally determined data to only the pure second-order kinetics equation with back (dissociation) reaction.

  14. Reverse osmosis transport of alkali halides and nickel salts through cellulose triacetate membranes. Performance prediction from NaCl experiments

    SciTech Connect

    Nirmal, J.D.; Pandya, V.P.; Desai, N.V.; Rangarajan, R. )

    1992-10-01

    The separation of alkali metal halides, nickel chloride, and nickel sulfate was determined for cellulose triacetate reverse osmosis (CTA RO) membranes. From transport analysis, the relative free energy parameters for transport of these salts through CTA membranes were determined. From these relative free energy parameters of salts, the solute separation by CTA membranes could be predicted from RO experiment with NaCl solution. The transport analysis and an illustration of how the concept is useful are presented in this paper.

  15. Physics of solid and liquid alkali halide surfaces near the melting point

    NASA Astrophysics Data System (ADS)

    Zykova-Timan, T.; Ceresoli, D.; Tartaglino, U.; Tosatti, E.

    2005-10-01

    This paper presents a broad theoretical and simulation study of the high-temperature behavior of crystalline alkali halide surfaces typified by NaCl(100), of the liquid NaCl surface near freezing, and of the very unusual partial wetting of the solid surface by the melt. Simulations are conducted using two-body rigid-ion Born-Mayer-Huggins-Fumi-Tosi (BMHFT) potentials, with full treatment of long-range Coulomb forces. After a preliminary check of the description of bulk NaCl provided by these potentials, which seems generally good even at the melting point, we carry out a new investigation of solid and liquid surfaces. Solid NaCl(100) is found in this model to be very anharmonic and yet exceptionally stable when hot. It is predicted by a thermodynamic integration calculation of the surface free energy that NaCl(100) should be a well-ordered, nonmelting surface, metastable even well above the melting point. By contrast, the simulated liquid NaCl surface is found to exhibit large thermal fluctuations and no layering order. In spite of that, it is shown to possess a relatively large surface free energy. The latter is traced to a surface entropy deficit, reflecting some kind of surface short-range order. We show that the surface short-range order is most likely caused by the continuous transition of the bulk ionic melt into the vapor, made of NaCl molecules and dimers rather than of single ions. Finally, the solid-liquid interface free energy is derived through Young's equation from direct simulation of partial wetting of NaCl(100) by a liquid droplet. The resulting interface free energy is large, in line with the conspicuous solid-liquid 27% density difference. A partial wetting angle near 50 close to the experimental value of 48 is obtained in the process. It is concluded that three elements, namely, the exceptional anharmonic stability of the solid (100) surface, the molecular short-range order at the liquid surface, and the costly solid-liquid interface, all conspire to cause the anomalously poor wetting of the (100) surface by its own melt in the BMHFT model of NaCland most likely also in real alkali halide surfaces.

  16. Vibrational Relaxation Dynamics of AN Infrared Laser-Excited Molecular Impurity Mode in Alkali Halide Lattices.

    NASA Astrophysics Data System (ADS)

    Moerner, William Esco

    1982-03-01

    The vibrational relaxation dynamics of spherical top ReO(,4)('-) molecules have been investigated under conditions of nonequilibrium laser excitation. Previous studies of relaxation mechanisms for molecular impurity modes in crystalline solids have chiefly utilized the techniques of low-power, linear spectroscopy. In this work, the nonequilibrium techniques of incoherent laser saturation and high resolution hole-burning spectroscopy have been used to measure the relaxation times T(,1) and T(,2) for the inhomogeneously broadened (nu)(,3) internal mode of ReO(,4)('-) as functions of temperature and host lattice. In addition, long-lived non-photochemical holes (with lifetimes greater than 10 minutes at 1.4 K) have been observed, indicating for the first time the presence of ground state optical pumping processes for a high symmetry impurity in a cubic crystal. The CO(,2) laser saturation measurements yielded values for the saturation intensity, I(,s), and hence the T(,1) T(,2) product in various hosts. The hole-burning measurements of T(,2) utilized a CO(,2) laser as a saturating pump and either a Pb salt diode laser or another CO(,2) laser as the tunable probe. Holes as narrow as 10 MHz (FWHM) were observed in inhomogeneously broadened lines extending over a frequency interval of several cm('-1). Above 10K, the dominant dephasing (T(,2)) mechanism is acoustic phonon scattering, while below 10K, T(,2) achieves the fundamental upper limit of 2T(,1) signifying that dephasing is lifetime-limited. Study of the alkali halide dependence of the (nu)(,3) excited state decay rate suggests that a combination of molecular internal modes, local modes of the lattice-impurity complex, and band phonons represents the dominant decay channel, rather than the previously expected multiphonon decay. The discovery of long-lived holes for a spherical top molecule at a cubic substitutional site suggests that the molecular ground state consists of at least two quasi-equivalent orientations, which are coupled only by excitation to the (nu)(,3) mode excited state. These studies of the vibrational relaxation dynamics of the ReO(,4)('-) molecule in alkali halides demonstrate the power of nonequilibrium laser techniques and provide a basis for future investigations of molecular impurity modes in solids.

  17. Stable geometries of the self-trapped exciton in alkali halide crystals

    NASA Astrophysics Data System (ADS)

    Song, K. S.; Baetzold, R. C.; Kong, F.

    1994-06-01

    According to recent works, the self-trapped excitons (STE) in alkali halides are grouped in three different types. In some (e.g. RbI), a population transfer is observed among coexisting types as temperature is raised. In others (NaBr and NaI) extra type emission bands have been observed under dilational strain. We studied the adiabatic potential energy surface (APES) of the STE under the effect of expanded or compressed lattices, and of rotation of the Vk core in several directions, based on both extended-ion and ab initio Hartree-Fock methods. A critical study of the zero field splitting parameter D of the spin Hamiltonian is made in assessing the effect of rotation. It is shown that: (a) the potential barrier separating the adjacent local minima on the APES becomes smaller as the lattice is dilated; (b) the APES associated with rotation of the halogen molecule-ion axis from [110] toward [001], upto about 30°, is flat; Rotations in other directions are stiff, however; (c) the observed anomaly of the D parameter in NaCl is compatible with the rotation described in (b) above. The geometries of the three types are discussed on the basis of this study.

  18. Physics of solid and liquid alkali halide surfaces near the melting point

    NASA Astrophysics Data System (ADS)

    Zykova-Timan, Tatyana; Ceresoli, Davide; Tartaglino, Ugo; Tosatti, Erio

    2006-03-01

    NaCl (and other alkali halide) crystal surfaces have the peculiar property of repelling their own melt. As a result they let themselves be wetted only partially by their own liquid at the melting point TM. We recently investigated the physical reasons for this unusual behavior. We found them through theory and molecular dynamics simulation to stem from the conspiracy of three factors. First, the solid NaCl(100) surface is exceptionally anharmonic,but also exceptionally stable. It can in fact survive even well above the melting point, for unlike most other surfaces it does not spontaneously melt. Second, the solid-liquid interface is very costly, due to a 27% density difference between solid and liquid. Third, the surface tension of liquid NaCl is relatively high. This last feature is due to an unexpected entropy deficit, that can in turn be traced to incipient molecular charge order in the outermost regions of the molten salt surface[1,2].[1] T. Zykova-Timan, D. Ceresoli, U. Tartaglino, E. Tosatti, Phys. Rev. Lett. 94, 176105 (2005) [2] T. Zykova-Timan, D. Ceresoli, U. Tartaglino, E. Tosatti, J. Chem. Phys. 123, 164701 (2005)

  19. Angular dependence of static and kinetic friction on alkali halide surfaces

    NASA Astrophysics Data System (ADS)

    Steiner, Pascal; Roth, Raphael; Gnecco, Enrico; Baratoff, Alexis; Meyer, Ernst

    2010-11-01

    The angular dependence of the lateral forces acting on an atomically sharp tip slowly pulled by an elastic spring along a crystal surface with square symmetry is investigated in the framework of a separable two-dimensional tip-surface interaction potential. In the stick-slip regime kinetic friction is proportional to (cos?+|sin?|) , ? being the angle between the scan direction and a particular symmetry axis. For a high enough normal force, static friction is proportional to 1/cos? , whereas for intermediate loads it shows a ? -dependent spread of possible values. Continuous sliding with ultralow friction sets in below a load-dependent corrugation amplitude. Numerical simulations help interpret those analytic results in terms of the zigzag motion of a friction force microscope tip sliding on the (001) surface of a rocksalt crystal. The influence of the offset between the start of a scan and the center of the corresponding unit cell, in particular, for scans along ?100? directions is also elucidated. The predicted ratio of kinetic friction along the ?100? and ?110? directions agrees best with values measured on alkali halides with similar cation and anion radii. This ratio, as well as the angular dependence of the static friction may be used to determine fine details of the lateral tip-sample interaction.

  20. Silicon halide-alkali metal flames as a source of solar grade silicon

    NASA Technical Reports Server (NTRS)

    Olson, D. B.; Miller, W. J.; Gould, R. K.

    1980-01-01

    The feasibility of using continuous high-temperature reactions of alkali metals and silicon halides to produce silicon in large quantities and of suitable purity for use in the production of photovoltaic solar cells was demonstrated. Low pressure experiments were performed demonstrating the production of free silicon and providing experience with the construction of reactant vapor generators. Further experiments at higher reagent flow rates were performed in a low temperature flow tube configuration with co-axial injection of reagents and relatively pure silicon was produced. A high temperature graphite flow tube was built and continuous separation of Si from NaCl was demonstrated. A larger scaled well stirred reactor was built. Experiments were performed to investigate the compatability of graphite based reactor materials of construction with sodium. At 1100 to 1200 K none of these materials were found to be suitable. At 1700 K the graphites performed well with little damage except to coatings of pyrolytic graphite and silicon carbide which were damaged.

  1. Performance of a multi-anode photomultiplier employing an ultra bi-alkali photo-cathode and rugged dynodes

    NASA Astrophysics Data System (ADS)

    Toizumi, T.; Inagawa, S.; Nakamori, T.; Kataoka, J.; Tsubuku, Y.; Yatsu, Y.; Shimokawabe, T.; Kawai, N.; Okada, T.; Ohtsu, I.

    2009-06-01

    We report on the performance testing of a multi-anode photomultiplier (MAPMT), the R8900-200-M16MOD-UBA, newly developed by Hamamatsu Photonics K.K. Although the R8900 series offers the great advantage of a highly sensitive surface ( ?80% of physical area), the quantum efficiency (Q.E.) was relatively low (at up to 20%). This paper describes two substantial changes we have made to the R8900-200-M16MOD-UBA: (1) improving the Q.E. to the 40% level by employing an ultra bi-alkali (UBA) photo-cathode and (2) constructing a rugged dynode that can withstand vibration for future use in space. We measured each pixel signal at the single photoelectron level and the signals of scintillation photons by using a 16-pixel plastic scintillator array. Thanks to high Q.E., good energy resolution of 29.9% (FWHM) was obtained for 59.5 keV ?-rays. We also demonstrated tolerance to vibration up to 17 Grms in possible launching vehicles.

  2. Alkali halide solutions under thermal gradients: soret coefficients and heat transfer mechanisms.

    PubMed

    Rmer, Frank; Wang, Zilin; Wiegand, Simone; Bresme, Fernando

    2013-07-11

    We report an extensive analysis of the non-equilibrium response of alkali halide aqueous solutions (Na(+)/K(+)-Cl(-)) to thermal gradients using state of the art non-equilibrium molecular dynamics simulations and thermal diffusion forced Rayleigh scattering experiments. The coupling between the thermal gradient and the resulting ionic salt mass flux is quantified through the Soret coefficient. We find the Soret coefficient is of the order of 10(-3) K(-1) for a wide range of concentrations. These relatively simple solutions feature a very rich behavior. The Soret coefficient decreases with concentration at high temperatures (higher than T ? 315 K), whereas it increases at lower temperatures. In agreement with previous experiments, we find evidence for sign inversion in the Soret coefficient of NaCl and KCl solutions. We use an atomistic non-equilibrium molecular dynamics approach to compute the Soret coefficients in a wide range of conditions and to attain further microscopic insight on the heat transport mechanism and the behavior of the Soret coefficient in aqueous solutions. The models employed in this work reproduce the magnitude of the Soret coefficient, and the general dependence of this coefficient with temperature and salt concentration. We use the computer simulations as a microscopic approach to establish a correlation between the sign and magnitude of the Soret coefficients and ionic solvation and hydrogen bond structure of the solutions. Finally, we report an analysis of heat transport in ionic solution by quantifying the solution thermal conductivity as a function of concentration. The simulations accurately reproduce the decrease of the thermal conductivity with increasing salt concentration that is observed in experiments. An explanation of this behavior is provided. PMID:23758489

  3. Optical properties of alkali halide crystals from all-electron hybrid TD-DFT calculations

    SciTech Connect

    Webster, R. Harrison, N. M.; Bernasconi, L.

    2015-06-07

    We present a study of the electronic and optical properties of a series of alkali halide crystals AX, with A = Li, Na, K, Rb and X = F, Cl, Br based on a recent implementation of hybrid-exchange time-dependent density functional theory (TD-DFT) (TD-B3LYP) in the all-electron Gaussian basis set code CRYSTAL. We examine, in particular, the impact of basis set size and quality on the prediction of the optical gap and exciton binding energy. The formation of bound excitons by photoexcitation is observed in all the studied systems and this is shown to be correlated to specific features of the Hartree-Fock exchange component of the TD-DFT response kernel. All computed optical gaps and exciton binding energies are however markedly below estimated experimental and, where available, 2-particle Green’s function (GW-Bethe-Salpeter equation, GW-BSE) values. We attribute this reduced exciton binding to the incorrect asymptotics of the B3LYP exchange correlation ground state functional and of the TD-B3LYP response kernel, which lead to a large underestimation of the Coulomb interaction between the excited electron and hole wavefunctions. Considering LiF as an example, we correlate the asymptotic behaviour of the TD-B3LYP kernel to the fraction of Fock exchange admixed in the ground state functional c{sub HF} and show that there exists one value of c{sub HF} (∼0.32) that reproduces at least semi-quantitatively the optical gap of this material.

  4. Simple electrolyte solutions: Comparison of DRISM and molecular dynamics results for alkali halide solutions

    PubMed Central

    Joung, In Suk; Luchko, Tyler; Case, David A.

    2013-01-01

    Using the dielectrically consistent reference interaction site model (DRISM) of molecular solvation, we have calculated structural and thermodynamic information of alkali-halide salts in aqueous solution, as a function of salt concentration. The impact of varying the closure relation used with DRISM is investigated using the partial series expansion of order-n (PSE-n) family of closures, which includes the commonly used hypernetted-chain equation (HNC) and Kovalenko-Hirata closures. Results are compared to explicit molecular dynamics (MD) simulations, using the same force fields, and to experiment. The mean activity coefficients of ions predicted by DRISM agree well with experimental values at concentrations below 0.5 m, especially when using the HNC closure. As individual ion activities (and the corresponding solvation free energies) are not known from experiment, only DRISM and MD results are directly compared and found to have reasonably good agreement. The activity of water directly estimated from DRISM is nearly consistent with values derived from the DRISM ion activities and the Gibbs-Duhem equation, but the changes in the computed pressure as a function of salt concentration dominate these comparisons. Good agreement with experiment is obtained if these pressure changes are ignored. Radial distribution functions of NaCl solution at three concentrations were compared between DRISM and MD simulations. DRISM shows comparable water distribution around the cation, but water structures around the anion deviate from the MD results; this may also be related to the high pressure of the system. Despite some problems, DRISM-PSE-n is an effective tool for investigating thermodynamic properties of simple electrolytes. PMID:23387564

  5. Crystal lattice properties fully determine short-range interaction parameters for alkali and halide ions

    NASA Astrophysics Data System (ADS)

    Mao, Albert H.; Pappu, Rohit V.

    2012-08-01

    Accurate models of alkali and halide ions in aqueous solution are necessary for computer simulations of a broad variety of systems. Previous efforts to develop ion force fields have generally focused on reproducing experimental measurements of aqueous solution properties such as hydration free energies and ion-water distribution functions. This dependency limits transferability of the resulting parameters because of the variety and known limitations of water models. We present a solvent-independent approach to calibrating ion parameters based exclusively on crystal lattice properties. Our procedure relies on minimization of lattice sums to calculate lattice energies and interionic distances instead of equilibrium ensemble simulations of dense fluids. The gain in computational efficiency enables simultaneous optimization of all parameters for Li+, Na+, K+, Rb+, Cs+, F-, Cl-, Br-, and I- subject to constraints that enforce consistency with periodic table trends. We demonstrate the method by presenting lattice-derived parameters for the primitive model and the Lennard-Jones model with Lorentz-Berthelot mixing rules. The resulting parameters successfully reproduce the lattice properties used to derive them and are free from the influence of any water model. To assess the transferability of the Lennard-Jones parameters to aqueous systems, we used them to estimate hydration free energies and found that the results were in quantitative agreement with experimentally measured values. These lattice-derived parameters are applicable in simulations where coupling of ion parameters to a particular solvent model is undesirable. The simplicity and low computational demands of the calibration procedure make it suitable for parametrization of crystallizable ions in a variety of force fields.

  6. Empirically derived formula for the energies of the first ultraviolet absorption maxima of 20 alkali-halide crystals

    NASA Astrophysics Data System (ADS)

    Woodruff, Truman O.

    1983-04-01

    Hilsch and Pohl noted long ago (1928-1930) that the energy of the first ultraviolet absorption maximum in an alkali halide crystal is well approximated by the energy required to transfer an electron from the halide ion to the alkali ion. However, they did not justify their way of including the contribution of the Madelung term to this energy. A more consistent treatment of the Madelung energy by Wolf and Herzfeld led to a modified form of the Hilsch-Pohl expression which, unfortunately, agreed less well with experiment. In the present work, the electron-transfer model was retained, but a more complete analysis led to a simple formula which is in excellent agreement with most of the present experimental data. That analysis, involving theoretical as well as empirical considerations, is presented here together with a detailed quantitative discussion of ways to choose the single adjustable constant determining the two parameters entering the formula. Two such choices were considered; the results of applying each to the twenty alkali halide crystals which can be made from Li, Na, K, Rb, Cs as cations and F, Cl, Br, I as anions are tabulated. With the more successful of the two methods, the data for six of the crystals are reproduced by the formula with an accuracy of one millihartree (0.037 eV) or better; for eleven of the other crystals, to within less than 0.4 eV. For the remaining three (NaF, CsCl and CsI), the error is less than 0.6 eV. The second of the two methods for adjusting the single constant led to a reasonable fit in all 20 cases (f.c.c. and s.c.).

  7. Infrared Vibrational Fluorescence and Persistent Spectral Hole Burning from Negatively Charged Cyanogen Molecules in Alkali Halides.

    NASA Astrophysics Data System (ADS)

    Spitzer, Ronnie Claudette

    1988-12-01

    The union of IR semiconductor diode laser and Fourier transform interferometric methods has produced two new spectroscopic probes for investigating the dynamics of matrix isolated molecules: vibrational fluorescence and persistent spectral hole burning. In this thesis, we investigate a single system, CN^- doped ionic crystals, with both low power techniques. High resolution measurements of the IR vibrational fluorescence from CN^- molecules matrix isolated in alkali halide hosts at low temperatures reveal an up-the-ladder cascade of remarkable range. The CN^- fundamental absorption line is pumped with a CW tunable diode laser near 5 ?m and the vibrational fluorescence analyzed with the high resolution (0.04 cm^{ -1}) interferometer. We find high-lying vibrational levels of CN^- (up to v = 16) are populated at 1.7 K by an electric dipole mediated V-V energy transfer process. At our high resolution, new aspects of the system emerge. Emission features from defect centers composed of a CN^- molecule associated with another nearby impurity ion dominate the spectrum at high CN^- concentrations. The most important center is the CN^- pair defect. At elevated temperatures population of the CN^- pair defect vibrational levels in the ground electronic state have been observed at ultraviolet energies for all hosts. Our results show that energy preferentially accumulates at the pair defect because one member of the pair is always in the ground state ready to accept an excitation from a neighboring center. By using the diode laser as a high brightness probe, a new photophysical hole burning mechanism has been identified. Persistent spectral holes form during laser excitation of the Na^+:CN ^- defect's vibrational mode, when the CN ^- molecule occasionally reorients by 180^circ to an inequivalent lattice orientation generated by the nearby Na ^+ ion. A lattice barrier to reorientation blocks relaxation back to the original ground state at low temperatures. By combining persistent spectral hole burning with broadband FT spectroscopy, the CN ^- dynamics are identified. A solid state linear vibrational Stark effect, observed here for the first time, probes the local lattice configuration.

  8. Low-Energy Grazing Ion-Scattering From Alkali-Halide Surfaces: A Novel Approach To C-14 Detection

    NASA Astrophysics Data System (ADS)

    Meyer, F. W.; Galutschek, E.; Hotchkis, M.

    2009-03-01

    Carbon-14 labeled compounds are widely used in the pharmaceutical industry, e.g., as tracers to determine the fate of these compounds in vivo. Conventional accelerator mass spectrometry (AMS) is one approach that offers sufficiently high sensitivity to avoid radiological waste and contamination issues in such studies, but requires large, expensive facilities that are usually not solely dedicated to this task. At the ORNL Multicharged Ion Research Facility (MIRF) we are exploring a small size, low cost alternative to AMS for biomedical 14C tracer studies that utilizes ECR-ion-source-generated keV-energy-range multicharged C beams grazingly incident on an alkali halide target, where efficient negative ion production by multiple electron capture takes place. By using C ion charge states of +3 or higher, the molecular isobar interference at mass 14, e.g. 12CH2 and 13CH, is eliminated. The negatively charged ions in the beam scattered from the alkali halide surface are separated from other scattered charge states by two large acceptance (15 msr) stages of electrostatic analysis. The N-14 isobar interference is thus removed, since N does not support a stable negative ion. Initial results for C-14 detection obtained using C-14 enriched CO2 from ANSTO will be described.

  9. Low-Energy Grazing Ion-Scattering from Alkali-Halide Surfaces: A Novel Approach to C-14 Detection

    SciTech Connect

    Meyer, Fred W; Galutschek, Ernst; Hotchkis, Michael

    2009-01-01

    Carbon-14 labeled compounds are widely used in the pharmaceutical industry, e.g., as tracers to determine the fate of these compounds in vivo. Conventional accelerator mass spectrometry (AMS) is one approach that offers sufficiently high sensitivity to avoid radiological waste and contamination issues in such studies, but requires large, expensive facilities that are usually not solely dedicated to this task. At the ORNL Multicharged Ion Research Facility (MIRF) we are exploring a small size, low cost alternative to AMS for biomedical 14C tracer studies that utilizes ECR-ion-source-generated keV-energy-range multicharged C beams grazingly incident on an alkali halide target, where efficient negative ion production by multiple electron capture takes place. By using C ion charge states of +3 or higher, the molecular isobar interference at mass 14, e.g. 12CH2 and 13CH, is eliminated. The negatively charged ions in the beam scattered from the alkali halide surface are separated from other scattered charge states by two large acceptance ({approx}15 msr) stages of electrostatic analysis. The N-14 isobar interference is thus removed, since N does not support a stable negative ion. Initial results for C-14 detection obtained using C-14 enriched CO2 from ANSTO will be described.

  10. Low-Energy Grazing Ion-Scattering From Alkali-Halide Surfaces: A Novel Approach To C-14 Detection

    SciTech Connect

    Meyer, F. W.; Galutschek, E.; Hotchkis, M.

    2009-03-10

    Carbon-14 labeled compounds are widely used in the pharmaceutical industry, e.g., as tracers to determine the fate of these compounds in vivo. Conventional accelerator mass spectrometry (AMS) is one approach that offers sufficiently high sensitivity to avoid radiological waste and contamination issues in such studies, but requires large, expensive facilities that are usually not solely dedicated to this task. At the ORNL Multicharged Ion Research Facility (MIRF) we are exploring a small size, low cost alternative to AMS for biomedical {sup 14}C tracer studies that utilizes ECR-ion-source-generated keV-energy-range multicharged C beams grazingly incident on an alkali halide target, where efficient negative ion production by multiple electron capture takes place. By using C ion charge states of +3 or higher, the molecular isobar interference at mass 14, e.g. {sup 12}CH{sub 2} and {sup 13}CH, is eliminated. The negatively charged ions in the beam scattered from the alkali halide surface are separated from other scattered charge states by two large acceptance ({approx}15 msr) stages of electrostatic analysis. The N-14 isobar interference is thus removed, since N does not support a stable negative ion. Initial results for C-14 detection obtained using C-14 enriched CO{sub 2} from ANSTO will be described.

  11. Development of processes for the production of solar grade silicon from halides and alkali metals, phase 1 and phase 2

    NASA Technical Reports Server (NTRS)

    Dickson, C. R.; Gould, R. K.; Felder, W.

    1981-01-01

    High temperature reactions of silicon halides with alkali metals for the production of solar grade silicon are described. Product separation and collection processes were evaluated, measure heat release parameters for scaling purposes and effects of reactants and/or products on materials of reactor construction were determined, and preliminary engineering and economic analysis of a scaled up process were made. The feasibility of the basic process to make and collect silicon was demonstrated. The jet impaction/separation process was demonstrated to be a purification process. The rate at which gas phase species from silicon particle precursors, the time required for silane decomposition to produce particles, and the competing rate of growth of silicon seed particles injected into a decomposing silane environment were determined. The extent of silane decomposition as a function of residence time, temperature, and pressure was measured by infrared absorption spectroscopy. A simplistic model is presented to explain the growth of silicon in a decomposing silane enviroment.

  12. Sensitivity of alkali halide scintillating calorimeters with particle identification to investigate the DAMA dark matter detection claim

    NASA Astrophysics Data System (ADS)

    Nadeau, P.; Clark, M.; Di Stefano, P. C. F.; Lanfranchi, J.-C.; Roth, S.; von Sivers, M.; Yavin, I.

    2015-07-01

    Scintillating calorimeters are cryogenic detectors combining a measurement of scintillation with one of phonons to provide particle identification. In view of developing alkali halide devices of this type able to check the DAMA/LIBRA claim for the observation of dark matter, we have simulated detector performances to determine their sensitivity by two methods with little model-dependence. We conclude that if performance of the phonon channel can be brought in line with those of other materials, an exposure of 10 kg-days would suffice to check the DAMA/LIBRA claim in standard astrophysical scenarios. Additionally, a fairly modest array of 5 kg with background rejection would be able to directly check the DAMA/LIBRA modulation result in 2 years.

  13. Boosting the photocurrent density of p-type solar cells based on organometal halide perovskite-sensitized mesoporous NiO photocathodes.

    PubMed

    Wang, Huan; Zeng, Xianwei; Huang, Zhanfeng; Zhang, Wenjun; Qiao, Xianfeng; Hu, Bin; Zou, Xiaoping; Wang, Mingkui; Cheng, Yi-Bing; Chen, Wei

    2014-08-13

    The p-n tandem design of a sensitized solar cell is a novel concept holding the potential to overcome the efficiency limitation of conventional single-junction sensitized solar cells. Significant improvement of the photocurrent density (Jsc) of the p-type half-cell is a prerequisite for the realization of a highly efficient p-n tandem cell in the future. This study has demonstrated effective photocathodes based on novel organometal halide perovskite-sensitized mesoporous NiO in liquid-electrolyte-based p-type solar cells. An acceptably high Jsc up to 9.47 mA cm(-2) and efficiency up to 0.71% have been achieved on the basis of the CH3NH3PbI3/NiO solar cell at 100 mW cm(-2) light intensity, which are significantly higher than those of any previously reported liquid-electrolyte-based p-type solar cells based on sensitizers of organic dyes or inorganic quantum dots. The dense blocking layer made by spray pyrolysis of nickel acetylacetonate holds the key to determining the current flow direction of the solar cells. High hole injection efficiency at the perovskite/NiO interface and high hole collection efficiency through the mesoporous NiO network have been proved by time-resolved photoluminescence and transient photocurrent/photovoltage decay measurements. The limitation of these p-type solar cells primarily rests with the adverse light absorption by the NiO mesoporous film; the secondary limitation arises from the highly viscous ethyl acetate-based electrolyte, which is helpful for the solar cell stability but hinders fluent diffusion into the pore channels, giving rise to a nonlinear dependence of Jsc on the light intensity. PMID:24972278

  14. EPR study of electron bombarded alkali- and alkaline-earth halide crystal surfaces

    NASA Technical Reports Server (NTRS)

    Fryburg, G. C.; Lad, R. A.

    1975-01-01

    An EPR study of electron bombarded LiF, NaCl, KCl, CaF2 and BaF2 polycrystalline surfaces has shown that small metal particles are formed on the surfaces of the crystals. Identification was made from CESR signals. The symmetric line-shape of the signals, even at 77 K, indicated that the particles were less than 0.5 micron in diameter. Signals due to F centers were observed in LiF but not in the other halides. Implications to metal deposition are considered.

  15. Lattice model calculation of elastic and thermodynamic properties at high pressure and temperature. [for alkali halides in NaCl lattice

    NASA Technical Reports Server (NTRS)

    Demarest, H. H., Jr.

    1972-01-01

    The elastic constants and the entire frequency spectrum were calculated up to high pressure for the alkali halides in the NaCl lattice, based on an assumed functional form of the inter-atomic potential. The quasiharmonic approximation is used to calculate the vibrational contribution to the pressure and the elastic constants at arbitrary temperature. By explicitly accounting for the effect of thermal and zero point motion, the adjustable parameters in the potential are determined to a high degree of accuracy from the elastic constants and their pressure derivatives measured at zero pressure. The calculated Gruneisen parameter, the elastic constants and their pressure derivatives are in good agreement with experimental results up to about 600 K. The model predicts that for some alkali halides the Grunesen parameter may decrease monotonically with pressure, while for others it may increase with pressure, after an initial decrease.

  16. An Investigation of Ion-Pairing of Alkali Metal Halides in Aqueous Solutions Using the Electrical Conductivity and the Monte Carlo Computer Simulation Methods

    PubMed Central

    Gujt, Jure; Bešter-Rogač, Marija; Hribar-Lee, Barbara

    2013-01-01

    The ion pairing is, in very dilute aqueous solutions, of rather small importance for solutions’ properties, which renders its precise quantification quite a laborious task. Here we studied the ion pairing of alkali halides in water by using the precise electric conductivity measurements in dilute solutions, and in a wide temperature range. The low-concentration chemical model was used to analyze the results, and to estimate the association constant of different alkali halide salts. It has been shown that the association constant is related to the solubility of salts in water and produces a ’volcano relationship’, when plotted against the difference between the free energy of hydration of the corresponding individual ions. The computer simulation, using the simple MB+dipole water model, were used to interprete the results, to find a microscopic basis for Collins’ law of matching water affinities. PMID:24526801

  17. Universal scaling of potential energy functions describing intermolecular interactions. II. The halide-water and alkali metal-water interactions

    SciTech Connect

    Werhahn, Jasper C.; Akase, Dai; Xantheas, Sotiris S.

    2014-08-14

    The scaled forms of the newly introduced generalized potential energy functions (PEFs) describing intermolecular interactions [J. Chem. Phys. xx, yyyyy (2011)] have been used to fit the ab-initio minimum energy paths (MEPs) for the halide- and alkali metal-water systems X-(H2O), X=F, Cl, Br, I, and M+(H2O), M=Li, Na, K, Rb, Cs. These generalized forms produce fits to the ab-initio data that are between one and two orders of magnitude better in the χ2 than the original forms of the PEFs. They were found to describe both the long-range, minimum and repulsive wall of the potential energy surface quite well. Overall the 4-parameter extended Morse (eM) and generalized Buckingham exponential-6 (gB-e6) potentials were found to best fit the ab-initio data. Furthermore, a single set of parameters of the reduced form was found to describe all candidates within each class of interactions. The fact that in reduced coordinates a whole class of interactions can be represented by a single PEF, yields the simple relationship between the molecular parameters associated with energy (well depth, ε), structure (equilibrium distance, rm) and spectroscopy (anharmonic frequency, ν):€ν = A⋅ (ε /μ)1/ 2 /rm + B⋅ε /rm 3 , where A and B are constants depending on the underlying PEF. This more general case of Badger’s rule has been validated using the experimentally measured frequencies of the hydrogen bonded OH stretching vibrations in the halide-water series.

  18. Ca-Fe and Alkali-Halide Alteration of an Allende Type B CAI: Aqueous Alteration in Nebular or Asteroidal Settings

    NASA Technical Reports Server (NTRS)

    Ross, D. K.; Simon, J. I.; Simon, S. B.; Grossman, L.

    2012-01-01

    Ca-Fe and alkali-halide alteration of CAIs is often attributed to aqueous alteration by fluids circulating on asteroidal parent bodies after the various chondritic components have been assembled, although debate continues about the roles of asteroidal vs. nebular modification processes [1-7]. Here we report de-tailed observations of alteration products in a large Type B2 CAI, TS4 from Allende, one of the oxidized subgroup of CV3s, and propose a speculative model for aqueous alteration of CAIs in a nebular setting. Ca-Fe alteration in this CAI consists predominantly of end-member hedenbergite, end-member andradite, and compositionally variable, magnesian high-Ca pyroxene. These phases are strongly concentrated in an unusual "nodule" enclosed within the interior of the CAI (Fig. 1). The Ca, Fe-rich nodule superficially resembles a clast that pre-dated and was engulfed by the CAI, but closer inspection shows that relic spinel grains are enclosed in the nodule, and corroded CAI primary phases interfinger with the Fe-rich phases at the nodule s margins. This CAI also contains abundant sodalite and nepheline (alkali-halide) alteration that occurs around the rims of the CAI, but also penetrates more deeply into the CAI. The two types of alteration (Ca-Fe and alkali-halide) are adjacent, and very fine-grained Fe-rich phases are associated with sodalite-rich regions. Both types of alteration appear to be replacive; if that is true, it would require substantial introduction of Fe, and transport of elements (Ti, Al and Mg) out of the nodule, and introduction of Na and Cl into alkali-halide rich zones. Parts of the CAI have been extensively metasomatized.

  19. Thermodynamics of small alkali metal halide cluster ions: comparison of classical molecular simulations with experiment and quantum chemistry.

    PubMed

    Vlcek, Lukas; Uhlik, Filip; Moucka, Filip; Nezbeda, Ivo; Chialvo, Ariel A

    2015-01-22

    We evaluate the ability of selected classical molecular models to describe the thermodynamic and structural aspects of gas-phase hydration of alkali metal halide ions and the formation of small water clusters. To understand the effect of many-body interactions (polarization) and charge penetration effects on the accuracy of a force field, we perform Monte Carlo simulations with three rigid water models using different functional forms to account for these effects: (i) point charge nonpolarizable SPC/E, (ii) Drude point charge polarizable SWM4-DP, and (iii) Drude Gaussian charge polarizable BK3. Model predictions are compared with experimental Gibbs free energies and enthalpies of ion hydration, and with microscopic structural properties obtained from quantum DFT calculations. We find that all three models provide comparable predictions for pure water clusters and cation hydration but differ significantly in their description of anion hydration. None of the investigated classical force fields can consistently and quantitatively reproduce the experimental gas-phase hydration thermodynamics. The outcome of this study highlights the relation between the functional form that describes the effective intermolecular interactions and the accuracy of the resulting ion hydration properties. PMID:25513841

  20. N ,N'-dimethylperylene-3,4,9,10-bis(dicarboximide) on alkali halide (001) surfaces

    NASA Astrophysics Data System (ADS)

    Fendrich, Markus; Lange, Manfred; Weiss, Christian; Kunstmann, Tobias; Mller, Rolf

    2009-05-01

    The growth of N ,N'-dimethylperylene-3,4,9,10-bis(dicarboximide) (DiMe-PTCDI) on KBr(001) and NaCl(001) surfaces has been studied. Experimental results have been achieved using frequency modulation atomic force microscopy at room temperature under ultrahigh vacuum conditions. On both substrates, DiMe-PTCDI forms molecular wires with a width of 10nm, typically, and a length of up to 600nm at low coverages. All wires grow along either the [110] direction (or [110] direction, respectively) of the alkali halide (001) substrates. There is no wetting layer of molecules: atomic resolution of the substrates can be achieved between the wires. The wires are mobile on KBr but substantially more stable on NaCl. A p(22) superstructure in a brickwall arrangement on the ionic crystal surfaces is proposed based on electrostatic considerations. Calculations and Monte Carlo simulations using empirical potentials reveal possible growth mechanisms for molecules within the first layer for both substrates, also showing a significantly higher binding energy for NaCl(001). For KBr, the p(22) superstructure is confirmed by the simulations; for NaCl, a less dense, incommensurate superstructure is predicted.

  1. Interaction of wide band gap single crystals with 248 nm excimer laser radiation. XII. The emission of negative atomic ions from alkali halides

    SciTech Connect

    Kimura, Kenichi; Langford, S. C.; Dickinson, J. T.

    2007-12-01

    Many wide band gap materials yield charged and neutral emissions when exposed to sub-band-gap laser radiation at power densities below the threshold for optical breakdown and plume formation. In this work, we report the observation of negative alkali ions from several alkali halides under comparable conditions. We observe no evidence for negative halogen ions, in spite of the high electron affinities of the halogens. Significantly, the positive and negative alkali ions show a high degree of spatial and temporal overlap. A detailed study of all the relevant particle emissions from potassium chloride (KCl) suggests that K{sup -} is formed by the sequential attachment of two electrons to K{sup +}.

  2. Thermal diffusivity of alkali and silver halide crystals as a function of temperature

    NASA Astrophysics Data System (ADS)

    Yu, Xueyang; Hofmeister, Anne M.

    2011-02-01

    The phonon component of thermal diffusivity (D) for ten synthetic single-crystals (LiF, NaCl, NaI, NaI:Tl, KCl, KBr, CsI, CsI:Tl, AgCl, and AgBr) with the B1 and B2 structures was measured from ambient temperature (T) up to 1093 K using contact-free, laser-flash analysis, from which effects of ballistic radiative transfer were removed. We investigated optical flats from different manufacturers as well as pellets made from compressed powders of most of the above chemical compositions plus LiI, NaBr, KI, RbCl, RbBr, RbI, CsCl, CsBr, and AgI. Impurities were characterized using various spectroscopic methods. With increasing T ,D decreases such that near melting the derivatives ?D/?T are low, -0.00060.0004 mm2 s-1 K-1. Our results are 16% lower than D298 previously obtained with contact methods, which are elevated by ballistic radiative transfer for these infrared (IR) windows, and are well described by either D-1 following a low order polynomial in T, or by D-1?T+n, where n ranges from 1.0294 to 1.9429. Inverse correlations were found between D298 and both density and thermal expansivity (?). Primitive lattice constant times compressional velocity correlates directly with D but changes much more slowly with temperature. Instead, D(T ) is proportional to (T?L)-1 from 0 K up to the limit of measurements, in accord with these physical properties being anharmonic. On average, the damped harmonic oscillator-phonon gas model reproduces D298 based on two physical properties: compressional velocity and the damping coefficient (? ) from analysis of IR reflectivity data. Given large uncertainties in ?(T ), D-1(T) is reproduced for LiF, NaCl, MgO, and the silver halides, for which IR reflectivity data are available. Our correlations show that optical phonons largely govern heat transport of insulators, and permit prediction of D and thus thermal conductivity for simple, diatomic solids.

  3. Evidence for New Excess Electron Localization Sites in Na{sub {ital n}}F{sub {ital n}{minus}1 } Alkali-Halide Clusters

    SciTech Connect

    Durand, G.; Spiegelmann, F.; Labastie, P.; LHermite, J.; Poncharal, P.

    1997-07-01

    This Letter examines new types of localization sites for an excess electron in finite alkali-halide clusters resulting from defects on cuboidal structures, namely {open_quotes}edge states,{close_quotes} R center, and other surface defects. We present theoretical calculations on Na{sub n}F {sub n{minus}1} clusters with one excess electron. Comparisons with experimental results are presented for different cluster sizes (n=17 , 23, 28, and 29). Structures with edge or surface defects are relevant for n=23 , 28, and 29. {copyright} {ital 1997} {ital The American Physical Society}

  4. Temperature-dependent solubilities and mean ionic activity coefficients of alkali halides in water from molecular dynamics simulations

    NASA Astrophysics Data System (ADS)

    Mester, Zoltan; Panagiotopoulos, Athanassios Z.

    2015-07-01

    The mean ionic activity coefficients of aqueous KCl, NaF, NaI, and NaCl solutions of varying concentrations have been obtained from molecular dynamics simulations following a recently developed methodology based on gradual insertions of salt molecules [Z. Mester and A. Z. Panagiotopoulos, J. Chem. Phys. 142, 044507 (2015)]. The non-polarizable ion models of Weerasinghe and Smith [J. Chem. Phys. 119, 11342 (2003)], Gee et al. [J. Chem. Theory Comput. 7, 1369 (2011)], Reiser et al. [J. Chem. Phys. 140, 044504 (2014)], and Joung and Cheatham [J. Phys. Chem. B 112, 9020 (2008)] were used along with the extended simple point charge (SPC/E) water model [Berendsen et al., J. Phys. Chem. 91, 6269 (1987)] in the simulations. In addition to the chemical potentials in solution used to obtain the activity coefficients, we also calculated the chemical potentials of salt crystals and used them to obtain the solubility of these alkali halide models in SPC/E water. The models of Weerasinghe and Smith [J. Chem. Phys. 119, 11342 (2003)] and Gee et al. [J. Chem. Theory Comput. 7, 1369 (2011)] provide excellent predictions of the mean ionic activity coefficients at 298.15 K and 1 bar, but significantly underpredict or overpredict the solubilities. The other two models generally predicted the mean ionic activity coefficients only qualitatively. With the exception of NaF for which the solubility is significantly overpredicted, the model of Joung and Cheatham predicts salt solubilities that are approximately 40%-60% of the experimental values. The models of Reiser et al. [J. Chem. Phys. 140, 044504 (2014)] make good predictions for the NaCl and NaI solubilities, but significantly underpredict the solubilities for KCl and NaF. We also tested the transferability of the models to temperatures much higher than were used to parametrize them by performing simulations for NaCl at 373.15 K and 1 bar, and at 473.15 K and 15.5 bar. All models overpredict the drop in the values of mean ionic activity coefficients with increased temperature seen in experiments. The present results, together with earlier calculations for a number of models for NaCl aqueous solutions at 298.15 K, point to the strong need for development of improved intermolecular potential models for classical simulations of electrolyte solutions.

  5. Temperature-dependent solubilities and mean ionic activity coefficients of alkali halides in water from molecular dynamics simulations.

    PubMed

    Mester, Zoltan; Panagiotopoulos, Athanassios Z

    2015-07-28

    The mean ionic activity coefficients of aqueous KCl, NaF, NaI, and NaCl solutions of varying concentrations have been obtained from molecular dynamics simulations following a recently developed methodology based on gradual insertions of salt molecules [Z. Mester and A. Z. Panagiotopoulos, J. Chem. Phys. 142, 044507 (2015)]. The non-polarizable ion models of Weerasinghe and Smith [J. Chem. Phys. 119, 11342 (2003)], Gee et al. [J. Chem. Theory Comput. 7, 1369 (2011)], Reiser et al. [J. Chem. Phys. 140, 044504 (2014)], and Joung and Cheatham [J. Phys. Chem. B 112, 9020 (2008)] were used along with the extended simple point charge (SPC/E) water model [Berendsen et al., J. Phys. Chem. 91, 6269 (1987)] in the simulations. In addition to the chemical potentials in solution used to obtain the activity coefficients, we also calculated the chemical potentials of salt crystals and used them to obtain the solubility of these alkali halide models in SPC/E water. The models of Weerasinghe and Smith [J. Chem. Phys. 119, 11342 (2003)] and Gee et al. [J. Chem. Theory Comput. 7, 1369 (2011)] provide excellent predictions of the mean ionic activity coefficients at 298.15 K and 1 bar, but significantly underpredict or overpredict the solubilities. The other two models generally predicted the mean ionic activity coefficients only qualitatively. With the exception of NaF for which the solubility is significantly overpredicted, the model of Joung and Cheatham predicts salt solubilities that are approximately 40%-60% of the experimental values. The models of Reiser et al. [J. Chem. Phys. 140, 044504 (2014)] make good predictions for the NaCl and NaI solubilities, but significantly underpredict the solubilities for KCl and NaF. We also tested the transferability of the models to temperatures much higher than were used to parametrize them by performing simulations for NaCl at 373.15 K and 1 bar, and at 473.15 K and 15.5 bar. All models overpredict the drop in the values of mean ionic activity coefficients with increased temperature seen in experiments. The present results, together with earlier calculations for a number of models for NaCl aqueous solutions at 298.15 K, point to the strong need for development of improved intermolecular potential models for classical simulations of electrolyte solutions. PMID:26233143

  6. Photocathode aging in MCP PMT

    NASA Astrophysics Data System (ADS)

    Barnyakov, M. Yu; Mironov, A. V.

    2011-12-01

    We study aging of alkali-antimonide photocathodes in the microchannel plate photomultiplier tubes (MCP PMT) manufactured in Novosibirsk by ``Ekran FEP'' company. Such PMTs are used in the particle identification systems of KEDR, SND and CMD-3 experiments carried out at e+e- colliders VEPP-4M and VEPP-2000 in the Budker Institute of Nuclear Physics. The quantum efficiency (QE) degradation of a PMT equipped with MCP Chevron has been measured at different photon counting rates from 4?107 to 6?1010 s-1cm-2. It is found that the QE decrease is proportional to the charge extracted from the MCP nearest to the photocathode rather than to the output charge. The comparison of different types of alkali-antimonide photocathodes has shown that the treatment of photocathode with vapors of cesium and antimony can dramatically reduce the photocathode aging rate. The photocathode lifetime of the best MCP PMT sample has been measured at the photon counting rate of 107 cm-2s-1 and the initial gain of 106. The peak quantum efficiency degraded by 20% after accumulation of 3.3 C/cm2 anode charge.

  7. Development of processes for the production of solar grade silicon from halides and alkali metals, Phase 1 and Phase 2. Final report, October 1979 - February 1981

    SciTech Connect

    Dickson, C.R.; Gould, R.K.; Felder, W.

    1981-03-01

    High temperature reactions of silicon halides with alkali metals for the production of solar grade silicon are described. Product separation and collection processes were evaluated, measure heat release parameters for scaling purposes and effects of reactants and/or products on materials of reactor construction were determined, and preliminary engineering and economic analysis of a scaled up process were made. The feasibility of the basic process to make and collect silicon was demonstrated. The jet impaction/separation process was demonstrated to be a purification process. The rate at which gas phase species from silicon particle precursors, the time required for silane decomposition to produce particles, and the competing rate of growth of silicon seed particles injected into a decomposing silane environment were determined. The extent of silane decomposition as a function of residence time, temperature, and pressure was measured by infrared absorption spectroscopy. A simplistic model is presented to explain the growth of silicon in a decomposing silane enviroment.

  8. Mass spectrometry of oligopeptides in the presence of large amounts of alkali halides using desorption/ionization induced by neutral cluster impact.

    PubMed

    Portz, André; Baur, Markus; Gebhardt, Christoph R; Dürr, Michael

    2016-01-01

    Oligopeptides in the presence of large amounts of salt were desorbed and ionized using desorption/ionization induced by neutral clusters (DINeC) for further analysis by means of mass spectrometry (MS). Using oligopeptides in alkali halide solutions as a model system, DINeC was shown to yield clear and fragmentation free mass spectra of the biomolecules even from environments with a large excess of salt. The results were traced back to a phase separation between salt and biomolecules during sample preparation. The ratio between alkali metal complexes [M+A](+) and bare biomolecules [M+H](+) was controlled using different preparation schemes. DINeC was applied to the products of a tryptic digest of bovine serum albumin in the presence of sodium chloride; the results of a mass fingerprint analysis did not show a major difference for the spectra with and without salt in the original solution. The metal-ion/peptide interaction was further investigated by means of tandem-MS. PMID:26825286

  9. The Transient Absorption Due to Self-Trapped Excitons Localized at Iodine Dimers in Alkali Halide Crystals

    NASA Astrophysics Data System (ADS)

    Hirota, Shoichi; Edamatsu, Keiichi; Kondo, Yasuhiro; Hirai, Masamitsu

    1994-07-01

    The transient absorption spectra of a self-trapped exciton (STE) localized at iodine dimers (I22-*) in iodine-doped alkali chloride and bromide crystals (AX:I; A=Na, K, Rb; X=Cl, Br) have been investigated. The absorption bands due to electron-transitions appear below 1 eV, and the bands due to hole-transitions around 1.5 and 3.0 eV. The absorption bands due to the electron-transitions are located in much lower energy region than those of intrinsic STEs in nominally pure alkali chloride or bromide crystals. The bands due to the hole-transitions are very similar to those of V k (I2-) centers in alkali iodide crystals. These results suggest that the STE localized at iodine dimers is in the on-center configuration and its electronic state is diffused in comparison with that of off-center type STE.

  10. Band-structure calculations of noble-gas and alkali halide solids using accurate Kohn-Sham potentials with self-interaction correction

    SciTech Connect

    Li, Y.; Krieger, J.B. ); Norman, M.R. ); Iafrate, G.J. )

    1991-11-15

    The optimized-effective-potential (OEP) method and a method developed recently by Krieger, Li, and Iafrate (KLI) are applied to the band-structure calculations of noble-gas and alkali halide solids employing the self-interaction-corrected (SIC) local-spin-density (LSD) approximation for the exchange-correlation energy functional. The resulting band gaps from both calculations are found to be in fair agreement with the experimental values. The discrepancies are typically within a few percent with results that are nearly the same as those of previously published orbital-dependent multipotential SIC calculations, whereas the LSD results underestimate the band gaps by as much as 40%. As in the LSD---and it is believed to be the case even for the exact Kohn-Sham potential---both the OEP and KLI predict valence-band widths which are narrower than those of experiment. In all cases, the KLI method yields essentially the same results as the OEP.

  11. Biological photocathodes.

    PubMed Central

    Griffith, O H; Habliston, D L; Birrell, G B; Skoczylas, W P; Hedberg, K K

    1989-01-01

    Biological surfaces emit electrons when subjected to UV light. This emission is increased greatly after exposure to cesium vapor. Increases from 2 to 3 orders of magnitude are observed, depending on the biochemicals present. Heme and chlorophyll exhibit unusually high photoemission currents, which are increased further after cesiation. Photoemission from proteins and lipids is much less but also is increased by exposure to cesium. The formation of photocathodes with cesium greatly increases the practical magnifications attainable in photoelectron microscopy of organic and biological specimens. Photoelectron micrographs taken at magnifications greater than or equal to X 100,000 of chlorophyll-rich thylakoid membranes and of colloidal gold-labeled cytoskeleton preparations of cultured epithelial cells demonstrate the improvement in magnification. The selectivity and stability of the photocathodes suggest the possibility of detecting chromophore binding proteins in membranes and the design of photoelectron labels for tagging specific sites on biological surfaces. Images PMID:2928305

  12. SUPERCONDUCTING PHOTOCATHODES.

    SciTech Connect

    SMEDLEY, J.; RAO, T.; WARREN, J.; SEKUTOWICZ, LANGNER, J.; STRZYZEWSKI, P.; LEFFERS, R.; LIPSKI, A.

    2005-10-09

    We present the results of our investigation of lead and niobium as suitable photocathode materials for superconducting RF injectors. Quantum efficiencies (QE) have been measured for a range of incident photon energies and a variety of cathode preparation methods, including various lead plating techniques on a niobium substrate. The effects of operating at ambient and cryogenic temperatures and different vacuum levels on the cathode QE have also been studied.

  13. Characterization of an Alkali- and Halide-Resistant Laccase Expressed in E. coli: CotA from Bacillus clausii

    PubMed Central

    Brander, Søren; Mikkelsen, Jørn D.; Kepp, Kasper P.

    2014-01-01

    The limitations of fungal laccases at higher pH and salt concentrations have intensified the search for new extremophilic bacterial laccases. We report the cloning, expression, and characterization of the bacterial cotA from Bacillus clausii, a supposed alkalophilic ortholog of cotA from B. subtilis. Both laccases were expressed in E. coli strain BL21(DE3) and characterized fully in parallel for strict benchmarking. We report activity on ABTS, SGZ, DMP, caffeic acid, promazine, phenyl hydrazine, tannic acid, and bilirubin at variable pH. Whereas ABTS, promazine, and phenyl hydrazine activities vs. pH were similar, the activity of B. clausii cotA was shifted upwards by ∼0.5–2 pH units for the simple phenolic substrates DMP, SGZ, and caffeic acid. This shift is not due to substrate affinity (KM) but to pH dependence of catalytic turnover: The kcat of B. clausii cotA was 1 s−1 at pH 6 and 5 s−1 at pH 8 in contrast to 6 s−1 at pH 6 and 2 s−1 at pH 8 for of B. subtilis cotA. Overall, kcat/KM was 10-fold higher for B. subtilis cotA at pHopt. While both proteins were heat activated, activation increased with pH and was larger in cotA from B. clausii. NaCl inhibited activity at acidic pH, but not up to 500–700 mM NaCl in alkaline pH, a further advantage of the alkali regime in laccase applications. The B. clausii cotA had ∼20 minutes half-life at 80°C, less than the ∼50 minutes at 80°C for cotA from B. subtilis. While cotA from B. subtilis had optimal stability at pH∼8, the cotA from B. clausii displayed higher combined salt- and alkali-resistance. This resistance is possibly caused by two substitutions (S427Q and V110E) that could repel anions to reduce anion-copper interactions at the expense of catalytic proficiency, a trade-off of potential relevance to laccase optimization. PMID:24915287

  14. Characterization of an alkali- and halide-resistant laccase expressed in E. coli: CotA from Bacillus clausii.

    PubMed

    Brander, Sren; Mikkelsen, Jrn D; Kepp, Kasper P

    2014-01-01

    The limitations of fungal laccases at higher pH and salt concentrations have intensified the search for new extremophilic bacterial laccases. We report the cloning, expression, and characterization of the bacterial cotA from Bacillus clausii, a supposed alkalophilic ortholog of cotA from B. subtilis. Both laccases were expressed in E. coli strain BL21(DE3) and characterized fully in parallel for strict benchmarking. We report activity on ABTS, SGZ, DMP, caffeic acid, promazine, phenyl hydrazine, tannic acid, and bilirubin at variable pH. Whereas ABTS, promazine, and phenyl hydrazine activities vs. pH were similar, the activity of B. clausii cotA was shifted upwards by ~0.5-2 pH units for the simple phenolic substrates DMP, SGZ, and caffeic acid. This shift is not due to substrate affinity (K(M)) but to pH dependence of catalytic turnover: The k(cat) of B. clausii cotA was 1 s? at pH 6 and 5 s? at pH 8 in contrast to 6 s? at pH 6 and 2 s? at pH 8 for of B. subtilis cotA. Overall, k(cat)/K(M) was 10-fold higher for B. subtilis cotA at pH(opt). While both proteins were heat activated, activation increased with pH and was larger in cotA from B. clausii. NaCl inhibited activity at acidic pH, but not up to 500-700 mM NaCl in alkaline pH, a further advantage of the alkali regime in laccase applications. The B. clausii cotA had ~20 minutes half-life at 80C, less than the ~50 minutes at 80C for cotA from B. subtilis. While cotA from B. subtilis had optimal stability at pH~8, the cotA from B. clausii displayed higher combined salt- and alkali-resistance. This resistance is possibly caused by two substitutions (S427Q and V110E) that could repel anions to reduce anion-copper interactions at the expense of catalytic proficiency, a trade-off of potential relevance to laccase optimization. PMID:24915287

  15. Correlation of CsK{sub 2}Sb photocathode lifetime with antimony thickness

    SciTech Connect

    Mamun, M. A. Elmustafa, A. A.; Hernandez-Garcia, C.; Poelker, M.

    2015-06-01

    CsK{sub 2}Sb photocathodes with quantum efficiency on the order of 10% at 532 nm, and lifetime greater than 90 days at low voltage, were successfully manufactured via co-deposition of alkali species emanating from an effusion source. Photocathodes were characterized as a function of antimony layer thickness and alkali consumption, inside a vacuum chamber that was initially baked, but frequently vented without re-baking. Photocathode lifetime measured at low voltage is correlated with the antimony layer thickness. Photocathodes manufactured with comparatively thick antimony layers exhibited the best lifetime. We speculate that the antimony layer serves as a reservoir, or sponge, for the alkali.

  16. Correlation of CsK2Sb photocathode lifetime with antimony thickness

    NASA Astrophysics Data System (ADS)

    Mamun, M. A.; Hernandez-Garcia, C.; Poelker, M.; Elmustafa, A. A.

    2015-06-01

    CsK2Sb photocathodes with quantum efficiency on the order of 10% at 532 nm, and lifetime greater than 90 days at low voltage, were successfully manufactured via co-deposition of alkali species emanating from an effusion source. Photocathodes were characterized as a function of antimony layer thickness and alkali consumption, inside a vacuum chamber that was initially baked, but frequently vented without re-baking. Photocathode lifetime measured at low voltage is correlated with the antimony layer thickness. Photocathodes manufactured with comparatively thick antimony layers exhibited the best lifetime. We speculate that the antimony layer serves as a reservoir, or sponge, for the alkali.

  17. Electrolytic systems and methods for making metal halides and refining metals

    SciTech Connect

    Holland, Justin M.; Cecala, David M.

    2015-05-26

    Disclosed are electrochemical cells and methods for producing a halide of a non-alkali metal and for electrorefining the halide. The systems typically involve an electrochemical cell having a cathode structure configured for dissolving a hydrogen halide that forms the halide into a molten salt of the halogen and an alkali metal. Typically a direct current voltage is applied across the cathode and an anode that is fabricated with the non-alkali metal such that the halide of the non-alkali metal is formed adjacent the anode. Electrorefining cells and methods involve applying a direct current voltage across the anode where the halide of the non-alkali metal is formed and the cathode where the non-alkali metal is electro-deposited. In a representative embodiment the halogen is chlorine, the alkali metal is lithium and the non-alkali metal is uranium.

  18. Masked Photocathode for Photoinjector

    SciTech Connect

    Qiang, Ji

    2010-01-21

    In this research note, we propose a scheme to insert a photocathode inside a photoinjector for generating high brightness electron beam. Instead of mounting the photocathode onto the electrode, a masked electrode with small hole is used to shield the photocathode from the accelerating vacuum chamber. Using such a masked photocathode will make the replacement of photocathode material very simple by rotating the photocathode behind the mask into the hole. This will significantly increase the usage lifetime of a photocathode. Furthermore, this also helps reduce the dark current or secondary electron emission from the photocathode. The hole on the mask also provides a transverse cut-off to the Gaussian laser profile which can be beneficial from the beam dynamics point of view.

  19. Prototype dispenser photocathode: Demonstration and comparison to theory

    NASA Astrophysics Data System (ADS)

    Moody, N. A.; Jensen, K. L.; Feldman, D. W.; O'Shea, P. G.; Montgomery, E. J.

    2007-03-01

    A method to significantly extend the operational lifetime of alkali-based photocathodes by diffusing cesium to the surface at moderate temperature is presented and shown to restore the quantum efficiency (QE) of cesiated tungsten. Experimental measurements of QE as a function of surface cesium coverage compare exceptionally well with a recent theoretical photoemission model, notably without the use of adjustable parameters. A prototype cesium dispenser cell is demonstrated and validates the concept upon which long-life dispenser photocathodes can be based.

  20. Activation Layer Stabilization of High Polarization Photocathodes in Sub-Optimal RF Gun Environments

    SciTech Connect

    Mulhollan, Gregory; /SLAC /Saxed Surface Science, Austin, TX

    2010-08-25

    We have developed an activation procedure by which the reactivity to CO{sub 2}, a principal cause of yield decay for GaAs photocathodes, is greatly reduced. The use of a second alkali in the activation process is responsible for the increased immunity of the activated surface. The best immunity was obtained by using a combination of Cs and Li without any loss in near bandgap yield. Optimally activated photocathodes have nearly equal quantities of both alkalis.

  1. A Masked Photocathode in Photoinjector

    SciTech Connect

    Qiang, Ji

    2010-12-14

    In this paper, we propose a masked photocathode inside the photoinjector for generating high brightness election beam. Instead of mounting the photocathode onto an electrode, an electrode with small hole is used as a mask to shield the photocathode from the accelerating vacuum chamber. Using such a masked photocathode will make the replacement of photocathode material easy by rotating the photocathode behind the electrode into the hole. Furthermore, this helps reduce the dark current or secondary electron emission from the photocathode material. The masked photocathode also provides transverse cut-off to a Gaussian laser beam that reduces electron beam emittance growth from nonlinear space-charge effects.

  2. Photocathode research at SLAC

    SciTech Connect

    Mulhollan, G.; Clendenin, J.; Garwin, E.; Kirby, R.; Maruyama, T.; Tang, H.; Prepost, R.

    1998-01-01

    GaAs based photocathode research at SLAC will be described. Recent efforts have focused on both immediate applications and fundamental photocathode properties. This includes revisiting some old measurements with state-of-the-art instrumentation. {copyright} {ital 1998 American Institute of Physics.}

  3. Piezoelectrically Enhanced Photocathodes

    NASA Technical Reports Server (NTRS)

    Beach, Robert A.; Nikzad, Shouleh; Bell, Lloyd Douglas; Strittmatter, Robert

    2011-01-01

    Doping of photocathodes with materials that have large piezoelectric coefficients has been proposed as an alternative means of increasing the desired photoemission of electrons. Treating cathode materials to increase emission of electrons is called "activation" in the art. It has been common practice to activate photocathodes by depositing thin layers of suitable metals (usually, cesium). Because cesium is unstable in air, fabrication of cesiated photocathodes and devices that contain them must be performed in sealed tubes under vacuum. It is difficult and costly to perform fabrication processes in enclosed, evacuated spaces. The proposed piezoelectrically enhanced photocathodes would have electron-emission properties similar to those of cesiated photocathodes but would be stable in air, and therefore could be fabricated more easily and at lower cost. Candidate photocathodes include nitrides of elements in column III of the periodic table . especially compounds of the general formula Al(x)Ga(1.x)N (where 0< or = x < or =.1). These compounds have high piezoelectric coefficients and are suitable for obtaining response to ultraviolet light. Fabrication of a photocathode according to the proposal would include inducement of strain in cathode layers during growth of the layers on a substrate. The strain would be induced by exploiting structural mismatches among the various constituent materials of the cathode. Because of the piezoelectric effect in this material, the strain would give rise to strong electric fields that, in turn, would give rise to a high concentration of charge near the surface. Examples of devices in which piezoelectrically enhanced photocathodes could be used include microchannel plates, electron- bombarded charge-coupled devices, image tubes, and night-vision goggles. Piezoelectrically enhanced photocathode materials could also be used in making highly efficient monolithic photodetectors. Highly efficient and stable piezoelectrically enhanced, ultraviolet-sensitive photocathodes and photodetectors could be fabricated by use of novel techniques for growing piezoelectrically enhanced layers, in conjunction with thinning and dopant-selective etching techniques.

  4. Oxidation of hydrogen halides to elemental halogens

    DOEpatents

    Rohrmann, Charles A. (Kennewick, WA); Fullam, Harold T. (Richland, WA)

    1985-01-01

    A process for oxidizing hydrogen halides having substantially no sulfur impurities by means of a catalytically active molten salt is disclosed. A mixture of the subject hydrogen halide and an oxygen bearing gas is contacted with a molten salt containing an oxidizing catalyst and alkali metal normal sulfates and pyrosulfates to produce an effluent gas stream rich in the elemental halogen and substantially free of sulfur oxide gases.

  5. Mesh-based semitransparent photocathodes.

    PubMed

    Carruthers, G R

    1975-07-01

    Semitransparent photocathodes consisting of vacuum-deposited layers of CsI on electroformed nickel meshes with 40 and 60 lines/mm spacing have been investigated for applications in vacuum-ultraviolet electronic imaging devices. These photocathodes are found to have about half the quantum yield of an opaque CsI photocathode, but a factor of 2 to 3 greater quantum yield than a conventional semitransparent CsI photocathode. The limitations of window materials on short-wavelength spectral response, and their disadvantages in an energetic charged-particle environment, are eliminated. Unlike conventional opaque photocathodes, the mesh photocathodes can be used interchangeably with conventional semitransparent photocathodes in a wide variety of electronic imaging devices. Tests of mesh photocathodes in laboratory electrographic cameras indicate that best results for most applications are obtained if the output electron image has a somewhat poorer resolution than that corresponding to the mesh spacing. PMID:20154888

  6. Acicular photomultiplier photocathode structure

    DOEpatents

    Craig, Richard A.; Bliss, Mary

    2003-09-30

    A method and apparatus for increasing the quantum efficiency of a photomultiplier tube by providing a photocathode with an increased surface-to-volume ratio. The photocathode includes a transparent substrate, upon one major side of which is formed one or more large aspect-ratio structures, such as needles, cones, fibers, prisms, or pyramids. The large aspect-ratio structures are at least partially composed of a photoelectron emitting material, i.e., a material that emits a photoelectron upon absorption of an optical photon. The large aspect-ratio structures may be substantially composed of the photoelectron emitting material (i.e., formed as such upon the surface of a relatively flat substrate) or be only partially composed of a photoelectron emitting material (i.e., the photoelectron emitting material is coated over large aspect-ratio structures formed from the substrate material itself.) The large aspect-ratio nature of the photocathode surface allows for an effective increase in the thickness of the photocathode relative the absorption of optical photons, thereby increasing the absorption rate of incident photons, without substantially increasing the effective thickness of the photocathode relative the escape incidence of the photoelectrons.

  7. Molecular compressibility of some halides in alcohols

    NASA Technical Reports Server (NTRS)

    Serban, C.; Auslaender, D.

    1974-01-01

    After measuring ultrasonic velocity and density, the molecular compressibility values from Wada's formula were calculated, for alkali metal halide solutions in methyl, ethyl, butyl, and glycol alcohol. The temperature and concentration dependence were studied, finding deviations due to the hydrogen bonds of the solvent.

  8. Low-workfunction photocathodes based on acetylide compounds

    SciTech Connect

    Terdik, Joseph Z; Spentzouris, Linda; Terry, Jr., Jeffrey H; Harkay, Katherine C; Nemeth, Karoly; Srajer, George

    2014-05-20

    A low-workfunction photocathode includes a photoemissive material employed as a coating on the photocathode. The photoemissive material includes A.sub.nMC.sub.2, where A is a first metal element, the first element is an alkali metal, an alkali-earth element or the element Al; n is an integer that is 0, 1, 2, 3 or 4; M is a second metal element, the second metal element is a transition metal or a metal stand-in; and C.sub.2 is the acetylide ion C.sub.2.sup.2-. The photoemissive material includes a crystalline structure or non-crystalline structure of rod-like or curvy 1-dimensional polymeric substructures with MC.sub.2 repeating units embedded in a matrix of A.

  9. Computation of methodology-independent single-ion solvation properties from molecular simulations. IV. Optimized Lennard-Jones interaction parameter sets for the alkali and halide ions in water

    NASA Astrophysics Data System (ADS)

    Reif, Maria M.; Hnenberger, Philippe H.

    2011-04-01

    The raw single-ion solvation free energies computed from atomistic (explicit-solvent) simulations are extremely sensitive to the boundary conditions and treatment of electrostatic interactions used during these simulations. However, as shown recently [M. A. Kastenholz and P. H. Hnenberger, J. Chem. Phys. 124, 224501 (2006), 10.1529/biophysj.106.083667; M. M. Reif and P. H. Hnenberger, J. Chem. Phys. 134, 144103 (2010)], the application of appropriate correction terms permits to obtain methodology-independent results. The corrected values are then exclusively characteristic of the underlying molecular model including in particular the ion-solvent van der Waals interaction parameters, determining the effective ion size and the magnitude of its dispersion interactions. In the present study, the comparison of calculated (corrected) hydration free energies with experimental data (along with the consideration of ionic polarizabilities) is used to calibrate new sets of ion-solvent van der Waals (Lennard-Jones) interaction parameters for the alkali (Li+, Na+, K+, Rb+, Cs+) and halide (F-, Cl-, Br-, I-) ions along with either the SPC or the SPC/E water models. The experimental dataset is defined by conventional single-ion hydration free energies [Tissandier et al., J. Phys. Chem. A 102, 7787 (1998), 10.1021/jp982638r; Fawcett, J. Phys. Chem. B 103, 11181] along with three plausible choices for the (experimentally elusive) value of the absolute (intrinsic) hydration free energy of the proton, namely, ? G_hyd^{ominus }[H+] = -1100, -1075 or -1050 kJ mol-1, resulting in three sets L, M, and H for the SPC water model and three sets LE, ME, and HE for the SPC/E water model (alternative sets can easily be interpolated to intermediate ? G_hyd^{ominus }[H+] values). The residual sensitivity of the calculated (corrected) hydration free energies on the volume-pressure boundary conditions and on the effective ionic radius entering into the calculation of the correction terms is also evaluated and found to be very limited. Ultimately, it is expected that comparison with other experimental ionic properties (e.g., derivative single-ion solvation properties, as well as data concerning ionic crystals, melts, solutions at finite concentrations, or nonaqueous solutions) will permit to validate one specific set and thus, the associated ? G_hyd^{ominus }[H+] value (atomistic consistency assumption). Preliminary results (first-peak positions in the ion-water radial distribution functions, partial molar volumes of ionic salts in water, and structural properties of ionic crystals) support a value of ? G_hyd^{ominus }[H+] close to -1100 kJ.mol-1.

  10. Piezoelectrically enhanced photocathode

    NASA Technical Reports Server (NTRS)

    Beach, Robert A. (Inventor); Nikzad, Shouleh (Inventor); Strittmatter, Robert P. (Inventor); Bell, Lloyd Douglas (Inventor)

    2009-01-01

    A photocathode, for generating electrons in response to incident photons in a photodetector, includes a base layer having a first lattice structure and an active layer having a second lattice structure and epitaxially formed on the base layer, the first and second lattice structures being sufficiently different to create a strain in the active layer with a corresponding piezoelectrically induced polarization field in the active layer, the active layer having a band gap energy corresponding to a desired photon energy.

  11. Defects induced melting in alkali halides

    NASA Astrophysics Data System (ADS)

    Chauhan, R. S.; Snehlata, K.; Singh, C. P.

    2011-02-01

    In the present paper we study the pressure dependence of melting of NaCl and CsCl crystals. A formulation has been presented for the pressure dependence of melting temperature on the basis of the vacancy model using the expression for the pressure dependence of the volume of Schottky defects from the Roy-Roy equation of state. Values of pressure derivatives of melting temperature have been calculated at elevated pressures to determine the rate of change of melting temperature with increase in pressures using the data of vacancy formation energy and effective volume of Schottky defects. The vacancy model revised in the present study takes into account the variation of bulk modulus with pressure, whereas in the Ksiazek and Gorecki model, it was treated constant. Results for pressure derivative of melting temperature are calculated for the solids under study. The melting curves have also been obtained and found to compare well with results based on molecular dynamics simulation and experimental data reported in recent literature.

  12. Computation of methodology-independent single-ion solvation properties from molecular simulations. IV. Optimized Lennard-Jones interaction parameter sets for the alkali and halide ions in water

    SciTech Connect

    Reif, Maria M.; Huenenberger, Philippe H.

    2011-04-14

    The raw single-ion solvation free energies computed from atomistic (explicit-solvent) simulations are extremely sensitive to the boundary conditions and treatment of electrostatic interactions used during these simulations. However, as shown recently [M. A. Kastenholz and P. H. Huenenberger, J. Chem. Phys. 124, 224501 (2006); M. M. Reif and P. H. Huenenberger, J. Chem. Phys. 134, 144103 (2010)], the application of appropriate correction terms permits to obtain methodology-independent results. The corrected values are then exclusively characteristic of the underlying molecular model including in particular the ion-solvent van der Waals interaction parameters, determining the effective ion size and the magnitude of its dispersion interactions. In the present study, the comparison of calculated (corrected) hydration free energies with experimental data (along with the consideration of ionic polarizabilities) is used to calibrate new sets of ion-solvent van der Waals (Lennard-Jones) interaction parameters for the alkali (Li{sup +}, Na{sup +}, K{sup +}, Rb{sup +}, Cs{sup +}) and halide (F{sup -}, Cl{sup -}, Br{sup -}, I{sup -}) ions along with either the SPC or the SPC/E water models. The experimental dataset is defined by conventional single-ion hydration free energies [Tissandier et al., J. Phys. Chem. A 102, 7787 (1998); Fawcett, J. Phys. Chem. B 103, 11181] along with three plausible choices for the (experimentally elusive) value of the absolute (intrinsic) hydration free energy of the proton, namely, {Delta}G{sub hyd} {sup O-minus} [H{sup +}]=-1100, -1075 or -1050 kJ mol{sup -1}, resulting in three sets L, M, and H for the SPC water model and three sets L{sub E}, M{sub E}, and H{sub E} for the SPC/E water model (alternative sets can easily be interpolated to intermediate {Delta}G{sub hyd} {sup O-minus} [H{sup +}] values). The residual sensitivity of the calculated (corrected) hydration free energies on the volume-pressure boundary conditions and on the effective ionic radius entering into the calculation of the correction terms is also evaluated and found to be very limited. Ultimately, it is expected that comparison with other experimental ionic properties (e.g., derivative single-ion solvation properties, as well as data concerning ionic crystals, melts, solutions at finite concentrations, or nonaqueous solutions) will permit to validate one specific set and thus, the associated {Delta}G{sub hyd} {sup O-minus} [H{sup +}] value (atomistic consistency assumption). Preliminary results (first-peak positions in the ion-water radial distribution functions, partial molar volumes of ionic salts in water, and structural properties of ionic crystals) support a value of {Delta}G{sub hyd} {sup O-minus} [H{sup +}] close to -1100 kJ{center_dot}mol{sup -1}.

  13. Robust activation method for negative electron affinity photocathodes

    DOEpatents

    Mulhollan, Gregory A. (Dripping Springs, TX); Bierman, John C. (Austin, TX)

    2011-09-13

    A method by which photocathodes(201), single crystal, amorphous, or otherwise ordered, can be surface modified to a robust state of lowered and in best cases negative, electron affinity has been discovered. Conventional methods employ the use of Cs(203) and an oxidizing agent(207), typically carried by diatomic oxygen or by more complex molecules, for example nitrogen trifluoride, to achieve a lowered electron affinity(404). In the improved activation method, a second alkali, other than Cs(205), is introduced onto the surface during the activation process, either by co-deposition, yo-yo, or sporadic or intermittent application. Best effect for GaAs photocathodes has been found through the use of Li(402) as the second alkali, though nearly the same effect can be found by employing Na(406). Suitable photocathodes are those which are grown, cut from boules, implanted, rolled, deposited or otherwise fabricated in a fashion and shape desired for test or manufacture independently supported or atop a support structure or within a framework or otherwise affixed or suspended in the place and position required for use.

  14. Final Report, Photocathodes for High Repetition Rate Light Sources

    SciTech Connect

    Ben-Zvi, Ilan

    2014-04-20

    This proposal brought together teams at Brookhaven National Laboratory (BNL), Lawrence Berkeley National Laboratory (LBNL) and Stony Brook University (SBU) to study photocathodes for high repetition rate light sources such as Free Electron Lasers (FEL) and Energy Recovery Linacs (ERL). The work done under this grant comprises a comprehensive program on critical aspects of the production of the electron beams needed for future user facilities. Our program pioneered in situ and in operando diagnostics for alkali antimonide growth. The focus is on development of photocathodes for high repetition rate Free Electron Lasers (FELs) and Energy Recovery Linacs (ERLs), including testing SRF photoguns, both normal-conducting and superconducting. Teams from BNL, LBNL and Stony Brook University (SBU) led this research, and coordinated their work over a range of topics. The work leveraged a robust infrastructure of existing facilities and the support was used for carrying out the research at these facilities. The program concentrated in three areas: a) Physics and chemistry of alkali-antimonide cathodes b) Development and testing of a diamond amplifier for photocathodes c) Tests of both cathodes in superconducting RF photoguns and copper RF photoguns

  15. DIAMOND AMPLIFIED PHOTOCATHODES.

    SciTech Connect

    SMEDLEY,J.; BEN-ZVI, I.; BOHON, J.; CHANG, X.; GROVER, R.; ISAKOVIC, A.; RAO, T.; WU, Q.

    2007-11-26

    High-average-current linear electron accelerators require photoinjectors capable of delivering tens to hundreds of mA average current, with peak currents of hundreds of amps. Standard photocathodes face significant challenges in meeting these requirements, and often have short operational lifetimes in an accelerator environment. We report on recent progress toward development of secondary emission amplifiers for photocathodes, which are intended to increase the achievable average current while protecting the cathode from the accelerator. The amplifier is a thin diamond wafer which converts energetic (few keV) primary electrons into hundreds of electron-hole pairs via secondary electron emission. The electrons drift through the diamond under an external bias and are emitted into vacuum via a hydrogen-terminated surface with negative electron affinity (NEA). Secondary emission gain of over 200 has been achieved. Two methods of patterning diamond, laser ablation and reactive-ion etching (RIE), are being developed to produce the required geometry. A variety of diagnostic techniques, including FTIR, SEM and AFM, have been used to characterize the diamonds.

  16. DIAMOND AMPLIFIER FOR PHOTOCATHODES.

    SciTech Connect

    RAO,T.; BEN-ZVI,I.; BURRILL,A.; CHANG,X.; HULBERT,S.; JOHNSON,P.D.; KEWISCH,J.

    2004-06-21

    We report a new approach to the generation of high-current, high-brightness electron beams. Primary electrons are produced by a photocathode (or other means) and are accelerated to a few thousand electron-volts, then strike a specially prepared diamond window. The large Secondary Electron Yield (SEY) provides a multiplication of the number of electrons by about two orders of magnitude. The secondary electrons drift through the diamond under an electric field and emerge into the accelerating proper of the ''gun'' through a Negative Electron Affinity surface of the diamond. The advantages of the new approach include the following: (1) Reduction of the number of primary electrons by the large SEY, i.e. a very low laser power in a photocathode producing the primaries. (2) Low thermal emittance due to the NEA surface and the rapid thermalization of the electrons. (3) Protection of the cathode from possible contamination from the gun, allowing the use of large quantum efficiency but sensitive cathodes. (4) Protection of the gun from possible contamination by the cathode, allowing the use of superconducting gun cavities. (5) Production of high average currents, up to ampere class. (6) Encapsulated design, making the ''load-lock'' systems unnecessary. This paper presents the criteria that need to be taken into account in designing the amplifier.

  17. Infrared-sensitive photocathode

    DOEpatents

    Mariella, R.P. Jr.; Cooper, G.A.

    1995-04-04

    A single-crystal, multi-layer device is described incorporating an IR absorbing layer that is compositionally different from the Ga{sub x}Al{sub 1{minus}x}Sb layer which acts as the electron emitter. Many different IR absorbing layers can be envisioned for use in this embodiment, limited only by the ability to grow quality material on a chosen substrate. A non-exclusive list of possible IR absorbing layers would include GaSb, InAs and InAs/Ga{sub w}In{sub y}Al{sub 1{minus}y{minus}w}Sb superlattices. The absorption of the IR photon excites an electron into the conduction band of the IR absorber. An externally applied electric field then transports electrons from the conduction band of the absorber into the conduction band of the Ga{sub x}Al{sub 1{minus}x}Sb, from which they are ejected into vacuum. Because the band alignments of Ga{sub x}Al{sub 1{minus}x}Sb can be made the same as that of GaAs, emitting efficiencies comparable to GaAs photocathodes are obtainable. The present invention provides a photocathode that is responsive to wavelengths within the range of 0.9 {mu}m to at least 10 {mu}m. 9 figures.

  18. Infrared-sensitive photocathode

    DOEpatents

    Mariella, Jr., Raymond P. (Danville, CA); Cooper, Gregory A. (Pleasant Hill, CA)

    1995-01-01

    A single-crystal, multi-layer device incorporating an IR absorbing layer that is compositionally different from the Ga.sub.x Al.sub.1-x Sb layer which acts as the electron emitter. Many different IR absorbing layers can be envisioned for use in this embodiment, limited only by the ability to grow quality material on a chosen substrate. A non-exclusive list of possible IR absorbing layers would include GaSb, InAs and InAs/Ga.sub.w In.sub.y Al.sub.1-y-w Sb superlattices. The absorption of the IR photon excites an electron into the conduction band of the IR absorber. An externally applied electric field then transports electrons from the conduction band of the absorber into the conduction band of the Ga.sub.x Al.sub.1-x Sb, from which they are ejected into vacuum. Because the band alignments of Ga.sub.x Al.sub.1-x Sb can be made the same as that of GaAs, emitting efficiencies comparable to GaAs photocathodes are obtainable. The present invention provides a photocathode that is responsive to wavelengths within the range of 0.9 .mu.m to at least 10 .mu.m.

  19. Photocathodes for free electron lasers

    SciTech Connect

    Kong, S.H.; Kinross-Wright, J.; Nuguyen, D.C.; Sheffield, R.L.

    1994-09-01

    Many different photocathodes have been used as electron sources for FELs and other electron accelerator systems. In choosing one, a compromise between lifetime and quantum efficiency have been unavoidable. High quantum efficiency photocathodes such as CsK{sub 2}Sb, Cs{sub 3}Sb, and cesiated GaAs have short operational lifetimes and require an ultrahigh-vacuum environment. Long lifetime photocathodes such as LaB{sub 6}, Cu, and Y have relatively low quantum efficiencies. However, recently, cesium telluride was found to be an exception. Initial results from CERN and now at Los Alamos have shown that Cs{sub 2}Te is reasonably rugged with a high quantum efficiency below 270 nm. Further studies were carried out at Los Alamos in determining its performance as an electron source for the Los Alamos Advanced FEL. The Los Alamos Advanced FEL was successfully operated at 5-6 microns with a Cs{sub 2}Te photocathode driven by a frequency quadrupled Nd:YLF laser as the electron source. Cs{sub 2}Te photocathodes with quantum efficiencies of 12-18% at 254 mn were fabricated in an ultrahigh-vacuum chamber and transferred under high vacuum to the FEL. The authors estimated that the operational lifetime of Cs{sub 2}Te photocathodes to be at least 20 times that for K{sub 2}CsSb photocathodes. Furthermore, experiments in the fabrication chamber have shown that heating to 150-200{degrees}C photocathodes exposed for one hour at 2{times}10{sup {minus}4} torr of air was sufficient to revive the quantum efficiency from below 1% to about 10%. The electron beam for the FEL extracted from a cesium telluride target was also characterized. The emittance, response time, saturation level and dark current of cesium telluride photocathodes was determined to be sufficient for FEL applications.

  20. Ionic structure and physicochemical properties of molten halides

    SciTech Connect

    Smirnov, M.V.; Stepanov, V.P.; Khokhlov, V.A.

    1988-05-01

    A large body of experimental data on different physicochemical (thermodynamic, transport, surface) properties of molten halides is summarized. Trends in their variation during transition from typical ionic liquids, which are molten halides of alkali metals, to mixed ionic-covalent liquids, which contain halides of polyvalent metals, are demonstrated. It is concluded that for qualitative explanation and quantitative description of the temperature and concentration dependences of the physicochemical properties of molten halides, it is necessary to consider their actual ionic compositions, i.e., the existence also of clustered particles (clusters, groups of ions) besides the elemental ions. Such an approach allows us to accurately predict the physicochemical properties of molten halides of given chemical compositions.

  1. Metal-halide mixtures for latent heat energy storage

    NASA Technical Reports Server (NTRS)

    Chen, K.; Manvi, R.

    1981-01-01

    Alkali metal and alkali halide mixtures are identified which may be suitable for thermal energy storage at temperatures above 600 C. The use of metal-halides is appropriate because of their tendency to form two immiscible melts with a density difference, which reduces scale formation and solidification on heat transfer surfaces. Also, the accumulation of phase change material along the melt interface is avoided by the self-dispersing characteristic of some metal-halides, in particular Sr-SrCl2, Ba-BaCl2, and Ba-BaBr2 mixtures. Further advantages lie in their high thermal conductivities, ability to cope with thermal shock, corrosion inhibition, and possibly higher energy densities.

  2. Prevention of electron field emission from molybdenum substrates for photocathodes by the native oxide layer

    NASA Astrophysics Data System (ADS)

    Lagotzky, Stefan; Barday, Roman; Jankowiak, Andreas; Kamps, Thorsten; Klimm, Carola; Knobloch, Jens; Mller, Gnter; Senkovskiy, Boris; Siewert, Frank

    2015-05-01

    Comprehensive investigations of the electron field emission (FE) properties of annealed single crystal and polycrystalline molybdenum plugs, which are used as substrates for actual alkali-based photocathodes were performed with a FE scanning microscope. Well-polished and dry-ice cleaned Mo samples with native oxide did not show parasitic FE up to a field level of 50 MV/m required for photoinjector cavities. In situ heat treatments (HT) above 400 C, which are usual before photocathode deposition, activated field emission at lower field strength. Oxygen loading into the Mo surface, however, partially weakened these emitters. X-ray photoelectron spectroscopy of comparable Mo samples showed the dissolution of the native oxide during such heat treatments. These results reveal the suppression of field emission by native Mo oxides. Possible improvements for the photocathode preparation will be discussed.

  3. Alkali Metal/Salt Thermal-Energy-Storage Systems

    NASA Technical Reports Server (NTRS)

    Phillips, Wayne W.; Stearns, John W.

    1987-01-01

    Proposed thermal-energy-storage system based on mixture of alkali metal and one of its halide salts; metal and salt form slurry of two immiscible melts. Use of slurry expected to prevent incrustations of solidified salts on heat-transfer surfaces that occur where salts alone used. Since incrustations impede heat transfer, system performance improved. In system, charging heat-exchanger surface immersed in lower liquid, rich in halide-salt, phase-charge material. Discharging heat exchanger surface immersed in upper liquid, rich in alkali metal.

  4. Factors affecting performance of dispenser photocathodes

    NASA Astrophysics Data System (ADS)

    Moody, Nathan A.; Jensen, Kevin L.; Feldman, Donald W.; Montgomery, Eric J.; O'Shea, Patrick G.

    2007-11-01

    Usable lifetime has long been a limitation of high efficiency photocathodes in high average current accelerator applications such as free electron lasers, where poor vacuum conditions and high incident laser power contribute to early degradation in electron beam emission. Recent progress has been made in adapting well known thermionic dispenser techniques to photocathodes, resulting in a dispenser photocathode whose photosensitive surface coating of cesium can be periodically replenished to extend effective lifetime. This article details the design and fabrication process of a prototype cesium dispenser photocathode and describes in detail the dominant factors affecting its performance: activation procedure, surface cleanliness, temperature, and substrate microstructure.

  5. Metal-halide mixtures for latent heat energy storage

    NASA Technical Reports Server (NTRS)

    Chen, K.; Manvi, R.

    1981-01-01

    Some candidates for alkali metal and alkali halide mixtures suitable for thermal energy storage at temperatures 600 C are identified. A solar thermal system application which offer advantages such as precipitation of salt crystals away from heat transfer surfaces, increased thermal conductivity of phase change materials, corrosion inhibition, and a constant monotectic temperature, independent of mixture concentrations. By using the lighters, metal rich phase as a heat transfer medium and the denser, salt rich phase as a phase change material for latent heat storage, undesirable solidification on the heat transfer surface may be prevented, is presented.

  6. Bio-conventional bleaching of kadam kraft-AQ pulp by thermo-alkali-tolerant xylanases from two strains of Coprinellus disseminatus for extenuating adsorbable organic halides and improving strength with optical properties and energy conservation.

    PubMed

    Lal, Mohan; Dutt, Dharm; Tyagi, C H

    2012-04-01

    Two novel thermo-alkali-tolerant crude xylanases namely MLK-01 (enzyme-A) and MLK-07 (enzyme-B) from Coprinellus disseminatus mitigated kappa numbers of Anthocephalus cadamba kraft-AQ pulps by 32.5 and 34.38%, improved brightness by 1.5 and 1.6% and viscosity by 5.75 and 6.47% after (A)XE(1) and (B)XE(1)-stages, respectively. The release of reducing sugars and chromophores was the highest during prebleaching of A. cadamba kraft-AQ pulp at enzyme doses of 5 and 10 IU/g, reaction times 90 and 120 min, reaction temperatures 75 and 65C and consistency 10% for MLK-01 and MLK-07, respectively. MLK-07 was more efficient than MLK01 in terms of producing pulp brightness, improving mechanical strength properties and reducing pollution load. MLK-01 and MLK-07 reduced AOX by 19.51 and 42.77%, respectively at 4% chlorine demands with an increase in COD and colour due to removal of lignin carbohydrates complexes. A. cadamba kraft-AQ pulps treated with xylanases from MLK-01 to MLK-07 and followed by CEHH bleaching at half chlorine demand (2%) showed a drastic reduction in brightness with slight improvement in mechanical strength properties compared to pulp bleached at 4% chlorine demand. MLK-01 reduced AOX, COD and colour by 43.83, 39.03 and 27.71% and MLK-07 by 38.34, 40.48 and 30.77%, respectively at half chlorine demand compared to full chlorine demand (4%). pH variation during prebleaching of A. cadamba kraft-AQ pulps with strains MLK-01 and MLK-07 followed by CEHH bleaching sequences showed a decrease in pulp brightness, AOX, COD and colour with an increase in mechanical strength properties, pulp viscosity and PFI revolutions to get a beating level of 35 1 SR at full chlorine demand. PMID:22805918

  7. Binary technetium halides

    NASA Astrophysics Data System (ADS)

    Johnstone, Erik Vaughan

    In this work, the synthetic and coordination chemistry as well as the physico-chemical properties of binary technetium (Tc) chlorides, bromides, and iodides were investigated. Resulting from these studies was the discovery of five new binary Tc halide phases: alpha/beta-TcCl3, alpha/beta-TcCl 2, and TcI3, and the reinvestigation of the chemistries of TcBr3 and TcX4 (X = Cl, Br). Prior to 2009, the chemistry of binary Tc halides was poorly studied and defined by only three compounds, i.e., TcF6, TcF5, and TcCl4. Today, ten phases are known (i.e., TcF6, TcF5, TcCl4, TcBr 4, TcBr3, TcI3, alpha/beta-TcCl3 and alpha/beta-TcCl2) making the binary halide system of Tc comparable to those of its neighboring elements. Technetium binary halides were synthesized using three methods: reactions of the elements in sealed tubes, reactions of flowing HX(g) (X = Cl, Br, and I) with Tc2(O2CCH3)4Cl2, and thermal decompositions of TcX4 (X = Cl, Br) and alpha-TcCl 3 in sealed tubes under vacuum. Binary Tc halides can be found in various dimensionalities such as molecular solids (TcF6), extended chains (TcF5, TcCl4, alpha/beta-TcCl2, TcBr 3, TcI3), infinite layers (beta-TcCl3), and bidimensional networks of clusters (alpha-TcCl3); eight structure-types with varying degrees of metal-metal interactions are now known. The coordination chemistry of Tc binary halides can resemble that of the adjacent elements: molybdenum and ruthenium (beta-TcCl3, TcBr3, TcI 3), rhenium (TcF5, alpha-TcCl3), platinum (TcCl 4, TcBr4), or can be unique (alpha-TcCl2 and beta-TcCl 2) in respect to other known transition metal binary halides. Technetium binary halides display a range of interesting physical properties that are manifested from their electronic and structural configurations. The thermochemistry of binary Tc halides is extensive. These compounds can selectively volatilize, decompose, disproportionate, or convert to other phases. Ultimately, binary Tc halides may find application in the nuclear fuel cycle and as precursors in inorganic and organometallic chemistry.

  8. Process for oxidation of hydrogen halides to elemental halogens

    DOEpatents

    Lyke, Stephen E.

    1992-01-01

    An improved process for generating an elemental halogen selected from chlorine, bromine or iodine, from a corresponding hydrogen halide by absorbing a molten salt mixture, which includes sulfur, alkali metals and oxygen with a sulfur to metal molar ratio between 0.9 and 1.1 and includes a dissolved oxygen compound capable of reacting with hydrogen halide to produce elemental halogen, into a porous, relatively inert substrate to produce a substrate-supported salt mixture. Thereafter, the substrate-supported salt mixture is contacted (stage 1) with a hydrogen halide while maintaining the substrate-supported salt mixture during the contacting at an elevated temperature sufficient to sustain a reaction between the oxygen compound and the hydrogen halide to produce a gaseous elemental halogen product. This is followed by purging the substrate-supported salt mixture with steam (stage 2) thereby recovering any unreacted hydrogen halide and additional elemental halogen for recycle to stage 1. The dissolved oxygen compound is regenerated in a high temperature (stage 3) and an optical intermediate temperature stage (stage 4) by contacting the substrate-supported salt mixture with a gas containing oxygen whereby the dissolved oxygen compound in the substrate-supported salt mixture is regenerated by being oxidized to a higher valence state.

  9. Vitrification of IFR and MSBR halide salt reprocessing wastes

    SciTech Connect

    Siemer, D.D.

    2013-07-01

    Both of the genuinely sustainable (breeder) nuclear fuel cycles (IFR - Integral Fast Reactor - and MSBR - Molten Salt Breeder Reactor -) studied by the USA's national laboratories would generate high level reprocessing waste (HLRW) streams consisting of a relatively small amount ( about 4 mole %) of fission product halide (chloride or fluoride) salts in a matrix comprised primarily (about 95 mole %) of non radioactive alkali metal halide salts. Because leach resistant glasses cannot accommodate much of any of the halides, most of the treatment scenarios previously envisioned for such HLRW have assumed a monolithic waste form comprised of a synthetic analog of an insoluble crystalline halide mineral. In practice, this translates to making a 'substituted' sodalite ('Ceramic Waste Form') of the IFR's chloride salt-based wastes and fluoroapatite of the MSBR's fluoride salt-based wastes. This paper discusses my experimental studies of an alternative waste management scenario for both fuel cycles that would separate/recycle the waste's halide and immobilize everything else in iron phosphate (Fe-P) glass. It will describe both how the work was done and what its results indicate about how a treatment process for both of those wastes should be implemented (fluoride and chloride behave differently). In either case, this scenario's primary advantages include much higher waste loadings, much lower overall cost, and the generation of a product (glass) that is more consistent with current waste management practices. (author)

  10. Photocathodes for the energy recovery linacs

    NASA Astrophysics Data System (ADS)

    Rao, T.; Burrill, A.; Chang, X. Y.; Smedley, J.; Nishitani, T.; Hernandez Garcia, C.; Poelker, M.; Seddon, E.; Hannon, F. E.; Sinclair, C. K.; Lewellen, J.; Feldman, D.

    2006-02-01

    This paper presents an overview of existing and emerging technologies on electron sources that can service various energy recovering linacs under consideration. Photocathodes that can deliver average currents from 1 mA to 1 A, the pros and cons associated with these cathodes are addressed. Status of emerging technologies such as secondary emitters, cesiated dispenser cathodes, field and photon assisted field emitters and super lattice photocathodes are also reviewed.

  11. Photocathodes for the energy recovery linacs

    SciTech Connect

    Rao, T; Burrill, A; Chang, X Y; Smedley, J; Nishitani, T; Garcia, C Hernandez; Poelker, M; Seddon, E; Hannon, F E; Sinclair, C K; Lewellen, J; Feldman, D

    2005-03-19

    This paper presents an overview of existing and emerging technologies on electron sources that can service various Energy Recovering Linacs under consideration. Photocathodes that can deliver average currents from 1 mA to 1 A, the pros and cons associated with these cathodes are addressed. Status of emerging technologies such as secondary emitters, cesiated dispenser cathodes, field and photon assisted field emitters and super lattice photocathodes are also reviewed.

  12. PHOTOCATHODES FOR THE ENERGY RECOVERY LINACS.

    SciTech Connect

    RAO, T.; BURRILL, A.; CHANG, X.Y.; SMEDLEY, J.; ET AL.

    2005-03-19

    This paper presents an overview of existing and emerging technologies on electron sources that can service various Energy Recovering Linacs under consideration. Photocathodes that can deliver average currents from 1 mA to 1 A, the pros and cons associated with these cathodes are addressed. Status of emerging technologies such as secondary emitters, cesiated dispenser cathodes, field and photon assisted field emitters and super lattice photocathodes are also reviewed.

  13. Advanced photocathode simulation and theory

    NASA Astrophysics Data System (ADS)

    Jensen, K. L.; Feldman, D. W.; O'Shea, P. G.

    2003-07-01

    A low work function dispenser type photocathode that is self-annealing or repairing would have a substantial impact on Free Electron Lasers (FELs). On such a cathode, the emitting surface is constantly renewed by replenishment of low-work-function material. A photo-dispenser cathode should operate at a relatively low temperature compared to a conventional dispenser cathode and is anticipated to be robust and long-lived. Coatings cause a reduction in the transport barrier experienced by the electrons through a complex modification of the potential at the surface, e.g., a reduction in work function due to dipole effects. In this work, we describe our theoretical program to address such effects, as part of a program concurrent with experimental efforts to develop dispenser cathodes for use in high power RF photoinjectors. In particular, we discuss the development of a generalised Transmission Coefficient approach, its application to photoemission from metals, and progress towards developing a methodology for the determination of the general emission barrier profile.

  14. High Biomass Specific Methyl Halide Production Rates of Selected Coastal Marsh Plants and its Relationship to Halide Content

    NASA Astrophysics Data System (ADS)

    Manley, S. L.; Wang, N.; Cicerone, R. J.

    2002-12-01

    Salt tolerant coastal marsh plants (halophytes) have previously been shown to be globally significant producers of methyl chloride (MeCl) and methyl bromide (MeBr). While halophytes are known for their high salt content, there are few reports of their halide content. Our studies have attempted to quantify biomass specific methyl halide (MeX) production from these plants and relate it to tissue halide levels. MeCl, MeBr and MeI production rates and tissue chloride, bromide and iodide concentrations from selected coastal marsh plants were measured for nearly a year. Certain halophyte species (i.e. Batis and Frankenia) have very high summer biomass specific production rates for MeX (e.g. Frankenia: 1 ug MeCl /gfwt/hr; 80 ng MeBr/gfwt/hr; 8 ng MeI/gfwt/hr). These rates of MeCl and MeBr production are much higher than those from other coastal marsh plants or seaweeds. Plant halide levels remain high throughout the year, while MeX production peaks at a high level in mid summer falling to low winter rates. This implies a linkage to plant growth. Higher levels of chloride and bromide were seen in the fleshy marsh plants such as Batis (saltwort, approximately 20 percent dry wt chloride, 0.4 percent dry wt bromide) and Salicornia (pickleweed) than in the others such as Frankenia (alkali heath) approx 7 percent dry wt chloride, 0.1 percent dry wt bromide) or Spartina (cordgrass). No such trend was seen for iodide, which ranged from 4 - 10 ppm. Calculations show the daily halide losses from MeX production are far less than the variability in tissue halide content. MeX production removes a small fraction of the total tissue halide from these plants suggesting that MeX production is not a mechanism used by these species to control internal halide levels. Saltwort cell-free extracts incubated with bromide or iodide in the presence of S-adenosyl-L-methionine (SAM) produced the corresponding MeX. MeBr production was inhibited by caffeic acid the substrate of lignin-specific O-methyl transferase. MeX production may be a result of non-specific methylation of halides by SAM utilizing methyl transferases used in other biosynthetic pathways.

  15. RF Gun Photocathode Research at SLAC

    SciTech Connect

    Jongewaard, E.; Akre, R.; Brachmann, A.; Corbett, J.; Gilevich, S.; Grouev, K.; Hering, P.; P.Krejcik,; Lewandowski, J.; Loos, H.; Montagne, T.; Sheppard, J.C.; Stefan, P.; Vlieks, A.; Weathersby, S.; Zhou, F.; /SLAC

    2012-05-16

    LCLS is presently operating with a third copper photocathode in the original rf gun, with a quantum efficiency (QE) of {approx}1 x 10{sup -4} and projected emittance {gamma}{var_epsilon}{sub x,y} = 0.45 {micro}m at 250 pC bunch charge. The spare LCLS gun is installed in the SLAC Accelerator Structure Test Area (ASTA), fully processed to high rf power. As part of a wider photocathode R and D program, a UV laser system and additional gun diagnostics are being installed at ASTA to measure QE, QE lifetime, and electron beam emittance under a variety of operating conditions. The near-term goals are to test and verify the spare photocathode production/installation sequence, including transfer from the final holding chamber to the rf gun. Mid- and longer-term goals include development of a rigorous understanding of plasma and laser-assisted surface conditioning and investigation of new, high-QE photocathode materials. In parallel, an x-ray photoemission spectroscopy station is nearing completion, to analyze Cu photocathode surface chemistry. In this paper we review the status and anticipated operating parameters of ASTA and the spectroscopy test chamber.

  16. Gallium nitride photocathode development for imaging detectors

    NASA Astrophysics Data System (ADS)

    Siegmund, Oswald H. W.; Tremsin, Anton S.; Vallerga, John V.; McPhate, Jason B.; Hull, Jeffrey S.; Malloy, James; Dabiran, Amir M.

    2008-07-01

    Recent progress in Gallium Nitride (GaN, AlGaN, InGaN) photocathodes show great promise for future detector applications in Astrophysical instruments. Efforts with opaque GaN photocathodes have yielded quantum efficiencies up to 70% at 120 nm and cutoffs at ~380 nm, with low out of band response, and high stability. Previous work with semitransparent GaN photocathodes produced relatively low quantum efficiencies in transmission mode (4%). We now have preliminary data showing that quantum efficiency improvements of a factor of 5 can be achieved. We have also performed two dimensional photon counting imaging with 25mm diameter semitransparent GaN photocathodes in close proximity to a microchannel plate stack and a cross delay line readout. The imaging performance achieves spatial resolution of ~50?m with low intrinsic background (below 1 event sec-1 cm-2) and reasonable image uniformity. GaN photocathodes with significant quantum efficiency have been fabricated on ceramic MCP substrates. In addition GaN has been deposited at low temperature onto quartz substrates, also achieving substantial quantum efficiency.

  17. Production and properties of perrhenate-doped alkali halide crystals

    SciTech Connect

    Nestor, O.H.; Figueira, J.F.

    1987-01-01

    The growth and selected properties of single crystals of KCl doped with ReO/sub 4//minus// is described. The crystals have been used as saturable absorbers to modulate and control CO/sub 2/ laser radiation. ReO/sub 4//minus// ion concentrations in excess of 10/sup 17/ cm/sup /minus/3/ were achieved in KCl with good optical quality. The room temperature absorption of the ReO/sub 4//minus// ion in KCl was centered at 936.8 cm/sup /minus/1/ with 1.5 cm/sup (minus/1/ linewidth and with absorption cross section determined to be (0.46 + 0.02) /times/ 10 /sup /minus/16/ cm/sup 2/. The addition of Li/sup /plus// as a second dopant resulted in a splitting of the ReO/sub 4//minus// resonance into two components at 957.5 cm/sup /minus/1/ and 900.7 cm/sup /minus/1/. The characteristically sharp resonance of ReO/sub 4/minus// was not detected in NaCl grown with NaReO/sub 4/ additions to the melt. Only with addition of Ca/sup ++/ as a co-dopant was the ReO/sub 4/minus// resonance observed. The absorption, detected as a very weak resonance through a 92 mm path length, was centered at 946.0 cm/sup /minus/1/ with linewidth of 5 cm/sup /minus/1/ with linewidth of 5 cm/sup /minus/1/, overlapping the P(20) transition in the 10 micron CO/sub 2/ band. 6 refs., 10 figs.

  18. Cold ablation driven by localized forces in alkali halides.

    PubMed

    Hada, Masaki; Zhang, Dongfang; Pichugin, Kostyantyn; Hirscht, Julian; Kochman, Micha? A; Hayes, Stuart A; Manz, Stephanie; Gengler, Regis Y N; Wann, Derek A; Seki, Toshio; Moriena, Gustavo; Morrison, Carole A; Matsuo, Jiro; Sciaini, Germn; Miller, R J Dwayne

    2014-01-01

    Laser ablation has been widely used for a variety of applications. Since the mechanisms for ablation are strongly dependent on the photoexcitation level, so called cold material processing has relied on the use of high-peak-power laser fluences for which nonthermal processes become dominant; often reaching the universal threshold for plasma formation of ~1 J cm(-2) in most solids. Here we show single-shot time-resolved femtosecond electron diffraction, femtosecond optical reflectivity and ion detection experiments to study the evolution of the ablation process that follows femtosecond 400 nm laser excitation in crystalline sodium chloride, caesium iodide and potassium iodide. The phenomenon in this class of materials occurs well below the threshold for plasma formation and even below the melting point. The results reveal fast electronic and localized structural changes that lead to the ejection of particulates and the formation of micron-deep craters, reflecting the very nature of the strong repulsive forces at play. PMID:24835317

  19. An electron-lens for opaque photocathodes.

    NASA Technical Reports Server (NTRS)

    Johnson, C. B.; Hallam, K. L.

    1973-01-01

    It is possible to employ opaque photocathodes in image tubes having a special electromagnetic lens without the use of special internal image-forming optical lenses or mirrors. The special electron lens, having flat object and image planes, is found to provide excellent quality electron-optical image transfer. Stray light reflection inside the tube is expected to be less serious in this electron lens than in a conventional magnetically focused image tube lens due to the offset image plane, and due to the increased absorption of photons in opaque photocathode applications.

  20. Graphene shield enhanced photocathodes and methods for making the same

    DOEpatents

    Moody, Nathan Andrew

    2014-09-02

    Disclosed are graphene shield enhanced photocathodes, such as high QE photocathodes. In certain embodiments, a monolayer graphene shield membrane ruggedizes a high quantum efficiency photoemission electron source by protecting a photosensitive film of the photocathode, extending operational lifetime and simplifying its integration in practical electron sources. In certain embodiments of the disclosed graphene shield enhanced photocathodes, the graphene serves as a transparent shield that does not inhibit photon or electron transmission but isolates the photosensitive film of the photocathode from reactive gas species, preventing contamination and yielding longer lifetime.

  1. Alkali metal nitrate purification

    DOEpatents

    Fiorucci, Louis C. (Hamden, CT); Morgan, Michael J. (Guilford, CT)

    1986-02-04

    A process is disclosed for removing contaminants from impure alkali metal nitrates containing them. The process comprises heating the impure alkali metal nitrates in solution form or molten form at a temperature and for a time sufficient to effect precipitation of solid impurities and separating the solid impurities from the resulting purified alkali metal nitrates. The resulting purified alkali metal nitrates in solution form may be heated to evaporate water therefrom to produce purified molten alkali metal nitrates suitable for use as a heat transfer medium. If desired, the purified molten form may be granulated and cooled to form discrete solid particles of purified alkali metal nitrates.

  2. Wire ageing with the TEA photocathode

    SciTech Connect

    Va`vra, J.

    1996-06-01

    Recently several RICH protypes successfully tested a gaseous TEA photocathode. However, its wire ageing behavior is unknown. In principle, TEA is a more strongly bonded molecule than TMAE, and, as a result, one would expect better wire ageing behavior. This paper explores this question.

  3. Silver-halide gelatin holograms

    NASA Astrophysics Data System (ADS)

    Chang, B. J.; Winick, K.

    1980-05-01

    The use of a silver-halide gelatin for volume phase holograms having a wide spectral response and lower exposure requirements than alternatives and using commercially available silver salts, is proposed. The main difference between the dichromated gelatin and silver-halide processes is the creation of a hologram latent image, which is given in the form of a hardness differential between exposed and unexposed regions in the silver halide hologram; the differential is in turn created by the reaction products of either tanning development or tanning bleach, which harden the gelatin with link-bonds between molecules.

  4. Actinide halide complexes

    SciTech Connect

    Avens, L.R.; Zwick, B.D.; Sattelberger, A.P.; Clark, D.L.; Watkin, J.G.

    1991-02-07

    A compound of the formula MX{sub n}L{sub m} wherein M = Th, Pu, Np,or Am thorium, X = a halide atom, n = 3 or 4, L is a coordinating ligand selected from the group consisting of aprotic Lewis bases having an oxygen-, nitrogen-, sulfur-, or phosphorus-donor, and m is 3 or 4 for monodentate ligands or is 2 for bidentate ligands, where n + m = 7 or 8 for monodentate ligands or 5 or 6 for bidentate ligands, a compound of the formula MX{sub n} wherein M, X, and n are as previously defined, and a process of preparing such actinide metal compounds including admixing the actinide metal in an aprotic Lewis base as a coordinating solvent in the presence of a halogen-containing oxidant, are provided.

  5. A Summary of the 2010 Photocathode Physics for Photoinjectors Workshop

    SciTech Connect

    Bazarov, I; Dowell, D; Hannon, Fay; Harkay, K; Garcia, C H; Padmore, H; Rao, T; Smedley, J

    2010-10-01

    This contribution contains a summary and some highlights from the Photocathode Physics for Photoinjectors (P3) Workshop [1]. This workshop, held at Brookhaven National Laboratory in Ocotber of 2010, was aimed at bringing the photocathode community together to discuss and explore the current state of the art in accelerator photocathodes, from both a theoretical and a materials science perspective. All types of photocathode materials were discussed, including metals, NEA and PEA semiconductors, and "designer" photocathodes with bespoke properties. Topics of the workshop included: Current status of photocathodes for accelerator applications Current fabrication methods Applications of modern materials science to the growth and analysis of cathodes Photoemission spectroscopy as a diagnostic of cathode performance Utilization of modern user facilities Photoemission theory Novel ideas in cathode development Discussion forum on future collaboration for cathode growth, analysis and testing

  6. Multialkali photocathodes grown by molecular beam epitaxy technique

    NASA Astrophysics Data System (ADS)

    Dubovoi, I. A.; Chernikov, A. S.; Prokhorov, Alexander M.; Schelev, Mikhail Y.; Ushakov, Victor N.

    1991-04-01

    A new technique of bialkali photocathodes growth by molecular beam epitaxy (MI3E) has been developed. The photocathode film was deposited onto the substrate from molecular beams produced by simultaneously operating molecular sources of Sb, Na and K. Thus suggested procedure is noticeably differed from the classical one. Growth rate was about 1 A/sec and complete cycle of photocathode fabrication was 15-20 minutes. A special ultra high vacuum (UHV) chamber for MBE of multialkali photocathodes has been designed. The chamber is a part of UHV system consisting of an analysis vessel supplied with Auger and ESCA electron spectrometer and low energy electron diffractometer (LEED), the MBE chamber itself and a chamber for cold sealing of photocathodes with device body through indium ring. The system gives a possibility to carry out investigations of multialkali photocathode physics and to produce commercial devices. Developed technique can be used for fabrication of vacuum devices including streak tubes.

  7. Atomistic simulation of ion solvation in water explains surface preference of halides

    PubMed Central

    Caleman, Carl; Hub, Jochen S.; van Maaren, Paul J.; van der Spoel, David

    2011-01-01

    Water is a demanding partner. It strongly attracts ions, yet some halide anionschloride, bromide, and iodideare expelled to the air/water interface. This has important implications for chemistry in the atmosphere, including the ozone cycle. We present a quantitative analysis of the energetics of ion solvation based on molecular simulations of all stable alkali and halide ions in water droplets. The potentials of mean force for Cl-, Br-, and I- have shallow minima near the surface. We demonstrate that these minima derive from more favorable waterwater interaction energy when the ions are partially desolvated. Alkali cations are on the inside because of the favorable ionwater energy, whereas F- is driven inside by entropy. Models attempting to explain the surface preference based on one or more ion properties such as polarizability or size are shown to lead to qualitative and quantitative errors, prompting a paradigm shift in chemistry away from such simplifications.

  8. Progress on lead photocathodes for superconducting injectors

    SciTech Connect

    Smedley, John; Rao, Triveni; Sekutowicz, Jacek; Kneisel, Peter; Langner, J; Strzyzewski, P; Lefferts, Richard; Lipski, Andrzej

    2005-05-16

    We present the results of our investigation of bulk lead, along with various types of lead films, as suitable photocathode materials for superconducting RF injectors. The quantum efficiency of each sample is presented as a function of the photon energy of the incident light, from 3.9 eV to 6.5 eV. Quantum efficiencies of 0.5% have been obtained. Production of a niobium cavity with a lead plated cathode is underway.

  9. PROGRESS ON LEAD PHOTOCATHODES FOR SUPERCONDUCTING INJECTORS.

    SciTech Connect

    SMEDLEY, J.; RAO, T.; SEKUTOWICZ, J.; KNEISEL, P.; LANGNER, J.; STRZYZEWSKI, P.; LEFFERTS, R.; LIPSKI, A.

    2005-05-16

    We present the results of our investigation of bulk lead, along with various types of lead films, as suitable photocathode materials for superconducting RF injectors. The quantum efficiency of each sample is presented as a function of the photon energy of the incident light, from 3.9 eV to 6.5 eV. Quantum efficiencies of 0.5% have been obtained. Production of a niobium cavity with a lead-plated cathode is underway.

  10. Activation Layer Stabilization of High Polarization Photocathodes in Sub-Optimal RF Gun Environments

    SciTech Connect

    Gregory A. Mulhollan

    2010-11-16

    Specific activation recipes for bulk, 100 nm thick MBE grown and high polarization III-V photocathode material have been developed which mitigate the effects of exposure to background gasses. Lifetime data using four representative gasses were acquired for bulk GaAs, 100 nm unstrained GaAs and strained superlattice GaAs/GaAsP, all activated both with Cs and then Cs and Li (bi-alkali). Each photoemitter showed marked resilience improvement when activated using the bi-alkali recipe compared to the standard single alkali recipe. A dual alkali activation system at SLAC was constructed, baked and commissioned with the purpose of performing spin-polarization measurements on electrons emitted from the bi-alkali activated surfaces. An end station at SSRL was configured with the required sources for energy resolved photoemission measurements on the bi-alkali activated and CO2 dosed surfaces. The bi-alkali recipes were successfully implemented at SLAC/SSRL. Measurements at SLAC of the photoelectron spin-polarization from the modified activation surface showed no sign of a change in value compared to the standard activated material, i.e., no ill effects. Analysis of photoemission data indicates that the addition of Li to the activation layer results in a multi-layer structure. The presence of Li in the activation layer also acts as an inhibitor to CO2 absorption, hence better lifetimes in worse vacuum were achieved. The bi-alkali activation has been tested on O2 activated GaAs for comparison with NF3 activated surfaces. Comparable resilience to CO2 exposure was achieved for the O2 activated surface. An RF PECVD amorphous silicon growth system was modified to allow high temperature heat cleaning of GaAs substrates prior to film deposition. Growth versus thickness data were collected. Very thin amorphous silicon germanium layers were optimized to exhibit good behavior as an electron emitter. Growth of the amorphous silicon germanium films on the above substrates was fine tuned with respect to time and power to moderate plasma damage to the photo-generating layer. Auger electron spectroscopy was used to analyze the composition and thickness of the emitter layers. AFM studies showed conformal growth on the GaAs substrates. Measurements at SLAC on the photoemitted electrons from high polarization substrates coated with amorphous silicon germanium indicated an ~10% relative drop in spin-polarization at the wavelength corresponding to the maximum spin-polarization when compared to the uncoated material,

  11. Methyl Halide Production by Fungi

    NASA Astrophysics Data System (ADS)

    Dailey, G. D.; Varner, R. K.; Blanchard, R. O.; Sive, B. C.; Crill, P. M.

    2005-12-01

    Methyl chloride (CH3Cl), methyl bromide (CH3Br) and methyl iodide (CH3I) are methyl halide gases that contribute significant amounts of halogen radicals to the atmosphere. In an effort to better understand the global budget of methyl halides and their impact on the atmosphere, we need to identify the natural sources in addition to the known anthropogenic sources of these compounds. We are investigating the role of fungi in the production of methyl halides in the soils and wetlands in southern New Hampshire, USA. Previous research has shown that wood decay fungi and ectomycorrhizal fungi, which are within a group of fungi called basidiomycetes, emit methyl halides. In our study, measurements of headspace gas extracted from flasks containing fungi grown in culture demonstrate that a variety of fungi, including basidiomycetes and non-basidiomycetes, emit methyl halides. Our research sites include four ecosystems: an agricultural field, a temperate forest, a fresh water wetland, and coastal salt marshes. We have collected and isolated fungi at each site by culturing tissue samples of fruiting bodies and plant material, by using wood baits, and from the direct culture of soil. We compared the rates of methyl halide emissions from the fungi in the four ecosystems. In addition, we measured emissions from previously assayed fungal isolates after reintroducing them to sterilized soils that were collected from their original environments. Fungal biomass was determined by substrate-induced respiration (SIR). The emission rate by the fungus was determined by a linear regression of the concentration of methyl halide in the sample headspace over time divided by the fungal biomass.

  12. Actinide halide complexes

    DOEpatents

    Avens, Larry R.; Zwick, Bill D.; Sattelberger, Alfred P.; Clark, David L.; Watkin, John G.

    1992-01-01

    A compound of the formula MX.sub.n L.sub.m wherein M is a metal atom selected from the group consisting of thorium, plutonium, neptunium or americium, X is a halide atom, n is an integer selected from the group of three or four, L is a coordinating ligand selected from the group consisting of aprotic Lewis bases having an oxygen-, nitrogen-, sulfur-, or phosphorus-donor, and m is an integer selected from the group of three or four for monodentate ligands or is the integer two for bidentate ligands, where the sum of n+m equals seven or eight for monodentate ligands or five or six for bidentate ligands, a compound of the formula MX.sub.n wherein M, X, and n are as previously defined, and a process of preparing such actinide metal compounds including admixing the actinide metal in an aprotic Lewis base as a coordinating solvent in the presence of a halogen-containing oxidant, are provided.

  13. Actinide halide complexes

    DOEpatents

    Avens, L.R.; Zwick, B.D.; Sattelberger, A.P.; Clark, D.L.; Watkin, J.G.

    1992-11-24

    A compound is described of the formula MX[sub n]L[sub m] wherein M is a metal atom selected from the group consisting of thorium, plutonium, neptunium or americium, X is a halide atom, n is an integer selected from the group of three or four, L is a coordinating ligand selected from the group consisting of aprotic Lewis bases having an oxygen-, nitrogen-, sulfur-, or phosphorus-donor, and m is an integer selected from the group of three or four for monodentate ligands or is the integer two for bidentate ligands, where the sum of n+m equals seven or eight for monodentate ligands or five or six for bidentate ligands. A compound of the formula MX[sub n] wherein M, X, and n are as previously defined, and a process of preparing such actinide metal compounds are described including admixing the actinide metal in an aprotic Lewis base as a coordinating solvent in the presence of a halogen-containing oxidant.

  14. Photoemission Spectroscopic Study of Cesium Telluride Thin Film Photocathode

    SciTech Connect

    Sugiyama, Harue; Ogawa, Koji; Azuma, Junpei; Takahashi, Kazutoshi; Kamada, Masao

    2009-08-04

    The photoemission spectroscopy using synchrotron radiation has been carried out to study the high quantum efficiency and long working lifetime of cesium telluride (Cs{sub x}Te{sub y}) thin film photocathode. The electron affinity derived from the observed energy-distribution curves provides an important hint for long persistency of the photocathode.

  15. Preparation of cerium halide solvate complexes

    DOEpatents

    Vasudevan, Kalyan V; Smith, Nickolaus A; Gordon, John C; McKigney, Edward A; Muenchaussen, Ross E

    2013-08-06

    Crystals of a solvated cerium(III) halide solvate complex resulted from a process of forming a paste of a cerium(III) halide in an ionic liquid, adding a solvent to the paste, removing any undissolved solid, and then cooling the liquid phase. Diffusing a solvent vapor into the liquid phase also resulted in crystals of a solvated cerium(III) halide complex.

  16. Radiochemical synthesis of pure anhydrous metal halides

    NASA Technical Reports Server (NTRS)

    Philipp, W. H.; Marsik, S. J.; May, C. E.

    1973-01-01

    Method uses radiation chemistry as practical tool for inorganic preparations and in particular deposition of metals by irradiation of their aqueous metal salt solutions with high energy electrons. Higher valence metal halide is dissolved in organic liquid and exposed to high energy electrons. This causes metal halide to be reduced to a lower valence metal halide.

  17. Structure-Tuned Lead Halide Perovskite Nanocrystals.

    PubMed

    Hassan, Yasser; Song, Yin; Pensack, Ryan D; Abdelrahman, Ahmed I; Kobayashi, Yoichi; Winnik, Mitchell A; Scholes, Gregory D

    2016-01-01

    Colloidally stable suspensions of lead halide perovskite nanocrystals are prepared from high-quality lead halide nanocrystal seeds. Perovskite nanocrystals with different layered crystal structures are reported. These systems are well suited for investigations of the intrinsic photophysics and spectroscopy of organic-inorganic metal halide perovskites. PMID:26596245

  18. Development of Polarized Photocathodes for the Linear Collider

    SciTech Connect

    Richard Prepost

    2009-12-22

    In prior years a Wisconsin-SLAC collaboration developed polarized photocathodes which were used for the SLAC SLD and fixed target programs. Currently, the R&D program goal is the development of a polarized electron source (PES) which meets the ILC requirements for polarization, charge, lifetime, and pulse structure. There are two parts to this program. One part is the continued improvement of photocathode structures with higher polarization. The second part is the design and development of the laser system used to drive the photocathode. The long pulse train for the ILC introduces new challenges for the PES. More reliable and stable operation of the PES may be achievable if appropriate R&D is carried out for higher voltage operation and for a simpler photocathode load-lock system. The collaboration with SLAC is through the Polarized Photocathode Research Collaboration (PPRC). Senior SLAC personnel include T. Maruyama, J. Clendenin, R. Kirby, and A. Brachmann.

  19. Advances in DC photocathode electron guns

    SciTech Connect

    Bruce M. Dunham; P. Heartmann; Reza Kazimi; Hongxiu Liu; B. M. Poelker; J. S. Price; P. M. Rutt; W. J. Schneider; Charles K. Sinclair

    1998-07-01

    At Jefferson Lab, a DC photoemission gun using GaAs and GaAs-like cathodes provides a source of polarized electrons for the main accelerator. The gun is required to produce high average current with long operational lifetimes and high system throughout. Recent work has shown that careful control of the parameters affecting cathode lifetime lead to dramatic improvements in source operation. These conditions include vacuum and the related effect of ion backbombardment, and precise control of all of the electrons emitted from the cathode. In this paper, the authors will review recent results and discuss implications for future photocathode guns.

  20. STATUS OF DIAMOND SECONDARY EMISSION ENHANCED PHOTOCATHODE

    SciTech Connect

    RAO,T.; BEN-ZVI, I.; CHANG, X.; GRIMES, J.; GROVER, R.; ISAKOVIC, A.; SMEDLEY, J.; TODD, R.; WARREN, J.; WU, Q.

    2007-05-25

    The diamond secondary emission enhanced photocathode (SEEP) provides an attractive alternative for simple photo cathodes in high average current electron injectors. It reduces the laser power required to drive the cathode, simultaneously isolating the cathode and the FW cavity from each other, thereby protecting them from contamination and increasing their life time. In this paper, we present the latest results on the secondary electron yield using pulsed thermionic and photo cathodes as primary electron sources, shaping the diamond using laser ablation and reactive ion etching as well as the theoretical underpinning of secondary electron generation and preliminary results of modeling.

  1. Performance of photocathode rf gun electron accelerators

    SciTech Connect

    Ben-Zvi, I.

    1993-07-01

    In Photo-Injectors (PI) electron guns, electrons are emitted from a photocathode by a short laser pulse and then accelerated by intense rf fields in a resonant cavity. The best known advantage of this technique is the high peak current with a good emittance (high brightness). This is important for short wavelength Free-Electron Lasers and linear colliders. PIs are in operation in many electron accelerator facilities and a large number of new guns are under construction. Some applications have emerged, providing, for example, very high pulse charges. PIs have been operated over a wide range of frequencies, from 144 to 3000 MHz (a 17 GHz gun is being developed). An exciting new possibility is the development of superconducting PIs. A significant body of experimental and theoretical work exists by now, indicating the criticality of the accelerator elements that follow the gun for the preservation of the PI`s performance as well as possible avenues of improvements in brightness. Considerable research is being done on the laser and photocathode material of the PI, and improvement is expected in this area.

  2. Performance of photocathode rf gun electron accelerators

    SciTech Connect

    Ben-Zvi, I.

    1993-01-01

    In Photo-Injectors (PI) electron guns, electrons are emitted from a photocathode by a short laser pulse and then accelerated by intense rf fields in a resonant cavity. The best known advantage of this technique is the high peak current with a good emittance (high brightness). This is important for short wavelength Free-Electron Lasers and linear colliders. PIs are in operation in many electron accelerator facilities and a large number of new guns are under construction. Some applications have emerged, providing, for example, very high pulse charges. PIs have been operated over a wide range of frequencies, from 144 to 3000 MHz (a 17 GHz gun is being developed). An exciting new possibility is the development of superconducting PIs. A significant body of experimental and theoretical work exists by now, indicating the criticality of the accelerator elements that follow the gun for the preservation of the PI's performance as well as possible avenues of improvements in brightness. Considerable research is being done on the laser and photocathode material of the PI, and improvement is expected in this area.

  3. Modern theory and applications of photocathodes

    SciTech Connect

    Spicer, W.E.; Herrera-Gomez, A.

    1993-08-01

    Over the last thirty years, the Spicer Three-Step model has provided a very useful description of the process of photoemission for both fundamental and practical applications. By treating photoemission in terms of three successive steps-optical absorption, electron transport, and escape across the surface this theory allows photoemission to be related to parameters of the emitter, such as the optical absorption coefficient, electron scattering mechanisms, and the height of the potential barrier at the surface. Using simple equations and established parameters, the Three-Step model predicts the performance of cathodes and provides detailed understanding of the unexpected phenomena that appear when photocathodes are pushed into new practical domains. As an example, time responses are estimated for existing cathodes, and are found to cover a range of six orders of magnitude. Further, the time response is found to be directly related to the sensitivity (i.e., quantum efficiency) of the cathode. The quantum yield systematically decreases with the time response. Thus, metals are predicted to have the shortest time response (as little as 10{sup {minus}15} sec) and the smallest quantum efficiency (as little as 10{sup {minus}4} electrons per photon), whereas the negative affinity photocathodes have high yield (as high as 0.6 electrons per photon) but long response times (as long as 10{sup {minus}9} sec). Other applications of the Three-Step model are discussed.

  4. Development of Halide and Oxy-Halides for Isotopic Separations

    SciTech Connect

    Leigh R. Martin; Aaron T. Johnson; Jana Pfeiffer; Martha R. Finck

    2014-10-01

    The goal of this project was to synthesize a volatile form of Np for introduction into mass spectrometers at INL. Volatile solids of the 5f elements are typically those of the halides (e.g. UF6), however fluorine is highly corrosive to the sensitive internal components of the mass separator, and the other volatile halides exist as several different stable isotopes in nature. However, iodide is both mono-isotopic and volatile, and as such presents an avenue for creation of a form of Np suitable for introduction into the mass separator. To accomplish this goal, the technical work in the project sought to establish a novel synthetic route for the conversion NpO2+ (dissolved in nitric acid) to NpI3 and NpI4.

  5. Milk-alkali syndrome

    MedlinePLUS

    ... the dynamics of calcium homeostasis. Clin J Am Soc Nephrol . 1006;1:641– 654. Grubb M, Gaurav ... Welcome to the calcium-alkali syndrome. J Am Soc Nephrol. 2010;21:1440-1443. Yoshizawa H, Morishita ...

  6. Studies of Self-Trapped Exciton Luminescence in Ammonium Halides

    NASA Astrophysics Data System (ADS)

    Itoh, Minoru

    1988-01-01

    Intrinsic luminescence of ammonium halides has been studied under excitation with UV light or N2 laser pulse and also under red light stimulation during exposure to UV light. In NH4Br, a broad luminescence is observed at 4.18 eV and attributed to the radiative decay of self-trapped exciton (STE). Its intensity, decay time and linear polarization are measured as a function of temperature between 10 and 70 K. These data are well interpreted in terms of an energy-level structure of STEs in which a singlet state is located approximately 10 meV above a triplet state. In NH4Cl, it is confirmed that the 4.91 eV luminescence arising from singlet STEs is intensely excited with UV light in the exciton region as well as the band-to-band region. The above results will be discussed in comparison with those obtained in the alkali halides.

  7. High gradient rf gun studies of CsBr photocathodes

    SciTech Connect

    Vecchione, Theodore; Maldonado, Juan R.; Gierman, Stephen; Corbett, Jeff; Hartmann, Nick; Pianetta, Piero A.; Hesselink, Lambertus; Schmerge, John F.

    2015-04-03

    CsBr photocathodes have 10 times higher quantum efficiency with only 3 times larger intrinsic transverse emittance than copper. They are robust and can withstand 80 MV/m fields without breaking down or emitting dark current. They can operate in 210?? torr vacuum and survive exposure to air. They are well suited for generating high pulse charge in rf guns without a photocathode transfer system.

  8. High gradient rf gun studies of CsBr photocathodes

    DOE PAGESBeta

    Vecchione, Theodore; Maldonado, Juan R.; Gierman, Stephen; Corbett, Jeff; Hartmann, Nick; Pianetta, Piero A.; Hesselink, Lambertus; Schmerge, John F.

    2015-04-03

    CsBr photocathodes have 10 times higher quantum efficiency with only 3 times larger intrinsic transverse emittance than copper. They are robust and can withstand 80 MV/m fields without breaking down or emitting dark current. They can operate in 2×10⁻⁹ torr vacuum and survive exposure to air. They are well suited for generating high pulse charge in rf guns without a photocathode transfer system.

  9. Advanced 3D Photocathode Modeling and Simulations Final Report

    SciTech Connect

    Dimitre A Dimitrov; David L Bruhwiler

    2005-06-06

    High brightness electron beams required by the proposed Next Linear Collider demand strong advances in photocathode electron gun performance. Significant improvement in the production of such beams with rf photocathode electron guns is hampered by the lack high-fidelity simulations. The critical missing piece in existing gun codes is a physics-based, detailed treatment of the very complex and highly nonlinear photoemission process.

  10. High gradient rf gun studies of CsBr photocathodes

    NASA Astrophysics Data System (ADS)

    Vecchione, Theodore; Maldonado, Juan R.; Gierman, Stephen; Corbett, Jeff; Hartmann, Nick; Pianetta, Piero A.; Hesselink, Lambertus; Schmerge, John F.

    2015-04-01

    CsBr photocathodes have 10 times higher quantum efficiency with only 3 times larger intrinsic transverse emittance than copper. They are robust and can withstand 80 MV /m fields without breaking down or emitting dark current. They can operate in 2 ×10-9 torr vacuum and survive exposure to air. They are well suited for generating high pulse charge in rf guns without a photocathode transfer system.

  11. Atomic forces between noble gas atoms, alkali ions, and halogen ions for surface interactions

    NASA Technical Reports Server (NTRS)

    Wilson, J. W.; Outlaw, R. A.; Heinbockel, J. H.

    1988-01-01

    The components of the physical forces between noble gas atoms, alkali ions, and halogen ions are analyzed and a data base developed from analysis of the two-body potential data, the alkali-halide molecular data, and the noble gas crystal and salt crystal data. A satisfactory global fit to this molecular and crystal data is then reproduced by the model to within several percent. Surface potentials are evaluated for noble gas atoms on noble gas surfaces and salt crystal surfaces with surface tension neglected. Within this context, the noble gas surface potentials on noble gas and salt crystals are considered to be accurate to within several percent.

  12. R&D ERL: Photocathode Deposition and Transport System

    SciTech Connect

    Pate, D.; Ben-Zvi, I.; Rao, T.; Burrill, R.; Todd, R.; Smedley, J.; Holmes, D.

    2010-01-01

    The purpose of the photocathode deposition and transport system is to (1) produce a robust, high yield multialkali photocathode and (2) have a method of transporting the multialkali photocathode for insertion into a super conducting RF electron gun. This process is only successful if a sufficient quantum efficiency lifetime of the cathode, which is inserted in the SRF electron gun, is maintained. One important element in producing a multialkali photocathode is the strict vacuum requirements of 10{sup -11} torr to assure success in the production of longlived photocathodes that will not have their QE or lifetime depleted due to residual gas poisoning in a poor vacuum. A cutaway view of our third generation deposition system is shown in figure 1. There are certain design criteria and principles required. One must be able to install, remove, rejuvenate and replace a cathode without exposing the source or cathode to atmosphere. The system must allow one to deposit Cs, K, and Sb on a cathode tip surface at pressures in the 10{sup -10} to 10{sup -9} torr range. The cathode needs to be heated to as high as 850 C for cleaning and maintained at 130 C to 150 C during deposition. There should also be the capability for in-situ QE measurements. In addition the preparation of dispenser photocathodes must be accounted for, thus requiring an ion source for cathode cleaning. Finally the transport cart must be mobile and be able to negotiate the ERL facility labyrinth.

  13. Metal Photocathodes for Free Electron Laser Applications

    NASA Astrophysics Data System (ADS)

    Greaves, Corin Michael Ricardo

    Synchrotron x-ray radiation sources have revolutionized many areas of science from elucidating the atomic structure of proteins to understanding the electronic structure of complex materials such as the cuprate superconductors. In a Free Electron Laser (FEL), the main difference to the synchrotron radiation mechanism is that the light field acts on the electron beam, over a long distance in an undulator, and causes electron bunching at the optical wavelength. Electrons in different parts of the electron bunch are therefore correlated, and so emit coherently, with a brightness that scales as the square of the number of electrons. In order to lase, the electron beam in a FEL must have a transverse geometric emittance less than the wavelength of the light to be produced. For the generation of x-ray wavelengths, this is one of the most difficult challenges in the design and construction of a FEL. The geometric emittance can be "compressed" by acceleration to very high energy, but with the penalty of very large physical size and very large cost. The motivation for this work was provided by the desire to investigate the fundamental origin of the emittance of an electron beam as it is born at a photocathode. If this initial, or "thermal" emittance can be reduced, the energy, scale and cost of accelerators potentially would be reduced. As the LCLS used copper as its photocathode, this material was the one studied in this work. Copper was used in the LCLS as it represented a "robust" material that could stand the very high accelerating gradients used in the photoinjector of the FEL. Metals are also prompt photoemitters, and so can be used to produce very short electron bunches. This can be a useful property for creation of extremely short FEL pulses, and also for creation of beams that are allowed to expand under space charge forces, but in a way that results in linear fields, allowing subsequent recompression. An ideal photocathode for FEL photoinjector should have high quantum efficiency (QE), small emittance, fast temporal response, long lifetime, and minimal complexity. High QE of cathodes require less power for driving laser and also reduce the risk of damaging the cathode materials. Small emittance reduce the scale of the accelerator, therefore, the cost. Metal photocathodes such as copper exhibit long lifetime and fast response, but have quite low quantum efficiency ( < 10-4). The aim in this work was to understand the quantum yield of the metal, and the transverse momentum spectrum, as the product of the latter and the cathode beam spot size gives the transverse emittance. Initial x-ray diffraction work provided evidence that the LCLS photocathode consisted of large low index single crystal grains, and so work focused on the study of single crystals that could be produced with atomically ordered surfaces, rather than a polycrystalline material. Present theories of quantum yield and transverse emittance assume the basic premise that the metal is entirely disordered, and work here shows that this is fundamentally incorrect, and that the order of the surface plays a critical role in determining the characteristics of emission. In order to investigate these surfaces, I constructed a laser-based ultra-low energy angle resolved photoemission system, capable of measuring the momentum spectrum of the emission and wavelength and angle dependent electron yield. This system has been commissioned, and data taken on low index surfaces of copper. Results from this work on single crystal copper demonstrates that emitted electrons from the band structure of a material can exhibit small emittance and high quantum efficiency. We show that the emission from the Cu(111) surface state is highly correlated between angle of incidence and excitation energy. This manifests itself in the form of a truncated emission cone, rather than the isotropic emission predicted from the normal model. This clearly then reduces the emittance from the normal values. It also results in extremely strong polarization dependence, wi

  14. Apparatus enables accurate determination of alkali oxides in alkali metals

    NASA Technical Reports Server (NTRS)

    Dupraw, W. A.; Gahn, R. F.; Graab, J. W.; Maple, W. E.; Rosenblum, L.

    1966-01-01

    Evacuated apparatus determines the alkali oxide content of an alkali metal by separating the metal from the oxide by amalgamation with mercury. The apparatus prevents oxygen and moisture from inadvertently entering the system during the sampling and analytical procedure.

  15. Fabrication and measurement of regenerable low work function dispenser photocathodes

    NASA Astrophysics Data System (ADS)

    Moody, Nathan A.

    Laser-switched photoemitters are a source of electrons for high current applications such as free electron lasers. Laser-modulated photoemission permits rapid switching of the electron beam, far surpassing what can be achieved using electric-field gated emission. Photoinjector systems consist of a drive laser producing short bunches of photons and an efficient photocathode, which converts photon bunches into electron beam pulses. Development of both technologies is required, but the scope of this project is restricted to improvement of the photocathode. Most high-efficiency photocathodes employ cesium-based surface coatings to reduce work function and enable efficient electron emission in the visible range. Lifetime is severely limited by the loss of this delicate coating, which degrades rapidly in practical vacuum environments. More robust photocathodes exist, but have much lower efficiency, and place unrealistic demands on drive laser power and stability. This research proposes a novel dispenser concept that dramatically extends the lifetime of high efficiency cesium-based cathodes by continuously or periodically restoring the cesium surface monolayer during an in situ rejuvenation process. Sintered tungsten provides an interface between a cesium reservoir and the photoemitting surface. During temperature-controlled rejuvenation, cesium diffuses through and across the sintered tungsten to create and sustain a low-work function photocathode. The prototype dispenser cathode was fabricated and tested for two modes of operation: continuous and periodic near-room temperature rejuvenation. The data are compared with a photoemission model of partially covered surfaces under design for integration with existing beam simulations. Overall performance suggests that this cesium-delivery mechanism can significantly enhance the efficiency and operational lifetime of a wide variety of present and future cesium-based photocathodes. Also reported are surface characterization, ion beam cleaning, and fabrication techniques used to optimize performance of the dispenser photocathode.

  16. Synthesis of aryl halides via organoborane chemistry

    SciTech Connect

    Kabalka, G.W.; Sastry, K.A.R.; Sastry, U.; Somayaji, V.

    1982-01-01

    A method for the rapid synthesis of a variety of substituted aryl halides by the reaction of organoboranes with halide ions in the presence of chloramine-T is described in detail. The products were purified by column chromatography on silica gel using a mixture of petroleum ether-ethyl acetate as eluent.

  17. Alkalis and Skin.

    PubMed

    Greenwood, John E; Tan, Jin Lin; Ming, Justin Choong Tzen; Abell, Andrew D

    2016-01-01

    The aim of this editorial is to provide an overview of the chemical interactions occurring in the skin of our patients on contact with alkaline agents. Strongly basic alkali is highly aggressive and will readily hydrolyze (or cleave) key biological molecules such as lipids and proteins. This phenomenon is known as saponification in the case of lipids and liquefactive denaturation for peptides and proteins. A short section on current first-aid concepts is included. A better understanding of the basic science behind alkali burns will make us better teachers and provide an insight into the urgency needed in treating these common and dangerous chemical injuries. PMID:26182072

  18. Ideas about Acids and Alkalis.

    ERIC Educational Resources Information Center

    Toplis, Rob

    1998-01-01

    Investigates students' ideas, conceptions, and misconceptions about acids and alkalis before and after a teaching sequence in a small-scale research project. Concludes that student understanding of acids and alkalis is lacking. (DDR)

  19. Alkali metal ion battery with bimetallic electrode

    DOEpatents

    Boysen, Dane A; Bradwell, David J; Jiang, Kai; Kim, Hojong; Ortiz, Luis A; Sadoway, Donald R; Tomaszowska, Alina A; Wei, Weifeng; Wang, Kangli

    2015-04-07

    Electrochemical cells having molten electrodes having an alkali metal provide receipt and delivery of power by transporting atoms of the alkali metal between electrode environments of disparate chemical potentials through an electrochemical pathway comprising a salt of the alkali metal. The chemical potential of the alkali metal is decreased when combined with one or more non-alkali metals, thus producing a voltage between an electrode comprising the molten the alkali metal and the electrode comprising the combined alkali/non-alkali metals.

  20. Hygroscopicity Evaluation of Halide Scintillators

    SciTech Connect

    Zhuravleva, M; Stand, L; Wei, H; Hobbs, C. L.; Boatner, Lynn A; Ramey, Joanne Oxendine; Burger, Arnold; Rowe, E; Bhattacharya, P.; Tupitsyn, E; Melcher, Charles L

    2014-01-01

    A collaborative study of relative hygroscopicity of anhydrous halide scintillators grown at various laboratories is presented. We have developed a technique to evaluate moisture sensitivity of both raw materials and grown crystals, in which the moisture absorption rate is measured using a gravimetric analysis. Degradation of the scintillation performance was investigated by recording gamma-ray spectra and monitoring the photopeak position, count rate and energy resolution. The accompanying physical degradation of the samples exposed to ambient atmosphere was photographically recorded as well. The results were compared with ben

  1. Progress on diamond amplified photo-cathode

    SciTech Connect

    Wang, E.; Ben-Zvi, I.; Burrill, A.; Kewisch, J.; Chang, X.; Rao, T.; Smedley, J.; Wu, Q.; Muller, E.; Xin, T.

    2011-03-28

    Two years ago, we obtained an emission gain of 40 from the Diamond Amplifier Cathode (DAC) in our test system. In our current systematic study of hydrogenation, the highest gain we registered in emission scanning was 178. We proved that our treatments for improving the diamond amplifiers are reproducible. Upcoming tests planned include testing DAC in a RF cavity. Already, we have designed a system for these tests using our 112 MHz superconducting cavity, wherein we will measure DAC parameters, such as the limit, if any, on emission current density, the bunch charge, and the bunch length. The diamond-amplified photocathode, that promises to support a high average current, low emittance, and a highly stable electron beam with a long lifetime, is under development for an electron source. The diamond, functioning as a secondary emitter amplifies the primary current, with a few KeV energy, that comes from the traditional cathode. Earlier, our group recorded a maximum gain of 40 in the secondary electron emission from a diamond amplifier. In this article, we detail our optimization of the hydrogenation process for a diamond amplifier that resulted in a stable emission gain of 140. We proved that these characteristics are reproducible. We now are designing a system to test the diamond amplifier cathode using an 112MHz SRF gun to measure the limits of the emission current's density, and on the bunch charge and bunch length.

  2. Methods of recovering alkali metals

    DOEpatents

    Krumhansl, James L; Rigali, Mark J

    2014-03-04

    Approaches for alkali metal extraction, sequestration and recovery are described. For example, a method of recovering alkali metals includes providing a CST or CST-like (e.g., small pore zeolite) material. The alkali metal species is scavenged from the liquid mixture by the CST or CST-like material. The alkali metal species is extracted from the CST or CST-like material.

  3. Photocathode Optimization for a Dynamic Transmission Electron Microscope: Final Report

    SciTech Connect

    Ellis, P; Flom, Z; Heinselman, K; Nguyen, T; Tung, S; Haskell, R; Reed, B W; LaGrange, T

    2011-08-04

    The Dynamic Transmission Electron Microscope (DTEM) team at Harvey Mudd College has been sponsored by LLNL to design and build a test setup for optimizing the performance of the DTEM's electron source. Unlike a traditional TEM, the DTEM achieves much faster exposure times by using photoemission from a photocathode to produce electrons for imaging. The DTEM team's work is motivated by the need to improve the coherence and current density of the electron cloud produced by the electron gun in order to increase the image resolution and contrast achievable by DTEM. The photoemission test setup is nearly complete and the team will soon complete baseline tests of electron gun performance. The photoemission laser and high voltage power supply have been repaired; the optics path for relaying the laser to the photocathode has been finalized, assembled, and aligned; the internal setup of the vacuum chamber has been finalized and mostly implemented; and system control, synchronization, and data acquisition has been implemented in LabVIEW. Immediate future work includes determining a consistent alignment procedure to place the laser waist on the photocathode, and taking baseline performance measurements of the tantalum photocathode. Future research will examine the performance of the electron gun as a function of the photoemission laser profile, the photocathode material, and the geometry and voltages of the accelerating and focusing components in the electron gun. This report presents the team's progress and outlines the work that remains.

  4. Chlor-Alkali Technology.

    ERIC Educational Resources Information Center

    Venkatesh, S.; Tilak, B. V.

    1983-01-01

    Chlor-alkali technology is one of the largest electrochemical industries in the world, the main products being chlorine and caustic soda (sodium hydroxide) generated simultaneously by the electrolysis of sodium chloride. This technology is reviewed in terms of electrochemical principles and manufacturing processes involved. (Author/JN)

  5. Impurity segregation in zone-refined precursors for crystalline halide scintillators

    NASA Astrophysics Data System (ADS)

    Swider, S.; Lam, S.; Motakef, S.; Donohoe, E.; Coers, L.; Taylor, S.; Spencer, S.

    2015-06-01

    Successful growth of halide scintillator crystals depends on a supply of ultra-high purity (UHP) precursor materials. Metallic interstitials and substitutions may provide traps that quench luminescence. Oxygen impurities can create competing compounds within a matrix, such as oxyhalides, that disrupt crystallinity and nucleate cracks. Using mass spectroscopy and oxygen combustion analysis, we analyzed impurities in SrI2, EuI2, and YCl3 precursors before and after zone refining. The data show most alkali and alkali earth impurities segregated easily. However, with the exception of iron, many transition metals were incorporated into the solid. Reliable oxygen measurements proved difficult to achieve. Additional oxygen was measured in nitrates and sulfates, via ion chromatography. Zone refining reduced the overall impurity content, but levels remained above a 10 ppm target.

  6. Characterization of diamond film and bare metal photocathodes as a function of temperature and surface preparation

    SciTech Connect

    Shurter, R.P.; Moir, D.C.; Devlin, D.J.

    1996-07-01

    High current photocathodes using bare metal and polycrystalline diamond films illuminated by ultraviolet lasers are being developed at Los Alamos for use in a new generation of linear induction accelerators. These photocathodes must be able to produce multiple 60 ns pulses separated by several to tens of nanoseconds. The vacuum environment in which the photocathodes must operate is 10{sup -5} torr.

  7. Study of photoemission mechanism for varied doping GaN photocathode

    NASA Astrophysics Data System (ADS)

    Qiao, Jianliang; Xu, Yuan; Niu, Jun; Gao, Youtang; Chang, Benkang

    2015-10-01

    Negative electron affinity (NEA) GaN photocathode has many virtues, such as high quantum efficiency, low dark current, concentrated electrons energy distribution and angle distribution, adjustive threshold and so on. The quantum efficiency is an important parameter for the preparation and evaluation of NEA GaN photocathode. The varied doping GaN photocathode has the directional inside electric field within the material, so the higher quantum efficiency can be obtained. The varied doping NEA GaN photocathode has better photoemission performance. According to the photoemission theory of NEA GaN photocathode, the quantum efficiency formulas for uniform doping and varied doping NEA GaN photocathodes were given. In the certain condition, the quantum efficiency formula for varied doping GaN photocathode consists with the uniform doping. The activation experiment was finished for varied doping GaN photocathode. The cleaning method and technics for varied doping GaN photocathode were given in detail. To get an atom clean surface, the heat cleaning must be done after the chemical cleaning. Using the activation and evaluation system for NEA photocathode, the varied doping GaN photocathode was activated with Cs and O, and the photocurrent curve for varied doping GaN photocathode was gotten.

  8. Polarized Photocathode R&D for Future Linear Collliders

    SciTech Connect

    Zhou, F; Brachmann, A.; Maruyama, T.; Sheppard, J.C.; /SLAC

    2009-01-23

    It is a challenge to generate full charge electrons from the electron sources without compromising polarization for the proposed ILC and CLIC. It is essential to advance polarized photocathodes to meet the requirements. SLAC has worldwide unique dedicated test facilities, Cathode Test System and dc-Gun Test Laboratory, to fully characterize polarized photocathodes. Recent systematic measurements on a strained-well InAlGaAs/AlGaAs cathode at the facilities show that 87% polarization and 0.3% QE are achieved. The QE can be increased to {approx}1.0% with atomic hydrogen cleaning. The surface charge limit at a very low current intensity and the clear dependence of the polarization on the surface charge limit are observed for the first time. On-going programs to develop photocathodes for the ILC and CLIC are briefly introduced.

  9. FEMTO SECOND ELECTRON BEAM DIFFRACTION USING A PHOTOCATHODE RF GUN.

    SciTech Connect

    WANG,X.J.WU,Z.IHEE,H.

    2003-05-12

    One of the 21st century scientific frontiers is to explore the molecule structure transition on the femtosecond time scale. X-ray free electron laser (XFEL) is one of the tools now under development for investigating femto-second structure transition. We are proposing an alternative technique--femto-second electron diffraction based on a photocathode RF gun. We will present a design of a kHz femto-seconds electron diffraction system based on a photocathode RF gun. Our simulation shows that, the photocathode RF gun can produce 100 fs (FWHM) electron bunch with millions electrons at about 2 MeV. This is at least one order of magnitude reduction in bunch length, and two orders of magnitude increase in number of electrons comparing to present time-resolved electron diffraction system. We will also discuss various issues and limitations related to MeV electron diffraction.

  10. Photoemission characteristics of thin GaAs-based heterojunction photocathodes

    SciTech Connect

    Feng, Cheng; Zhang, Yijun Qian, Yunsheng; Shi, Feng; Zou, Jijun; Zeng, Yugang

    2015-01-14

    To better understand the different photoemission mechanism of thin heterojunction photocathodes, the quantum efficiency models of reflection-mode and transmission-mode GaAs-based heterojunction photocathodes are revised based on one-dimensional continuity equations, wherein photoelectrons generated from both the emission layer and buffer layer are taken into account. By comparison of simulated results between the revised and conventional models, it is found that the electron contribution from the buffer layer to shortwave quantum efficiency is closely related to some factors, such as the thicknesses of emission layer and buffer layer and the interface recombination velocity. Besides, the experimental quantum efficiency data of reflection-mode and transmission-mode AlGaAs/GaAs photocathodes are well fitted to the revised models, which confirm the applicability of the revised quantum efficiency models.

  11. Hydrothermal alkali metal recovery process

    DOEpatents

    Wolfs, Denise Y.; Clavenna, Le Roy R.; Eakman, James M.; Kalina, Theodore

    1980-01-01

    In a coal gasification operation or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein solid particles containing alkali metal residues are produced, alkali metal constituents are recovered from the particles by treating them with a calcium or magnesium-containing compound in the presence of water at a temperature between about 250.degree. F. and about 700.degree. F. and in the presence of an added base to establish a pH during the treatment step that is higher than would otherwise be possible without the addition of the base. During the treating process the relatively high pH facilitates the conversion of water-insoluble alkali metal compounds in the alkali metal residues into water-soluble alkali metal constituents. The resultant aqueous solution containing water-soluble alkali metal constituents is then separated from the residue solids, which consist of the treated particles and any insoluble materials formed during the treatment step, and recycled to the gasification process where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst. Preferably, the base that is added during the treatment step is an alkali metal hydroxide obtained by water washing the residue solids produced during the treatment step.

  12. Emission properties of body-centered cubic elemental metal photocathodes

    SciTech Connect

    Li, Tuo; Rickman, Benjamin L. Schroeder, W. Andreas

    2015-04-07

    A first principles analysis of photoemission is developed to explain the lower than expected rms transverse electron momentum measured using the solenoid scan technique for the body-centered cubic Group Vb (V, Nb, and Ta) and Group VIb (Cr, Mo, and W) metallic photocathodes. The density functional theory based analysis elucidates the fundamental role that the electronic band structure (and its dispersion) plays in determining the emission properties of solid-state photocathodes and includes evaluation of work function anisotropy using a thin-slab method.

  13. Alkali-vapor lasers

    NASA Astrophysics Data System (ADS)

    Zweiback, J.; Komashko, A.; Krupke, W. F.

    2010-02-01

    We report on the results from several of our alkali laser systems. We show highly efficient performance from an alexandrite-pumped rubidium laser. Using a laser diode stack as a pump source, we demonstrate up to 145 W of average power from a CW system. We present a design for a transversely pumped demonstration system that will show all of the required laser physics for a high power system.

  14. Toxicity of organometal halide perovskite solar cells

    NASA Astrophysics Data System (ADS)

    Babayigit, Aslihan; Ethirajan, Anitha; Muller, Marc; Conings, Bert

    2016-03-01

    In the last few years, the advent of metal halide perovskite solar cells has revolutionized the prospects of next-generation photovoltaics. As this technology is maturing at an exceptional rate, research on its environmental impact is becoming increasingly relevant.

  15. Effects of the fluence of implanted potassium ions on the photoelectric sensitivity of tungsten photocathodes

    NASA Astrophysics Data System (ADS)

    Afif, M.; Girardeau-Montaut, J. P.; Delafond, J.; Templier, C.

    1998-04-01

    Measurements of single-photon photoelectric emission sensitivity of polycrystalline tungsten surface implanted by potassium ions, with incident fluences 1, 2, 3, 4, and 5 10 17 K cm -2, are reported and compared to the data for pure tungsten under the same experimental conditions. The photoelectric performance of these photocathodes has been measured at 213 nm for different incidence angles of p-polarized and 16 ps pulses produced by harmonic generation from a Nd:YAG mode-locked laser. Significant improvements of the photoelectric efficiency of tungsten implanted with alkali ions have been demonstrated, as well as a good stability of performance during more than a full month irradiation. The enhancement depends both on the effective density of potassium atoms and on the microstructure of the implanted layer. At last, the enhancements of the photoelectric yield are principally related to a shift of the work function (WF) at the surface of implanted tungsten, observations supported by a recent model of which the main features are recalled.

  16. SUPPRESSION OF AFTERPULSING IN PHOTOMULTIPLIERS BY GATING THE PHOTOCATHODE

    EPA Science Inventory

    A number of gating schemes to minimize the long-term afterpulse signal in photomultipliers have been evaluated. Blocking the excitation pulse by gating the photocathode was found to reduce the gate-on afterpulse background by a factor of 230 over that for nongated operation. Thi...

  17. Metal-Insulator Photocathode Heterojunction for Directed Electron Emission

    SciTech Connect

    Droubay, Timothy C.; Chambers, Scott A.; Joly, Alan G.; Hess, Wayne P.; Nemeth, Karoly; Harkay, Katherine C.; Spentzouris, Linda

    2014-02-14

    New photocathode materials capable of producing intense and directed electron pulses are needed for development of next generation light sources and dynamic transmission electron microscopy. Ideal photocathodes should have high photoemission quantum efficiency (QE) and be capable of delivering collimated and well-shaped pulses of consistent charge under high-field operating conditions. High-brightness and low-intrinsic emittance electron pulses have been predicted for hybrid metal-insulator photocathode designs constructed from three to four monolayer MgO films on atomically flat silver. Here we use angle-resolved photoelectron spectroscopy to confirm directional photoemission and a large increase in QE under ultraviolet laser excitation of an ultrathin MgO film on Ag(001). We observe new low-binding energy photoemission, not seen for Ag(001), and greater electron emission in the normal direction. Under 4.66 eV laser excitation, the photoemission quantum efficiency of the MgO/Ag(001) hybrid photocathode is a factor of seven greater than that for clean Ag(001).

  18. New Photocathode materials for electron-ion-colliders

    SciTech Connect

    Lukaszew, Rosa A.

    2015-02-25

    Our aim has been to explore new photocathode materials and schemes to develop strategies and technologies for next generation nuclear physics accelerator capabilities, particularly for Electron Ion Colliders (EIC). Thus, we investigated thin film deposition and ensuing properties for several adequate magnetic materials applicable to spin-polarized photocathodes. We also implemented a full experimental setup for light incidence at an acute angle onto the photocathode surface in order to excite surface Plasmon resonance hence increasing light absorption by a metallic surface. We successfully tested the setup with a thermionic cathode as well as Plasmonic silver-MgO samples and obtained very encouraging results. Our first results are very encouraging since the photocurrent measured on this preliminary plasmonic Ag-MgO sample under low power (~ 1mW) cw red light from a HeNe laser was 256 pA, thus two orders magnitude larger than that reported by others following also plasmonic approaches. We extended our studies to shorter wavelengths and we also started preliminary work on chemically ordered MnAl thin films –a component of the tertiary Ag-Mn-Al (silmanal) alloy in order to develop spin-polarized photocathodes capable of sustaining surface Plasmon resonance. It is worthwhile mentioning that a graduate student has been directly involved during this project ensuring the training of next generation of scientists in this area of research.

  19. Progress in the fabrication of GaN photocathodes

    NASA Astrophysics Data System (ADS)

    Ulmer, Melville P.; Wessels, Bruce W.; Shahedipour, Fatemeh; Korotokov, Roman Y.; Joseph, Charles L.; Nihashi, Tokuaki

    2001-06-01

    Currently, photo-cathodes hold the highest promise in the near term (next few years) of being able to detect low light level UV signals at high QE while being nearly blind to visible wavelengths. We briefly discuss the requirements for UV detection for astronomical applications, and then we describe our work on producing GaN based photo-cathodes. The p-type GaN films were grown on sapphire at Northwestern University. The films were then converted into opaque photo-cathodes inside photo-tubes at Hamamatsu. Hamamatsu tested detective quantum efficiencies (DQE) of these detectors to be as high as 30% at 200 nm. The ratio of peak DQE at 200 nm to the minimum DQE at 500 nm was measured to be about 6 X 103. We found a dramatic increase in the DQE at 200 nm versus the conductivity, with the break point being near 0.13 1/(Ohm-cm). Based on this dramatic increase, we believe that further improvement in photo-cathode quantum efficiencies can be achieved by increasing the conductivity. We have recently achieved more than an order of magnitude increase in conductivity by co-doping techniques. Improvements in the solar blindness of the devices depend both on characteristics of the film and its surface properties. A detailed discussion of decreasing the visible response and producing a sharper wave-length cutoff is beyond the scope of this work, but we briefly discuss the attributes that most likely affect the wavelength dependence of the photo-cathode response.

  20. Novel lithium halide battery structure

    SciTech Connect

    Harney, M.J.; Icore, B.; O'Boyle, M.

    1980-12-30

    The present invention relates to a lithium halide battery structure comprising an outer metal envelope and top portion which is hermetically sealed to the envelope. The top portion includes an insulator conforming to and positioned thereon to the base configuration of the top portion and a support means having a base configuration substantially the same as the insulator. The support means also includes a flange depending from the support base and a pair of spaced apart post holders integral with said flange. First and second posts are positioned in the post holders with a metal anode collector screen positioned between and attached to said posts. The first post extends through the support means, insulator and top portion to define the anode terminal. The second post terminates in the associated post holder. A first and second pair of lithium anodes are pressure bonded together to sandwich therebetween the support means and anode collector screen. First and second depolarizer pellets are positioned between and in coextensive contact with the first and second anodes and the inner surface of the envelope.

  1. Dimming of metal halide lamps

    NASA Technical Reports Server (NTRS)

    Schurer, Kees

    1994-01-01

    We ran some tests on the effect of dimming of metal halide (MH) lamps upon the stability and the spectral quality of the light output. Lamps used were a new Philips lamp HPI-T 250W, a similar Philips lamp with a few thousand burning hours and a new Osram lamp HQI-T 250W/D. The ballast was a BBC type DJ 250/2KS, the starter a BAS TORGI type MZN 250 SE and the dimmer an Elstrom Control System type ERHQ-T 250. Power was derived from a Philips stabilizer, type PE 1602. Lamp output was monitored with a PAR meter. Spectra were taken at 100% and at 50% output as measured with the PAR meter. Lamps were allowed to stabilize at any setting for 30 minutes before measurements were made. Lamp manufacturers advise against dimming for fear of poor stability and intolerable changes of the spectrum. However, none of the lamps showed a decrease in stability, no flicker or wandering of the discharge, and the changes of the spectrum were not negligible, but certainly not dramatic. Lamps of either manufacture retain their white color, relative peak heights of spectral lines did shift, but no gaps in the spectrum occurred. Spectra taken at 50% with 30 minutes intervals coincided. Differences between the new and the older Philips lamp were noticeable, but not really significant.

  2. Preparation of alkali metal dispersions

    NASA Technical Reports Server (NTRS)

    Rembaum, A.; Landel, R. F. (inventors)

    1968-01-01

    A method is described for producing alkali metal dispersions of high purity. The dispersions are prepared by varying the equilibrium solubility of the alkali metal in a suitable organic solvent in the presence of aromatic hydrocarbons. The equilibrium variation is produced by temperature change. The size of the particles is controlled by controlling the rate of temperature change.

  3. The Remarkable Reactivity of Aryl Halides with Nucleophiles

    ERIC Educational Resources Information Center

    Bunnett, Joseph F.

    1974-01-01

    Discusses the reactivity of aryl halides with nucleophilic or basic reagents, including nucleophilic attacks on carbon, hydrogen, halogen, and arynes. Suggestions are made concerning revisions of the sections on aryl halide chemistry courses and the corresponding chapters in textbooks. (CC)

  4. Purification of alkali metal nitrates

    DOEpatents

    Fiorucci, Louis C. (Hamden, CT); Gregory, Kevin M. (Woodridge, IL)

    1985-05-14

    A process is disclosed for removing heavy metal contaminants from impure alkali metal nitrates containing them. The process comprises mixing the impure nitrates with sufficient water to form a concentrated aqueous solution of the impure nitrates, adjusting the pH of the resulting solution to within the range of between about 2 and about 7, adding sufficient reducing agent to react with heavy metal contaminants within said solution, adjusting the pH of the solution containing reducing agent to effect precipitation of heavy metal impurities and separating the solid impurities from the resulting purified aqueous solution of alkali metal nitrates. The resulting purified solution of alkali metal nitrates may be heated to evaporate water therefrom to produce purified molten alkali metal nitrate suitable for use as a heat transfer medium. If desired, the purified molten form may be granulated and cooled to form discrete solid particles of alkali metal nitrates.

  5. The effect of surface cleaning on quantum efficiency in AlGaN photocathode

    NASA Astrophysics Data System (ADS)

    Hao, Guanghui; Zhang, Yijun; Jin, Muchun; Feng, Cheng; Chen, Xinlong; Chang, Benkang

    2015-01-01

    To improve the quantum efficiency of AlGaN photocathode, various surfaces cleaning techniques for the removal of alumina and carbon from AlGaN photocathode surface were investigated. The atomic compositions of AlGaN photocathode structure and surface were measured by the X-ray photoelectron spectroscopy and Ar+ ion sputtering. It is found that the boiling KOH solution and the mixture of sulfuric acid and hydrogen peroxide, coupled with the thermal cleaning at 850 C can effectively remove the alumina and carbon from the AlGaN photocathode surface. The quantum efficiency of AlGaN photocathode is improved to 35.1% at 240 nm, an increase of 50% over the AlGaN photocathode chemically cleaned by only the mixed solution of sulfuric acid and hydrogen peroxide and thermally cleaned at 710 C.

  6. DC photogun vacuum characterization through photocathode lifetime studies

    SciTech Connect

    Marcy Stutzman; Joseph Grames; Matt Poelker; Kenneth Surles-Law; Philip Adderley

    2007-07-02

    Excellent vacuum is essential for long photocathode lifetimes in DC high voltage photoelectron guns. Vacuum Research at Thomas Jefferson National Accelerator Facility has focused on characterizing the existing vacuum systems at the CEBAF polarized photoinjector and on quantifying improvements for new systems. Vacuum chamber preprocessing, full activation of NEG pumps and NEG coating the chamber walls should improve the vacuum within the electron gun, however, pressure measurement is difficult at pressures approaching the extreme-high-vacuum (XHV) region and extractor gauge readings are not significantly different between the improved and original systems. The ultimate test of vacuum in a DC high voltage photogun is the photocathode lifetime, which is limited by the ionization and back-bombardment of residual gasses. Discussion will include our new load-locked gun design as well as lifetime measurements in both our operational and new photo-guns, and the correlations between measured vacuum and lifetimes will be investigated.

  7. Photocathode performance measurements for the SLC polarized electron gun

    SciTech Connect

    Garden, C.L.; Hoyt, E.W.; Schultz, D.C.; Tang, H.

    1993-04-01

    A low-voltage test system is used to qualify various III-V semiconductor materials as photocathodes for the SLC. The system features a load lock to introduce samples, high pumping speed, a sensitive residual gas analyzer, and an infrared temperature detector. Heat cleaning, cesiation, and oxidation procedures have been studied to optimize cathode activation for achieving an optimum NEA surface. VGF GaAs, MBE-grown AlGaAs, MBE GaAs layered on AlGaAs, and MOCVD GaAsP cathodes with different active layer thicknesses and doping concentrations have been tested for quantum efficiency and lifetime. New higher-polarization strained-layer GaAs on GaAsP photocathodes have also been tested. Results and operational experience are discussed.

  8. Extreme ultraviolet quantum detection efficiency of rubidium bromide opaque photocathodes

    NASA Technical Reports Server (NTRS)

    Siegmund, Oswald H. W.; Gaines, Geoffrey A.

    1990-01-01

    Measurements are presented of the quantum detection efficiency (QDE) of three samples of RbBr photocathode layers over the 44-150-A wavelength range. The QDE of RbBr-coated microchannel plate (MCP) was measured using a back-to-back Z-stack MCP configuration in a detector with a wedge and strip position-sensitive anode, of the type described by Siegmund et al. (1984). To assess the stability of RbBr layer, the RbBr photocathode was exposed to air at about 30 percent humidity for 20 hr. It was found that the QDE values for the aged cathode were within the QDE measurement errors of the original values. A simple QDE model was developed, and it was found that its predictions are in accord with the QDE measurements.

  9. High-Yield Metal Materials for Photocathode RF Gun

    SciTech Connect

    Wang, X.J.; Ben-Zvi, I.; Smedley, J.; Srinivasan-Rao, T.; Woodle, M.; Palmer, D.T.; Miller, R.H.

    1997-11-01

    Significant progress has been made in both improving the quantum efficiency and understanding the physics process of photoemission of metal photocathode materials under high electric field. Metal material, copper and magnesium were installed on the photocathode RF gun, and experimentally investigated using frequency quadrupled Nd:Yag laser (266 nm). A systemic procedure was developed for preparing cathode; this involves diamond polishing, ultrasonic cleaning and high temperature vacuum bake out. Using laser cleaning and explosive electron emission cleaning, the highest quantum efficiency measured for copper and magnesium are 0.02% and 0.3%, respectively. The Schottky effect was experimental investigated, the quantum efficiency of the Cu is dominated by the Schottky effect since the work function of the copper is almost equal to the photon energy used (4.66 eV). The quantum efficiency of the magnesium is significant enhanced by the Schottky effect.

  10. Method for recovering hydrocarbons from molten metal halides

    DOEpatents

    Pell, Melvyn B.

    1979-01-01

    In a process for hydrocracking heavy carbonaceous materials by contacting such carbonaceous materials with hydrogen in the presence of a molten metal halide catalyst to produce hydrocarbons having lower molecular weights and thereafter recovering the hydrocarbons so produced from the molten metal halide, an improvement comprising injecting into the spent molten metal halide, a liquid low-boiling hydrocarbon stream is disclosed.

  11. Applications of Laser and Synchrotron Based ARPES to Photocathode Research

    SciTech Connect

    Rameau J.; Smedley J.; Muller, E.; Kidd, T.; Johnson, P.; Allen, P.; Carr, L.; Valla, T.

    2010-10-12

    Laser angle resolved photoelectron spectroscopy (ARPES) provides unique information about angle and energy distribution of photoelectrons. Laser ARPES gives unique insight into how NEA materials work. ARPES combined with some ancillary measurements gives a very complete picture of system electronic physics. For H:C[100] there is now a clear program for engineering as well as development analogous systems. ARPES well suited for identifying 'ideal' photocathodes with intrinsically low emittance and high QE.

  12. High Brightness and high polarization electron source using transmission photocathode

    SciTech Connect

    Yamamoto, Naoto; Jin Xiuguang; Ujihara, Toru; Takeda, Yoshikazu; Mano, Atsushi; Nakagawa, Yasuhide; Nakanishi, Tsutomu; Okumi, Shoji; Yamamoto, Masahiro; Konomi, Taro; Ohshima, Takashi; Saka, Takashi; Kato, Toshihiro; Horinaka, Hiromichi; Yasue, Tsuneo; Koshikawa, Takanori

    2009-08-04

    A transmission photocathode was fabricated based on GaAs-GaAsP strained superlattice layers on a GaP substrate and a 20 kV-gun was built to generate the polarized electron beams with the diameter of a few micro-meter. As the results, the reduced brightness of 1.3x10{sup 7} A/cm{sup 2}/sr and the polarization of 90% were achieved.

  13. Highly efficient photocathodes for dye-sensitized tandem solar cells.

    PubMed

    Nattestad, A; Mozer, A J; Fischer, M K R; Cheng, Y-B; Mishra, A; Bäuerle, P; Bach, U

    2010-01-01

    Thin-film dye-sensitized solar cells (DSCs) based on mesoporous semiconductor electrodes are low-cost alternatives to conventional silicon devices. High-efficiency DSCs typically operate as photoanodes (n-DSCs), where photocurrents result from dye-sensitized electron injection into n-type semiconductors. Dye-sensitized photocathodes (p-DSCs) operate in an inverse mode, where dye-excitation is followed by rapid electron transfer from a p-type semiconductor to the dye (dye-sensitized hole injection). Such p-DSCs and n-DSCs can be combined to construct tandem solar cells (pn-DSCs) with a theoretical efficiency limitation well beyond that of single-junction DSCs (ref. 4). Nevertheless, the efficiencies of such tandem pn-DSCs have so far been hampered by the poor performance of the available p-DSCs (refs 3, 5-15). Here we show for the first time that p-DSCs can convert absorbed photons to electrons with yields of up to 96%, resulting in a sevenfold increase in energy conversion efficiency compared with previously reported photocathodes. The donor-acceptor dyes, studied as photocathodic sensitizers, comprise a variable-length oligothiophene bridge, which provides control over the spatial separation of the photogenerated charge carriers. As a result, charge recombination is decelerated by several orders of magnitude and tandem pn-DSCs can be constructed that exceed the efficiency of their individual components. PMID:19946281

  14. Performance of Au transmission photocathode on a microchannel plate detector

    SciTech Connect

    Lowenstern, M. E.; Harding, E. C.; Huntington, C. M.; Visco, A. J.; Rathore, G.; Drake, R. P.

    2008-10-15

    X-ray framing cameras, employing microchannel plates (MCPs) for detection and signal amplification, play a key role in research in high-energy-density physics. These instruments convert radiographic x-rays into electrons produced by plasma during such experiments into electrons that are amplified in the channels and then detected by a phosphor material. The separation of detection from signal amplification offers potential improvements in sensitivity and noise properties. We have implemented a suspended Au transmission photocathode (160 A thick) on a MCP and are evaluating it using a 1.5 keV Al K{alpha} x-ray source. We find an approximately twofold increase in the ratio of detected events to incident photons when the photocathode-to-MCP voltage difference is sufficiently large. Our calculations indicate that this increase is probably caused by a combination of signal produced by the photocathode and an increase in the efficiency of detection of x-rays that reach the MCP surface through modification of the local electric field.

  15. Advanced Laser Technologies for High-brightness Photocathode Electron Gun

    NASA Astrophysics Data System (ADS)

    Tomizawa, Hiromitsu

    A laser-excited photocathode RF gun is one of the most reliable high-brightness electron beam sources for XFELs. Several 3D laser shaping methods have been developed as ideal photocathode illumination sources at SPring-8 since 2001. To suppress the emittance growth caused by nonlinear space-charge forces, the 3D cylindrical UV-pulse was optimized spatially as a flattop and temporally as squarely stacked chirped pulses. This shaping system is a serial combination of a deformable mirror that adaptively shapes the spatial profile with a genetic algorithm and a UV-pulse stacker that consists of four birefringent ?-BBO crystal rods for temporal shaping. Using this 3D-shaped pulse, a normalized emittance of 1.4 ? mm mrad was obtained in 2006. Utilizing laser's Z-polarization, Schottky-effect-gated photocathode gun was proposed in 2006. The cathode work functions are reduced by a laser-induced Schottky effect. As a result of focusing a radially polarized laser pulse with a hollow lens in vacuum, the Z-field (Z-polarization) is generated at the cathode.

  16. Unraveling halide hydration: A high dilution approach

    NASA Astrophysics Data System (ADS)

    Migliorati, Valentina; Sessa, Francesco; Aquilanti, Giuliana; D'Angelo, Paola

    2014-07-01

    The hydration properties of halide aqua ions have been investigated combining classical Molecular Dynamics (MD) with Extended X-ray Absorption Fine Structure (EXAFS) spectroscopy. Three halide-water interaction potentials recently developed [M. M. Reif and P. H. Hnenberger, J. Chem. Phys. 134, 144104 (2011)], along with three plausible choices for the value of the absolute hydration free energy of the proton (? G^{ominus }_{hyd}[H^+]), have been checked for their capability to properly describe the structural properties of halide aqueous solutions, by comparing the MD structural results with EXAFS experimental data. A very good agreement between theory and experiment has been obtained with one parameter set, namely LE, thus strengthening preliminary evidences for a ? G^{ominus }_{hyd}[H^+] value of -1100 kJ mol-1 [M. M. Reif and P. H. Hnenberger, J. Chem. Phys. 134, 144104 (2011)]. The Cl-, Br-, and I- ions have been found to form an unstructured and disordered first hydration shell in aqueous solution, with a broad distribution of instantaneous coordination numbers. Conversely, the F- ion shows more ordered and defined first solvation shell, with only two statistically relevant coordination geometries (six and sevenfold complexes). Our thorough investigation on the effect of halide ions on the microscopic structure of water highlights that the perturbation induced by the Cl-, Br-, and I- ions does not extend beyond the ion first hydration shell, and the structure of water in the F- second shell is also substantially unaffected by the ion.

  17. Upgrading platform using alkali metals

    DOEpatents

    Gordon, John Howard

    2014-09-09

    A process for removing sulfur, nitrogen or metals from an oil feedstock (such as heavy oil, bitumen, shale oil, etc.) The method involves reacting the oil feedstock with an alkali metal and a radical capping substance. The alkali metal reacts with the metal, sulfur or nitrogen content to form one or more inorganic products and the radical capping substance reacts with the carbon and hydrogen content to form a hydrocarbon phase. The inorganic products may then be separated out from the hydrocarbon phase.

  18. Development and characterization of diamond film and compound metal surface high current photocathodes

    SciTech Connect

    Shurter, R.P.; Moir, D.C.; Devlin, D.J.; Springer, R.W.; Archuleta, T.A.

    1997-09-01

    High current photocathodes operating in vacuum environments as high as 8xE-5 torr are being developed at Los Alamos for use in a new generation of linear induction accelerators. We report quantum efficiencies in wide bandgap semiconductors, pure metals, and compound metal surfaces photocathode materials illuminated by ultraviolet laser radiation.

  19. Spectroscopic studies of Sb3 + color centers in alkali halide single crystals

    NASA Astrophysics Data System (ADS)

    Choi, K. O.; Lee, S. W.; Bae, H. K.; Jung, S. H.; Chang, C. K.; Kang, J. G.

    1991-05-01

    The emission from KCl: Sb3+ and KI: Sb3+ excited in the A-absorption band was measured as a function of exciting photon energy and temperature. The A-band excitation produced two emission bands for KCl: Sb3+ and a single band for KI: Sb3+. The definitive assignment of these bands is presented in terms of the adiabatic potential energy surface (APES), in which the effect of the spin-orbit interaction (SO) on the Jahn-Teller (JT) interaction coupling to the Eg mode is taken into account. The polarization spectrum and the angular dependence of polarization ratio of the A-band emission were also studied to determine the symmetry axes of the Sb3+ -vacancies complex. The results indicate that the anisotropy is associated with the relaxed excited state (RES) of Sb3+. It is also found that the JT interaction coupling to the T2g mode and the vacancies, situated in the next-nearest-neighbor (nnn) and the nearest-neighbor (nn) positions to the Sb3+ ion, give rise to an additive perturbation.

  20. Two types of self-trapped excitons in alkali halide crystals

    NASA Astrophysics Data System (ADS)

    Shluger, A. L.; Itoh, N.; Puchin, V. E.; Heifets, E. N.

    1991-07-01

    We have carried out ab initio many-electron variational calculations of the adiabatic potential-energy surface (APES) for the lowest triplet state of the self-trapped exciton (STE) in KCl and LiCl. For KCl, it is found that at the APES minimum, the Cl-2 molecular ion comprising the STE hole is displaced along the <110> axis by about 0.90 Å from its symmetrical position. The STE electron and hole are shifted in the direction opposite to that of the Cl-2 displacement. The calculated optical-transition energies due to electron and hole excitations of the STE at the APES minimum, and the luminescence energy due to the transition to the crystal ground state agree well with the experimental results. It is found that the <110> displacement of the Cl-2 molecular ion at the APES minimum from its symmetrical position for LiCl is 0.07 Å, much smaller than that in KCl, and that the direction of the shift of the electron and hole is opposite to that for KCl; the electron and hole are localized near one of the Cl-2 ions located closer to the lattice site. It is shown that, for a small shift of the Cl-2 molecular ion from its symmetrical position, the states in which electron and hole are shifted to opposite directions appear in both LiCl and KCl crystals within energy intervals less than 0.8 eV. It is pointed out that the configuration interaction between the two states with the electron and hole shifted in opposite directions should be included for more precise APES calculations at small off-center displacements, and that the electron-hole correlation is important to determine the electronic structure of the STE.

  1. The aluminum electrode in AlCl3-alkali-halide melts

    NASA Technical Reports Server (NTRS)

    Holleck, G. L.; Giner, J.

    1972-01-01

    Passivation phenomena were observed upon cathodic and anodic polarization of the Al electrode in AlCl3-KCl-NaCl melts between 100 and 160 C. They are caused by formation of a solid salt layer at the electrode surface resulting from concentration changes upon current flow. The anodic limiting currents increased with temperature and with decreasing AlCl3 content of the melt. Current voltage curves obtained on a rotating aluminum disk showed a linear relationship between the anodic limiting current and 1/sq root of 2 pi (rps). Upon cathodic polarization dentrite formation occurs at the Al electrode. The activation overvoltage in AlCl3-KCl-NaCl (57.5-12.5-20 mol%) was determined by galvanostatic current step methods. An apparent exchange current density of 270 mA/cm2 at 130 C and a double layer capacity of 40 plus or minus 10 microfarad/cm2 were measured.

  2. Building foundations for molecular electronics: Growth of organic molecules on alkali halides as prototypical insulating substrates

    NASA Astrophysics Data System (ADS)

    Burke, Sarah A.

    The epitaxy and growth of a series of organic molecules deposited on insulating surfaces were investigated by noncontact atomic force microscopy (nc-AFM). The molecules studied, C60, 3,4,9,10-perylene tetracarboxylic dianhydride (PTCDA), 3,4,9,10-perylene tetracarboxlylic diimide (PTCDI), and copper (II) phthalocyanine (CuPc), were selected to investigate the effect of different molecular geometries, charge distributions and intermolecular interactions and as interesting candidates in molecular electronic applications. As it is known that the properties of molecules are influenced by their structural arrangements, an understanding of the interactions of molecules with substrates of interest as well as the dominant processes involved in growth are of great interest. Model insulating substrates KBr and NaCl were used for growth studies, due to the necessity of insulators in electrically isolating device regions. Dewetting processes were observed in several of these systems: C 60 on KBr and NaCl, PTCDA on NaCl and PTCDI on NaCl. The specific influences of de- wetting are discussed for each system, in particular the morphological impact of dewetting and the driving of dewetting by strained metastable monolayers. For C60 deposits, interesting branched structures are formed in the process of dewetting which are remarkably stable once formed, yet do not represent the equilibrium growth morphology. A determination of the large cell coincident epitaxy reveals a small, yet significant discrepancy between the observed overlayer and calculated stable adsorption sites indicating a dominance of the intermolecular interaction over the molecule---substrate interaction. For both PTCDA and PTCDI on NaCl, strained metastable monolayer epitaxies were observed giving rise to a transition in both interface structure and morphology: a dewetting transition. A comparison of the observed molecular scale structures and growth modalities is made in order to build a framework for understanding the prevalence of dewetting for molecules on ionic surfaces. Finally, in order to better understand the connection between molecular scale structures and interesting opto-electronic properties, the application of a hybrid-electrostatic characterization technique by nc-AFM is discussed. Using this technique, the opto-electrostatic response of three different PTCDA arrangements on a nanotemplated NaCl surface are shown to differ according to the degree of intermolecular interaction permitted by the structure.

  3. Shear viscosity of molten alkali halides from equilibrium and nonequilibrium molecular-dynamics simulations

    NASA Astrophysics Data System (ADS)

    Galamba, N.; Nieto de Castro, C. A.; Ely, James F.

    2005-06-01

    The shear viscosity of molten NaCl and KCl was calculated through equilibrium (EMD) and nonequilibrium molecular-dynamics (NEMD) simulations in the canonical (N,V,T) ensemble. Two rigid-ion potentials were investigated, namely, the Born-Mayer-Huggins-Tosi-Fumi potential and the Michielsen-Woerlee-Graaf-Ketelaar potential with the parameters proposed by Ladd. The NEMD simulations were performed using the SLLOD equations of motion [D. J. Evans and G. P. Morriss, Phys. Rev. A 30, 1528 (1984)] with a Gaussian isokinetic thermostat and the results are compared with those obtained from Green-Kubo EMD (N,V,T) simulations and experimental shear viscosity data. The NEMD zero strain rate shear viscosity, ?(0), was obtained by fitting a simplified Carreau-type equation and by application of mode-coupling theory, i.e., a ?-?1/2 linear relationship. The values obtained from the first method are found to be significantly lower than those predicted by the second. The agreement between the EMD and NEMD results with experimental data is satisfactory for the two potentials investigated. The ion-ion radial distribution functions obtained with the two rigid-ion potentials for both molten salts are discussed in terms of the differences between the two models.

  4. Equilibrium and nonequilibrium molecular dynamics simulations of the thermal conductivity of molten alkali halides

    NASA Astrophysics Data System (ADS)

    Galamba, N.; Nieto de Castro, C. A.; Ely, James F.

    2007-05-01

    The thermal conductivity of molten NaCl and KCl was calculated through the Evans-Gillan nonequilibrium molecular dynamics (NEMD) algorithm and Green-Kubo equilibrium molecular dynamics (EMD) simulations. The EMD simulations were performed for a "binary" ionic mixture and the NEMD simulations assumed a pure system for reasons discussed in this work. The cross thermoelectric coefficient obtained from Green-Kubo EMD simulations is discussed in terms of the homogeneous thermoelectric power or Seebeck coefficient of these materials. The thermal conductivity obtained from NEMD simulations is found to be in very good agreement with that obtained through Green-Kubo EMD simulations for a binary ionic mixture. This result points to a possible cancellation between the neglected "partial enthalpy" contribution to the heat flux associated with the interdiffusion of one species through the other and that part of the thermal conductivity related to the coupled fluxes of charge and heat in "binary" ionic mixtures.

  5. Thermal conductivity of molten alkali halides from equilibrium molecular dynamics simulations.

    PubMed

    Galamba, N; Nieto de Castro, C A; Ely, J F

    2004-05-01

    The thermal conductivity of molten sodium chloride and potassium chloride has been computed through equilibrium molecular dynamics Green-Kubo simulations in the microcanonical ensemble (N,V,E). In order to access the temperature dependence of the thermal conductivity coefficient of these materials, the simulations were performed at five different state points. The form of the microscopic energy flux for ionic systems whose Coulombic interactions are calculated through the Ewald method is discussed in detail and an efficient formula is used by analogy with the methods used to evaluate the stress tensor in Coulombic systems. The results show that the Born-Mayer-Huggins-Tosi-Fumi potential predicts a weak negative temperature dependence for the thermal conductivity of NaCl and KCl. The simulation results are in agreement with part of the experimental data available in the literature with simulation values generally overpredicting the thermal conductivity by 10%-20%. PMID:15267797

  6. Is surface layering of aqueous alkali halides determined by ion pairing in the bulk solution?

    NASA Astrophysics Data System (ADS)

    Brandes, Eva; Stage, Christiane; Motschmann, Hubert; Rieder, Julian; Buchner, Richard

    2014-11-01

    This contribution aims to elucidate the connection between ion-ion-solvent interactions in the bulk of aqueous electrolyte solutions and the properties of their liquid-air interface. In particular, we were interested in the conditions under which ion pairs form at the surface and whether this is linked to ion pairing in the bulk. For this reason different combinations of hard (Cl-, Li+) and soft ions (I-, Cs+) were investigated. Ion hydration and possible ion association in the bulk was probed with dielectric relaxation spectroscopy. This technique monitors the cooperative reorientation of the dipolar solvent molecules and detects all ion-pair species possibly present in the solution. At the interface, the formation of contact ion pairs was investigated by infrared-visible-sum frequency spectroscopy (SFG). This nonlinear optical technique possesses an inherent surface specificity and can be used for the characterization of interfacial water. The intensity of the SFG-active vibrational stretching modes depends on the number of oriented water molecules. The electric field at the surface of a charged aqueous interface aligns the water dipoles, which in turn increases the SFG response. Hence, the enhancement of the oscillator strengths of the water vibrational modes can be used to draw some conclusions on the strengths and geometrical extension of the electric field. The formation of ion pairs at the interface reduces the intensity of the band associated with hydrogen-bonded water. The underlying theory is presented. The combined data show that there are no contact ion pairs in the bulk of the fluid andat bestonly small amounts of solvent shared ion pairs. On the other hand, the combination of hard/hard or soft/soft ions leads to the formation of ion pairs at the liquid-air interface.

  7. Alkali Halide Opacity in Brown Dwarf and Cool Stellar Atmospheres: A Study of Lithium Chloride

    NASA Astrophysics Data System (ADS)

    Kirby, K.; Weck, P. F.; Schweitzer, A.; Stancil, P. C.; Hauschildt, P. H.

    2003-12-01

    Recent thermochemical equilibrium calculations have revealed the important role played by lithium chloride in the lithium chemistry of cool dwarf atmospheres (K. Lodders 1999, ApJ 519, 793). Indeed, LiCl appears to be the dominant Li-bearing gas over an extended domain of the (P,T) diagram, typically for temperatures below 1500 K. LiCl has a large dipole moment in its ground electronic state which can give rise to intense rovibrational line spectra. In addition, LiCl can make dipole transitions to several low-lying unbound excited states, causing dissociation of the molecule. For these reasons, LiCl may be a significant source of line and continuum opacity in brown dwarf and cool stellar atmospheres. In this work, we report calculations of complete lists of line oscillator strengths and photodissociation cross sections for the low-lying electronic states of LiCl. We have performed single- and double-excitation configuration interaction calculations using the ALCHEMY ab initio package (Mc Lean et al. 1991, MOTECC 91, Elsevier, Leiden) and obtained the potential curves and the corresponding dipole transition moment functions between the X 1? ^+ ground state and the B 1? ^+ and A 1? excited states. The resulting line oscillator strengths and molecular photodissociation cross sections have been included in the PHOENIX stellar atmosphere code (Hauschildt & Baron 1999, J. Comput. App. Math. 102, 41). The new models, calculated using spherical geometry for all gravities considered, also incorporate our latest database of nearly 670 million molecular lines, and updated equations of state (EOS). This work was supported in part by NSF grants AST-9720704 and AST-0086246, NASA grants NAG5-8425, NAG5-9222, and NAG5-10551 as well as NASA/JPL grant 961582.

  8. Electronic line-up in light-emitting diodes with alkali-halide/metal cathodes

    NASA Astrophysics Data System (ADS)

    Brown, T. M.; Friend, R. H.; Millard, I. S.; Lacey, D. J.; Butler, T.; Burroughes, J. H.; Cacialli, F.

    2003-05-01

    The electronic nature of metal-semiconductor contacts is a fundamental issue in the understanding of semiconductor device physics, because such contacts control charge injection, and therefore play a major role in determining the electron/hole population in the semiconductor itself. This role is particularly important for organic semiconductors as they are generally used in their pristine, undoped form. Here, we review our progress in the understanding of the energy level line-up in finished, blue-emitting, polyfluorene-based light-emitting diodes, which exploit LiF and CsF thin films in combination with Ca and Al to obtain cathodes with low injection barriers. We have used electroabsorption measurements, as they allow the noninvasive determination of the built-in potential when changing the cathode. This provides precious experimental information on the alteration of the polymer/cathode interfacial energy level line-up. The latter is found to depend strongly on the electrode work function. Thus, the Schottky-Mott model for the energy level alignment is found to be a better first-order approximation than those models where strong pinning or large interface dipoles determine the alignment (e.g., Bardeen model), except for electrodes that extensively react with the polymer, and introduce deep gap states. In addition, we show results that validate the approximation of rigid tilting of polymer energy levels with bias (for biases for which no significant injection of carriers occurs). To investigate further the consequences of the electronic line-up on device operation, we complemented the electroabsorption measurements with characterization of the emissive and transport properties of the light-emitting diodes, and confirmed that the cathodic barrier lowering in CsF/Ca/Al and LiF/Ca/Al electrodes leads to the best improvements in electron injection. We found that luminance and overall current are greatly affected by the barrier-reducing cathodes, indicating a truly bipolar transport, with comparable electron and hole currents. We also found significant indications of CsF/Ca/Al cathodes strongly reacting with the polymer, which is suggestive of CsF dissociation and diffusion in the bulk of the polymer.

  9. Amorphous Si thin film based photocathodes with high photovoltage for efficient hydrogen production.

    PubMed

    Lin, Yongjing; Battaglia, Corsin; Boccard, Mathieu; Hettick, Mark; Yu, Zhibin; Ballif, Christophe; Ager, Joel W; Javey, Ali

    2013-01-01

    An amorphous Si thin film with TiO2 encapsulation layer is demonstrated as a highly promising and stable photocathode for solar hydrogen production. With platinum as prototypical cocatalyst, a photocurrent onset potential of 0.93 V vs RHE and saturation photocurrent of 11.6 mA/cm(2) are measured. Importantly, the a-Si photocathodes exhibit impressive photocurrent of ~6.1 mA/cm(2) at a large positive bias of 0.8 V vs RHE, which is the highest for all reported photocathodes at such positive potential. Ni-Mo alloy is demonstrated as an alternative low-cost catalyst with onset potential and saturation current similar to those obtained with platinum. This low-cost photocathode with high photovoltage and current is a highly promising photocathode for solar hydrogen production. PMID:24079390

  10. Characterization of x-ray photocathode in transmission mode for imaging application

    SciTech Connect

    Ikeura-Sekiguchi, Hiromi; Sekiguchi, Tetsuhiro; Koike, Masaki; Yagi-Watanabe, Kazutoshi

    2009-09-15

    The performance of an Al x-ray transmission photocathode was experimentally characterized by measuring the total electron yield from backsurface photocathodes of varying thickness. It was demonstrated that the backsurface electron yield is proportional to the x-ray photocurrent transmitted through the photocathode for thicknesses thicker than the optimum thickness. The optimum photocathode thickness with the highest conversion efficiency was found to be approximately 70 nm at 2.963 keV. An escape depth of the secondary electrons was determined to be approximately 13 nm from the yield-versus-thickness data fitted with a semiempirical equation. Using this parameter, the dependence of the optimum photocathode thickness on the x-ray energy was calculated for the 30-10000 eV range. As one example of imaging applications, different photoemission images in the transmission and reflection modes are also presented.

  11. Effects of atomic hydrogen and deuterium exposure on high polarization GaAs photocathodes

    SciTech Connect

    M. Baylac; P. Adderley; J. Brittian; J. Clark; T. Day; J. Grames; J. Hansknecht; M. Poelker; M. Stutzman; A. T. Wu; A. S. Terekhov

    2005-12-01

    Strained-layer GaAs and strained-superlattice GaAs photocathodes are used at Jefferson Laboratory to create high average current beams of highly spin-polarized electrons. High electron yield, or quantum efficiency (QE), is obtained only when the photocathode surface is atomically clean. For years, exposure to atomic hydrogen or deuterium has been the photocathode cleaning technique employed at Jefferson Laboratory. This work demonstrates that atomic hydrogen cleaning is not necessary when precautions are taken to ensure that clean photocathode material from the vendor is not inadvertently dirtied while samples are prepared for installation inside photoemission guns. Moreover, this work demonstrates that QE and beam polarization can be significantly reduced when clean high-polarization photocathode material is exposed to atomic hydrogen from an rf dissociator-style atomic hydrogen source. Surface analysis provides some insight into the mechanisms that degrade QE and polarization due to atomic hydrogen cleaning.

  12. Mean transverse energy and response time measurements of GaInP based photocathodes

    SciTech Connect

    Jin, Xiuguang; Yamamoto, Masahiro; Miyajima, Tsukasa; Honda, Yosuke; Uchiyama, Takashi; Tabuchi, Masao; Takeda, Yoshikazu

    2014-08-14

    GaInP, which has a wider band gap than GaAs, is introduced as a photocathode for energy recovery linac (ERL). The wide band gap of material is expected to reduce the heating effect in the thermal relaxation process after high energy excitation. GaInP photocathodes exhibited higher quantum efficiency than GaAs and low thermal emittance as the same as GaAs photocathodes under green laser light irradiation. A short picosecond electron pulse was also achieved with the GaInP photocathode under 532 nm pulse laser irradiation. These experimental results demonstrate that the GaInP photocathode is an important candidate for ERL.

  13. Modeling the quantum efficiency of controlled porosity dispenser photocathodes

    NASA Astrophysics Data System (ADS)

    Pan, Z.; Jensen, K.; O'Shea, P.

    2012-01-01

    A theoretical model of diffusion, evaporation, and rejuvenation of cesium on the surface of a controlled porosity dispenser photocathode is developed. The model applies a novel hexagonal meshgrid for increased numerical accuracy. For activation temperatures within the range of 400 K-1000 K, simulation found differences of less than 5% between the quantum efficiency (QE) maximum and minimum over ideal homogenous surfaces. Simulations suggest more variation for real cases to include real surface non uniformity. Changes in the QE map across the surface suggest that the emittance can change depending on temperature. Extensions to the model as well as connections to experiment are discussed.

  14. High voltage switch triggered by a laser-photocathode subsystem

    DOEpatents

    Chen, Ping; Lundquist, Martin L.; Yu, David U. L.

    2013-01-08

    A spark gap switch for controlling the output of a high voltage pulse from a high voltage source, for example, a capacitor bank or a pulse forming network, to an external load such as a high gradient electron gun, laser, pulsed power accelerator or wide band radar. The combination of a UV laser and a high vacuum quartz cell, in which a photocathode and an anode are installed, is utilized as triggering devices to switch the spark gap from a non-conducting state to a conducting state with low delay and low jitter.

  15. Characterization of quantum well structures using a photocathode electron microscope

    NASA Technical Reports Server (NTRS)

    Spencer, Michael G.; Scott, Craig J.

    1989-01-01

    Present day integrated circuits pose a challenge to conventional electronic and mechanical test methods. Feature sizes in the submicron and nanometric regime require radical approaches in order to facilitate electrical contact to circuits and devices being tested. In addition, microwave operating frequencies require careful attention to distributed effects when considering the electrical signal paths within and external to the device under test. An alternative testing approach which combines the best of electrical and optical time domain testing is presented, namely photocathode electron microscope quantitative voltage contrast (PEMQVC).

  16. RECENT PROGRESS ON THE DIAMOND AMPLIFIED PHOTO-CATHODE EXPERIMENT.

    SciTech Connect

    CHANG,X.; BEN-ZVI, I.; BURRILL, A.; GRIMES, J.; RAO, T.; SEGALOV, Z.; SMEDLEY, J.; WU, Q.

    2007-06-25

    We report recent progress on the Diamond Amplified Photo-cathode (DAP). The use of a pulsed electron gun provides detailed information about the DAP physics. The secondary electron gain has been measured under various electric fields. We have achieved gains of a few hundred in the transmission mode and observed evidence of emission of electrons from the surface. A model based on recombination of electrons and holes during generation well describes the field dependence of the gain. The emittance measurement system for the DAP has been designed, constructed and is ready for use. The capsule design of the DAP is also being studied in parallel.

  17. Nanosecond length electron pulses from a laser-excited photocathode

    SciTech Connect

    Young, A.T.; D'Etat, B.; Stutzin, G.C.; Leung, K.N.; Kunkel, W.B.

    1989-06-01

    A photocathode made from polycrystalline lanthanum hexaboride (LaB{sub 6}) has produced nanosecond length electron pulses when excited by an excimer laser at 308nm. Peak currents in excess of 1A have been observed, with quantum yields of 4 {times} 10{sup {minus}5} being measured. A method for extracting the electrons from an emission-limited cathode, plasma extraction, has been demonstrated. This technique uses a low power continuous discharge to provide the electric field needed to extract the photoelectrons. This technique may be useful in producing high repetition rate short pulse ion sources. 10 refs., 4 figs.

  18. Alkali metal cluster theory

    SciTech Connect

    Chen, J.

    1990-01-01

    The tight-binding Hubbard model has been applied to alkali metal clusters with Hartree-Fock self-consistent methods and perturbation methods for the numerical calculations. The relaxation has been studied between the equilibrium structures and the range of the hopping matrix elements in the Hubbard Hamiltonian. The structures are not sensitive to the interaction range but are determined by the number of valence electrons each atom has. Inertia tensors are used to analyze the symmetries of the clusters. The principal axes of the clusters are determined to be the axes of rotational symmetries of clusters if the clusters have any. The eigenvalues of inertia tensors are compared between this model and the ellipsoidal jellium model. The agreement is good for large clusters. At a finite temperature, the thermal motion fluctuates the structures. A fluctuation function has been defined with the distance matrix of a cluster. The fluctuation has been studied with the Monte Carlo simulation method. Energy levels of clusters are calculated from the Hubbard model. Ionization potentials and magic numbers are also obtained from these energy levels. The results confirm that the Hubbard model is a good approximation for a small cluster. The excitation energy is presented by the difference between the original level and excited level, and the electron-hole interactions. The author also studied cooling of clusters between the nozzle and detector in molecular beam apparatus with three cooling mechanisms, adiabatic expansion, photon emission and cluster decay. The adiabatic expansion and the photon emission do not affect mass abundances of clusters. The studies show that cluster decay cooling produces a shift in the mass spectra. The shift is dependent on the temperature of the beam and increases as the temperature increases.

  19. Polarization and charge limit studies of strained GaAs photocathodes

    SciTech Connect

    Saez, P.J.

    1997-03-01

    This thesis presents studies on the polarization and charge limit behavior of electron beams produced by strained GaAs photocathodes. These photocathodes are the source of high-intensity, high-polarization electron beams used for a variety of high-energy physics experiments at the Stanford Linear Accelerator Center. Recent developments on P-type, biaxially-strained GaAs photocathodes have produced longitudinal polarization in excess of 80% while yielding beam intensities of {approximately} 2.5 A/cm{sup 2} at an operating voltage of 120 kV. The SLAC Gun Test Laboratory, which has a replica of the SLAC injector, was upgraded with a Mott polarimeter to study the polarization properties of photocathodes operating in a high-voltage DC gun. Both the maximum beam polarization and the maximum charge obtainable from these photocathodes have shown a strong dependence on the wavelength of illumination, on the doping concentration, and on the negative electron affinity levels. The experiments performed for this thesis included studying the effects of temperature, cesiation, quantum efficiency, and laser intensity on the polarization of high-intensity beams. It was found that, although low temperatures have been shown to reduce the spin relaxation rate in bulk semiconductors, they don`t have a large impact on the polarization of thin photocathodes. It seems that the short active region in thin photocathodes does not allow spin relaxation mechanisms enough time to cause depolarization. Previous observations that lower QE areas on the photocathode yield higher polarization beams were confirmed. In addition, high-intensity, small-area laser pulses were shown to produce lower polarization beams. Based on these results, together with some findings in the existing literature, a new proposal for a high-intensity, high-polarization photocathode is given. It is hoped that the results of this thesis will promote further investigation on the properties of GaAs photocathodes.

  20. Lanthanide-halide based humidity indicators

    DOEpatents

    Beitz, James V.; Williams, Clayton W.

    2008-01-01

    The present invention discloses a lanthanide-halide based humidity indicator and method of producing such indicator. The color of the present invention indicates the humidity of an atmosphere to which it is exposed. For example, impregnating an adsorbent support such as silica gel with an aqueous solution of the europium-containing reagent solution described herein, and dehydrating the support to dryness forms a substance with a yellow color. When this substance is exposed to a humid atmosphere the water vapor from the air is adsorbed into the coating on the pore surface of the silica gel. As the water content of the coating increases, the visual color of the coated silica gel changes from yellow to white. The color change is due to the water combining with the lanthanide-halide complex on the pores of the gel.

  1. Morphology-Controlled Synthesis of Organometal Halide Perovskite Inverse Opals.

    PubMed

    Chen, Kun; Tüysüz, Harun

    2015-11-01

    The booming development of organometal halide perovskites in recent years has prompted the exploration of morphology-control strategies to improve their performance in photovoltaic, photonic, and optoelectronic applications. However, the preparation of organometal halide perovskites with high hierarchical architecture is still highly challenging and a general morphology-control method for various organometal halide perovskites has not been achieved. A mild and scalable method to prepare organometal halide perovskites in inverse opal morphology is presented that uses a polystyrene-based artificial opal as hard template. Our method is flexible and compatible with different halides and organic ammonium compositions. Thus, the perovskite inverse opal maintains the advantage of straightforward structure and band gap engineering. Furthermore, optoelectronic investigations reveal that morphology exerted influence on the conducting nature of organometal halide perovskites. PMID:26376773

  2. Unraveling halide hydration: A high dilution approach

    SciTech Connect

    Migliorati, Valentina Sessa, Francesco; DAngelo, Paola; Aquilanti, Giuliana

    2014-07-28

    The hydration properties of halide aqua ions have been investigated combining classical Molecular Dynamics (MD) with Extended X-ray Absorption Fine Structure (EXAFS) spectroscopy. Three halide-water interaction potentials recently developed [M. M. Reif and P. H. Hnenberger, J. Chem. Phys. 134, 144104 (2011)], along with three plausible choices for the value of the absolute hydration free energy of the proton (?G{sub hyd}{sup ?}[H{sup +}]), have been checked for their capability to properly describe the structural properties of halide aqueous solutions, by comparing the MD structural results with EXAFS experimental data. A very good agreement between theory and experiment has been obtained with one parameter set, namely L{sub E}, thus strengthening preliminary evidences for a ?G{sub hyd}{sup ?}[H{sup +}] value of ?1100 kJ mol{sup ?1} [M. M. Reif and P. H. Hnenberger, J. Chem. Phys. 134, 144104 (2011)]. The Cl{sup ?}, Br{sup ?}, and I{sup ?} ions have been found to form an unstructured and disordered first hydration shell in aqueous solution, with a broad distribution of instantaneous coordination numbers. Conversely, the F{sup ?} ion shows more ordered and defined first solvation shell, with only two statistically relevant coordination geometries (six and sevenfold complexes). Our thorough investigation on the effect of halide ions on the microscopic structure of water highlights that the perturbation induced by the Cl{sup ?}, Br{sup ?}, and I{sup ?} ions does not extend beyond the ion first hydration shell, and the structure of water in the F{sup ?} second shell is also substantially unaffected by the ion.

  3. Hydrothermal alkali metal catalyst recovery process

    DOEpatents

    Eakman, James M.; Clavenna, LeRoy R.

    1979-01-01

    In a coal gasification operation or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein solid particles containing alkali metal residues are produced, alkali metal constituents are recovered from the particles primarily in the form of water soluble alkali metal formates by treating the particles with a calcium or magnesium-containing compound in the presence of water at a temperature between about 250.degree. F. and about 700.degree. F. and in the presence of added carbon monoxide. During the treating process the water insoluble alkali metal compounds comprising the insoluble alkali metal residues are converted into water soluble alkali metal formates. The resultant aqueous solution containing water soluble alkali metal formates is then separated from the treated particles and any insoluble materials formed during the treatment process, and recycled to the gasification process where the alkali metal formates serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst. This process permits increased recovery of alkali metal constituents, thereby decreasing the overall cost of the gasification process by reducing the amount of makeup alkali metal compounds necessary.

  4. Highly active oxide photocathode for photoelectrochemical water reduction

    NASA Astrophysics Data System (ADS)

    Paracchino, Adriana; Laporte, Vincent; Sivula, Kevin; Grtzel, Michael; Thimsen, Elijah

    2011-06-01

    A clean and efficient way to overcome the limited supply of fossil fuels and the greenhouse effect is the production of hydrogen fuel from sunlight and water through the semiconductor/water junction of a photoelectrochemical cell, where energy collection and water electrolysis are combined into a single semiconductor electrode. We present a highly active photocathode for solar H2 production, consisting of electrodeposited cuprous oxide, which was protected against photocathodic decomposition in water by nanolayers of Al-doped zinc oxide and titanium oxide and activated for hydrogen evolution with electrodeposited Pt nanoparticles. The roles of the different surface protection components were investigated, and in the best case electrodes showed photocurrents of up to -7.6?mA?cm-2 at a potential of 0?V versus the reversible hydrogen electrode at mild pH. The electrodes remained active after 1?h of testing, cuprous oxide was found to be stable during the water reduction reaction and the Faradaic efficiency was estimated to be close to 100%.

  5. The upgraded photocathode laser of the TESLA Test Facility

    NASA Astrophysics Data System (ADS)

    Will, I.; Koss, G.; Templin, I.

    2005-04-01

    This paper describes the photocathode laser of the TESLA Test Facility (TTF). The laser system generates trains of ultraviolet picosecond pulses with 262 nm wavelength. Special measures were required to allow for stable and reliable generation of these pulse trains that are up to 800 μs long and can contain up to 800 micropulses at 1 MHz repetition rate, alternatively, up to 2400 micropulses at 3 MHz repetition rate within the train. The duration of the individual micropulses is 11 ps FWHM ( σ˜4.5 ps). In the 1 MHz mode the micropulse energy at 262 nm wavelength reaches 54 μJ. Laser pulses are generated synchronously to the RF system of the TTF-2 linear accelerators (linac) with synchronization accuracy better than 1 ps. The laser is able to run at 10 Hz repetition rate with full remote control. It illuminates the photocathode of an RF gun to generate the electron bunches which are subsequently accelerated in the TTF linac.

  6. AlGaN/InGaN Photocathode Development

    NASA Astrophysics Data System (ADS)

    Buckley, J. H.; Leopold, D. J.

    2008-12-01

    An increase in quantum efficiency in photodetectors could result in a proportional reduction in the area of atmospheric Cherenkov telescopes and an even larger reduction in cost. We report on the development of high quantum efficiency, high gain, UV/blue photon-counting detectors based on AlGaN/InGaN photocathode heterostructures grown by molecular beam epitaxy. This research could eventually result in nearly ideal light detectors with a number of distinct advantages over existing technologies for numerous applications in high-energy physics and particle astrophysics. Potential advantages include much lower noise detection, better stability and radiation resistance than other cathode structures, high VUV sensitivity and very low radioactive background levels for deep underground experiments, and high detection efficiency for the detection of individual VUV-visible photons. We are also developing photocathodes with intrinsic gain, initially improving the detection efficiency of hybrid semiconductor-vacuum tube devices and eventually leading to a new type of all-solid-state photomultiplier device.

  7. Highly active oxide photocathode for photoelectrochemical water reduction.

    PubMed

    Paracchino, Adriana; Laporte, Vincent; Sivula, Kevin; Grtzel, Michael; Thimsen, Elijah

    2011-06-01

    A clean and efficient way to overcome the limited supply of fossil fuels and the greenhouse effect is the production of hydrogen fuel from sunlight and water through the semiconductor/water junction of a photoelectrochemical cell, where energy collection and water electrolysis are combined into a single semiconductor electrode. We present a highly active photocathode for solar H(2) production, consisting of electrodeposited cuprous oxide, which was protected against photocathodic decomposition in water by nanolayers of Al-doped zinc oxide and titanium oxide and activated for hydrogen evolution with electrodeposited Pt nanoparticles. The roles of the different surface protection components were investigated, and in the best case electrodes showed photocurrents of up to -7.6 mA cm(-2) at a potential of 0 V versus the reversible hydrogen electrode at mild pH. The electrodes remained active after 1 h of testing, cuprous oxide was found to be stable during the water reduction reaction and the Faradaic efficiency was estimated to be close to 100%. PMID:21552270

  8. AlGaN/InGaN Photocathode Development

    SciTech Connect

    Buckley, J. H.; Leopold, D. J.

    2008-12-24

    An increase in quantum efficiency in photodetectors could result in a proportional reduction in the area of atmospheric Cherenkov telescopes and an even larger reduction in cost. We report on the development of high quantum efficiency, high gain, UV/blue photon-counting detectors based on AlGaN/InGaN photocathode heterostructures grown by molecular beam epitaxy. This research could eventually result in nearly ideal light detectors with a number of distinct advantages over existing technologies for numerous applications in high-energy physics and particle astrophysics. Potential advantages include much lower noise detection, better stability and radiation resistance than other cathode structures, high VUV sensitivity and very low radioactive background levels for deep underground experiments, and high detection efficiency for the detection of individual VUV-visible photons. We are also developing photocathodes with intrinsic gain, initially improving the detection efficiency of hybrid semiconductor-vacuum tube devices and eventually leading to a new type of all-solid-state photomultiplier device.

  9. Influence of air exposure on CsI photocathodes

    NASA Astrophysics Data System (ADS)

    Xie, Yuguang; Zhang, Aiwu; Liu, Yingbiao; Liu, Hongbang; Hu, Tao; Zhou, Li; Cai, Xiao; Fang, Jian; Yu, Boxiang; Ge, Yongshuai; L, Qiwen; Sun, Xilei; Sun, Lijun; Xue, Zheng; Xie, Yigang; Zheng, Yangheng; L, Junguang

    2012-10-01

    We investigate the influence of air exposure on the quantum efficiency (QE) and surface morphology of CsI photocathodes (PCs), at relative humidities (RH) higher than 80% down to nearly 3% (both at room temperature) and a 60 C baking condition. By atomic force microscopy (AFM) surface analysis, it is clearly seen that RH >60% speeds up water film formation and CsI dissolution on the surface of the photocathode at the minute scale, while both grain size and QE change slowly at RH <30% at the hour scale. In the baking environment, the peak QE decreases less than 1.5% (absolute) within one week, and a stainless steel substrate and electron beam evaporation technique tend to effectively weaken the influence of air. With an Au-coated FR-4 substrate, the QE degradation is found to strongly depend on wavelength in the range of 120-210 nm. According to spectra of X-ray photoelectron spectroscopy (XPS), an excess of cesium was observed and the chemical reaction between water and CsI when exposed to humid air is proved. It is found that carbon, and not H2O or O2, is the main pollutant in the baking condition.

  10. EVALUATION OF METHODS FOR THE DETERMINATION OF TOTAL ORGANIC HALIDE IN WATER AND WASTE

    EPA Science Inventory

    Various methods for the determination of total organic halides (TOX) in groundwater and in waste oil samples have been evaluated. Of three inorganic halide species generation approaches and three inorganic halide determinative techniques evaluated for groundwater analyses, one co...

  11. Process and composition for drying of gaseous hydrogen halides

    DOEpatents

    Tom, Glenn M.; Brown, Duncan W.

    1989-08-01

    A process for drying a gaseous hydrogen halide of the formula HX, wherein X is selected from the group consisting of bromine, chlorine, fluorine, and iodine, to remove water impurity therefrom, comprising: contacting the water impurity-containing gaseous hydrogen halide with a scavenger including a support having associated therewith one or more members of the group consisting of: (a) an active scavenging moiety selected from one or more members of the group consisting of: (i) metal halide compounds dispersed in the support, of the formula MX.sub.y ; and (ii) metal halide pendant functional groups of the formula -MX.sub.y-1 covalently bonded to the support, wherein M is a y-valent metal, and y is an integer whose value is from 1 to 3; (b) corresponding partially or fully alkylated compounds and/or pendant functional groups, of the metal halide compounds and/or pendant functional groups of (a); wherein the alkylated compounds and/or pendant functional groups, when present, are reactive with the gaseous hydrogen halide to form the corresponding halide compounds and/or pendant functional groups of (a); and M being selected such that the heat of formation, .DELTA.H.sub.f of its hydrated halide, MX.sub.y.(H.sub.2 O).sub.n, is governed by the relationship: .DELTA.H.sub.f .gtoreq.n.times.10.1 kilocalories/mole of such hydrated halide compound wherein n is the number of water molecules bound to the metal halide in the metal halide hydrate. Also disclosed is an appertaining scavenger composition and a contacting apparatus wherein the scavenger is deployed in a bed for contacting with the water impurity-containing gaseous hydrogen halide.

  12. Anomalous Alloy Properties in Mixed Halide Perovskites.

    PubMed

    Yin, Wan-Jian; Yan, Yanfa; Wei, Su-Huai

    2014-11-01

    Engineering halide perovskite through mixing halogen elements, such as CH3NH3PbI3-xClx and CH3NH3PbI3-xBrx, is a viable way to tune its electronic and optical properties. Despite many emerging experiments on mixed halide perovskites, the basic electronic and structural properties of the alloys have not been understood and some crucial questions remain, for example, how much Cl can be incorporated into CH3NH3PbI3 is still unclear. In this Letter, we chose CsPbX3 (X = I, Br, Cl) as an example and use a first-principle calculation together with cluster-expansion methods to systematically study the structural, electronic, and optical properties of mixed halide perovskites and find that unlike conventional semiconductor alloys, they exhibit many anomalous alloy properties such as small or even negative formation energies at some concentrations and negligible or even negative band gap bowing parameters at high temperature. We further show that mixed-(I,Cl) perovskite is hard to form at temperature below 625 K, whereas forming mixed-(Br,Cl) and (I,Br) alloys are easy at room temperature. PMID:26278729

  13. Short-arc metal halide lamp suitable for projector application

    NASA Astrophysics Data System (ADS)

    Kawai, Kouji; Matsumoto, Masayuki

    1995-04-01

    Recently, progress has been made in the development of projectors used for large screen displays. Projection systems employing high luminous efficiency Metal Halide Lamps as a light source demonstrate unique and desirable features. For example, compared to conventional lamps, a Metal Halide Lamp has longer life, higher luminous efficiency, the shortest arc length possible, and higher color-rendering characteristics, resulting in an overall superior performance. Several lamps, including Metal Halide, Xenon, and Halogen lamps, are used in HDTV (High Definition Television). Recently, Metal Halide Lamps have become accepted as the light source of choice. The reason for this is the high brightness, color balance, and long life of the Metal Halide Lamp. The fundamental operating principal for Metal Halide Lamps is almost the same as that of Mercury lamps. A Metal Halide Lamp has very different characteristics in that, the spectrum of illumination can be varied by varying the mixture of Metal Halide generated in the lamp. For these lamps, we have improved the electrode, the chemical composition of the Metal Halide, and the glass envelope. We have achieved a longer average life (greater than 2500 hours) for a compact, single-bulb, projection-type lamp.

  14. Lanthanide doped strontium-barium cesium halide scintillators

    DOEpatents

    Bizarri, Gregory; Bourret-Courchesne, Edith; Derenzo, Stephen E.; Borade, Ramesh B.; Gundiah, Gautam; Yan, Zewu; Hanrahan, Stephen M.; Chaudhry, Anurag; Canning, Andrew

    2015-06-09

    The present invention provides for a composition comprising an inorganic scintillator comprising an optionally lanthanide-doped strontium-barium, optionally cesium, halide, useful for detecting nuclear material.

  15. Observation of Significant Quantum Efficiency Enhancement from a Polarized Photocathode with Distributed Brag Reflector

    SciTech Connect

    Zhang, Shukui; Poelker, Matthew; Stutzman, Marcy L.; Chen, Yiqiao; Moy, Aaron

    2015-09-01

    Polarized photocathodes with higher Quantum efficiency (QE) would help to reduce the technological challenge associated with producing polarized beams at milliampere levels, because less laser light would be required, which simplifies photocathode cooling requirements. And for a given amount of available laser power, higher QE would extend the photogun operating lifetime. The distributed Bragg reflector (DBR) concept was proposed to enhance the QE of strained-superlattice photocathodes by increasing the absorption of the incident photons using a Fabry-Perot cavity formed between the front surface of the photocathode and the substrate that includes a DBR, without compromising electron polarization. Here we present recent results showing QE enhancement of a GaAs/GaAsP strained-superlattice photocathode made with a DBR structure. Typically, a GaAs/GaAsP strained-superlattice photocathode without DBR provides a QE of 1%, at a laser wavelength corresponding to peak polarization. In comparison, the GaAs/GaAsP strained-superlattice photocathodes with DBR exhibited an enhancement of over 2 when the incident laser wavelength was tuned to meet the resonant condition for the Fabry-Perot resonator.

  16. Surface Science Analysis of GaAs Photocathodes Following Sustained Electron Beam Delivery

    SciTech Connect

    Shutthanandan, V.; Zhu, Zihua; Stutzman, Marcy L.; Hannon, Fay; Hernandez-Garcia, Carlos; Nandasiri, Manjula I.; Kuchibhatla, Satyanarayana V N T; Thevuthasan, Suntharampillai; Hess, Wayne P.

    2012-06-12

    Degradation of the photocathode materials employed in photoinjectors represents a challenge for sustained operation of nuclear physics accelerators and high power Free Electron Lasers (FEL). Several photocathode degradation processes are suspected, including defect formation by ion back bombardment, photochemistry of surface adsorbed species and irradiation-induced surface defect formation. To better understand the mechanisms of photocathode degradation, we have conducted surface and bulk analysis studies of two GaAs photocathodes removed from the FEL photoinjector after delivering electron beam for a few years. The analysis techniques include Helium Ion Microscopy (HIM), Rutherford Backscattering Spectrometry (RBS), Atomic Force Microscopy (AFM) and Secondary Ion Mass Spectrometry (SIMS). In addition, strained super-lattice GaAs photocathode samples, removed from the CEBAF photoinjector were analyzed using Transmission Electron Microscopy (TEM) and SIMS. This analysis of photocathode degradation during nominal photoinjector operating conditions represents first steps towards developing robust new photocathode designs necessary for generating sub-micron emittance electron beams required for both fourth generation light sources and intense polarized CW electron beams for nuclear and high energy physics facilities.

  17. Making and Breaking of Lead Halide Perovskites.

    PubMed

    Manser, Joseph S; Saidaminov, Makhsud I; Christians, Jeffrey A; Bakr, Osman M; Kamat, Prashant V

    2016-02-16

    A new front-runner has emerged in the field of next-generation photovoltaics. A unique class of materials, known as organic metal halide perovskites, bridges the gap between low-cost fabrication and exceptional device performance. These compounds can be processed at low temperature (typically in the range 80-150 °C) and readily self-assemble from the solution phase into high-quality semiconductor thin films. The low energetic barrier for crystal formation has mixed consequences. On one hand, it enables inexpensive processing and both optical and electronic tunability. The caveat, however, is that many as-formed lead halide perovskite thin films lack chemical and structural stability, undergoing rapid degradation in the presence of moisture or heat. To date, improvements in perovskite solar cell efficiency have resulted primarily from better control over thin film morphology, manipulation of the stoichiometry and chemistry of lead halide and alkylammonium halide precursors, and the choice of solvent treatment. Proper characterization and tuning of processing parameters can aid in rational optimization of perovskite devices. Likewise, gaining a comprehensive understanding of the degradation mechanism and identifying components of the perovskite structure that may be particularly susceptible to attack by moisture are vital to mitigate device degradation under operating conditions. This Account provides insight into the lifecycle of organic-inorganic lead halide perovskites, including (i) the nature of the precursor solution, (ii) formation of solid-state perovskite thin films and single crystals, and (iii) transformation of perovskites into hydrated phases upon exposure to moisture. In particular, spectroscopic and structural characterization techniques shed light on the thermally driven evolution of the perovskite structure. By tuning precursor stoichiometry and chemistry, and thus the lead halide charge-transfer complexes present in solution, crystallization kinetics can be tailored to yield improved thin film homogeneity. Because degradation of the as-formed perovskite film is in many ways analogous to its initial formation, the same suite of monitoring techniques reveals the moisture-induced transformation of low band gap methylammonium lead iodide (CH3NH3PbI3) to wide band gap hydrate compounds. The rate of degradation is increased upon exposure to light. Interestingly, the hydration process is reversible under certain conditions. This facile formation and subsequent chemical lability raises the question of whether CH3NH3PbI3 and its analogues are thermodynamically stable phases, thus posing a significant challenge to the development of transformative perovskite photovoltaics. Adequately addressing issues of structural and chemical stability under real-world operating conditions is paramount if perovskite solar cells are to make an impact beyond the benchtop. Expanding our fundamental knowledge of lead halide perovskite formation and degradation pathways can facilitate fabrication of stable, high-quality perovskite thin films for the next generation of photovoltaic and light emitting devices. PMID:26789596

  18. Electrolytic method to make alkali alcoholates using ion conducting alkali electrolyte/separator

    DOEpatents

    Joshi, Ashok V.; Balagopal, Shekar; Pendelton, Justin

    2011-12-13

    Alkali alcoholates, also called alkali alkoxides, are produced from alkali metal salt solutions and alcohol using a three-compartment electrolytic cell. The electrolytic cell includes an anolyte compartment configured with an anode, a buffer compartment, and a catholyte compartment configured with a cathode. An alkali ion conducting solid electrolyte configured to selectively transport alkali ions is positioned between the anolyte compartment and the buffer compartment. An alkali ion permeable separator is positioned between the buffer compartment and the catholyte compartment. The catholyte solution may include an alkali alcoholate and alcohol. The anolyte solution may include at least one alkali salt. The buffer compartment solution may include a soluble alkali salt and an alkali alcoholate in alcohol.

  19. Mechanism and Selectivity in Nickel-Catalyzed Cross-Electrophile Coupling of Aryl Halides with Alkyl Halides

    PubMed Central

    Biswas, Soumik; Weix, Daniel J.

    2013-01-01

    The direct cross-coupling of two different electrophiles, such as an aryl halide with an alkyl halide, offers many advantages over conventional cross-coupling methods that require a carbon nucleophile. Despite its promise as a versatile synthetic strategy, a limited understanding of the mechanism and origin of cross selectivity has hindered progress in reaction development and design. Herein, we shed light on the mechanism for the nickel-catalyzed cross-electrophile coupling of aryl halides with alkyl halides and demonstrate that the selectivity arises from an unusual catalytic cycle that combines both polar and radical steps to form the new C-C bond. PMID:23952217

  20. A novel system for measurement of the transverse electron momentum distribution from photocathodes

    SciTech Connect

    Feng, J.; Nasiatka, J.; Wan, W.; Padmore, H. A.; Vecchione, T.

    2015-01-15

    The transverse momentum of electrons produced by a photocathode contributes significantly to the performance of several different types of accelerator-based light sources, such as Free Electron Lasers, as well as systems designed for ultrafast electron diffraction and dynamic transmission electron microscopy. Minimization of the transverse emittance from photocathodes is the subject of intensive research, and therefore measurement of this parameter is of great importance. Here, we describe a simple system that offers real time measurements of transverse emittance and can be easily integrated into the photocathode fabrication process.

  1. Alkali and transition metal phospholides

    NASA Astrophysics Data System (ADS)

    Bezkishko, I. A.; Zagidullin, A. A.; Milyukov, V. A.; Sinyashin, O. G.

    2014-06-01

    Major tendencies in modern chemistry of alkali and transition metal phospholides (phosphacyclopentadienides) are systematized, analyzed and generalized. Basic methods of synthesis of these compounds are presented. Their chemical properties are considered with a special focus on their complexing ability. Potential applications of phospholides and their derivatives are discussed. The bibliography includes 184 references.

  2. Measurement of photocathode spectral response at cryogenic temperature

    NASA Astrophysics Data System (ADS)

    Menegolli, A.; Prata, M.; Prata, M. C.; Raselli, G. L.; Vignoli, C.

    2007-03-01

    Noble-gas liquids, such as xenon and argon, have been recently proposed as light scintillators in some experiments dedicated to neutrino physics and dark matter research. These experiments need the use of photomultiplier tubes directly immersed in the liquid phase and operating at cryogenic temperatures. We carried out an investigation about the spectral response and its variation from room to cryogenic temperature for two different kind of cryogenic photocathodes manufactured by Electron Tubes Ltd. and Hamamatsu Photonics K.K. Measurements were carried out by means of a xenon continuous lamp and a UV-VIS monocromator which allows the analysis from 300 to 700 nm with 5 nm resolution. Cryogenic tests were made at the liquid nitrogen temperature (77 K).

  3. Reproducible, rugged, and inexpensive photocathode x-ray diode

    SciTech Connect

    Idzorek, G. C.; Tierney, T. E.; Lockard, T. E.; Moy, K. J.; Keister, J. W.

    2008-10-15

    The photoemissive cathode type of x-ray diode (XRD) is popular for measuring time and spectrally resolved output of pulsed power experiments. Vitreous carbon XRDs currently used on the Sandia National Laboratories Z-machine were designed in the early 1980s and use materials and processes no longer available. Additionally cathodes used in the high x-ray flux and dirty vacuum environment of a machine such as Z suffer from response changes requiring recalibration. In searching for a suitable replacement cathode, we discovered very high purity vitreous-carbon planchets are commercially available for use as biological substrates in scanning electron microscope (SEM) work. After simplifying the photocathode mounting to use commercially available components, we constructed a set of 20 XRDs using SEM planchets that were then calibrated at the National Synchrotron Light Source at Brookhaven National Laboratory. We present comparisons of the reproducibility and absolute calibrations between the current vitreous-carbon XRDs and our new design.

  4. Atomic hydrogen cleaning of GaAS Photocathodes

    SciTech Connect

    M. Poelker; J. Price; C. Sinclair

    1997-01-01

    It is well known that surface contaminants on semiconductors can be removed when samples are exposed to atomic hydrogen. Atomic H reacts with oxides and carbides on the surface, forming compounds that are liberated and subsequently pumped away. Experiments at Jefferson lab with bulk GaAs in a low-voltage ultra-high vacuum H cleaning chamber have resulted in the production of photocathodes with high photoelectron yield (i.e., quantum efficiency) and long lifetime. A small, portable H cleaning apparatus also has been constructed to successfully clean GaAs samples that are later removed from the vacuum apparatus, transported through air and installed in a high-voltage laser-driven spin-polarized electron source. These results indicate that this method is a versatile and robust alternative to conventional wet chemical etching procedures usually employed to clean bulk GaAs.

  5. [Emissions of methyl halides from coastal salt marshes: A review].

    PubMed

    Xie, Wen-xia; Zhao, Quan-sheng; Cui, Yu-qian; Du, Hui-na; Ye, Si-yuan

    2015-11-01

    Methyl halides are the major carrier of halogens in the atmosphere, and they play an important role in tropospheric and stratospheric ozone depletion. Meanwhile, methyl halides can act as greenhouse gases in the atmosphere, and they are also environmentally significant because of their toxicity. Coastal salt marshes, the important intertidal ecosystems at the land-ocean interface, have been considered to be a large potential natural source of methyl halides. In this paper, the research status of the natural source or sink of methyl halides, the mechanisms of their emission from coastal salt marshes and affecting factors were summarized. In view of this, the following research fields need to be strengthened in the future: 1) Long time-scale and large region-range researches about the emission of methyl halides and the evaluation of their source and sink function, 2) Accurate quantification of contribution rates of different plant species and various biological types to fluxes of methyl halides, 3) Further researches on effects of the tidal fluctuation process and flooding duration on methyl halides emission, 4) Effects of the global change and human activities on methyl halides emission. PMID:26915215

  6. How specific halide adsorption varies hydrophobic interactions.

    PubMed

    Stock, Philipp; Müller, Melanie; Utzig, Thomas; Valtiner, Markus

    2016-01-01

    Hydrophobic interactions (HI) are driven by the water structure around hydrophobes in aqueous electrolytes. How water structures at hydrophobic interfaces and how this influences the HI was subject to numerous studies. However, the effect of specific ion adsorption on HI and hydrophobic interfaces remains largely unexplored or controversial. Here, the authors utilized atomic force microscopy force spectroscopy at well-defined nanoscopic hydrophobic interfaces to experimentally address how specific ion adsorption of halide ions as well as NH4 (+), Cs(+), and Na(+) cations alters interaction forces across hydrophobic interfaces. Our data demonstrate that iodide adsorption at hydrophobic interfaces profoundly varies the hydrophobic interaction potential. A long-range and strong hydration repulsion at distances D > 3 nm, is followed by an instability which could be explained by a subsequent rapid ejection of adsorbed iodides from approaching hydrophobic interfaces. In addition, the authors find only a weakly pronounced influence of bromide, and as expected no influence of chloride. Also, all tested cations do not have any significant influence on HI. Complementary, x-ray photoelectron spectroscopy and quartz-crystal-microbalance with dissipation monitoring showed a clear adsorption of large halide ions (Br(-)/I(-)) onto hydrophobic self-assembled monolayers (SAMs). Interestingly, iodide can even lead to a full disintegration of SAMs due to specific and strong interactions of iodide with gold. Our data suggest that hydrophobic surfaces are not intrinsically charged negatively by hydroxide adsorption, as it was generally believed. Hydrophobic surfaces rather interact strongly with negatively charged large halide ions, leading to a surface charging and significant variation of interaction forces. PMID:26753786

  7. Towards a Robust, Efficient Dispenser Photocathode: the Effect of Recesiation on Quantum Efficiency

    SciTech Connect

    Montgomery, Eric J.; Pan Zhigang; Leung, Jessica; Feldman, Donald W.; O'Shea, Patrick G.; Jensen, Kevin L.

    2009-01-22

    Future electron accelerators and Free Electron Lasers (FELs) require high brightness electron sources; photocathodes for such devices are challenged to maintain long life and high electron emission efficiency (high quantum efficiency, or QE). The UMD dispenser photocathode design addresses this tradeoff of robustness and QE. In such a dispenser, a cesium-based surface layer is deposited on a porous substrate. The surface layer can be replenished from a subsurface cesium reservoir under gentle heating, allowing cesium to diffuse controllably to the surface and providing demonstrably more robust photocathodes. In support of the premise that recesiation is able to restore contaminated photocathodes, we here report controlled contamination of cesium-based surface layers with subsequent recesiation and the resulting effect on QE. Contaminant gases investigated include examples known from the vacuum environment of typical electron guns.

  8. Spectral response, carrier lifetime, and photocurrents of SiC photocathodes

    NASA Astrophysics Data System (ADS)

    Kato, Masashi; Miyake, Keiko; Yasuda, Tomonari; Ichimura, Masaya; Hatayama, Tomoaki; Ohshima, Takeshi

    2016-01-01

    Silicon carbide (SiC) photocathode is one of the candidates for energy conversion from the solar light to hydrogen gas. The conversion efficiencies using SiC photocathodes are still low for practical use. In this study, to find origins of low conversion efficiency, we evaluated carrier lifetimes and depletion layer widths in SiC photocathodes and examined relationship of them with photocurrents. In addition, we observed spectral response of the photocurrents from the photocathodes. From these results, we found that enhancement of the carrier lifetime and the depletion layer width is effective for increase of the conversion efficiency for 4H- and 6H-SiC. 3C-SiC would have defects reducing the effective carrier lifetime, and thus decrease of such defects is essential for increase of the conversion efficiency using 3C-SiC.

  9. Towards a Robust, Efficient Dispenser Photocathode: the Effect of Recesiation on Quantum Efficiency

    NASA Astrophysics Data System (ADS)

    Montgomery, Eric J.; Pan, Zhigang; Leung, Jessica; Feldman, Donald W.; O'Shea, Patrick G.; Jensen, Kevin L.

    2009-01-01

    Future electron accelerators and Free Electron Lasers (FELs) require high brightness electron sources; photocathodes for such devices are challenged to maintain long life and high electron emission efficiency (high quantum efficiency, or QE). The UMD dispenser photocathode design addresses this tradeoff of robustness and QE. In such a dispenser, a cesium-based surface layer is deposited on a porous substrate. The surface layer can be replenished from a subsurface cesium reservoir under gentle heating, allowing cesium to diffuse controllably to the surface and providing demonstrably more robust photocathodes. In support of the premise that recesiation is able to restore contaminated photocathodes, we here report controlled contamination of cesium-based surface layers with subsequent recesiation and the resulting effect on QE. Contaminant gases investigated include examples known from the vacuum environment of typical electron guns.

  10. Molecular Catalyst Immobilized Photocathodes for Water/Proton and Carbon Dioxide Reduction.

    PubMed

    Tian, Haining

    2015-11-01

    As one of the components in a tandem photoelectrochemical cell for solar-fuel production, the photocathode carries out the reduction reaction to convert solar light and the corresponding substrate (e.g., proton and CO2) into target fuels. Immobilizing molecular catalysts onto the photocathode is a promising strategy to enhance the interfacial electron/hole-transfer process and to improve the stability of the catalysts. Furthermore, the molecular catalysts are beneficial in improving the selectivity of the reduction reaction, particularly for CO2 reduction. On the photocathode, the binding mode of the catalysts and the arrangement between the photosensitizer and the catalyst also play crucial roles in the performance and stability of the final device. How to firmly and effectively immobilize the catalyst on the photoelectrode is now becoming a scientific question. Recent publications on molecular catalyst immobilized photocathodes are therefore surveyed. PMID:26437747

  11. Performance and operational upgrades of x-ray streak camera photocathode assemblies at NIF

    NASA Astrophysics Data System (ADS)

    Hatch, Ben; Palmer, Nathan; Ayers, Shannon; Browning, Don; Felker, Brian; Holder, Joe; Homoelle, Doug; Khan, Shahab; Kimbrough, Joe; MacPhee, Andrew; Petre, Robert B.; Perfect, Brad; Throop, Alan; Wong, J. N.

    2014-09-01

    X-ray streak cameras are used at the National Ignition Facility for time-resolved measurements of inertial confinement fusion metrics such as capsule implosion velocity, self-emission burn width, and x-ray bang time (time of brightest x-ray emission). Recently a design effort was undertaken to improve the performance and operation of the streak camera photocathode and related assemblies. The performance improvements include a new optical design for the input of UV timing fiducial pulses that increases collection efficiency of electrons off the photocathode, repeatability and precision of the photocathode pack assembly, and increase the input field of view for upcoming experiments. The operational improvements will provide the ability to replace photocathode packs between experiments in the field without removing the diagnostic from the Diagnostic Instrument Manipulator (DIM). The new design and preliminary results are presented.

  12. Evaluation of chemical cleaning for Ga1-xAlxAs photocathode by spectral response

    NASA Astrophysics Data System (ADS)

    Chen, Xinlong; Chang, Benkang; Zhao, Jing; Hao, Guanghui; Jin, Muchun; Xu, Yuan

    2013-11-01

    The spectral response has been used to evaluate the chemical cleaning for Ga1-xAlxAs photocathode by an on-line spectral response measurement system. The spectral response curves of Ga1-xAlxAs photocathodes treated by different chemical cleaning methods are measured and analyzed in detail. We use the quantum efficiency formulas to fit the experimental curves transforming from the spectral response curves, and obtain the related performance parameters such as the surface electron escape probability, the back-interface recombination velocity, the electron diffusion length, and the thickness of the etching GaAs layer. The results show that the GaAs photocathode cleaned by the HF solution could obtain a good photoemission effect, while the Ga0.37Al0.63As photocathode could be well cleaned by the solution of sulfuric acid and hydrogen peroxide.

  13. Nanoscale investigation of organic - inorganic halide perovskites

    NASA Astrophysics Data System (ADS)

    Cacovich, S.; Divitini, G.; Vru?ini?, M.; Sadhanala, A.; Friend, R. H.; Sirringhaus, H.; Deschler, F.; Ducati, C.

    2015-10-01

    Over the last few years organic - inorganic halide perovskite-based solar cells have exhibited a rapid evolution, reaching certified power conversion efficiencies now surpassing 20%. Nevertheless the understanding of the optical and electronic properties of such systems on the nanoscale is still an open problem. In this work we investigate two model perovskite systems (based on iodine - CH3NH3PbI3 and bromine - CH3NH3PbBr3), analysing the local elemental composition and crystallinity and identifying chemical inhomogeneities.

  14. Color separation in metal halide lamps

    NASA Astrophysics Data System (ADS)

    Stoffels, W. W.; Nimalasuriya, T.; Flikweert, A. J.; Brok, W. J. M.; Mullen, J. J. A. M.; Kroesen, G. M. W.; Haverlag, M.

    2006-10-01

    Metal halide discharge lamps are efficient lighting sources. However their widespread application is hindered by several problems. One problem is color separation. This is caused by a non-homogeneous distribution of radiating species within the lamp. It is believed to be the result of a complex interplay between diffusion and convection processes. In this contribution convection in the lamp is varied by placing the lamp in a rotating centrifuge. The resulting centrifugal force of up to ten times the normal gravitational force enhances the convection within the lamp and allows studying its effect on the color separation.

  15. Alkali and alkali-earth ions in 4He systems

    NASA Astrophysics Data System (ADS)

    Rossi, M.; Verona, M.; Galli, D. E.; Reatto, L.

    2004-06-01

    We study with variational Monte Carlo simulations a single ion impurity in nanodroplets and in liquid 4He . Within the shadow wave function (SWF) approach we have studied alkali-earth ion doped 4He systems ( Be+ and Mg+ ) and we have also improved our previous variational results for alkali ion impurities ( Na+ , K+ , and Cs+ ). The new SWF allows for anisotropic correlations between 4He atoms and the ion. The first shell of 4He atoms around the ions has always a well defined solidlike structure, which is remarkably different for each ion but it does not depend on the 4He system (bulk liquid or cluster). We also give results for the chemical potential, the single particle excitation spectrum, and the effective mass of the ions in the bulk.

  16. Optical Design Considerations Relevant to Reflective UV Launch Gratings for Photocathode Irradiation

    SciTech Connect

    Bolton, Paul

    2010-12-07

    The characteristics of photoelectron microbunches emitted from a photocathode in response to laser irradiation determine many of the incident laser pulse requirements. RF photocathode designs based on grazing incidence of the irradiation benefit from the removal of launch optics from the electron beamline and enhanced absorption at Brewster angles. However, this also introduces two well known complexities in the laser pulse 'launch' requirements: (i) a transverse spatial anamorphism to guarantee that the projected transverse spatial profile of the irradiation is circular (in the plane of the photocathode) and (ii) a 'time slew' or tilted amplitude front on the laser pulse that is incident on the photocathode to guarantee that the temporal (longitudinal) profiles are synchronous across the entire transverse irradiation profile in the photocathode plane. A single diffraction grating can be used to fulfill these combined requirements. This reported work focuses on grating behavior only. It does not address imaging requirements associated with relayed optical transport from the grating to the photocathode. Because the grating is a highly dispersive optical element by design, the dispersive aspects of all launch requirements are important.

  17. Positron-alkali atom scattering

    NASA Technical Reports Server (NTRS)

    Mceachran, R. P.; Horbatsch, M.; Stauffer, A. D.; Ward, S. J.

    1990-01-01

    Positron-alkali atom scattering was recently investigated both theoretically and experimentally in the energy range from a few eV up to 100 eV. On the theoretical side calculations of the integrated elastic and excitation cross sections as well as total cross sections for Li, Na and K were based upon either the close-coupling method or the modified Glauber approximation. These theoretical results are in good agreement with experimental measurements of the total cross section for both Na and K. Resonance structures were also found in the L = 0, 1 and 2 partial waves for positron scattering from the alkalis. The structure of these resonances appears to be quite complex and, as expected, they occur in conjunction with the atomic excitation thresholds. Currently both theoretical and experimental work is in progress on positron-Rb scattering in the same energy range.

  18. Methyl halide production associated with kelp

    NASA Technical Reports Server (NTRS)

    Dastoor, Minoo N.; Manley, Steven L.

    1985-01-01

    Methyl halides (MeX) are important trace constituents of the atmosphere because they, mostly MeCl, have a major impact on the atmospheric ozone layer. Also, MeCl may account for 5 pct. of the total Cl budget and MeI may have a central role in the biogeochemical cycling of iodine. High MeI concentrations were found in seawater from kelp beds and it has been suggested that MeI is produced by kelps and that MeI and MeBr along with numerous other halocarbons were released by non-kelp marine macroalgae. The objective was to determine if kelps (and other seaweeds) are sources of MeX and to assess their contribution to the estimated global source strength (EGSS) of MeX. Although the production of MeX appears to be associated with kelp, microbes involved with kelp degradation also produce MeX. Microbial MeX production may be of global significance. The microbial MeX production potential, assuming annual kelp production equals kelp degradation and 100 pct. conversion of kelp halides to MeX, is approx. 2 x the EGSS. This is not achieved but indicates that microbial production of MeX may be of global significance.

  19. Resolution characteristics of graded band-gap reflection-mode AlGaAs/GaAs photocathodes

    NASA Astrophysics Data System (ADS)

    Deng, Wenjuan; Zhang, Daoli; Zou, Jijun; Peng, Xincun; Wang, Weilu; Zhang, Yijun; Chang, Benkang

    2015-12-01

    The modulation transfer function (MTF) of graded band-gap AlGaAs/GaAs reflection-mode photocathodes was determined using two-dimensional Poisson and continuity equations through numerical method. Based on the MTF model, we calculated the theoretical MTF of graded and uniform band-gap reflection-mode photocathodes. We then analyzed the effects of Al composition, wavelength of incident photon, and thicknesses of AlGaAs and GaAs layer on the resolution. Calculation results show that graded band-gap structures can increase the resolution of reflection-mode photocathodes. When the spatial frequency is 800 lp/mm and wavelength is 600 nm, the resolution of graded band-gap photocathodes generally increases by 15.4-29.6%. The resolution improvement of graded band-gap photocathodes is attributed to the fact that the built-in electric field in graded band-gap photocathodes reduces the lateral diffusion distance of photoelectrons.

  20. 10 CFR 429.54 - Metal halide lamp ballasts and fixtures.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 10 Energy 3 2014-01-01 2014-01-01 false Metal halide lamp ballasts and fixtures. 429.54 Section... CONSUMER PRODUCTS AND COMMERCIAL AND INDUSTRIAL EQUIPMENT Certification § 429.54 Metal halide lamp ballasts... are applicable to metal halide lamp ballasts; and (2) For each basic model of metal halide...

  1. 10 CFR 429.54 - Metal halide lamp ballasts and fixtures.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 10 Energy 3 2012-01-01 2012-01-01 false Metal halide lamp ballasts and fixtures. 429.54 Section... CONSUMER PRODUCTS AND COMMERCIAL AND INDUSTRIAL EQUIPMENT Certification § 429.54 Metal halide lamp ballasts... are applicable to metal halide lamp ballasts; and (2) For each basic model of metal halide...

  2. 10 CFR 429.54 - Metal halide lamp ballasts and fixtures.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 10 Energy 3 2013-01-01 2013-01-01 false Metal halide lamp ballasts and fixtures. 429.54 Section... CONSUMER PRODUCTS AND COMMERCIAL AND INDUSTRIAL EQUIPMENT Certification § 429.54 Metal halide lamp ballasts... are applicable to metal halide lamp ballasts; and (2) For each basic model of metal halide...

  3. Alkali metal sources for OLED devices

    NASA Astrophysics Data System (ADS)

    Cattaneo, Lorena; Longoni, Giorgio; Bonucci, Antonio; Tominetti, Stefano

    2005-07-01

    In OLED organic layers electron injection is improved by using alkali metals as cathodes, to lower work function or, as dopants of organic layer at cathode interface. The creation of an alkali metal layer can be accomplished through conventional physical vapor deposition from a heated dispenser. However alkali metals are very reactive and must be handled in inert atmosphere all through the entire process. If a contamination takes place, it reduces the lithium deposition rate and also the lithium total yield in a not controlled way. An innovative alkali metal dispensing technology has been developed to overcome these problems and ensure OLED alkali metal cathode reliability. The alkali Metal dispenser, called Alkamax, will be able to release up to a few grams of alkali metals (in particular Li and Cs) throughout the adoption of a very stable form of the alkali metal. Lithium, for example, can be evaporated "on demand": the evaporation could be stopped and re-activated without losing alkali metal yield because the metal not yet consumed remains in its stable form. A full characterization of dispensing material, dispenser configuration and dispensing process has been carried out in order to optimize the evaporation and deposition dynamics of alkali metals layers. The study has been performed applying also inside developed simulations tools.

  4. The Surface Activation Layer of GaAs Negative Electron Affinity Photocathode Activated by Cs, Li and NF3

    SciTech Connect

    Sun, Yun; Kirby, R.E.; Maruyama, T.; Mulhollan, G.A.; Bierman, J.C.; Pianetta, P.; /SLAC, SSRL

    2009-12-11

    The lifetime of GaAs photocathodes can be greatly improved by introducing Li in the Cs+NF{sub 3} activation process. The surface activation layer of such photocathodes is studied by synchrotron radiation photoemission and is compared with GaAs photocathodes activated without Li. The charge distributions of N, F and Cs experience significant changes when Li is added in the activation. In addition, the presence of Li causes NF{sub x} molecules to take an orientation with F atoms on top. All these changes induced by Li hold the key for the lifetime improvement of GaAs photocathodes.

  5. Regenerable activated bauxite adsorbent alkali monitor probe

    DOEpatents

    Lee, S.H.D.

    1992-12-22

    A regenerable activated bauxite adsorber alkali monitor probe for field applications to provide reliable measurement of alkali-vapor concentration in combustion gas with special emphasis on pressurized fluidized-bed combustion (PFBC) off-gas. More particularly, the invention relates to the development of a easily regenerable bauxite adsorbent for use in a method to accurately determine the alkali-vapor content of PFBC exhaust gases. 6 figs.

  6. Unraveling the Role of Monovalent Halides in Mixed-Halide Organic-Inorganic Perovskites.

    PubMed

    Deepa, Melepurath; Ramos, F Javier; Shivaprasad, S M; Ahmad, Shahzada

    2016-03-16

    The performance of perovskite solar cells is strongly influenced by the composition and microstructure of the perovskite. A recent approach to improve the power conversion efficiencies utilized mixed-halide perovskites, but the halide ions and their roles were not directly studied. Unraveling their precise location in the perovskite layer is of paramount importance. Here, we investigated four different perovskites by using X-ray photoelectron spectroscopy, and found that among the three studied mixed-halide perovskites, CH3 NH3 Pb(I0.74 Br0.26 )3 and CH3 NH3 PbBr3-x Clx show peaks that unambiguously demonstrate the presence of iodide and bromide in the former, and bromide and chloride in the latter. The CH3 NH3 PbI3-x Clx perovskite shows anomalous behavior, the iodide content far outweighs that of the chloride; a small proportion of chloride, in all likelihood, resides deep within the TiO2 /absorber layer. Our study reveals that there are many distinguishable structural differences between these perovskites, and that these directly impact the photovoltaic performances. PMID:26717046

  7. Surface science analysis of GaAs photocathodes following sustained electron beam delivery

    SciTech Connect

    Carlos Hernandez-Garcia, Fay Hannon, Marcy Stutzman, V. Shutthanandan, Z. Zhu, M. Nandasri, S. V. Kuchibhatla, S. Thevuthasan, W. P. Hess

    2012-06-01

    Degradation of the photocathode materials employed in photoinjectors represents a challenge for sustained operation of nuclear physics accelerators and high power Free Electron Lasers (FEL). Photocathode quantum efficiency (QE) degradation is due to residual gasses in the electron source vacuum system being ionized and accelerated back to the photocathode. These investigations are a first attempt to characterize the nature of the photocathode degradation, and employ multiple surface and bulk analysis techniques to investigate damage mechanisms including sputtering of the Cs-oxidant surface monolayer, other surface chemistry effects, and ion implantation. Surface and bulk analysis studies were conducted on two GaAs photocathodes, which were removed from the JLab FEL DC photoemission gun after delivering electron beam, and two control samples. The analysis techniques include Helium Ion Microscopy (HIM), Rutherford Backscattering Spectrometry (RBS), Atomic Force Microscopy (AFM) and Secondary Ion Mass Spectrometry (SIMS). In addition, two high-polarization strained superlattice GaAs photocathode samples, one removed from the Continuous Electron Beam Accelerator Facility (CEBAF) photoinjector and one unused, were also analyzed using Transmission Electron Microscopy (TEM) and SIMS. It was found that heat cleaning the FEL GaAs wafer introduces surface roughness, which seems to be reduced by prolonged use. The bulk GaAs samples retained a fairly well organized crystalline structure after delivering beam but shows evidence of Cs depletion on the surface. Within the precision of the SIMS and RBS measurements the data showed no indication of hydrogen implantation or lattice damage from ion back bombardment in the bulk GaAs wafers. In contrast, SIMS and TEM measurements of the strained superlattice photocathode show clear crystal damage in the wafer from ion back bombardment.

  8. Tellurium halide IR fibers for remote spectroscopy

    NASA Astrophysics Data System (ADS)

    Zhang, Xhang H.; Ma, Hong Li; Blanchetiere, Chantal; Le Foulgoc, Karine; Lucas, Jacques; Heuze, Jean; Colardelle, P.; Froissard, P.; Picque, D.; Corrieu, G.

    1994-07-01

    The new family of IR transmitting glasses, the TeX glasses, based on the association of tellurium and halide (Cl, Br, or I) are characterized by a wide optical window extending from 2 to 18 micrometers and a strong stability towards devitrification. Optical fibers drawn from these glasses exhibit low losses in the 7 - 10 micrometers range (less than 1 dB/m for single index fibers, 1 - 2 dB/m for fibers having a core-clad structure). The TeX glass fibers have been used in a remote analysis set-up which is mainly composed of a FTIR spectrometer coupled with a HgCdTe detector. This prototype system permits qualitative and quantitative analysis in a wide wavelength region lying from 3 to 13 micrometers , covering the fundamental absorption of more organic species. The evolution of a lactic and an alcoholic fermentation has been monitored by means of this set-up.

  9. Fatigue of silver-halide fibers

    NASA Astrophysics Data System (ADS)

    Barkay, Nitzan; German, Alla; Shalem, Shaul; Katzir, Abraham

    1994-07-01

    The IR transmittance of silver-halide fibers was measured while they were undergoing various flexing procedures leading to mechanical fatigue. The fatigue experiments consisted of repetitive bending, going from small bending radii (plastic regime) to large bending radii (elastic regime). Various types of fibers have been investigated including unclad fibers, fibers with a core-clad structure, fibers of various AgClxBr1-x compositions and fibers of different diameters. The optical measurements which were done during the flexing experiments involved CO2-laser transmission and spectral (FTIR) transmission. The results for the various conditions are reported and discussed in terms of high-cycle and low- cycle fatigue. Such investigations are of practical importance in characterizing fibers useful for endoscopic surgery and IR detection.

  10. Passive particle dosimetry. [silver halide crystal growth

    NASA Technical Reports Server (NTRS)

    Childs, C. B.

    1977-01-01

    Present methods of dosimetry are reviewed with emphasis on the processes using silver chloride crystals for ionizing particle dosimetry. Differences between the ability of various crystals to record ionizing particle paths are directly related to impurities in the range of a few ppm (parts per million). To understand the roles of these impurities in the process, a method for consistent production of high purity silver chloride, and silver bromide was developed which yields silver halides with detectable impurity content less than 1 ppm. This high purity silver chloride was used in growing crystals with controlled doping. Crystals were grown by both the Czochalski method and the Bridgman method, and the Bridgman grown crystals were used for the experiments discussed. The distribution coefficients of ten divalent cations were determined for the Bridgman crystals. The best dosimeters were made with silver chloride crystals containing 5 to 10 ppm of lead; other impurities tested did not produce proper dosimeters.

  11. Beyond injection: Trojan horse underdense photocathode plasma wakefield acceleration

    SciTech Connect

    Hidding, B.; Rosenzweig, J. B.; Xi, Y.; O'Shea, B.; Andonian, G.; Schiller, D.; Barber, S.; Williams, O.; Pretzler, G.; Koenigstein, T.; Kleeschulte, F.; Hogan, M. J.; Litos, M.; Corde, S.; White, W. W.; Muggli, P.; Bruhwiler, D. L.; Lotov, K.

    2012-12-21

    An overview on the underlying principles of the hybrid plasma wakefield acceleration scheme dubbed 'Trojan Horse' acceleration is given. The concept is based on laser-controlled release of electrons directly into a particle-beam-driven plasma blowout, paving the way for controlled, shapeable electron bunches with ultralow emittance and ultrahigh brightness. Combining the virtues of a low-ionization-threshold underdense photocathode with the GV/m-scale electric fields of a practically dephasing-free beam-driven plasma blowout, this constitutes a 4th generation electron acceleration scheme. It is applicable as a beam brightness transformer for electron bunches from LWFA and PWFA systems alike. At FACET, the proof-of-concept experiment 'E-210: Trojan Horse Plasma Wakefield Acceleration' has recently been approved and is in preparation. At the same time, various LWFA facilities are currently considered to host experiments aiming at stabilizing and boosting the electron bunch output quality via a trojan horse afterburner stage. Since normalized emittance and brightness can be improved by many orders of magnitude, the scheme is an ideal candidate for light sources such as free-electron-lasers and those based on Thomson scattering and betatron radiation alike.

  12. Beyond injection: Trojan horse underdense photocathode plasma wakefield acceleration

    NASA Astrophysics Data System (ADS)

    Hidding, B.; Rosenzweig, J. B.; Xi, Y.; O'Shea, B.; Andonian, G.; Schiller, D.; Barber, S.; Williams, O.; Pretzler, G.; Königstein, T.; Kleeschulte, F.; Hogan, M. J.; Litos, M.; Corde, S.; White, W. W.; Muggli, P.; Bruhwiler, D. L.; Lotov, K.

    2012-12-01

    An overview on the underlying principles of the hybrid plasma wakefield acceleration scheme dubbed "Trojan Horse" acceleration is given. The concept is based on laser-controlled release of electrons directly into a particle-beam-driven plasma blowout, paving the way for controlled, shapeable electron bunches with ultralow emittance and ultrahigh brightness. Combining the virtues of a low-ionization-threshold underdense photocathode with the GV/m-scale electric fields of a practically dephasing-free beam-driven plasma blowout, this constitutes a 4th generation electron acceleration scheme. It is applicable as a beam brightness transformer for electron bunches from LWFA and PWFA systems alike. At FACET, the proof-of-concept experiment "E-210: Trojan Horse Plasma Wakefield Acceleration" has recently been approved and is in preparation. At the same time, various LWFA facilities are currently considered to host experiments aiming at stabilizing and boosting the electron bunch output quality via a trojan horse afterburner stage. Since normalized emittance and brightness can be improved by many orders of magnitude, the scheme is an ideal candidate for light sources such as free-electron-lasers and those based on Thomson scattering and betatron radiation alike.

  13. A mechanism of Cu work function reduction in CsBr/Cu photocathodes.

    PubMed

    Halliday, M T E; Hess, W P; Shluger, A L

    2016-03-01

    Thin films of CsBr deposited on Cu(100) have been proposed as next-generation photocathode materials for applications in particle accelerators and free-electron lasers. However, the mechanisms underlying an improved photocathode performance as well as their long-term stability remain poorly understood. We present Density Functional Theory (DFT) calculations of the work function reduction following the application of CsBr thin film coatings to Cu photocathodes. The effects of both flat and rough interface and van der Waals forces are examined. Calculations suggest that CsBr films can reduce the Cu(100) work function by about 1.5 eV, which would explain the observed increase in quantum efficiency (QE) of coated vs. uncoated photocathodes. A model explaining the experimentally observed laser activation of photocathodes is provided whereby the photo-induced creation of Br vacancies and Cs-Br di-vacancies and their subsequent diffusion to the Cu/CsBr interface lead to a further increase in QE after a period of laser irradiation. PMID:26899524

  14. Design of quantum efficiency measurement system for variable doping GaAs photocathode

    NASA Astrophysics Data System (ADS)

    Chen, Liang; Yang, Kai; Liu, HongLin; Chang, Benkang

    2008-03-01

    To achieve high quantum efficiency and good stability has been a main direction to develop GaAs photocathode recently. Through early research, we proved that variable doping structure is executable and practical, and has great potential. In order to optimize variable doping GaAs photocathode preparation techniques and study the variable doping theory deeply, a real-time quantum efficiency measurement system for GaAs Photocathode has been designed. The system uses FPGA (Field-programmable gate array) device, and high speed A/D converter to design a high signal noise ratio and high speed data acquisition card. ARM (Advanced RISC Machines) core processor s3c2410 and real-time embedded system are used to obtain and show measurement results. The measurement precision of photocurrent could reach 1nA, and measurement range of spectral response curve is within 400~1000nm. GaAs photocathode preparation process can be real-time monitored by using this system. This system could easily be added other functions to show the physic variation of photocathode during the preparation process more roundly in the future.

  15. Purification and Characterization of an Extracellular, Thermo-Alkali-Stable, Metal Tolerant Laccase from Bacillus tequilensis SN4

    PubMed Central

    Sondhi, Sonica; Sharma, Prince; Saini, Shilpa; Puri, Neena; Gupta, Naveen

    2014-01-01

    A novel extracellular thermo-alkali-stable laccase from Bacillus tequilensis SN4 (SN4LAC) was purified to homogeneity. The laccase was a monomeric protein of molecular weight 32 KDa. UV-visible spectrum and peptide mass fingerprinting results showed that SN4LAC is a multicopper oxidase. Laccase was active in broad range of phenolic and non-phenolic substrates. Catalytic efficiency (kcat/Km) showed that 2, 6-dimethoxyphenol was most efficiently oxidized by the enzyme. The enzyme was inhibited by conventional inhibitors of laccase like sodium azide, cysteine, dithiothreitol and ?-mercaptoethanol. SN4LAC was found to be highly thermostable, having temperature optimum at 85C and could retain more than 80% activity at 70C for 24 h. The optimum pH of activity for 2, 6-dimethoxyphenol, 2, 2?-azino bis[3-ethylbenzthiazoline-6-sulfonate], syringaldazine and guaiacol was 8.0, 5.5, 6.5 and 8.0 respectively. Enzyme was alkali-stable as it retained more than 75% activity at pH 9.0 for 24 h. Activity of the enzyme was significantly enhanced by Cu2+, Co2+, SDS and CTAB, while it was stable in the presence of halides, most of the other metal ions and surfactants. The extracellular nature and stability of SN4LAC in extreme conditions such as high temperature, pH, heavy metals, halides and detergents makes it a highly suitable candidate for biotechnological and industrial applications. PMID:24871763

  16. Tellurite glass as a waste form for mixed alkali-chloride waste streams: Candidate materials selection and initial testing

    NASA Astrophysics Data System (ADS)

    Riley, Brian J.; Rieck, Bennett T.; McCloy, John S.; Crum, Jarrod V.; Sundaram, S. K.; Vienna, John D.

    2012-05-01

    Tellurite glasses have historically been shown to host large concentrations of halides. They are here considered for the first time as a waste form for immobilizing chloride wastes, such as may be generated in the proposed molten alkali salt electrochemical separations step in nuclear fuel reprocessing. Key properties of several tellurite glasses are determined to assess acceptability as a chloride waste form. TeO2 glasses with other oxides (PbO, Al2O3 + B2O3, WO3, P2O5, or ZnO) were fabricated with and without 10 mass% of a simulated (non-radioactive) mixed alkali, alkaline-earth, and rare earth chloride waste. Measured chemical durability is compared for the glasses, as determined by the product consistency test (PCT), a common standardized chemical durability test often used to validate borosilicate glass waste forms. The glass with the most promise as a waste form is the TeO2-PbO system, as it offers good halide retention, a low sodium release (by PCT) comparable with high-level waste silicate glass waste forms, and a high storage density.

  17. Metal-nonmetal transition in indium-alkali metal and aluminum-alkali metal melts

    NASA Astrophysics Data System (ADS)

    Kiselev, A. I.

    2012-02-01

    The electrical resistivities of indium-alkali metal and aluminum-alkali metal melts are calculated. The Ziman theory of the electrical conductivity of metallic melts is shown to successfully describe the experimental effects of an increase in the electrical resistivity during a metal-nonmetal transition in the indium-alkali metal systems. This theory also predicts similar qualitative effects of a change in the electrical resistivities of aluminum-alkali metal melts. The melts of aluminum-alkali metal systems are assumed to undergo a metal-nonmetal transition.

  18. The alkali metals: 200 years of surprises.

    PubMed

    Dye, James L

    2015-03-13

    Alkali metal compounds have been known since antiquity. In 1807, Sir Humphry Davy surprised everyone by electrolytically preparing (and naming) potassium and sodium metals. In 1808, he noted their interaction with ammonia, which, 100 years later, was attributed to solvated electrons. After 1960, pulse radiolysis of nearly any solvent produced solvated electrons, which became one of the most studied species in chemistry. In 1968, alkali metal solutions in amines and ethers were shown to contain alkali metal anions in addition to solvated electrons. The advent of crown ethers and cryptands as complexants for alkali cations greatly enhanced alkali metal solubilities. This permitted us to prepare a crystalline salt of Na(-) in 1974, followed by 30 other alkalides with Na(-), K(-), Rb(-) and Cs(-) anions. This firmly established the -1 oxidation state of alkali metals. The synthesis of alkalides led to the crystallization of electrides, with trapped electrons as the anions. Electrides have a variety of electronic and magnetic properties, depending on the geometries and connectivities of the trapping sites. In 2009, the final surprise was the experimental demonstration that alkali metals under high pressure lose their metallic character as the electrons are localized in voids between the alkali cations to become high-pressure electrides! PMID:25666067

  19. Properties of mixed alkali germanate glasses

    NASA Astrophysics Data System (ADS)

    Ashton-Patton, Melissann Marie

    There is little data in the literature pertaining to mixed alkali germanate glasses. The majority of the data exists for the sodium-potassium-germanate glasses, and focuses on the density, glass transition temperature and vibrational spectra. This study explores three of the ten possible mixed alkali germanate glass systems: the lithium-cesium-germanium ternary, the sodium-potassium-germanium ternary, and the potassium-rubidium-germanium ternary. The mixed alkali effect was examined at two different concentrations of germania (85 and 90 mol %). To examine the mixed alkali effect on the germanate anomaly, the alkali oxides were held in a ratio of 1:1 and the germanium was varied from 100 to 75 mol %. The glass transition temperature and densities behavior of the mixed alkali germanate glasses in this study behaved as expected, exhibiting a maximum in Tg and no mixed alkali effect in density. The glasses with a 1:1 ratio of alkali exhibited properties between the end member glasses. The infrared spectra from this study show that the hydroxyl content increases as the amount of alkali in the glass increases. The cation identity does effect the band positions and intensities. The infrared bands between 1500 and 4000 cm-1 are shown to be a result of water. Electrical conductivity of mixed alkali germanate glasses exhibited unique behavior. Small additions of alkali (? 5 mol %) result in a positive or a linear deviation from additivity, in both the lithium-cesium-germanate system and the sodium-potassium-germanate system. With 10 mol % alkali oxide addition the deviation from additivity increases as the radius ratio of the cations increases. However, with 15 mol % alkali oxide addition, the greater the difference in the radius ratio of the cations, the smaller the deviation from additivity. A Kissinger study on the lithium-cesium-germanate glasses, yields activation energies consistent with crystallization studies in the literature for other mixed alkali germanate glasses. Glasses with a 1:1 ratio of cesium oxide to lithium oxide, or more cesium oxide than lithium oxide, crystallize into cesium germanium oxide crystals, however if there is more lithium the glasses crystallize into an unknown phase.

  20. Review of alkali laser research and development

    NASA Astrophysics Data System (ADS)

    Zhdanov, Boris V.; Knize, Randy J.

    2013-02-01

    In this review we present an analysis of optically pumped alkali laser research and development from the first proposal in 1958 by Schawlow and Townes to the current state. In spite of the long history, real interest in alkali vapor lasers has appeared in the past decade, after the demonstration of really efficient lasing in Rb and Cs vapors in 2003 and the first successful power scaling experiments. This interest was stimulated by the possibility of using efficient diode lasers for optical pumping of the alkali lasers and by the fact that these lasers can produce a high quality and high power output beam from a single aperture. We present a review of the most important achievements in high power alkali laser research and development, discuss some problems existing in this field, and provide future perspectives in diode pumped alkali laser development.

  1. Method of handling radioactive alkali metal waste

    DOEpatents

    Wolson, Raymond D. (Lockport, IL); McPheeters, Charles C. (Plainfield, IL)

    1980-01-01

    Radioactive alkali metal is mixed with particulate silica in a rotary drum reactor in which the alkali metal is converted to the monoxide during rotation of the reactor to produce particulate silica coated with the alkali metal monoxide suitable as a feed material to make a glass for storing radioactive material. Silica particles, the majority of which pass through a 95 mesh screen or preferably through a 200 mesh screen, are employed in this process, and the preferred weight ratio of silica to alkali metal is 7 to 1 in order to produce a feed material for the final glass product having a silica to alkali metal monoxide ratio of about 5 to 1.

  2. Photoemission Study of Cs-NF3 Activated GaAs(100) Negative Electron Affinity Photocathodes

    SciTech Connect

    Liu, Z.; Sun, Y.; Peterson, S.; Pianetta, P.

    2008-05-28

    GaAs based negative electron affinity photocathodes activated with Cs and NF{sub 3} are used as polarized electron sources for linear accelerators. It is generally believed that the activation layer consists of CsF. The activation layers of Cs-NF{sub 3} on GaAs photocathodes are herein investigated using synchrotron radiation photoelectron spectroscopy (SR-PES). F1s, N1s and other core levels are recorded at photon energies ranging from 70eV to 820eV. Surprisingly, a significant amount of nitrogen is observed in the activation layers. Two distinct species of nitrogen are observed, one of which decreases along with the Fluorine signal as the yield of the photocathode decays with time.

  3. Polarization studies of strained GaAs photocathodes at the SLAC Gun Test Laboratory

    SciTech Connect

    Saez, P.; Alley, R.; Clendenin, J.; Frisch, J.; Kirby, R.; Mair, R.; Maruyama, T.; Miller, R.; Mulhollan, G.; Prescott, C.

    1995-08-01

    The SLAC Gun Test Laboratory apparatus, the first two meters of which is a replica of the SLAC injector, is used to study the production of intense, highly-polarized electron beams required for the Stanford Linear Collider and future linear colliders. The facility has been upgraded with a Mott polarimeter in order to characterize the electron polarization from photocathodes operating in a DC gun. In particular, SLAC utilizes p-type, biaxially strained GaAs photocathodes which have produced longitudinal electron polarizations greater than 80% while yielding pulses of 5 A/sq cm at an operating voltage of 120 kV. Among the experiments performed include studying the influences of the active layer thickness, temperature, quantum efficiency and cessation on the polarization. The results might help to develop strained photocathodes with higher polarization.

  4. Temporal resolution limit estimation of x-ray streak cameras using a CsI photocathode

    NASA Astrophysics Data System (ADS)

    Li, Xiang; Gu, Li; Zong, Fangke; Zhang, Jingjin; Yang, Qinlao

    2015-08-01

    A Monte Carlo model is developed and implemented to calculate the characteristics of x-ray induced secondary electron (SE) emission from a CsI photocathode used in an x-ray streak camera. Time distributions of emitted SEs are investigated with an incident x-ray energy range from 1 to 30 keV and a CsI thickness range from 100 to 1000 nm. Simulation results indicate that SE time distribution curves have little dependence on the incident x-ray energy and CsI thickness. The calculated time dispersion within the CsI photocathode is about 70 fs, which should be the temporal resolution limit of x-ray streak cameras that use CsI as the photocathode material.

  5. Characterizing and Optimizing Photocathode Laser Distributions for Ultra-low Emittance Electron Beam Operations

    SciTech Connect

    Zhou, F.; Bohler, D.; Ding, Y.; Gilevich, S.; Huang, Z.; Loos, H.; Ratner, D.; Vetter, S.

    2015-12-07

    Photocathode RF gun has been widely used for generation of high-brightness electron beams for many different applications. We found that the drive laser distributions in such RF guns play important roles in minimizing the electron beam emittance. Characterizing the laser distributions with measurable parameters and optimizing beam emittance versus the laser distribution parameters in both spatial and temporal directions are highly desired for high-brightness electron beam operation. In this paper, we report systematic measurements and simulations of emittance dependence on the measurable parameters represented for spatial and temporal laser distributions at the photocathode RF gun systems of Linac Coherent Light Source. The tolerable parameter ranges for photocathode drive laser distributions in both directions are presented for ultra-low emittance beam operations.

  6. High quantum efficiency photocathode simulation for the investigation of novel structured designs

    SciTech Connect

    Opachich, Y. P. Ross, P. W.; Huffman, E.; Koch, J. A.; MacPhee, A. G.; Nagel, S. R.; Bell, P. M.; Bradley, D. K.; Landen, O. L.; Hilsabeck, T. J.

    2014-11-15

    A computer model in CST Studio Suite has been developed to evaluate several novel geometrically enhanced photocathode designs. This work was aimed at identifying a structure that would increase the total electron yield by a factor of two or greater in the 130 keV range. The modeling software was used to simulate the electric field and generate particle tracking for several potential structures. The final photocathode structure has been tailored to meet a set of detector performance requirements, namely, a spatial resolution of <40 ?m and a temporal spread of 110 ps. We present the details of the geometrically enhanced photocathode model and resulting static field and electron emission characteristics.

  7. High quantum efficiency photocathode simulation for the investigation of novel structured designsa)

    NASA Astrophysics Data System (ADS)

    Opachich, Y. P.; Ross, P. W.; MacPhee, A. G.; Hilsabeck, T. J.; Nagel, S. R.; Huffman, E.; Bell, P. M.; Bradley, D. K.; Koch, J. A.; Landen, O. L.

    2014-11-01

    A computer model in CST Studio Suite has been developed to evaluate several novel geometrically enhanced photocathode designs. This work was aimed at identifying a structure that would increase the total electron yield by a factor of two or greater in the 1-30 keV range. The modeling software was used to simulate the electric field and generate particle tracking for several potential structures. The final photocathode structure has been tailored to meet a set of detector performance requirements, namely, a spatial resolution of <40 ?m and a temporal spread of 1-10 ps. We present the details of the geometrically enhanced photocathode model and resulting static field and electron emission characteristics.

  8. High quantum efficiency photocathode simulation for the investigation of novel structured designs.

    PubMed

    Opachich, Y P; Ross, P W; MacPhee, A G; Hilsabeck, T J; Nagel, S R; Huffman, E; Bell, P M; Bradley, D K; Koch, J A; Landen, O L

    2014-11-01

    A computer model in CST Studio Suite has been developed to evaluate several novel geometrically enhanced photocathode designs. This work was aimed at identifying a structure that would increase the total electron yield by a factor of two or greater in the 1-30 keV range. The modeling software was used to simulate the electric field and generate particle tracking for several potential structures. The final photocathode structure has been tailored to meet a set of detector performance requirements, namely, a spatial resolution of <40 ?m and a temporal spread of 1-10 ps. We present the details of the geometrically enhanced photocathode model and resulting static field and electron emission characteristics. PMID:25430201

  9. High-brightness electron beam evolution following laser-based cleaning of a photocathode

    NASA Astrophysics Data System (ADS)

    Zhou, F.; Brachmann, A.; Decker, F.-J.; Emma, P.; Gilevich, S.; Iverson, R.; Stefan, P.; Turner, J.

    2012-09-01

    Laser-based techniques have been widely used for cleaning metal photocathodes to increase quantum efficiency (QE). However, the impact of laser cleaning on cathode uniformity and thereby on electron beam quality are less understood. We are evaluating whether this technique can be applied to revive photocathodes used for high-brightness electron sources in advanced x-ray free-electron laser (FEL) facilities, such as the Linac Coherent Light Source (LCLS) at the SLAC National Accelerator Laboratory. The laser-based cleaning was applied to two separate areas of the current LCLS photocathode on July 4 and July 26, 2011, respectively. The QE was increased by 8-10 times upon the laser cleaning. Since the cleaning, routine operation has exhibited a slow evolution of the QE improvement and comparatively rapid improvement of transverse emittance, with a factor of 3 QE enhancement over five months, and a significant emittance improvement over the initial 2-3 weeks following the cleaning. Currently, the QE of the LCLS photocathode is holding constant at about 1.210-4, with a normalized injector emittance of about 0.3?m for a 150-pC bunch charge. With the proper procedures, the laser-cleaning technique appears to be a viable tool to revive the LCLS photocathode. We present observations and analyses for the QE and emittance evolution in time following the laser-based cleaning of the LCLS photocathode, and comparison to the previous studies, the measured thermal emittance versus the QE and comparison to the theoretical model.

  10. High Pressure Electrochemistry: Application to silver halides

    NASA Astrophysics Data System (ADS)

    Havens, K.; Kavner, A.

    2007-12-01

    Electron and ion charge transfer processes help govern electrical conductivity and diffusive mass and heat transport properties in deep Earth minerals. In an attempt to understand how pressure influences charge transfer behavior, the halide silver bromide (AgBr) was studied under the influence of an electric potential difference applied across two electrodes in a diamond anvil cell. This study follows our previous work on AgI, which was found to dissociate to molecular iodine and silver metal due to pressure and voltage influences. We performed two sets of experiments on AgBr at high pressure in a diamond anvil cell: electrochemical dissociation and electrical resistance measurements. In our study, we were able to electrochemically dissociate AgBr at pressures of 0.25-1.6 GPa by applying a voltage across the electrodes in the diamond cell sample chamber. Ag metal grew visibly on the negatively-charged electrode when voltages varying from 0.1 V to 5 V were applied. Additionally, a dark blue color appeared in low pressure areas of the diamond cell and grew darker from both voltage application and light exposure, indicating photochemical effects. We found that the reaction area and growth rate of both metal and dark blue color strongly increased as voltage increased, but tended to decrease with greater pressure. The resistance across the cell was observed to be influenced by both pressure and light exposure. As the AgBr sample was exposed to visible light, the resistance dropped instantaneously, and after the light was turned off, the resistance increased on a timescale of 10's of seconds to minutes. Notably, at higher pressures, the AgBr showed less photosensitivity. Exploration of these metal halide systems has many potential applications. First, these experiments explore the pressure-dependence of photochemical and photovoltaic processes, and may spur development of pressure-tuned microscale electronic devices. Second, these experimental results can be used to constrain thermodynamic models of pressure-dependent electrochemical behavior of materials, which may then be applied to the high temperature, high pressure mineral phases of the deep Earth and planets.

  11. Characterization of quantum efficiency and robustness of cesium-based photocathodes

    NASA Astrophysics Data System (ADS)

    Montgomery, Eric J.

    High quantum efficiency, robust photocathodes produce picosecond-pulsed, high-current electron beams for photoinjection applications like free electron lasers. In photoinjectors, a pulsed drive laser incident on the photocathode causes photoemission of short, dense bunches of electrons, which are then accelerated into a relativistic, high quality beam. Future free electron lasers demand reliable photocathodes with long-lived quantum efficiency at suitable drive laser wavelengths to maintain high current density. But faced with contamination, heating, and ion back-bombardment, the highest efficiency photocathodes find their delicate cesium-based coatings inexorably lost. In answer, the work herein presents careful, focused studies on cesium-based photocathodes, particularly motivated by the cesium dispenser photocathode. This is a novel device comprised of an efficiently photoemissive, cesium-based coating deposited onto a porous sintered tungsten substrate, beneath which is a reservoir of elemental cesium. Under controlled heating cesium diffuses from the reservoir through the porous substrate and across the surface to replace cesium lost to harsh conditions---recently shown to significantly extend the lifetime of cesium-coated metal cathodes. This work first reports experiments on coated metals to validate and refine an advanced theory of photoemission already finding application in beam simulation codes. Second, it describes a new theory of photoemission from much higher quantum efficiency cesium-based semiconductors and verifies its predictions with independent experiment. Third, it investigates causes of cesium loss from both coated metal and semiconductor photocathodes and reports remarkable rejuvenation of full quantum efficiency for contaminated cesium-coated surfaces, affirming the dispenser prescription of cesium resupply. And fourth, it details continued advances in cesium dispenser design with much-improved operating characteristics: lower temperature and cleaner operation. Motivated by dispenser integration with semiconductor coatings, initial fabrication of those coatings are reported on dispenser-type substrates with measurement of quantum efficiency and analysis of thermal stability. Detailed investigations are performed on dispenser substrate preparation by ion beam cleaning and on dispenser pore structure by electron microscopy and focused ion beam milling. The dissertation concludes by discussing implications of all results for the demonstration and optimization of the future high quantum efficiency cesium dispenser photocathode.

  12. Compact narrow-band THz radiation source based on photocathode rf gun

    NASA Astrophysics Data System (ADS)

    Li, Wei-Wei; He, Zhi-Gang; Jia, Qi-Ka

    2014-04-01

    Narrow-band THz coherent Cherenkov radiation can be driven by a subpicosecond electron bunch traveling along the axis of a hollow cylindrical dielectric-lined waveguide. We present a scheme of compact THz radiation source based on the photocathode rf gun. On the basis of our analytic result, the subpicosecond electron bunch with high charge (800 pC) can be generated directly in the photocathode rf gun. According to the analytical and simulated results, a narrow emission spectrum peaked at 0.24 THz with 2 megawatt (MW) peak power is expected to gain in the proposed scheme (the length of the facility is about 1.2 m).

  13. An in-situ photocathode loading system for the SLC Polarized Electron Gun

    SciTech Connect

    Kirby, R.E.; Collet, G.J.; Skarpaas, K.

    1992-12-01

    An ultra-high vacuum loadlock system capable of operating at high voltage has been added to the SLC Polarized Electron Gun. The unit incorporates facilities for heat cleaning, activating and measuring the quantum efficiency of photocathodes. A tray of up to four photocathodes can be exchanged without bringing the activation unit or gun up to atmosphere. Low voltage quantum efficiencies of 20% have been obtained for bulk GaAs at 633 nm and 6% for a 0.3 micron GaAs layer at 755 nm. Results for other cathodes as well as operational characteristics are discussed.

  14. SRRC/ANL high current l-band single cell photocathode rf gun.

    SciTech Connect

    Ho, C. H.

    1998-07-16

    A high current L-band photocathode rf gun is under development at SRRC (Synchrotron Radiation Research Center, Taiwan) in collaboration with ANL (Argonne National Laboratory, USA). The goal is to produce up to 100 nC charge with the surface field gradient of over 90 MV/m at the center of the photocathode. In this report, they present the detailed design and initial test results. If successful, this gun will be used as the future AWA (Argonne Wakefield Accelerator)[1] high current gun.

  15. Noise sources in silver halide volume holograms

    NASA Astrophysics Data System (ADS)

    Fimia, Antonio; Carretero-Lopez, Luis; Belendez, Augusto

    1994-05-01

    Dichromated gelatin has been established as the most frequently used recording material for the obtention of holographic optical elements and new applications are being found for photopolymers in previously unexplored areas such as holographic interconnects. However, photographic emulsion from the beginning has been and continues to be the most used holographic recording material. This is due to the relatively high sensitivity and ease of processing of this material, improved processing chemistries, commercial films, and the repeatability of the results. In this paper we will analyze different sources of noise in photographic emulsions such as intermodulation noise, noise gratings and non-linear noise, and the influence of the photochemical process on the previously noise sources cited. Bleached emulsions by rehalogenating and solvent process will be considered and silver halide sensitized gelatin will be present as a solution in transmission holograms. At the same time, new developers and new noise models will be presented under the supposition that non-linear response of the recording material is due to the photochemical process.

  16. Charge carrier mobility in hybrid halide perovskites.

    PubMed

    Motta, Carlo; El-Mellouhi, Fedwa; Sanvito, Stefano

    2015-01-01

    The charge transport properties of hybrid halide perovskites are investigated with a combination of density functional theory including van der Waals interaction and the Boltzmann theory for diffusive transport in the relaxation time approximation. We find the mobility of electrons to be in the range 5-10 cm(2)V(-1)s(-1) and that for holes within 1-5 cm(2)V(-1)s(-1), where the variations depend on the crystal structure investigated and the level of doping. Such results, in good agreement with recent experiments, set the relaxation time to about 1 ps, which is the time-scale for the molecular rotation at room temperature. For the room temperature tetragonal phase we explore two possible orientations of the organic cations and find that the mobility has a significant asymmetry depending on the direction of the current with respect to the molecular axis. This is due mostly to the way the PbI3 octahedral symmetry is broken. Interestingly we find that substituting I with Cl has minor effects on the mobilities. Our analysis suggests that the carrier mobility is probably not a key factor in determining the high solar-harvesting efficiency of this class of materials. PMID:26235910

  17. Melt synthesis of inorganic nitrides and halides

    NASA Astrophysics Data System (ADS)

    Molstad, Jay Clark

    Novel halide chlorides Sr7Cl2H12, Sr 7Br2H12, and Ba2ClH3 were formed from sodium chloride and strontium metal in sodium metal melts at 900°C. Sr7Br2H12 crystallizes in the anti-Fe 12Zr2P7 structure type, and Sr7Cl 2H12 crystallizes in a slightly distorted variant of this structure. Ba2ClH3 crystallizes in a structure containing infinite two-dimensional sheets of edge-sharing Ba6Cl chlorine-centered octahedra. Single crystals of gallium nitride can be obtained by reaction of gallium metal and dinitrogen gas at 750°C. Small amounts of alkaline earth metals added to the reaction mixture promote the formation of large crystals. Polycrystalline GaN nucleates rapidly under these conditions on the surface of a stainless steel autoclave; nucleation is far less pronounced on tungsten surfaces. Trace concentrations of hydrogen greatly enhance GaN nucleation. Melts of magnesium metal with cerium, gadolinium, and lanthanum were exposed to ammonia and nitrogen gas at temperatures from 700°C to 900°C. Binary rare earth and magnesium nitrides and hydrides are formed, but no ternary compounds are seen. The absence of ternary compounds is discussed in the light of a thermodynamic model predicting ternary formation in these systems.

  18. Charge carrier mobility in hybrid halide perovskites

    PubMed Central

    Motta, Carlo; El-Mellouhi, Fedwa; Sanvito, Stefano

    2015-01-01

    The charge transport properties of hybrid halide perovskites are investigated with a combination of density functional theory including van der Waals interaction and the Boltzmann theory for diffusive transport in the relaxation time approximation. We find the mobility of electrons to be in the range 510?cm2V?1s?1 and that for holes within 15?cm2V?1s?1, where the variations depend on the crystal structure investigated and the level of doping. Such results, in good agreement with recent experiments, set the relaxation time to about 1?ps, which is the time-scale for the molecular rotation at room temperature. For the room temperature tetragonal phase we explore two possible orientations of the organic cations and find that the mobility has a significant asymmetry depending on the direction of the current with respect to the molecular axis. This is due mostly to the way the PbI3 octahedral symmetry is broken. Interestingly we find that substituting I with Cl has minor effects on the mobilities. Our analysis suggests that the carrier mobility is probably not a key factor in determining the high solar-harvesting efficiency of this class of materials. PMID:26235910

  19. Lead Halide Perovskites and Other Metal Halide Complexes As Inorganic Capping Ligands for Colloidal Nanocrystals

    PubMed Central

    2014-01-01

    Lead halide perovskites (CH3NH3PbX3, where X = I, Br) and other metal halide complexes (MXn, where M = Pb, Cd, In, Zn, Fe, Bi, Sb) have been studied as inorganic capping ligands for colloidal nanocrystals. We present the methodology for the surface functionalization via ligand-exchange reactions and the effect on the optical properties of IVVI, IIVI, and IIIV semiconductor nanocrystals. In particular, we show that the Lewis acidbase properties of the solvents, in addition to the solvent dielectric constant, must be properly adjusted for successful ligand exchange and colloidal stability. High luminescence quantum efficiencies of 2030% for near-infrared emitting CH3NH3PbI3-functionalized PbS nanocrystals and 5065% for red-emitting CH3NH3CdBr3- and (NH4)2ZnCl4-capped CdSe/CdS nanocrystals point to highly efficient electronic passivation of the nanocrystal surface. PMID:24746226

  20. Zintl cluster chemistry in the alkali-metal-gallium systems

    SciTech Connect

    Henning, R.

    1998-03-27

    Previous research into the alkali-metal-gallium systems has revealed a large variety of networked gallium deltahedra. The clusters are analogues to borane clusters and follow the same electronic requirements of 2n+2 skeletal electrons for closo-deltahedra. This work has focused on compounds that do not follow the typical electron counting rules. The first isolated gallium cluster was found in Cs{sub 8}Ga{sub 11}. The geometry of the Ga{sub 11}{sup 7{minus}} unit is not deltahedral but can be described as a penta-capped trigonal prism. The reduction of the charge from a closo-Ga{sub 11}{sup 13{minus}} to Ga{sub 11}{sup 7{minus}} is believed to be the driving force of the distortion. The compound is paramagnetic because of an extra electron but incorporation of a halide atom into the structure captures the unpaired electron and forms a diamagnetic compound. A second isolated cluster has been found in Na{sub 10}Ga{sub 10}Ni where the tetra-capped trigonal prismatic gallium is centered by nickel. Stabilization of the cluster occurs through Ni-Ga bonding. A simple two-dimensional network occurs in the binary K{sub 2}Ga{sub 3} Octahedra are connected through four waist atoms to form a layered structure with the potassium atoms sitting between the layers. Na{sub 30.5}Ga{sub 60{minus}x}Ag{sub x} is nonstoichiometric and needs only a small amount of silver to form (x {approximately} 2--6). The structure is composed of three different clusters which are interconnected to form a three-dimensional structure. The RbGa{sub 3{minus}x}Au{sub x} system is also nonstoichiometric with a three-dimensional structure composed of Ga{sub 8} dodecahedra and four-bonded gallium atoms. Unlike Na{sub 30.5}Ga{sub 60{minus}x}Ag{sub x}, the RbGa{sub 3} binary is also stable. The binary is formally a Zintl phase but the ternary is not. Some chemistry in the alkali-metal-indium system also has been explored. A new potassium-indium binary is discussed but the structure has not been completely characterized.

  1. Diode pumped alkali vapor fiber laser

    DOEpatents

    Payne, Stephen A.; Beach, Raymond J.; Dawson, Jay W.; Krupke, William F.

    2006-07-26

    A method and apparatus is provided for producing near-diffraction-limited laser light, or amplifying near-diffraction-limited light, in diode pumped alkali vapor photonic-band-gap fiber lasers or amplifiers. Laser light is both substantially generated and propagated in an alkali gas instead of a solid, allowing the nonlinear and damage limitations of conventional solid core fibers to be circumvented. Alkali vapor is introduced into the center hole of a photonic-band-gap fiber, which can then be pumped with light from a pump laser and operated as an oscillator with a seed beam, or can be configured as an amplifier.

  2. Diode pumped alkali vapor fiber laser

    DOEpatents

    Payne, Stephen A.; Beach, Raymond J.; Dawson, Jay W.; Krupke, William F.

    2007-10-23

    A method and apparatus is provided for producing near-diffraction-limited laser light, or amplifying near-diffraction-limited light, in diode pumped alkali vapor photonic-band-gap fiber lasers or amplifiers. Laser light is both substantially generated and propagated in an alkali gas instead of a solid, allowing the nonlinear and damage limitations of conventional solid core fibers to be circumvented. Alkali vapor is introduced into the center hole of a photonic-band-gap fiber, which can then be pumped with light from a pump laser and operated as an oscillator with a seed beam, or can be configured as an amplifier.

  3. Alkali Silicate Vehicle Forms Durable, Fireproof Paint

    NASA Technical Reports Server (NTRS)

    Schutt, John B.; Seindenberg, Benjamin

    1964-01-01

    The problem: To develop a paint for use on satellites or space vehicles that exhibits high resistance to cracking, peeling, or flaking when subjected to a wide range of temperatures. Organic coatings will partially meet the required specifications but have the inherent disadvantage of combustibility. Alkali-silicate binders, used in some industrial coatings and adhesives, show evidence of forming a fireproof paint, but the problem of high surface-tension, a characteristic of alkali silicates, has not been resolved. The solution: Use of a suitable non-ionic wetting agent combined with a paint incorporating alkali silicate as the binder.

  4. Uptake of haloacetyl and carbonyl halides by water surfaces

    SciTech Connect

    De Bruyn, W.J.; Shorter, J.A.; Davidovits, P.; Worsnop, D.R.; Zahniser, M.S.; Kolb, C.E.

    1995-05-01

    Gas-liquid uptake studies have been completed for the carbonyl halides CCl{sub 2}O and CF{sub 2}O and the haloacetyl halides CCl{sub 3}CCIO, CF{sub 3}CFO, and CF{sub 3}CCIO, which are intermediate products from gas phase oxidation of volatile halogen-containing species in the atmosphere. The fluorine-containing species result from the degradation of hydrochlorofluorocarbons (HCFCs) (proposed substitutes for chlorofluorocarbons, CFCs). The tropospheric lifetime of the halides depends on their dissolution in the aqueous phase, determined by Henry`s law solubility (H) and hydrolysis rate (k{sub hyd}). Using a bubble column apparatus, time-resolved gas-liquid interaction experiments measured the product Hk{sub hyd}{1/2}. Studies were performed at 278 K and pH = 1-13; for CCl{sub 3}CClO and CCl{sub 2}O, temperature was varied from 278 to 298 K. From this work and results from other laboratories, limits on values of the product Hk{sub hyd} were established and used to estimate a `global` cloud processing rate of these halides. A approximately 30-day upper limit to their tropospheric lifetime implies that tropospheric removal of the halide degradation products is fast enough not to contribute to the ozone depletion potential of the parent HCFCs. 39 refs., 6 figs., 1 tab.

  5. Genetic Control of Methyl Halide Production in Arabidopsis

    NASA Astrophysics Data System (ADS)

    Rhew, R. C.; Ostergaard, L.; Saltzman, E. S.; Yanofsky, M. F.

    2003-12-01

    Methyl chloride and methyl bromide are the primary carriers of natural chlorine and bromine to the stratosphere where they catalyze the destruction of ozone, whereas methyl iodide influences aerosol formation and ozone loss in the troposphere. Methyl bromide is also an agricultural fumigant whose use is scheduled to be phased out by international agreement. Despite the economic and environmental importance of these methyl halides, their natural sources and biological production mechanisms are poorly understood. Currently identified sources include oceans, biomass burning, industrial and agricultural use, fuel combustion, salt marshes, wetlands, rice paddies, certain terrestrial plants and fungi, and abiotic processes. We demonstrate that the model plant Arabidopsis thaliana produces and emits methyl halides and that the enzyme primarily responsible for the production is encoded by the HARMLESS TO OZONE LAYER (HOL) gene located on chromosome II. In mutant plants that have a disruption of the HOL gene, methyl halide production is largely eliminated. A phylogenetic analysis using the HOL gene suggests that the ability to produce methyl halides is widespread among vascular plants. This approach provides a genetic basis for understanding and predicting patterns of methyl halide production by plants.

  6. Alkali metal for ultraviolet band-pass filter

    NASA Technical Reports Server (NTRS)

    Mardesich, Nick (inventor); Fraschetti, George A. (inventor); Mccann, Timothy A. (inventor); Mayall, Sherwood D. (inventor); Dunn, Donald E. (inventor); Trauger, John T. (inventor)

    1993-01-01

    An alkali metal filter having a layer of metallic bismuth deposited onto the alkali metal is provided. The metallic bismuth acts to stabilize the surface of the alkali metal to prevent substantial surface migration from occurring on the alkali metal, which may degrade optical characteristics of the filter. To this end, a layer of metallic bismuth is deposited by vapor deposition over the alkali metal to a depth of approximately 5 to 10 A. A complete alkali metal filter is described along with a method for fabricating the alkali metal filter.

  7. Analysis of the physical atomic forces between noble gas atoms, alkali ions and halogen ions

    NASA Technical Reports Server (NTRS)

    Wilson, J. W.; Heinbockel, J. H.; Outlaw, R. A.

    1986-01-01

    The physical forces between atoms and molecules are important in a number of processes of practical importance, including line broadening in radiative processes, gas and crystal properties, adhesion, and thin films. The components of the physical forces between noble gas atoms, alkali ions, and halogen ions are analyzed and a data base for the dispersion forces is developed from the literature based on evaluations with the harmonic oscillator dispersion model for higher order coefficients. The Zener model of the repulsive core is used in the context of the recent asymptotic wave functions of Handler and Smith; and an effective ionization potential within the Handler and Smith wave functions is defined to analyze the two body potential data of Waldman and Gordon, the alkali-halide molecular data, and the noble gas crystal and salt crystal data. A satisfactory global fit to this molecular and crystal data is then reproduced by the model to within several percent. Surface potentials are evaluated for noble gas atoms on noble gas and salt crystal surfaces with surface tension neglected. Within this context, the noble gas surface potentials on noble gas and salt crystals are considered to be accurate to within several percent.

  8. Regeneration of zinc halide catalyst used in the hydrocracking of polynuclear hydrocarbons

    DOEpatents

    Gorin, Everett

    1978-01-01

    Improved recovery of spent molten zinc halide hydro-cracking catalyst is achieved in the oxidative vapor phase regeneration thereof by selective treatment of the zinc oxide carried over by the effluent vapors from the regeneration zone with hydrogen halide gas under conditions favoring the reaction of the zinc oxide with the hydrogen halide, whereby regenerated zinc halide is recovered in a solids-free state with little loss of zinc values.

  9. Measurement of charge limit in a strained lattice GaAs photocathode

    SciTech Connect

    Saez, P.; Alley, R.; Aoyagi, H.

    1993-04-01

    The SLAC Linear Collider (SLC) Polarized Electron Source (PES) photocathodes have shown a charge saturation when illuminated with a high intensity laser pulse. This charge limit in the cesium-activated GaAs crystal seems to be strongly dependent on its surface condition and on the incident light wavelength. Charge limit studies with highly polarized strained lattice GaAs materials are presented.

  10. Enhanced Raman scattering from cesium suboxides on silver particles and the structure of S-1 photocathodes

    NASA Technical Reports Server (NTRS)

    Bates, C. W., Jr.

    1984-01-01

    An explanation is given for the results of recent enhanced Raman scattering studies of photomultiplier tubes with S-1 photocathode surfaces which indicated the presence of Cs11O3 but not Cs2O. The reason for the discrepancy between the currently accepted model of the S-1 and this recent result is discussed.

  11. NREL Improves Hole Transport in Sensitized CdS-NiO Nanoparticle Photocathodes (Fact Sheet)

    SciTech Connect

    Not Available

    2012-01-01

    Significantly improved charge-collection efficiencies result from a general chemical approach to synthesizing photocathodes. It has been reported that a dye-sensitized nickel oxide (NiO) photocathode, when coupled to a dye-sensitized photoanode, could significantly increase overall solar conversion efficiency. However, the conversion efficiencies of these cells are still low. There has been much effort to improve the conversion efficiency by fabricating films with improved properties and developing more effective sensitizing dyes for p-type NiO. One of the factors limiting the use of NiO for solar cell application is the low hole conductivity in p-NiO. A team of researchers from the National Renewable Energy Laboratory (NREL) developed a general chemical approach to synthesize NiO-cadmium sulfide (CdS) core-shell nanoparticle films as photocathodes for p-type semiconductor-sensitized solar cells. Compared to dye-sensitized NiO photocathodes, the CdS-sensitized NiO cathodes exhibited two orders of magnitude faster hole transport (attributable to the passivation of surface traps by the CdS) and almost 100% charge-collection efficiencies.

  12. Photocathode electron beam sources using GaN and InGaN with NEA surface

    NASA Astrophysics Data System (ADS)

    Nishitani, T.; Maekawa, T.; Tabuchi, M.; Meguro, T.; Honda, Y.; Amano, H.

    2015-03-01

    A photocathode electron source using p-type GaN and p-type InGaN semiconductors with a negative electron affinity (NEA) surface has been studied for its ability to maintain an extended NEA state. The key technology of NEA photocathodes is the formation of electric dipoles by atoms on the surface, which makes it possible for photo excited electrons in the conduction band minimum to escape into the vacuum. This means that in order to keep the electron energy spread as small as possible, the excitation photon energy should be tuned to the band gap energy. However, the NEA surface is damaged by the adsorption of residual gas and the back-bombardment of ionized residual gas by photoelectrons. The p-type GaN and InGaN semiconductors were measured a lifetime of quantum yield of excitation energy corresponding to the band gap energy in comparison to the p-type GaAs as the conventional NEA photocathode. Lifetime of NEA-photocathodes using the GaN and InGaN were 21 times and 7.7 times longer respectively than that using the GaAs.

  13. Improved alkali-metal/silicate binders

    NASA Technical Reports Server (NTRS)

    Schutt, J.

    1978-01-01

    Family of inorganic binders utilizes potassium or sodium oxide/silicate dispersion and employs high mole ratio of silicon dioxide to alkali-metal binder. Binders are stable, inexpensive, extremely water resistant, and easy to apply.

  14. Alkali Metal Handling Practices at NASA MSFC

    NASA Technical Reports Server (NTRS)

    Salvail, Patrick G.; Carter, Robert R.

    2002-01-01

    NASA Marshall Space Flight Center (MSFC) is NASA s principle propulsion development center. Research and development is coordinated and carried out on not only the existing transportation systems, but also those that may be flown in the near future. Heat pipe cooled fast fission cores are among several concepts being considered for the Nuclear Systems Initiative. Marshall Space Flight Center has developed a capability to handle high-purity alkali metals for use in heat pipes or liquid metal heat transfer loops. This capability is a low budget prototype of an alkali metal handling system that would allow the production of flight qualified heat pipe modules or alkali metal loops. The processing approach used to introduce pure alkali metal into heat pipe modules and other test articles are described in this paper.

  15. Arsenic volatilization of GaAs photocathode at low temperature during thermal cleaning

    NASA Astrophysics Data System (ADS)

    Liu, Hui; Shi, Feng; Miao, Zhuang; Gao, Xiang; Cheng, Hong-chang; Niu, Sen; Wang, Long; Chen, Chang

    2014-09-01

    The gallium arsenide (GaAs) photocathode was generally cleaned by radiant heating, direct heating, ion bombardment annealing, and so on. In this paper, the radiant heating method, namely thermal cleaning method, was adopted for GaAs photocathode surface purification. Using this method could obtain an atomic clean surface, ensure the integrity of the GaAs surface lattice, and guarantee the uniformity of surface cleaning effect at the same time. But because the accurate measurement of the GaAs photocathode surface temperature in the vacuum system was very difficult, the residual gas analyzer (RGA) was used in this experiment to monitor the residual gas composition in ultrahigh vacuum during the thermal cleaning process and determine the thermal cleaning temperature by the partial pressure curves of As and Ga. It was found that the first peaks of As and Ga elements both appeared after heating about one hour, accompanied with H2O, N2/CO, CO2 and other common gas. According to partial pressure curves of H2O, N2/CO, CO2 and the heating time, it could be judged that the temperature at that time was not high, which should be under 150C.After thermal cleaning experiment of three GaAs photocathodes, it was found that the peak value of As partial pressure at low temperature was generally within 10-11mbar~10-10mbar, and the peak value was at 10-10mbar at high temperature. Sometimes it was appeared that the peak value of As partial pressure at low temperature was even higher than the peak value at high temperature. The As volatilization phenomenon occurred at low temperature indicated that the elemental As exist on the GaAs photocathode surface or near surface after the chemical etching process, and the As could volatilize from GaAs photocathode at low temperature in the beginning of thermal cleaning. This research has guiding significance for further understanding the thermal cleaning mechanism of GaAs photocathode and improving the thermal cleaning technology.

  16. Closed Loop Rare Gas Halide Laser Flow

    NASA Astrophysics Data System (ADS)

    Cassady, P. E.; Mullaney, G.; Byron, S. R.

    1981-11-01

    High pulse repetition frequency, rare gas halide lasers are potentially useful in laser photochemical processes such as laser isotope separation. For practical use in many of these applications, high pulse repetition frequency operation must be achieved with good optical beam quality. Ideally, such a laser should achieve good medium optical quality with a minimum gas recirculation power. Component reliability in the laser cavity, flow loop and electrical circuitry is also needed for long laser lifetime. A closed loop XeCl laser, named Mistral, has been constructed at Mathematical Sciences Northwest, Inc., (MSNW), to investigate acoustic damping and flow control techniques needed to achieve good optical quality in these lasers. The device uses a 20 cm long UV preionized laser cavity to produce power levels of order 100 W. The flow loop has been designed to minimize flow disturbances and to allow examination of the performance of various acoustic dampers located in the side-walls of the flow channel upstream and downstream of the discharge region. A burst of laser pulses at 1 to 2 kilohertz PRF is provided by a main discharge triggered spark gap switched PFN coupled to 8 ft.-long cable peaking capacitors. The test time is limited by the gas capacity of the triggered spark gap gas supply to about 2 minutes. The loop is constructed primarily of nickel plated stainless steel, and includes a centrifugal blower and heat exchanger. A description of the design, fabrication and operation of this facility is given together with the results of current experimental investigations.

  17. 40 CFR 721.10181 - Halide salt of an alkylamine (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Halide salt of an alkylamine (generic... Specific Chemical Substances 721.10181 Halide salt of an alkylamine (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as halide salt...

  18. 10 CFR 431.322 - Definitions concerning metal halide lamp ballasts and fixtures.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... starts a probe-start metal halide lamp that contains a third starting electrode (probe) in the arc tube... voltage. Pulse-start metal halide ballast means an electronic or electromagnetic ballast that starts a pulse-start metal halide lamp with high voltage pulses, where lamps shall be started by the...

  19. 10 CFR 431.322 - Definitions concerning metal halide lamp ballasts and fixtures.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... starts a probe-start metal halide lamp that contains a third starting electrode (probe) in the arc tube... voltage. Pulse-start metal halide ballast means an electronic or electromagnetic ballast that starts a pulse-start metal halide lamp with high voltage pulses, where lamps shall be started by the...

  20. 10 CFR 431.322 - Definitions concerning metal halide lamp ballasts and fixtures.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... starts a probe-start metal halide lamp that contains a third starting electrode (probe) in the arc tube... voltage. Pulse-start metal halide ballast means an electronic or electromagnetic ballast that starts a pulse-start metal halide lamp with high voltage pulses, where lamps shall be started by the...

  1. 40 CFR 721.10181 - Halide salt of an alkylamine (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Halide salt of an alkylamine (generic... Specific Chemical Substances § 721.10181 Halide salt of an alkylamine (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as halide salt...

  2. 40 CFR 721.10181 - Halide salt of an alkylamine (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Halide salt of an alkylamine (generic... Specific Chemical Substances 721.10181 Halide salt of an alkylamine (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as halide salt...

  3. 40 CFR 721.10181 - Halide salt of an alkylamine (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Halide salt of an alkylamine (generic... Specific Chemical Substances 721.10181 Halide salt of an alkylamine (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as halide salt...

  4. Desulfurizing Coal With an Alkali Treatment

    NASA Technical Reports Server (NTRS)

    Ravindram, M.; Kalvinskas, J. J.

    1987-01-01

    Experimental coal-desulfurization process uses alkalies and steam in fluidized-bed reactor. With highly volatile, high-sulfur bituminous coal, process removed 98 percent of pyritic sulfur and 47 percent of organic sulfur. Used in coal liquefaction and in production of clean solid fuels and synthetic liquid fuels. Nitrogen or steam flows through bed of coal in reactor. Alkalies react with sulfur, removing it from coal. Nitrogen flow fluidizes bed while heating or cooling; steam is fluidizing medium during reaction.

  5. Alkali metal intercalates of molybdenum disulfide.

    NASA Technical Reports Server (NTRS)

    Somoano, R. B.; Hadek, V.; Rembaum, A.

    1973-01-01

    Study of some of the physicochemical properties of compounds obtained by subjecting natural molybdenite and single crystals of molybdenum disulfide grown by chemical vapor transport to intercalation with the alkali group of metals (Li, Na, K, Rb, and Cs) by means of the liquid ammonia technique. Reported data and results include: (1) the intercalation of the entire alkali metal group, (2) stoichiometries and X-ray data on all of the compounds, and (3) superconductivity data for all the intercalation compounds.

  6. Fate of alkalis in coal combustion

    SciTech Connect

    Stewart, G.W.; Stinespring, C.D.; Davidovits, P.

    1982-01-01

    The results of these measurements and experiments provide a plausible way to begin an explanation for the distribution of alkali in the ash particulates. To summarize: (1) under typical coal combustion conditions in an atmosphere rich in CO/sub 2/ and/or SO/sub 2/, the alkalis in the organic fraction do not vaporize but remain bound in the ash as stable carbonates or sulfates; (2) the alkalis in the inorganic fraction diffuse to the surface producing enrichment by a factor of about 13 to a depth of about 100A. The results, however, do not provide conclusive evidence about the fate of the alkalis. The effect of water vapor in the combustion stream has not yet been studied. Clearly, water could have an important effect on the vaporization process. Furthermore, the reasoning we have followed to explain the absence of alkali enrichment in the submicron particles requires that the volatilization of the alkalis in both the organic and inorganic fraction not be significant (say less than 20%).

  7. Thallous halide materials for use in cryogenic applications

    NASA Technical Reports Server (NTRS)

    Lawless, William N. (Inventor)

    1981-01-01

    Thallous halides, either alone or in combination with other ceramic materials, are used in cryogenic applications such as heat exchange material for the regenerator section of a closed-cycle cryogenic refrigeration section, as stabilizing coatings for superconducting wires, and as dielectric insulating materials. The thallous halides possess unusually large specific heats at low temperatures, have large thermal conductivities, are nonmagnetic, and are nonconductors of electricity. They can be formed into a variety of shapes such as spheres, bars, rods, or the like and can be coated onto substrates.

  8. Alkali metal crystalline polymer electrolytes

    NASA Astrophysics Data System (ADS)

    Zhang, Chuhong; Gamble, Stephen; Ainsworth, David; Slawin, Alexandra M. Z.; Andreev, Yuri G.; Bruce, Peter G.

    2009-07-01

    Polymer electrolytes have been studied extensively because uniquely they combine ionic conductivity with solid yet flexible mechanical properties, rendering them important for all-solid-state devices including batteries, electrochromic displays and smart windows. For some 30 years, ionic conductivity in polymers was considered to occur only in the amorphous state above Tg. Crystalline polymers were believed to be insulators. This changed with the discovery of Li+ conductivity in crystalline poly(ethylene oxide)6:LiAsF6 (refs 4, 5). However, new crystalline polymer electrolytes have proved elusive, questioning whether the 6:1 complex has particular structural features making it a unique exception to the rule that only amorphous polymers conduct. Here, we demonstrate that ionic conductivity in crystalline polymers is not unique to the 6:1 complex by reporting several new crystalline polymer electrolytes containing different alkali metal salts (Na+, K+ and Rb+), including the best conductor poly(ethylene oxide)8:NaAsF6 discovered so far, with a conductivity 1.5 orders of magnitude higher than poly(ethylene oxide)6:LiAsF6. These are the first crystalline polymer electrolytes with a different composition and structures to that of the 6:1 Li+ complex.

  9. Alteration of alkali reactive aggregates autoclaved in different alkali solutions and application to alkali-aggregate reaction in concrete

    SciTech Connect

    Lu Duyou; Xu Zhongzi; Tang Mingshu; Fournier, Benoit

    2006-06-15

    Surface alteration of typical aggregates with alkali-silica reactivity and alkali-carbonate reactivity, i.e. Spratt limestone (SL) and Pittsburg dolomitic limestone (PL), were studied by XRD and SEM/EDS after autoclaving in KOH, NaOH and LiOH solutions at 150 deg. C for 150 h. The results indicate that: (1) NaOH shows the strongest attack on both ASR and ACR aggregates, the weakest attack is with LiOH. For both aggregates autoclaved in different alkali media, the crystalline degree, morphology and distribution of products are quite different. More crystalline products are formed on rock surfaces in KOH than that in NaOH solution, while almost no amorphous product is formed in LiOH solution; (2) in addition to dedolomitization of PL in KOH, NaOH and LiOH solutions, cryptocrystalline quartz in PL involves in reaction with alkaline solution and forms typical alkali-silica product in NaOH and KOH solutions, but forms lithium silicate (Li{sub 2}SiO{sub 3}) in LiOH solution; (3) in addition to massive alkali-silica product formed in SL autoclaved in different alkaline solutions, a small amount of dolomite existing in SL may simultaneously dedolomitize and possibly contribute to expansion; (4) it is promising to use the duplex effect of LiOH on ASR and ACR to distinguish the alkali-silica reactivity and alkali-carbonate reactivity of aggregate when both ASR and ACR might coexist.

  10. Structural diversity in solvated lanthanide halide complexes

    SciTech Connect

    Evans, W.J.; Shreeve, J.L.; Ziller, J.W.; Doedens, R.J.

    1995-02-01

    Crystallization of lanthanide trichlorides from neat {eta}-caprolactone (C{sub 6}H{sub 10}O{sub 2}) and caprolactone/THF mixtures has revealed a much more diverse structural chemistry for solvated lanthanide trichloride complexes than had previously been observed. As the metal is varied, different products preferentially crystallize under the same conditions to give a series of complexes which do not vary smoothly in composition as a function of radial size. The following compounds, in order of increasing radial size of the metal, have been structurally characterized: YbCl{sub 3}(C{sub 6}H{sub 10}O{sub 2})- (THF){sub 2}, 1; YCl{sub 3}(C{sub 6}H{sub 10}O{sub 2}){sub 3}, 2; [TbCl{sub 4}(THF){sub 2}]{sup -}[TbCl{sub 2}(THF){sub 5}]{sup +}, 3; [Cl{sub 3}Sm({mu}-Cl){sub 3}]{sup 3-}[Sm(C{sub 6}H{sub 10}O{sub 2}){sub 8}]{sup 3+}, 4;[Cl{sub 3}Nd({mu}-Cl){sub 3}NdCl{sub 3}]{sup 3-}[Nd(C{sup 6}H{sub 10}O{sub 2}){sub 8}]{sup 3+}, 5. In the course of these studies, the polymeric halides [NdCl({mu}-Cl){sub 2-}(THF){sub 2}]{sub n}, 6, and [CeCl({mu}-Cl){sub 2}(THF){sub 2}]{sub n}, 7, were also identified by X-ray crystallography. Although both 1 and 2 have octahedral geometries, they differ in the amount of caprolactone present and the fact that 1 is facial while 2 is meridional. The ion pair system 3 contains a six-coordinate anion with a trans octahedral geometry and a seven-coordinate cation with axial chloride ligands in a pentagonal bipyramidal structure. Complexes 4 and 5 contain bimetallic trianions devoid of caprolactone which adopt a face-sharing bioctahedral geometry. The eight-coordinate cations in 4 and 5 contain no chloride ligands and adopt a square antiprismatic geometry. Isostructure 6 and 7 contain seven-coordinate pentagonal bipyramidal metal centers surrounded by four bridging chloride atoms, one terminal chloride, and two terminal THF ligands.

  11. p-GaAs(Cs,O)-photocathodes: Demarcation of domains of validity for practical models of the activation layer

    SciTech Connect

    Bakin, V. V.; Toropetsky, K. V.; Scheibler, H. E.; Terekhov, A. S.; Jones, L. B.; Militsyn, B. L.; Noakes, T. C. Q.

    2015-05-04

    The (Cs,O)-activation procedure for p-GaAs(Cs,O)-photocathodes was studied with the aim of demarcating the domains of validity for the two practical models of the (Cs,O)-activation layer: The dipole layer (DL) model and the heterojunction (HJ) model. To do this, the photocathode was activated far beyond the normal maximum of quantum efficiency, and several photocathode parameters were measured periodically during this process. In doing so, the data obtained enabled us to determine the domains of validity for the DL- and HJ-models, to define more precisely the characteristic parameters of the photocathode within both of these domains and thus to reveal the peculiarities of the influence of the (Cs,O)-layer on the photoelectron escape probability.

  12. p-GaAs(Cs,O)-photocathodes: Demarcation of domains of validity for practical models of the activation layer

    NASA Astrophysics Data System (ADS)

    Bakin, V. V.; Toropetsky, K. V.; Scheibler, H. E.; Terekhov, A. S.; Jones, L. B.; Militsyn, B. L.; Noakes, T. C. Q.

    2015-05-01

    The (Cs,O)-activation procedure for p-GaAs(Cs,O)-photocathodes was studied with the aim of demarcating the domains of validity for the two practical models of the (Cs,O)-activation layer: The dipole layer (DL) model and the heterojunction (HJ) model. To do this, the photocathode was activated far beyond the normal maximum of quantum efficiency, and several photocathode parameters were measured periodically during this process. In doing so, the data obtained enabled us to determine the domains of validity for the DL- and HJ-models, to define more precisely the characteristic parameters of the photocathode within both of these domains and thus to reveal the peculiarities of the influence of the (Cs,O)-layer on the photoelectron escape probability.

  13. Students' Understanding of Alkyl Halide Reactions in Undergraduate Organic Chemistry

    ERIC Educational Resources Information Center

    Cruz-Ramirez de Arellano, Daniel

    2013-01-01

    Organic chemistry is an essential subject for many undergraduate students completing degrees in science, engineering, and pre-professional programs. However, students often struggle with the concepts and skills required to successfully solve organic chemistry exercises. Since alkyl halides are traditionally the first functional group that is

  14. Methyl halide emission estimates from domestic biomass burning in Africa

    NASA Astrophysics Data System (ADS)

    Mead, M. I.; Khan, M. A. H.; White, I. R.; Nickless, G.; Shallcross, D. E.

    Inventories of methyl halide emissions from domestic burning of biomass in Africa, from 1950 to the present day and projected to 2030, have been constructed. By combining emission factors from Andreae and Merlet [2001. Emission of trace gases and aerosols from biomass burning. Global Biogeochemical Cycles 15, 955-966], the biomass burning estimates from Yevich and Logan [2003. An assessment of biofuel use and burning of agricultural waste in the developing world. Global Biogeochemical Cycles 17(4), 1095, doi:10.1029/2002GB001952] and the population data from the UN population division, the emission of methyl halides from domestic biomass usage in Africa has been estimated. Data from this study suggest that methyl halide emissions from domestic biomass burning have increased by a factor of 4-5 from 1950 to 2005 and based on the expected population growth could double over the next 25 years. This estimated change has a non-negligible impact on the atmospheric budgets of methyl halides.

  15. Semiempirical and DFT Investigations of the Dissociation of Alkyl Halides

    ERIC Educational Resources Information Center

    Waas, Jack R.

    2006-01-01

    Enthalpy changes corresponding to the gas phase heats of dissociation of 12 organic halides were calculated using two semiempirical methods, the Hartree-Fock method, and two DFT methods. These calculated values were compared to experimental values where possible. All five methods agreed generally with the expected empirically known trends in the

  16. 40 CFR 721.10698 - Polyfluorinated alkyl halide (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10698 Polyfluorinated alkyl halide (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically...

  17. On the Boiling Points of the Alkyl Halides.

    ERIC Educational Resources Information Center

    Correia, John

    1988-01-01

    Discusses the variety of explanations in organic chemistry textbooks of a physical property of organic compounds. Focuses on those concepts explaining attractive forces between molecules. Concludes that induction interactions play a major role in alkyl halides and other polar organic molecules and should be given wider exposure in chemistry texts.

  18. Students' Understanding of Alkyl Halide Reactions in Undergraduate Organic Chemistry

    ERIC Educational Resources Information Center

    Cruz-Ramirez de Arellano, Daniel

    2013-01-01

    Organic chemistry is an essential subject for many undergraduate students completing degrees in science, engineering, and pre-professional programs. However, students often struggle with the concepts and skills required to successfully solve organic chemistry exercises. Since alkyl halides are traditionally the first functional group that is…

  19. Students' understanding of alkyl halide reactions in undergraduate organic chemistry

    NASA Astrophysics Data System (ADS)

    Cruz-Ramirez de Arellano, Daniel

    Organic chemistry is an essential subject for many undergraduate students completing degrees in science, engineering, and pre-professional programs. However, students often struggle with the concepts and skills required to successfully solve organic chemistry exercises. Since alkyl halides are traditionally the first functional group that is studied in undergraduate organic chemistry courses, establishing a robust understanding of the concepts and reactions related to them can be beneficial in assuring students' success in organic chemistry courses. Therefore, the purpose of this study was to elucidate and describe students' understanding of alkyl halide reactions in an undergraduate organic chemistry course. Participants were interviewed using a think-aloud protocol in which they were given a set of exercises dealing with reactions and mechanisms of alkyl halide molecules in order to shed light on the students' understanding of these reactions and elucidate any gaps in understanding and incorrect warrants that may be present. These interviews were transcribed and analyzed using qualitative inquiry approaches. In general, the findings from this study show that the students exhibited gaps in understanding and incorrect warrants dealing with: (1) classifying substances as bases and/or nucleophiles, (2) assessing the basic or nucleophilic strength of substances, (3) accurately describing the electron movement of the steps that take place during alkyl halide reaction mechanisms, and (4) assessing the viability of their proposed reactive intermediates and breakage of covalent bonds. In addition, implications for teaching and future research are proposed.

  20. Measurement of Surface Phonon Dispersion Curves of Alkali Halide Single Crystals by Time of Flight Spectroscopy of He Atom Beams

    NASA Astrophysics Data System (ADS)

    Toennies, J. Peter

    1982-01-01

    The development of highly expanded He nozzle beams with velocity half widths less than 1% has made it possible to observe the annihilation and creation of single surface phonons in time of flight spectra of the scattered atoms. Measurements have been carried out for a wide range of incident angles at a beam energy of about 20 meV for the following crystals and directions: LiF langle100rangle, LiF langle110rangle, NaF langle100rangle, KCl langle100rangle, NaCl langle100rangle, and MgO langle100rangle. In all cases the spectra show up to 5 sharp well resolved maxima. From the final angle and energy of each peak the parallel surface momentum component and frequency of the phonon is determined. The results show a predominant coupling with Rayleigh surface phonons with only a weak coupling with bulk phonons. Rayleigh dispersion curves have been measured out to the zone boundary for all crystals except LiF langle110rangle and MgO. There is also some evidence for excitation of modes of higher frequencies. Except for LiF langle100rangle at the zone boundary the results compare well with theoretical calculations. Benedek has been able to fit the new LiF He atom and previous neutron dispersion curves with a revised breathing shell model calculation.

  1. Cocrystallization of certain 4f and 5f elements in the bivalent state with alkali metal halides

    SciTech Connect

    Mikheev, N.B.; Kamenskaya, A.M.; Veleshko, I.E.; Kulyukhin, S.A.

    1987-01-01

    The cocrystallization of Fm/sup 2 +/, Es/sup 2 +/, Cf/sup 2 +/, Am/sup 2 +/, Yb/sup 2 +/, Eu/sup 2 +/ and Sr/sup 2 +/ with NaCl, KCl and KBr in tetrahydrofuran (THF), hexamethylphosphorotriamide (HMPA), and ethanol has been studied. It is shown that in water-ethanol medium An/sup 2 +/ cocrystallize with KCl by the formation of anomalous mixed crystals and Ln/sup 2 +/ do not cocrystallize. In HMPA neither Ln/sup 2 +/ nor An/sup 2 +/ are observed to transfer into the KBr solid phase, while in THF both Ln/sup 2 +/ and An/sup 2 +/ cocrystallize with NaCl. The change in the behavior on Ln/sup 2 +/ and An/sup 2 +/ cocrystallize with a change from one solvent to another is caused by the difference in the effective ionic radii of these elements, which arises from the large nephelauxetic effect for An/sup 2 +/ as well as by the different solvating power of these solvents.

  2. Different approaches for the calculation of electronic excited states of nonstoichiometric alkali halide clusters: the example of Na3F.

    PubMed

    Durand, G; Heitz, M-C; Spiegelman, F; Meier, C; Mitri?, R; Bonaci?-Kouteck, V; Pittner, J

    2004-11-22

    The electronic structure and excited states of the Na(3)F cluster are investigated using different approximate, but numerically efficient, computational schemes, such as a 2e hybrid quantum/classical pseudopotential model with full-configuration interaction or time-dependent density-functional theory. Various quantities such as geometries and transition energies are compared with results previously obtained by multireference configuration interaction calculations, taken as reference data. The potential energy surfaces of the lowest excited states are investigated and the finite-temperature absorption spectra are calculated. The good agreement with recent beam experiments [J.-M. L'Hermite, V. Blanchet, A. Le Padellec, B. Lamory, and P. Labastie, Eur. Phys. J. D 28, 361 (2004)] leads to the conclusion that the absorption spectrum observed experimentally corresponds to the lowest energy isomer which has a C(2v) planar rhombic geometry. PMID:15549863

  3. Different approaches for the calculation of electronic excited states of nonstoichiometric alkali halide clusters: The example of Na3F

    NASA Astrophysics Data System (ADS)

    Durand, G.; Heitz, M.-C.; Spiegelman, F.; Meier, C.; Mitri?, R.; Bona?i?-Kouteck, V.; Pittner, J.

    2004-11-01

    The electronic structure and excited states of the Na3F cluster are investigated using different approximate, but numerically efficient, computational schemes, such as a 2e hybrid quantum/classical pseudopotential model with full-configuration interaction or time-dependent density-functional theory. Various quantities such as geometries and transition energies are compared with results previously obtained by multireference configuration interaction calculations, taken as reference data. The potential energy surfaces of the lowest excited states are investigated and the finite-temperature absorption spectra are calculated. The good agreement with recent beam experiments [J.-M. L'Hermite, V. Blanchet, A. Le Padellec, B. Lamory, and P. Labastie, Eur. Phys. J. D 28, 361 (2004)] leads to the conclusion that the absorption spectrum observed experimentally corresponds to the lowest energy isomer which has a C2v planar rhombic geometry.

  4. Numerical modeling of alkali vapor lasers.

    PubMed

    Shu, Hong; Chen, Ying; Bass, Michael; Monjardin, J Fernando; Deile, Jochen

    2011-10-10

    Detailed numerical analyses are presented of a continuous wave (cw), single spatial mode alkali vapor laser pumped by a diffraction-limited Ti: Sapphire laser. These analyses provide insight into the operation of alkali vapor lasers to aid in the development of high power, diode laser pumped alkali vapor lasers. It is demonstrated that in the laser considered the laser spatial pattern is significantly changed after each pass through the gain medium, and the laser spatial pattern in steady state operation is also very different from that of the passive cavity mode. According to the calculation, lasing significantly improves the pump absorption efficiency and changes the absorbed pump distribution. The effect of varying the transverse size of the pumped region is also analyzed and an optimum pump beam waist radius is demonstrated. In addition, the shift of the pump beam waist location is also studied. The computation method and its convergence behavior are also described in detail. PMID:21996995

  5. Photo-cathode preparation system of the A0 photo-injector

    SciTech Connect

    Moyses Kuchnir et al.

    2002-08-23

    The A0 Photo-Injector is an electron accelerator located in the AZero high bay area of Fermilab. A pulsed laser system generates electron bunches by the photo-electric effect when hitting a photo-cathode in a 1.5-cell, 1.3 GHz RF gun. A 9-cell, 1.3 GHz superconducting resonant cavity then accelerates the electrons to 15 MeV. The 10 ps time resolved waveform of the laser pulses is transferred to the electron bunches. This report is focused on the first hardware component of this accelerator, the Photo-cathode Preparation System. The reason for its existence is in the nature of the photo-electric material film used: Cs{sub 2}Te (Cesium Telluride), a very reactive compound that once coated on the cathode requires that it be transported and used in ultra high vacuum (UHV), i.e. < 10{sup -9} Torr.

  6. Photoemission Studies of Metallic Photocathodes Prepared by Pulsed Laser Ablation Deposition Technique

    NASA Astrophysics Data System (ADS)

    Fasano, V.; Lorusso, A.; De Rosa, H.; Cultrera, L.; Perrone, A.

    2010-11-01

    We present the results of our investigation on metallic films as suitable photocathodes for the production of intense electron beams in RF photoinjector guns. Pulsed laser ablation deposition technique was used for growing Mg and Y thin films onto Si and Cu substrates in high vacuum and at room temperature. Different diagnostic methods were used to characterize the thin films deposited on Si with the aim to optimize the deposition process. Photoelectron performances were investigated on samples deposited on Cu substrate in an ultra high vacuum photodiode chamber at 10-7 Pa. Relatively high quantum efficiencies have been obtained for the deposited films, comparable to those of corresponding bulks. Samples could stay for several months in humid open air before being tested in a photodiode cell. The deposition process and the role of the photocathode surface contamination and its influence on the photoelectron performances are presented and discussed.

  7. Engineering Design and Fabrication of an Ampere-Class Superconducting Photocathode Electron Gun

    SciTech Connect

    Ben-Zvi,I.

    2008-11-17

    Over the past three years, Advanced Energy Systems and Brookhaven National Laboratory (BNL) have been collaborating on the design of an Ampere- class superconducting photocathode electron gun. BNL performed the physics design of the overall system and RF cavity under prior programs. Advanced Energy Systems (AES) is currently responsible for the engineering design and fabrication of the electron gun under contract to BNL. We will report on the engineering design and fabrication status of the superconducting photocathode electron gun. The overall configuration of the cryomodule will be reviewed. The layout of the hermitic string, space frame, shielding package, and cold mass will be discussed. The engineering design of the gun cavity and removable cathode will be presented in detail and areas of technical risk will be highlighted. Finally, the fabrication sequence and fabrication status of the gun cavity will be discussed.

  8. Use of MgF2 and LiF photocathodes in the extreme ultraviolet.

    NASA Technical Reports Server (NTRS)

    Lapson, L. B.; Timothy, J. G.

    1973-01-01

    The photoelectric yields of 2000-A thick samples of MgF2 and LiF have been measured at wavelengths in the range from 1216 to 461 A. Peak values of 43 and 34%, respectively, were obtained at wavelengths around 550 A at 45 deg incidence. Coating the cathode of a channel electron multiplier with 3000 A of MgF2 produced no significant deterioration in the electrical properties and increased the sensitivity by factors of 1.62, 2.76, and 2.60 at wavelengths of 742, 584, and 461 A, respectively. Since the stability of response of the MgF2 photocathodes appears to be equal to that of conventional metallic and semiconducting cathodes, it is concluded that MgF2 would be a practical, high-efficiency photocathode for use in the extreme ultraviolet.

  9. Method for resurrecting negative electron affinity photocathodes after exposure to an oxidizing gas

    SciTech Connect

    Mulhollan, Gregory A; Bierman, John C

    2012-10-30

    A method by which negative electron affinity photocathodes (201), single crystal, amorphous, or otherwise ordered, can be made to recover their quantum yield following exposure to an oxidizing gas has been discovered. Conventional recovery methods employ the use of cesium as a positive acting agent (104). In the improved recovery method, an electron beam (205), sufficiently energetic to generate a secondary electron cloud (207), is applied to the photocathode in need of recovery. The energetic beam, through the high secondary electron yield of the negative electron affinity surface (203), creates sufficient numbers of low energy electrons which act on the reduced-yield surface so as to negate the effects of absorbed oxidizing atoms thereby recovering the quantum yield to a pre-decay value.

  10. Large area polycrystalline diamond films as high current photocathodes for linear induction accelerators

    SciTech Connect

    Shurter, R.P.; Moir, D.C.; Devlin, D.J.; Springer, R.W.

    1997-08-01

    Investigations are underway at Los Alamos to develop a new generation of high current, low source temperature photo cathodes able to operate in vacuum environments with pressures above 10e-6 torr without poisoning or degradation of emission properties. Polycrystalline diamond films are emerging as the ideal material for these photocathodes. Robustness, high quantum efficiency and high thermal conductivity are fundamental necessary attributes that are found in diamond. The high electron/hole mobility in the boron doped diamond lattice and the ability to create a negative electron affinity surface through downward band bending allow for high current density emission with quantum efficiencies of 0.5% when illuminated by a ArF laser. We report the results to date toward the development of a four kiloampere photocathode with a source temperature below 5eV for the DARHT linear induction Accelerator

  11. Performance of a DC GaAs photocathode gun for the Jefferson lab FEL

    SciTech Connect

    Grippo, Albert; Yunn, Byung; Sinclair, Charles; Bohn, Courtlandt; Douglas, David; Bullard, Donald; Krafft, Geoffrey; Gubeli, Joseph; Siggins, Timothy

    2001-12-01

    The performance of the 320kV DC photocathode gun has met the design specifications for the 1kW IR Demo FEL at Jefferson Lab. This gun has shown theability to deliver high average current beam with outstanding lifetimes. The GaAs photocathode has delivered 135pC per bunch, at a bunch repetition rate of37.425MHz, corresponding to 5mA average CW current. In a recent cathode lifetime measurement, 20h of CW beam was delivered with an average currentof 3.1mA and 211C of total charge from a 0.283cm2 illuminated spot. The cathode showed a 1/e lifetime of 58h and a1/e extracted charge lifetime of 618C.We have achieved quantum efficiencies of 5% from a GaAs wafer that has been in service for 13 months delivering in excess 2400C with only three activationcycles.

  12. Structural and morphological properties of metallic thin films grown by pulsed laser deposition for photocathode application

    NASA Astrophysics Data System (ADS)

    Lorusso, A.; Gontad, F.; Caricato, A. P.; Chiadroni, E.; Broitman, E.; Perrone, A.

    2016-03-01

    In this work yttrium and lead thin films have been deposited by pulsed laser deposition technique and characterized by ex situ different diagnostic methods. All the films were adherent to the substrates and revealed a polycrystalline structure. Y films were uniform with a very low roughness and droplet density, while Pb thin films were characterized by a grain morphology with a relatively high roughness and droplet density. Such metallic materials are studied because they are proposed as a good alternative to copper and niobium photocathodes which are generally used in radiofrequency and superconducting radiofrequency guns, respectively. The photoemission performances of the photocathodes based on Y and Pb thin films have been also studied and discussed.

  13. Ultraviolet quantum detection efficiency of potassium bromide as an opaque photocathode applied to microchannel plates

    NASA Technical Reports Server (NTRS)

    Siegmund, Oswald H. W.; Everman, E.; Vallerga, J. V.; Sokolowski, J.; Lampton, M.

    1987-01-01

    The quantum detection efficiency (QDE) of potassium bromide as a photocathode applied directly to the surface of a microchannel plate over the 250-1600 A wavelength range has been measured. The contributions of the photocathode material in the channels and on the interchannel web to the QDE have been determined. Two broad peaks in the QDE centered at about 450 and about 1050 A are apparent, the former with about 50 percent peak QDE and the latter with about 40 percent peak QDE. The photoelectric threshold is observed at about 1600 A, and there is a narrow QDE minimum at about 750 A which correlates with 2X the band gap energy for KBr. The angular variation of the QDE from 0 to 40 deg to the channnel axis has also been examined. The stability of Kbr with time is shown to be good with no significant degradation of QDE at wavelengths below 1216 A over a 15-day period in air.

  14. Effect of humid air exposure on photoemissive and structural properties of KBr thin film photocathode

    NASA Astrophysics Data System (ADS)

    Rai, R.; Triloki; Ghosh, N.; Singh, B. K.

    2015-07-01

    We have investigated the influence of water molecule absorption on photoemissive and structural properties of potassium bromide (KBr) thin film photocathode under humid air exposure at relative humidity 62 ±3%. It is evident from photoemission measurement that the photoelectron yield of KBr photocathode is degraded exponentially with humid air exposed time. Structural studies of the "as-deposited" and "humid air aged" films reveal that there is no effect of relative humidity on film's crystalline face centered cubic structure. However, the crystallite size of "humid air aged" KBr film has been increased as compared to "as-deposited" one. In addition, topographical properties of KBr film are also examined by means of scanning electron microscope, transmission electron microscope and atomic force microscope and it is observed that granular characteristic of film has been altered, even for short exposure to humid atmosphere.

  15. Selection of non-adsorbing alkali components

    SciTech Connect

    Lee, S.H.D.; Natesan, K.; Swift, W.M.

    1992-01-01

    This project consists of three phases of laboratory experimental study. In phase I (screening), eight candidate materials, 304SS (serves as a base material for comparison), Hastelloy C-276, Hastelloy X, Haynes No. 188, Allonized 304SS, Pt-coated 304SS, and ceramic-coated 304SS, will be subjected to atmospheric TGA study under the simulated PFBC (oxidizing) environment with and without alkali vapor doping. Each candidate material will be evaluated for its resistance toward alkali-vapor capture. In addition, a post-test metallographic characterization of the sample will be performed to obtain a better understanding of the alkali capture mechanism and material behavior. The material(s) with little or no alkali-vapor adsorption will be selected as the promising material(s) for the Phase II study. In Phase II, the promising material(s) will be further tested in the TGA under elevated pressure to simulate the PFBC environment (in terms of temperature, pressure, and gas composition). The effect of pressure on the extent of alkali-vapor adsorption will be evaluated, and the test samples will be metallographically characterized. The most promising candidate material(s) will be identified and recommended for further tesfing in the actual PFBC environment. In Phase III, four materials will be selected from the eight candidate materials screened in the PFBC environment and will be evaluated for their alkali-vapor capture by atmospheric TGA under the coal gasification fuel gas (reducing) environment. The tested samples will also be metallographically characterized. The most promising material(s) will be identified and recommended for further testing in the actual coal gasification environment.

  16. Selection of non-adsorbing alkali components

    SciTech Connect

    Lee, S.H.D.; Natesan, K.; Swift, W.M.

    1992-11-01

    This project consists of three phases of laboratory experimental study. In phase I (screening), eight candidate materials, 304SS (serves as a base material for comparison), Hastelloy C-276, Hastelloy X, Haynes No. 188, Allonized 304SS, Pt-coated 304SS, and ceramic-coated 304SS, will be subjected to atmospheric TGA study under the simulated PFBC (oxidizing) environment with and without alkali vapor doping. Each candidate material will be evaluated for its resistance toward alkali-vapor capture. In addition, a post-test metallographic characterization of the sample will be performed to obtain a better understanding of the alkali capture mechanism and material behavior. The material(s) with little or no alkali-vapor adsorption will be selected as the promising material(s) for the Phase II study. In Phase II, the promising material(s) will be further tested in the TGA under elevated pressure to simulate the PFBC environment (in terms of temperature, pressure, and gas composition). The effect of pressure on the extent of alkali-vapor adsorption will be evaluated, and the test samples will be metallographically characterized. The most promising candidate material(s) will be identified and recommended for further tesfing in the actual PFBC environment. In Phase III, four materials will be selected from the eight candidate materials screened in the PFBC environment and will be evaluated for their alkali-vapor capture by atmospheric TGA under the coal gasification fuel gas (reducing) environment. The tested samples will also be metallographically characterized. The most promising material(s) will be identified and recommended for further testing in the actual coal gasification environment.

  17. Porous copper zinc tin sulfide thin film as photocathode for double junction photoelectrochemical solar cells.

    PubMed

    Dai, Pengcheng; Zhang, Guan; Chen, Yuncheng; Jiang, Hechun; Feng, Zhenyu; Lin, Zhaojun; Zhan, Jinhua

    2012-03-21

    Porous copper zinc tin sulfide (CZTS) thin film was prepared via a solvothermal approach. Compared with conventional dye-sensitized solar cells (DSSCs), double junction photoelectrochemical cells using dye-sensitized n-type TiO(2) (DS-TiO(2)) as the photoanode and porous p-type CZTS film as the photocathode shows an increased short circuit current, external quantum efficiency and power conversion efficiency. PMID:22322239

  18. Magnetic field effects on the photocathode uniformity of Hamamatsu R7081 photomultiplier tubes

    NASA Astrophysics Data System (ADS)

    Jeon, E. J.; Kim, J. Y.; Kim, Y. D.; Ma, K. J.; Nam, J. T.

    2013-01-01

    We tested the effects of magnetic fields on a photomultiplier tube (PMT), namely, Hamamatsu R7081, with a large surface area photocathode. The output signals of the PMT were affected in such a way that the magnetic fields deflected photoelectrons to the first dynode. We measured the effects produced by the orientation of the PMT relative to the magnetic fields and the variations in the output signals with respect to the incident light positions in the magnetic fields.

  19. Alkali metal vapors - Laser spectroscopy and applications

    NASA Technical Reports Server (NTRS)

    Stwalley, W. C.; Koch, M. E.

    1980-01-01

    The paper examines the rapidly expanding use of lasers for spectroscopic studies of alkali metal vapors. Since the alkali metals (lithium, sodium, potassium, rubidium and cesium) are theoretically simple ('visible hydrogen'), readily ionized, and strongly interacting with laser light, they represent ideal systems for quantitative understanding of microscopic interconversion mechanisms between photon (e.g., solar or laser), chemical, electrical and thermal energy. The possible implications of such understanding for a wide variety of practical applications (sodium lamps, thermionic converters, magnetohydrodynamic devices, new lasers, 'lithium waterfall' inertial confinement fusion reactors, etc.) are also discussed.

  20. Alkali activation of Australian slag cements

    SciTech Connect

    Bakharev, T.; Sanjayan, J.G.; Cheng, Y.B.

    1999-01-01

    Investigation of alkali activation of Australian slag (AAS) was carried out using sodium silicate, sodium hydroxide, sodium carbonate, sodium phosphate, and combinations of these activators. Compressive strengths in the range from 20 to 40 MPa were achieved for the pastes. The most effective activator was liquid sodium silicate. With this activator, the effect of curing at 60 C, modulus (M{sub s}) of sodium silicate solution and concentration of alkalis on the compressive strength and setting times have been studied. On the basis of this investigation, a sodium silicate solution with a low Na content and M{sub s} = 0.75 is recommended for formulation of AAS concrete.

  1. Recovery of alkali metal constituents from catalytic coal conversion residues

    DOEpatents

    Soung, W.Y.

    In a coal gasification operation (32) or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein particles containing alkali metal residues are produced, alkali metal constituents are recovered from the particles by contacting them with water or an aqueous solution to remove water-soluble alkali metal constituents and produce an aqueous solution enriched in said constituents. The aqueous solution thus produced is then contacted with carbon dioxide to precipitate silicon constituents, the pH of the resultant solution is increased, preferably to a value in the range between about 12.5 and about 15.0, and the solution of increased pH is evaporated to increase the alkali metal concentration. The concentrated aqueous solution is then recycled to the conversion process where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst.

  2. Alkali-aggregate reaction in concrete containing high-alkali cement and granite aggregate

    SciTech Connect

    Owsiak, Z

    2004-01-01

    The paper discusses results of the research into the influence of high-alkali Portland cement on granite aggregate. The deformation of the concrete structure occurred after 18 months. The research was carried out by means of a scanning electron microscope equipped with a high-energy dispersive X-ray analyzer that allowed observation of unpolished sections of concrete bars exhibiting the cracking pattern typical of the alkali-silica reaction. Both the microscopic observation and the X-ray elemental analysis confirm the presence of alkali-silica gel and secondary ettringite in the cracks.

  3. Nonepitaxial Thin-Film InP for Scalable and Efficient Photocathodes.

    PubMed

    Hettick, Mark; Zheng, Maxwell; Lin, Yongjing; Sutter-Fella, Carolin M; Ager, Joel W; Javey, Ali

    2015-06-18

    To date, some of the highest performance photocathodes of a photoelectrochemical (PEC) cell have been shown with single-crystalline p-type InP wafers, exhibiting half-cell solar-to-hydrogen conversion efficiencies of over 14%. However, the high cost of single-crystalline InP wafers may present a challenge for future large-scale industrial deployment. Analogous to solar cells, a thin-film approach could address the cost challenges by utilizing the benefits of the InP material while decreasing the use of expensive materials and processes. Here, we demonstrate this approach, using the newly developed thin-film vapor-liquid-solid (TF-VLS) nonepitaxial growth method combined with an atomic-layer deposition protection process to create thin-film InP photocathodes with large grain size and high performance, in the first reported solar device configuration generated by materials grown with this technique. Current-voltage measurements show a photocurrent (29.4 mA/cm(2)) and onset potential (630 mV) approaching single-crystalline wafers and an overall power conversion efficiency of 11.6%, making TF-VLS InP a promising photocathode for scalable and efficient solar hydrogen generation. PMID:26266588

  4. Modeling the resupply, diffusion, and evaporation of cesium on the surface of controlled porosity dispenser photocathodes

    NASA Astrophysics Data System (ADS)

    Pan, Zhigang; Jensen, Kevin L.; Montgomery, Eric J.

    2013-09-01

    A controlled porosity dispenser (CPD) photocathode is currently being explored and developed to replace the Cs during operation and increase photocathode lifetime. Experimental results from cesium (Cs) emission of a sintered-wire tungsten CPD are presented and are used to inform a theoretical model of Cs resupply, diffusion, and evaporation on the surface of the photocathode. The evaporation of Cs from a tungsten surface is modeled using an effective one-dimensional potential well representation of the binding energy. The model accounts for both local and global interactions of Cs with the surface metal as well as with other Cs atoms. It is found that for typical activation temperatures within the range of 500 K-750 K, differences of less than 5% between the quantum efficiency (QE) maximum and minimum over ideal homogenous surfaces occur, even when variations to mimic surface non-uniformity due to pore blockage are included. The theoretical evaporation rates of sub-monolayer surface coverage of Cs compare well to the data of Taylor and Langmuir [I. Langmuir and J. B. Taylor, Phys. Rev. 40, 463-464 (1932)] and reproduce the nonlinear behavior of evaporation with varying coverage and temperature.

  5. Significant Broadband Photocurrent Enhancement by Au-CZTS Core-Shell Nanostructured Photocathodes

    PubMed Central

    Zhang, Xuemei; Wu, Xu; Centeno, Anthony; Ryan, Mary P.; Alford, Neil M.; Riley, D. Jason; Xie, Fang

    2016-01-01

    Copper zinc tin sulfide (CZTS) is a promising material for harvesting solar energy due to its abundance and non-toxicity. However, its poor performance hinders their wide application. In this paper gold (Au) nanoparticles are successfully incorporated into CZTS to form Au@CZTS core-shell nanostructures. The photocathode of Au@CZTS nanostructures exhibits enhanced optical absorption characteristics and improved incident photon-to-current efficiency (IPCE) performance. It is demonstrated that using this photocathode there is a significant increase of the power conversion efficiency (PCE) of a photoelectrochemical solar cell of 100% compared to using a CZTS without Au core. More importantly, the PCE of Au@CZTS photocathode improved by 15.8% compared to standard platinum (Pt) counter electrode. The increased efficiency is attributed to plasmon resonance energy transfer (PRET) between the Au nanoparticle core and the CZTS shell at wavelengths shorter than the localized surface plasmon resonance (LSPR) peak of the Au and the semiconductor bandgap. PMID:26997140

  6. Effect of surface cleaning on spectral response for InGaAs photocathodes.

    PubMed

    Jin, Muchun; Zhang, Yijun; Chen, Xinlong; Hao, Guanghui; Chang, Benkang; Shi, Feng

    2015-12-20

    Photocathode surface treatment aims to obtain high sensitivity, where the key point is to acquire an atomically clean surface. Various surface cleaning methods for removing contamination from InGaAs photocathode surfaces were investigated. The atomic compositions of InGaAs photocathode structures and surfaces were measured by x-ray photoelectron spectroscopy and Ar ion sputtering. After surface cleaning, the InGaAs surface is arsenoxide-free, however, a small amount of Ga2O3 and In2O3 still can be found. The 1:1 mixed solution of hydrochloric acid to deionized water followed by thermal annealing at 525C has been demonstrated to be the best choice in dealing with the surface oxides. After the Cs/O activation, a surface model was proposed where the oxides on the surface will lead to a positive electron affinity, adversely affecting low-energy electrons escaping to the vacuum, which is reflected by the photocurrent curves and the spectral response curves. PMID:26837029

  7. Longitudinal Emittance Compensation In a Photocathode RF gun Injector - Analysis and Experiments

    NASA Astrophysics Data System (ADS)

    Wang, X. J.

    1997-05-01

    The concept of longitudinal emittance compensation in a photocathode RF gun injector is introduced first. The analysis shows that the arrangements of the transverse emittance compensation photocathode RF gun injector is well suited for longitudinal emittance compensation. By setting the laser phase relative to the RF field close to the zero crossing, the photoelectron beam produced at the gun exit will have short bunchlength and large energy spread, this beam was further compressed in the drift space followed the RF gun and solenoid. The linac after the drift space will preserve the short bunch and reduce the energy spread through acceleration. The solenoid magnet plays an important role in the bunch compression in the drift space to reduce the bunch lengthening caused by the beam divergence. Experiments performed at the Brookhaven Accelerator Test Facility (ATF) has produced a 370 fs electron beam with 40 pC using a 15 ps laser, more than a facto of 30 bunch compression. We will also discussed various effects may reduce the longitudinal emittance compensation in the photocathode RF gun injector.

  8. Nonlinear response of the photocathode of an x-ray streak camera to UV light

    SciTech Connect

    Kyrala, G.A.; Oro, D.M.; Studebaker, J.K.; Wood, W.M.; Schappert, G.T.; Watts, S.; Fulton, R.D.

    1994-09-01

    We have found that a potassium-iodide photocathode of an x-ray streak camera responds to UV light at {lambda}=308 nm. The photocathode surface work function, 6.5 eV, is larger than the 4 eV energy of the UV photon, hence the source of the response is interesting. We will present results on the response of a transmission type potassium-iodide photocathode to the UV light from a {lambda}308 nm, subpicosecond XeCl laser and from a {lambda}=326 nm HeCd laser. We will test for the nonlinearity of the yield to measure of the number of photons that are needed to be absorbed before a signal is recorded. We will present data on the effect of the UV irradiance on the yield, as well as on the temporal width of the recorded signal. We will give an explanation of the observation and its effect on the dynamic-range response of the streak-camera. We will show that the response is linear with the incident irradiance, up to an incident irradiance of 10{sup 8} W/cm{sup 2} and we will explain the observation.

  9. Polarization Possibilities of Small Spin-Orbit Interaction in Strained-Superlattice Photocathodes

    SciTech Connect

    Not Available

    2010-08-25

    Strained-superlattice photocathodes based on InGaP/GaAs were investigated. The photocathode performance is found highly dependent on the superlattice parameters. The electron confinement energy in superlattice appears important. The strained-superlattice structure based on GaAsP/GaAs, with a maximum polarization as high as 90% and more than 1% quantum efficiency, is presently the prime candidate for the ILC polarized electron photocathodes. A recent systematic study shows, however, that the peak polarization seems saturated even though the heavy-hole (HH) and light-hole (LH) band splitting is increased significantly, indicating that there is a material specific spin relaxation mechanism. It is widely accepted that the D'yakonov-Perel mechanism is the dominant spin relaxation mechanism in the III-V compound superlattice structures with a low p-doping ({le} 10{sup 17} cm{sup -3}), and that the spin relaxation may be reduced by choosing a material with a smaller spin-orbit interaction. As the spin-orbit interaction in phosphides is much smaller than in arsenides, strained-superlattice structure based on InGaP/GaAs were investigated. The computer code SPECCODE developed by Subashiev and Gerchikov has been used for calculating the band structures in superlattice.

  10. Dye-controlled interfacial electron transfer for high-current indium tin oxide photocathodes.

    PubMed

    Huang, Zhongjie; He, Mingfu; Yu, Mingzhe; Click, Kevin; Beauchamp, Damian; Wu, Yiying

    2015-06-01

    Efficient sensitized photocathodes are highly desired for solar fuels and tandem solar cells, yet the development is hindered by the scarcity of suitable p-type semiconductors. The generation of high cathodic photocurrents by sensitizing a degenerate n-type semiconductor (tin-doped indium oxide; ITO) is reported. The sensitized mesoporous ITO electrodes deliver cathodic photocurrents of up to 5.96±0.19 mA cm(-2), which are close to the highest record in conventional p-type sensitized photocathodes. This is realized by the rational selection of dyes with appropriate energy alignments with ITO. The energy level alignment between the highest occupied molecular orbital of the sensitizer and the conduction band of ITO is crucial for efficient hole injection. Transient absorption spectroscopy studies demonstrate that the cathodic photocurrent results from reduction of the photoexcited sensitizer by free electrons in ITO. Our results reveal a new perspective toward the selection of electrode materials for sensitized photocathodes. PMID:25907357

  11. Modeling Photoemission of Spin-Polarized Electrons from NEA GaAs Photocathodes

    NASA Astrophysics Data System (ADS)

    Chubenko, Oksana; Afanasev, Andrei

    2015-04-01

    At present, photoemission from strained GaAs activated to negative electron affinity (NEA) is a main source of polarized electrons for modern nuclear-physics and particle-physics facilities. Future experiments at advanced electron colliders will require high-current polarized electron beams, which could provide high polarization and luminosity. This sets new requirements for photocathodes in terms of high quantum efficiency (QE) (>>1%) and spin polarization (~85%). Detailed simulation and modeling of physics processes in photocathodes is important for optimization of their design in order to achieve high QE and reduce depolarization mechanisms. The purpose of the present work was to develop a semi-phenomenological model, which could predict photoemission and electron spin polarization from NEA GaAs photocathodes. Effect of the presence of nanostructures was also studied. Simulation results were compared to the experimental results obtained by the polarized electron source group at Thomas Jefferson National Accelerator Facility. Work supported by Thomas Jefferson Accelerator Facility and George Washington University.

  12. Significant Broadband Photocurrent Enhancement by Au-CZTS Core-Shell Nanostructured Photocathodes.

    PubMed

    Zhang, Xuemei; Wu, Xu; Centeno, Anthony; Ryan, Mary P; Alford, Neil M; Riley, D Jason; Xie, Fang

    2016-01-01

    Copper zinc tin sulfide (CZTS) is a promising material for harvesting solar energy due to its abundance and non-toxicity. However, its poor performance hinders their wide application. In this paper gold (Au) nanoparticles are successfully incorporated into CZTS to form Au@CZTS core-shell nanostructures. The photocathode of Au@CZTS nanostructures exhibits enhanced optical absorption characteristics and improved incident photon-to-current efficiency (IPCE) performance. It is demonstrated that using this photocathode there is a significant increase of the power conversion efficiency (PCE) of a photoelectrochemical solar cell of 100% compared to using a CZTS without Au core. More importantly, the PCE of Au@CZTS photocathode improved by 15.8% compared to standard platinum (Pt) counter electrode. The increased efficiency is attributed to plasmon resonance energy transfer (PRET) between the Au nanoparticle core and the CZTS shell at wavelengths shorter than the localized surface plasmon resonance (LSPR) peak of the Au and the semiconductor bandgap. PMID:26997140

  13. Detection of soft X-rays with NEA III-V photocathodes. [Negative Electron Affinity X-ray detector for astronomy

    NASA Technical Reports Server (NTRS)

    Bardas, D.; Kellogg, E.; Murray, S.; Enck, R., Jr.

    1978-01-01

    A description is presented of the results of tests on an X-ray photomultiplier containing a negative electron affinity (NEA) photocathode. This device makes it possible to investigate the response of the NEA photocathode to X-rays of various energies. The obtained data provide a basis for the determination of the photoelectron yield and energy resolution of the considered photocathode as a function of energy in the range from 0.8 to 3 keV. The investigation demonstrates the feasibility of using an NEA III-V photocathode for the detection of soft X-rays.

  14. Spectroscopic effects of disorder and vibrational localization in mixed-halide metal-halide chain solids

    SciTech Connect

    Love, S.P.; Scott, B.; Worl, L.A.; Huckett, S.C.; Saxena, A.; Huang, X.Z.; Bishop, A.R.; Swanson, B.I.

    1993-02-01

    Resonance Raman techniques, together with lattice-dynamics and Peierls-Hubbard modelling, are used to explore the electronic and vibrational dynamics of the quasi-one-dimensional metal-halogen chain solids [Pt(en){sub 2}][R(en){sub 2}X{sub 2}](ClO{sub 4}){sub 4}, (en = C{sub 2}H{sub 8}N{sub 2} and X=Cl, Br), abbreviated ``PLX.`` The mixed-halide materials PtCl{sub 1-x}Br{sub x} and PtCl{sub 1-x}I{sub x} consist of long mixed chains with heterojunctions between segments of the two constituent materials. Thus, in addition to providing mesoscale modulation of the chain electronic states, they serve as prototypes for elucidating the properties to be expected for macroscopic heterojunctions of these highly nonlinear materials. Once a detailed understanding of the various local vibrational modes occurring in these disordered solids is developed, the electronic structure of the chain segments and junctions can be probed by tuning the Raman excitation through their various electronic resonances.

  15. Matrix isolation infrared spectra of hydrogen halide and halogen complexes with nitrosyl halides

    NASA Technical Reports Server (NTRS)

    Allamandola, Louis J.; Lucas, Donald; Pimentel, George C.

    1982-01-01

    Matrix isolation infrared spectra of nitrosyl halide (XNO) complexes with HX and X2 (X = Cl, Br) are presented. The relative frequency shifts of the HX mode are modest (ClNO H-Cl, delta-nu/nu = -0.045; BrNO H-Br, delta-nu/nu = -0.026), indicating weak hydrogen bonds 1-3 kcal/mol. These shifts are accompanied by significant shifts to higher frequencies in the XN-O stretching mode (CIN-O HCl, delta-nu/nu = +0.016; BrN-O HBr, delta-nu/nu = +0.011). Similar shifts were observed for the XN-O X2 complexes (ClN-O Cl2, delta-nu/nu = +0.009; BrN-O-Br2, delta-nu/nu = +0.013). In all four complexes, the X-NO stretching mode relative shift is opposite in sign and about 1.6 times that of the NO stretching mode. These four complexes are considered to be similar in structure and charge distribution. The XN-O frequency shift suggests that complex formation is accompanied by charge withdrawal from the NO bond ranging from about .04 to .07 electron charges. The HX and X2 molecules act as electron acceptors, drawing electrons out of the antibonding orbital of NO and strengthening the XN-O bond. The implications of the pattern of vibrational shifts concerning the structure of the complexes are discussed.

  16. Salts of alkali metal anions and process of preparing same

    DOEpatents

    Dye, James L.; Ceraso, Joseph M.; Tehan, Frederick J.; Lok, Mei Tak

    1978-01-01

    Compounds of alkali metal anion salts of alkali metal cations in bicyclic polyoxadiamines are disclosed. The salts are prepared by contacting an excess of alkali metal with an alkali metal dissolving solution consisting of a bicyclic polyoxadiamine in a suitable solvent, and recovered by precipitation. The salts have a gold-color crystalline appearance and are stable in a vacuum at -10.degree. C. and below.

  17. 40 CFR 721.8900 - Substituted halogenated pyridinol, alkali salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ..., alkali salt. 721.8900 Section 721.8900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances 721.8900 Substituted halogenated pyridinol, alkali salt. (a) Chemical... as substituted halogenated pyridinols, alkali salts (PMNs P-88-1271 and P-88-1272) are subject...

  18. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  19. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  20. 40 CFR 721.8900 - Substituted halogenated pyridinol, alkali salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ..., alkali salt. 721.8900 Section 721.8900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.8900 Substituted halogenated pyridinol, alkali salt. (a) Chemical... as substituted halogenated pyridinols, alkali salts (PMNs P-88-1271 and P-88-1272) are subject...

  1. 40 CFR 721.4660 - Alcohol, alkali metal salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Alcohol, alkali metal salt. 721.4660... Substances § 721.4660 Alcohol, alkali metal salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance generically identified as alcohol, alkali metal salt (PMN P-91-151)...

  2. 40 CFR 721.4660 - Alcohol, alkali metal salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alcohol, alkali metal salt. 721.4660... Substances § 721.4660 Alcohol, alkali metal salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance generically identified as alcohol, alkali metal salt (PMN P-91-151)...

  3. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  4. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  5. 40 CFR 721.8900 - Substituted halogenated pyridinol, alkali salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ..., alkali salt. 721.8900 Section 721.8900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances 721.8900 Substituted halogenated pyridinol, alkali salt. (a) Chemical... as substituted halogenated pyridinols, alkali salts (PMNs P-88-1271 and P-88-1272) are subject...

  6. 40 CFR 721.8900 - Substituted halogenated pyridinol, alkali salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ..., alkali salt. 721.8900 Section 721.8900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances 721.8900 Substituted halogenated pyridinol, alkali salt. (a) Chemical... as substituted halogenated pyridinols, alkali salts (PMNs P-88-1271 and P-88-1272) are subject...

  7. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  8. 40 CFR 721.8900 - Substituted halogenated pyridinol, alkali salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ..., alkali salt. 721.8900 Section 721.8900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances 721.8900 Substituted halogenated pyridinol, alkali salt. (a) Chemical... as substituted halogenated pyridinols, alkali salts (PMNs P-88-1271 and P-88-1272) are subject...

  9. 40 CFR 721.1878 - Alkali metal alkyl borohydride (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Alkali metal alkyl borohydride... Specific Chemical Substances § 721.1878 Alkali metal alkyl borohydride (generic). (a) Chemical substance... alkali metal alkyl borohydride (PMN P-00-1089) is subject to reporting under this section for...

  10. 40 CFR 721.1878 - Alkali metal alkyl borohydride (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Alkali metal alkyl borohydride... Specific Chemical Substances § 721.1878 Alkali metal alkyl borohydride (generic). (a) Chemical substance... alkali metal alkyl borohydride (PMN P-00-1089) is subject to reporting under this section for...

  11. 40 CFR 721.1878 - Alkali metal alkyl borohydride (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Alkali metal alkyl borohydride... Specific Chemical Substances § 721.1878 Alkali metal alkyl borohydride (generic). (a) Chemical substance... alkali metal alkyl borohydride (PMN P-00-1089) is subject to reporting under this section for...

  12. 40 CFR 721.4660 - Alcohol, alkali metal salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Alcohol, alkali metal salt. 721.4660... Substances § 721.4660 Alcohol, alkali metal salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance generically identified as alcohol, alkali metal salt (PMN P-91-151)...

  13. 40 CFR 721.4660 - Alcohol, alkali metal salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Alcohol, alkali metal salt. 721.4660... Substances § 721.4660 Alcohol, alkali metal salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance generically identified as alcohol, alkali metal salt (PMN P-91-151)...

  14. 40 CFR 721.1878 - Alkali metal alkyl borohydride (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Alkali metal alkyl borohydride... Specific Chemical Substances § 721.1878 Alkali metal alkyl borohydride (generic). (a) Chemical substance... alkali metal alkyl borohydride (PMN P-00-1089) is subject to reporting under this section for...

  15. 40 CFR 721.1878 - Alkali metal alkyl borohydride (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alkali metal alkyl borohydride... Specific Chemical Substances § 721.1878 Alkali metal alkyl borohydride (generic). (a) Chemical substance... alkali metal alkyl borohydride (PMN P-00-1089) is subject to reporting under this section for...

  16. 40 CFR 721.4660 - Alcohol, alkali metal salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Alcohol, alkali metal salt. 721.4660... Substances § 721.4660 Alcohol, alkali metal salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance generically identified as alcohol, alkali metal salt (PMN P-91-151)...

  17. Analysis of Melting for Alkali Earth and Alkali Oxides Based on the Diffusional Force Theory

    NASA Astrophysics Data System (ADS)

    Liu, Quan; Chen, Li-Rong

    An analysis of the melting alkali earth and alkali oxides is presented using the concept of diffusional force. The calculations are performed by developing an ionic model based on Harrison's quantum mechanical treatment of overlap repulsive potential which takes into account the interactions up to second neighbors. Van der Waals dipole-dipole and dipole-quadrupole interactions calculated by more accurate methods are also included in the model. Using the formula by Fang, derived on the basis of thermodynamic analysis, the values of interionic distances for 8 alkali earth and alkali oxides at melting have been obtained. A simple model for melting is developed based on the diffusional force models. The values of Tm thus obtained are found to show fairly good agreement with experimental values of melting temperatures.

  18. Alkali resistant optical coatings for alkali lasers and methods of production thereof

    DOEpatents

    Soules, Thomas F; Beach, Raymond J; Mitchell, Scott C

    2014-11-18

    In one embodiment, a multilayer dielectric coating for use in an alkali laser includes two or more alternating layers of high and low refractive index materials, wherein an innermost layer includes a thicker, >500 nm, and dense, >97% of theoretical, layer of at least one of: alumina, zirconia, and hafnia for protecting subsequent layers of the two or more alternating layers of high and low index dielectric materials from alkali attack. In another embodiment, a method for forming an alkali resistant coating includes forming a first oxide material above a substrate and forming a second oxide material above the first oxide material to form a multilayer dielectric coating, wherein the second oxide material is on a side of the multilayer dielectric coating for contacting an alkali.

  19. Methods and Mechanisms for Cross-Electrophile Coupling of Csp(2) Halides with Alkyl Electrophiles.

    PubMed

    Weix, Daniel J

    2015-06-16

    Cross-electrophile coupling, the cross-coupling of two different electrophiles, avoids the need for preformed carbon nucleophiles, but development of general methods has lagged behind cross-coupling and C-H functionalization. A central reason for this slow development is the challenge of selectively coupling two substrates that are alike in reactivity. This Account describes the discovery of generally cross-selective reactions of aryl halides and acyl halides with alkyl halides, the mechanistic studies that illuminated the underlying principles of these reactions, and the use of these fundamental principles in the rational design of new cross-electrophile coupling reactions. Although the coupling of two different electrophiles under reducing conditions often leads primarily to symmetric dimers, the subtle differences in reactivity of aryl halides and alkyl halides with nickel catalysts allowed for generally cross-selective coupling reactions. These conditions could also be extended to the coupling of acyl halides with alkyl halides. These reactions are exceptionally functional group tolerant and can be assembled on the benchtop. A combination of stoichiometric and catalytic studies on the mechanism of these reactions revealed an unusual radical-chain mechanism and suggests that selectivity arises from (1) the preference of nickel(0) for oxidative addition to aryl halides and acyl halides over alkyl halides and (2) the greater propensity of alkyl halides to form free radicals. Bipyridine-ligated arylnickel intermediates react with alkyl radicals to efficiently form, after reductive elimination, new C-C bonds. Finally, the resulting nickel(I) species is proposed to regenerate an alkyl radical to carry the chain. Examples of new reactions designed using these principles include carbonylative coupling of aryl halides with alkyl halides to form ketones, arylation of epoxides to form ?-aryl alcohols, and coupling of benzyl sulfonate esters with aryl halides to form diarylmethanes. Arylnickel(II) intermediates can insert carbon monoxide to form acylnickel(II) intermediates that react with alkyl halides to form ketones, demonstrating the connection between the mechanisms of reactions of aryl halides and acid chlorides with alkyl halides. The low reactivity of epoxides with nickel can be overcome by the use of either titanium or iodide cocatalysis to facilitate radical generation and this can also be extended to enantioselective arylation of meso-epoxides. The high reactivity of benzyl bromide with nickel, which leads to the formation of bibenzyl in attempted reactions with bromobenzene, can be overcome by using a benzyl mesylate along with cobalt phthalocyanine cocatalysis to convert the mesylate into an alkyl radical. PMID:26011466

  20. Terahertz radiation in alkali vapor plasmas

    SciTech Connect

    Sun, Xuan; Zhang, X.-C.

    2014-05-12

    By taking advantage of low ionization potentials of alkali atoms, we demonstrate terahertz wave generation from cesium and rubidium vapor plasmas with an amplitude nearly one order of magnitude larger than that from nitrogen gas at low pressure (0.02–0.5 Torr). The observed phenomena are explained by the numerical modeling based upon electron tunneling ionization.

  1. Cohesive Energy of the Alkali Metals.

    ERIC Educational Resources Information Center

    Poole, R. T.

    1980-01-01

    Describes a method, considered appropriate for presentation to undergraduate students in materials science and related courses, for the calculation of cohesive energies of the alkali metals. Uses a description based on the free electron model and gives results to within 0.1 eV of the experimental values. (Author/GS)

  2. SO2 REMOVAL BY LIMESTONE DUAL ALKALI

    EPA Science Inventory

    The article gives results of testing (between February 1982 and March 1983) on a pilot-scale, limestone, dual-alkali, flue gas desulfurization (FGD) system at IERL-RTP, where testing started in 1979. These results that significant improvement in soda ash consumption and filter ca...

  3. Enhanced Born Charge and Proximity to Ferroelectricity in Thallium Halides

    SciTech Connect

    Du, Mao-Hua; Singh, David J

    2010-01-01

    Electronic structure and lattice dynamics calculations on thallium halides show that the Born effective charges in these compounds are more than twice larger than the nominal ionic charges. This is a result of cross-band-gap hybridization between Tl-p and halogen-p states. The large Born charges cause giant splitting between longitudinal and transverse optic phonon modes, bringing the lattice close to ferroelectric instability. Our calculations indeed show spontaneous lattice polarization upon lattice expansion starting at 2%. It is remarkable that the apparently ionic thallium halides with a simple cubic CsCl structure and large differences in electronegativity between cations and anions can be very close to ferroelectricity. This can lead to effective screening of defects and impurities that would otherwise be strong carrier traps and may therefore contribute to the relatively good carrier transport properties in TlBr radiation detectors.

  4. Solution-Phase Synthesis of Cesium Lead Halide Perovskite Nanowires.

    PubMed

    Zhang, Dandan; Eaton, Samuel W; Yu, Yi; Dou, Letian; Yang, Peidong

    2015-07-29

    Halide perovskites have attracted much attention over the past 5 years as a promising class of materials for optoelectronic applications. However, compared to hybrid organic-inorganic perovskites, the study of their pure inorganic counterparts, like cesium lead halides (CsPbX3), lags far behind. Here, a catalyst-free, solution-phase synthesis of CsPbX3 nanowires (NWs) is reported. These NWs are single-crystalline, with uniform growth direction, and crystallize in the orthorhombic phase. Both CsPbBr3 and CsPbI3 are photoluminescence active, with composition-dependent temperature and self-trapping behavior. These NWs with a well-defined morphology could serve as an ideal platform for the investigation of fundamental properties and the development of future applications in nanoscale optoelectronic devices based on all-inorganic perovskites. PMID:26181343

  5. Large methyl halide emissions from south Texas salt marshes

    NASA Astrophysics Data System (ADS)

    Rhew, R. C.; Whelan, M. E.; Min, D.-H.

    2014-11-01

    Coastal salt marshes are natural sources of methyl chloride (CH3Cl) and methyl bromide (CH3Br) to the atmosphere, but measured emission rates vary widely by geography. Here we report large methyl halide fluxes from subtropical salt marshes of south Texas. Sites with the halophytic plant, Batis maritima, emitted methyl halides at rates that are orders of magnitude greater than sites containing other vascular plants or macroalgae. B. maritima emissions were generally highest at midday; however, diurnal variability was more pronounced for CH3Br than CH3Cl, and surprisingly high nighttime CH3Cl fluxes were observed in July. Seasonal and intra-site variability were large, even taking into account biomass differences. Overall, these subtropical salt marsh sites show much higher emission rates than temperate salt marshes at similar times of the year, supporting the contention that low-latitude salt marshes are significant sources of CH3Cl and CH3Br.

  6. Large methyl halide emissions from south Texas salt marshes

    NASA Astrophysics Data System (ADS)

    Rhew, R. C.; Whelan, M. E.; Min, D.-H.

    2014-06-01

    Coastal salt marshes are natural sources of methyl chloride (CH3Cl) and methyl bromide (CH3Br) to the atmosphere, but measured emission rates vary widely by geography. Here we report large methyl halide fluxes from subtropical salt marshes of south Texas. Sites with the halophytic plant, Batis maritima, emitted methyl halides at rates that are orders of magnitude greater than sites containing other vascular plants or macroalgae. B. maritima emissions were generally highest at midday; however, diurnal variability was more pronounced for CH3Br than CH3Cl, and surprisingly high nighttime CH3Cl fluxes were observed in July. Seasonal and intra-site variability were large, even taking into account biomass differences. Overall, these subtropical salt marsh sites show much higher emission rates than temperate salt marshes at similar times of the year, supporting the contention that low-latitude salt marshes are significant sources of CH3Cl and CH3Br.

  7. Ni-catalyzed reductive addition of alkyl halides to isocyanides.

    PubMed

    Wang, Bo; Dai, Yijing; Tong, Weiqi; Gong, Hegui

    2015-12-21

    This paper highlights Ni-catalyzed reductive trapping of secondary and tertiary alkyl radicals with both electron-rich and electron-deficient aryl isocyanides using zinc as the terminal reductant, affording 6-alkylated phenanthridine in good yields. The employment of carbene ligands necessitates the alkyl radical process, and represents the first utility in the Ni-catalyzed reductive conditions for the generation of unactivated alkyl radicals from the halide precursors. PMID:26524544

  8. Copper-catalyzed arylation of alkyl halides with arylaluminum reagents

    PubMed Central

    Shrestha, Bijay

    2015-01-01

    Summary We report a Cu-catalyzed coupling between triarylaluminum reagents and alkyl halides to form arylalkanes. The reaction proceeds in the presence of N,N,N,N-tetramethyl-o-phenylenediamine (NN-1) as a ligand in combination with CuI as a catalyst. This catalyst system enables the coupling of primary alkyl iodides and bromides with electron-neutral and electron-rich triarylaluminum reagents and affords the cross-coupled products in good to excellent yields. PMID:26734088

  9. Palladium- (and nickel-) catalyzed vinylation of aryl halides

    PubMed Central

    Denmark, Scott E.; Butler, Christopher R.

    2009-01-01

    Functionalized styrenes are extremely useful building blocks for organic synthesis and for functional polymers. One of the most general syntheses of styrenes involves the combination of an aryl halide with a vinyl organometallic reagent under catalysis by palladium or nickel complexes. This Feature Article provides the first comprehensive summary of the vinylation methods currently available along with a critical comparison of the efficiency, cost and scope of the methods. PMID:19081992

  10. Halide-bridged binuclear HX-splitting catalysts.

    PubMed

    Powers, David C; Hwang, Seung Jun; Zheng, Shao-Liang; Nocera, Daniel G

    2014-09-01

    Two-electron mixed-valence compounds promote the rearrangement of the two-electron bond photochemically. Such complexes are especially effective at managing the activation of hydrohalic acids (HX). Closed HX-splitting cycles require proton reduction to H2 and halide oxidation to X2 to be both accomplished, the latter of which is thermodynamically and kinetically demanding. Phosphazane-bridged Rh2 catalysts have been especially effective at activating HX via photogenerated ligand-bridged intermediates; such intermediates are analogues of the classical ligand-bridged intermediates proposed in binuclear elimination reactions. Herein, a new family of phosphazane-bridged Rh2 photocatalysts has been developed where the halide-bridged geometry is designed into the ground state. The targeted geometries were accessed by replacing previously used alkyl isocyanides with aryl isocyanide ligands, which provided access to families of Rh2L1 complexes. H2 evolution with Rh2 catalysts typically proceeds via two-electron photoreduction, protonation to afford Rh hydrides, and photochemical H2 evolution. Herein, we have directly observed each of these steps in stoichiometric reactions. Reactivity differences between Rh2 chloride and bromide complexes have been delineated. H2 evolution from both HCl and HBr proceeds with a halide-bridged Rh2 hydride photoresting state. The H2-evolution efficiency of the new family of halide-bridged catalysts is compared to a related catalyst in which ligand-bridged geometries are not stabilized in the molecular ground state, and the new complexes are found to more efficiently facilitate H2 evolution. PMID:25137532

  11. Engaging Alkenyl Halides with Alkylsilicates via Photoredox Dual Catalysis.

    PubMed

    Patel, Niki R; Kelly, Christopher B; Jouffroy, Matthieu; Molander, Gary A

    2016-02-19

    Single-electron transmetalation via photoredox/nickel dual catalysis provides the opportunity for the construction of Csp(3)-Csp(2) bonds through the transfer of alkyl radicals under very mild reaction conditions. A general procedure for the cross-coupling of primary and secondary (bis-catecholato)alkylsilicates with alkenyl halides is presented. The developed method allows not only alkenyl bromides and iodides but also previously underexplored alkenyl chlorides to be employed. PMID:26828317

  12. The photolysis of acetylene halides reaction with oxygen

    SciTech Connect

    Hwang, Mei-Lee; Kuo, Yu-Ping

    1996-12-31

    The photolysis of chloro- and bromo-acetylene reactions at low temperature with Hg lamp are carried out. There is no new absorption band observed after in-situ photolysis of acetylene halides in Ar matrix. With the presence of oxygen, several new bands appeared. The new peaks at 2138 and 2342 cm{sup -1} were assigned as CO and CO{sub 2}, respectively. Further work is essential for the assignment of the other new bands.

  13. Colloidal nanocrystals with inorganic halide, pseudohalide, and halometallate ligands.

    PubMed

    Zhang, Hao; Jang, Jaeyoung; Liu, Wenyong; Talapin, Dmitri V

    2014-07-22

    We investigate simple halides and pseudohalides as an important class of inorganic ligands for nanocrystals (NCs) in solution phase ligand exchange. These short, robust, and easy to model ligands bind to the NC surface and provide electrostatic stabilization of NC dispersions in N-methylformamide. The replacement of organic ligands on NCs with compact halide and pseudohalide ligands greatly facilitates electronic communication between NCs. For example, a high electron mobility of ? ? 12 cm(2) V(-1) s(-1) has been observed in thin films made of I(-)-capped CdSe NCs. We also studied charge transport properties of thin films based on the pseudohalide N3(-)-capped InAs NCs, suggesting the possibility of obtaining "all III-V" NC solids. In addition, we extend the surface chemistry of halometallates (e.g., CH3NH3PbI3), which can stabilize colloidal solutions of lead chalcogenide NCs. These halide, pseudohalide, and halometallate ligands enrich the current family of inorganic ligands and can open up more opportunities for applications of NCs in the fields of electronics, optoelectronics, and thermoelectrics. PMID:24988140

  14. Depth profile of halide anions under highly charged biological membrane

    NASA Astrophysics Data System (ADS)

    Sung, Woongmo; Wang, Wenjie; Lee, Jonggwan; Vaknin, David; Kim, Doseok

    2015-03-01

    Halide ion (Cl- and I-) distribution under a cationic Langmuir monolayer consisting of 1,2-dipalmitoyl-3 trimethylammonium-propane (DPTAP) molecules was investigated by vibrational sum-frequency generation (VSFG) and X-ray spectroscopy. From VSFG spectra, it was observed that large halide anions (I-) screen surface charge more efficiently so that interfacial water alignment becomes more randomized. On the other hand, number density of ions directly measured by X-ray fluorescence spectroscopy at grazing incidence angle reveals that the ion densities within 6 ~ 8 nm are the same for both I- and Cl-. Since the observed ion densities in both cases are almost equal to the charge density of the DPTAP monolayer, we propose that larger halide anions are attracted closer to the surface making direct binding with the charged headgroups of the molecules in the monolayer, accomplishing charge neutrality in short distance. This direct adsorption of anions also disturbs the monolayer structure both in terms of the conformation of alkyl chains and the vertical configuration of the monolayer, with iodine having the stronger effect. Our study shows that the length scale that ions neutralize a charged interface varies significantly and specifically even between monovalent ions.

  15. Methyl halide emissions from greenhouse-grown mangroves

    NASA Astrophysics Data System (ADS)

    Manley, Steven L.; Wang, Nun-Yii; Walser, Maggie L.; Cicerone, Ralph J.

    2007-01-01

    Two mangrove species, Avicennia germinans and Rhizophora mangle, were greenhouse grown for nearly 1.5 years from saplings. A single individual of each species was monitored for the emission of methyl halides from aerial tissue. During the first 240 days, salinity was incrementally increased with the addition of seawater, and was maintained between 18 and 28‰ for the duration of the study. Exponential growth occurred after 180 days. Methyl halide emissions normalized to leaf area were measured throughout the study and varied dramatically. Emission rates normalized to land area (mg m-2 y-1), assuming a LAI = 5, yielded 82 and 29 for CH3Cl, 10 and 1.6 for CH3Br, and 26 and 11 for CH3I, for A. germinans and R. mangle, respectively. From these preliminary determinations, only CH3I emissions emerge as being of possible global atmospheric significance. This study emphasizes the need for field studies of methyl halide emissions from mangrove forests.

  16. Will Lanthanum Halide Scintillators Make NaI(Tl) Obsolete?

    NASA Astrophysics Data System (ADS)

    Milbrath, Brian

    2006-05-01

    The commercial availability of lanthanum halide scintillators (LaCl3:Ce and LaBr3:Ce) has been much anticipated due to their significantly better resolution (3-4% at 662 keV) relative to NaI(Tl). Unfortunately, our initial investigation of these scintillators revealed significant alpha contamination quite apparent in background spectra. Using measurements of the detector in coincidence with a HPGe detector, we identified the alpha-contaminant as Ac-227. Since this time, the alpha contamination has been substantially reduced so that a second contaminant, La-138 (a beta, gamma, and x-ray source) has become the dominant contaminant in the material. Commercially-available sizes of lanthanum halide scintillators have now reached sizes suitable for handheld Radioactive Isotope Identification Devices (RIIDs). To study the potential of this new material for RIIDs we performed a series of measurements comparing a 1.5'' x 1.5'' LaBr3 detector with an Exploranium GR-135 RIID, which contains a 1.5'' x 2.2'' NaI(Tl) detector. Measurements were taken for short timeframes of seconds to minutes, as typifies RIID usage. Measurements included examples of naturally occurring radioactive material (NORM) typically found in cargo. Of particular interest was the extent to which interference between the La-138 contaminant and K-40, a radioisotope commonly found in NORM, compromise the lanthanum halide performance. Example spectra, detector comparisons and results will be shown.

  17. Environmental controls over methyl halide emissions from rice paddies

    NASA Astrophysics Data System (ADS)

    Redeker, K. R.; Cicerone, R. J.

    2004-03-01

    This paper examines primary controlling factors that affect methyl halide emissions from rice paddy ecosystems. Observations of four cultivars under multiple growth conditions during studies in commercial fields and the University of California, Irvine, greenhouse lead to the conclusion that daily emissions of methyl halides are primarily determined by the growth stage of the rice plant, with the exception that methyl chloride emissions show no clear seasonal pattern. Methyl chloride emissions appear to be more from the paddy water and/or soil as opposed to the plants; however, in soils with high chloride content, these emissions appear to peak during the reproductive phase. Strong secondary influences include air temperature, soil halide concentration, and soil pore water saturation. The cultivars studied had statistically separate seasonally integrated emissions. Irradiant light and aboveground biomass appear to have little effect on emissions. Emissions of methyl chloride, methyl bromide, and methyl iodide are estimated to be 3.5, 2.3, and 48 mg/m2/yr, or 5.3, 3.5, and 72 Gg/yr, from rice paddies globally.

  18. Lasing in robust cesium lead halide perovskite nanowires.

    PubMed

    Eaton, Samuel W; Lai, Minliang; Gibson, Natalie A; Wong, Andrew B; Dou, Letian; Ma, Jie; Wang, Lin-Wang; Leone, Stephen R; Yang, Peidong

    2016-02-23

    The rapidly growing field of nanoscale lasers can be advanced through the discovery of new, tunable light sources. The emission wavelength tunability demonstrated in perovskite materials is an attractive property for nanoscale lasers. Whereas organic-inorganic lead halide perovskite materials are known for their instability, cesium lead halides offer a robust alternative without sacrificing emission tunability or ease of synthesis. Here, we report the low-temperature, solution-phase growth of cesium lead halide nanowires exhibiting low-threshold lasing and high stability. The as-grown nanowires are single crystalline with well-formed facets, and act as high-quality laser cavities. The nanowires display excellent stability while stored and handled under ambient conditions over the course of weeks. Upon optical excitation, Fabry-Pérot lasing occurs in CsPbBr3 nanowires with an onset of 5 μJ cm(-2) with the nanowire cavity displaying a maximum quality factor of 1,009 ± 5. Lasing under constant, pulsed excitation can be maintained for over 1 h, the equivalent of 10(9) excitation cycles, and lasing persists upon exposure to ambient atmosphere. Wavelength tunability in the green and blue regions of the spectrum in conjunction with excellent stability makes these nanowire lasers attractive for device fabrication. PMID:26862172

  19. Alkali metal recovery from carbonaceous material conversion process

    DOEpatents

    Sharp, David W.; Clavenna, LeRoy R.; Gorbaty, Martin L.; Tsou, Joe M.

    1980-01-01

    In a coal gasification operation or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein solid particles containing alkali metal residues are produced in the gasifier or similar reaction zone, alkali metal constitutents are recovered from the particles by withdrawing and passing the particles from the reaction zone to an alkali metal recovery zone in the substantial absence of molecular oxygen and treating the particles in the recovery zone with water or an aqueous solution in the substantial absence of molecular oxygen. The solution formed by treating the particles in the recovery zone will contain water-soluble alkali metal constituents and is recycled to the conversion process where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst. Preventing contact of the particles with oxygen as they are withdrawn from the reaction zone and during treatment in the recovery zone avoids the formation of undesirable alkali metal constituents in the aqueous solution produced in the recovery zone and insures maximum recovery of water-soluble alkali metal constituents from the alkali metal residues.

  20. Nanostructured Silicon Photocathodes for Solar Water Splitting Patterned by the Self-Assembly of Lamellar Block Copolymers.

    PubMed

    Shen, Lang; He, Chunlin; Qiu, Jing; Lee, Sung-Min; Kalita, Abinasha; Cronin, Stephen B; Stoykovich, Mark P; Yoon, Jongseung

    2015-12-01

    We studied a type of nanostructured silicon photocathode for solar water splitting, where one-dimensionally periodic lamellar nanopatterns derived from the self-assembly of symmetric poly(styrene-block-methyl methacrylate) block copolymers were incorporated on the surface of single-crystalline silicon in configurations with and without a buried metallurgical junction. The resulting nanostructured silicon photocathodes with the characteristic lamellar morphology provided suppressed front-surface reflection and increased surface area, which collectively contributed to the enhanced photocatalytic performance in the hydrogen evolution reaction. The augmented light absorption in the nanostructured silicon directly translated to the increase of the saturation current density, while the onset potential decreased with the etching depth because of the increased levels of surface recombination. The pp(+)-silicon photocathodes, compared to the n(+)pp(+)-silicon with a buried solid-state junction, exhibited a more pronounced shift of the current density-potential curves upon the introduction of the nanostructured surface owing to the corresponding increase in the liquid/silicon junction area. Systematic studies on the morphology, optical properties, and photoelectrochemical characteristics of nanostructured silicon photocathodes, in conjunction with optical modeling based on the finite-difference time-domain method, provide quantitative description and optimal design rules of lamellar-patterned silicon photocathodes for solar water splitting. PMID:26575400

  1. Development of High Quantum Efficiency UV/Blue Photocathode Epitaxial Semiconductor Heterostructures for Scintillation and Cherenkov Radiation Detection

    NASA Technical Reports Server (NTRS)

    Leopold, Daniel J.

    2002-01-01

    The primary goal of this research project was to further extend the use of advanced heteroepitaxial-semiconductor crystal growth techniques such as molecular beam epitaxy (MBE) and to demonstrate significant gains in UV/blue photonic detection by designing and fabricating atomically-tailored heteroepitaxial GaAlN/GaInN photocathode device structures. This NASA Explorer technology research program has focused on the development of photocathodes for Cherenkov and scintillation radiation detection. Support from the program allowed us to enhance our MBE system to include a nitrogen plasma source and a magnetic bearing turbomolecular pump for delivery and removal of high purity atomic nitrogen during GaAlN/GaInN film growth. Under this program we have also designed, built and incorporated a cesium activation stage. In addition, a connected UHV chamber with photocathode transfer/positioner components as well as a hybrid phototube stage was designed and built to make in-situ quantum efficiency measurements without ever having to remove the photocathodes from UHV conditions. Thus we have constructed a system with the capability to couple atomically-tailored MBE-grown photocathode heterostructures with real high gain readout devices for single photon detection evaluation.

  2. Systematic analysis of the unique band gap modulation of mixed halide perovskites.

    PubMed

    Kim, Jongseob; Lee, Sung-Hoon; Chung, Choong-Heui; Hong, Ki-Ha

    2016-02-01

    Solar cells based on organic-inorganic hybrid metal halide perovskites have been proven to be one of the most promising candidates for the next generation thin film photovoltaic cells. Mixing Br or Cl into I-based perovskites has been frequently tried to enhance the cell efficiency and stability. One of the advantages of mixed halides is the modulation of band gap by controlling the composition of the incorporated halides. However, the reported band gap transition behavior has not been resolved yet. Here a theoretical model is presented to understand the electronic structure variation of metal mixed-halide perovskites through hybrid density functional theory. Comparative calculations in this work suggest that the band gap correction including spin-orbit interaction is essential to describe the band gap changes of mixed halides. In our model, both the lattice variation and the orbital interactions between metal and halides play key roles to determine band gap changes and band alignments of mixed halides. It is also presented that the band gap of mixed halide thin films can be significantly affected by the distribution of halide composition. PMID:26791587

  3. Alkali element background reduction in laser ICP-MS

    NASA Astrophysics Data System (ADS)

    Magee, C. W., Jr.; Norris, C. A.

    2015-03-01

    Alkali backgrounds in laser ablation ICP-MS analyses can be enhanced by electron-induced ionisation of alkali contamination on the skimmer cone, reducing effective detection limits for these elements. Traditionally, this problem is addressed by isolating analyses of high-alkali materials onto a designated cone set, or by operating the ICP-MS in a "soft extraction" mode, which reduces the energy of electrons repelled into the potentially contaminated sampling cone by the extraction field. Here we present a novel approach, where we replace the traditional alkali glass tuning standards with synthetic low-alkali glass reference materials. Using this vitreous tuning solution, we find that this approach reduces the amount of alkali contamination produced, halving backgrounds for the heavy alkali elements without any change to analytical procedures. Using segregated cones is still the most effective method for reducing lithium backgrounds, but since the procedures are complimentary, both can easily be applied to the routine operations of an analytical lab.

  4. Effect of alkali lignins with different molecular weights from alkali pretreated rice straw hydrolyzate on enzymatic hydrolysis.

    PubMed

    Li, Yun; Qi, Benkun; Luo, Jianquan; Wan, Yinhua

    2016-01-01

    This study investigated the effect of alkali lignins with different molecular weights on enzymatic hydrolysis of lignocellulose. Different alkali lignins fractions, which were obtained from cascade ultrafiltration, were added into the dilute acid pretreated (DAP) and alkali pretreated (AP) rice straws respectively during enzymatic hydrolysis. The results showed that the addition of alkali lignins enhanced the hydrolysis and the enhancement for hydrolysis increased with increasing molecular weights of alkali lignins, with maximum enhancement being 28.69% for DAP and 20.05% for AP, respectively. The enhancement was partly attributed to the improved cellulase activity, and filter paper activity increased by 18.03% when adding lignin with highest molecular weight. It was found that the enhancement of enzymatic hydrolysis was correlated with the adsorption affinity of cellulase on alkali lignins, and the difference in surface charge and hydrophobicity of alkali lignins were responsible for the difference in affinity between cellulase and lignins. PMID:26496216

  5. Solar Hydrogen Production by Amorphous Silicon Photocathodes Coated with a Magnetron Sputter Deposited Mo2C Catalyst.

    PubMed

    Morales-Guio, Carlos G; Thorwarth, Kerstin; Niesen, Bjoern; Liardet, Laurent; Patscheider, Jörg; Ballif, Christophe; Hu, Xile

    2015-06-10

    Coupling of Earth-abundant hydrogen evolution catalysts to photoabsorbers is crucial for the production of hydrogen fuel using sunlight. In this work, we demonstrate the use of magnetron sputtering to deposit Mo2C as an efficient hydrogen evolution reaction catalyst onto surface-protected amorphous silicon (a-Si) photoabsorbers. The a-Si/Mo2C photocathode evolves hydrogen under simulated solar illumination in strongly acidic and alkaline electrolytes. Onsets of photocurrents are observed at potentials as positive as 0.85 V vs RHE. Under AM 1.5G (1 sun) illumination, the photocathodes reach current densities of -11.2 mA cm(-2) at the reversible hydrogen potential in 0.1 M H2SO4 and 1.0 M KOH. The high photovoltage and low-cost of the Mo2C/a-Si assembly make it a promising photocathode for solar hydrogen production. PMID:26005904

  6. A H2-evolving photocathode based on direct sensitization of MoS3 with an organic photovoltaic cell

    PubMed Central

    Bourgeteau, Tiphaine; Tondelier, Denis; Geffroy, Bernard; Brisse, Romain; Laberty-Robert, Christel; Campidelli, Stéphane; de Bettignies, Rémi; Artero, Vincent; Palacin, Serge; Jousselme, Bruno

    2013-01-01

    An organic solar cell based on a poly-3-hexylthiophene (P3HT): phenyl-C61-butyric acid (PCBM) bulk hetero-junction was directly coupled with molybdenum sulfide resulting in the design of a new type of photocathode for the production of hydrogen. Both the light-harvesting system and the catalyst were deposited by low-cost solution-processed methods, i.e. spin coating and spray coating respectively. Spray-coated MoS3 films are catalytically active in strongly acidic aqueous solutions with the best efficiencies for thicknesses of 40 to 90 nm. The photocathodes display photocurrents higher than reference samples, without catalyst or without coupling with a solar cell. Analysis by gas chromatography confirms the light-induced hydrogen evolution. The addition of titanium dioxide in the MoS3 film enhances electron transport and collection within thick films and therefore the performance of the photocathode. PMID:24404434

  7. A polarized photoluminescence study of strained layer GaAs photocathodes

    SciTech Connect

    Mair, R.A.

    1996-07-01

    Photoluminescence measurements have been made on a set of epitaxially grown strained GaAs photocathode structures. The photocathodes are designed to exhibit a strain-induced enhancement of the electron spin polarization obtainable by optical pumping with circularly polarized radiation of near band gap energy. For the case of non-strained GaAs, the degree of spin polarization is limited to 50% by crystal symmetry. Under an appropriate uniaxial compression or tension, however, the valence band structure near the gap minimum is modified such that a spin polarization of 100% is theoretically possible. A total of nine samples with biaxial compressive strains ranging from zero to {approximately}0.8% are studied. X-ray diffraction analysis, utilizing Bragg reflections, is used to determine the crystal lattice structure of the samples. Luminescence spectra and luminescence circular polarization data are obtained at room temperature, {approx}78 K and {approx}12 K. The degree of luminescence circular polarization is used as a relative measure of the photo-excited electron spin polarization. The room temperature luminescence circular polarization data is compared with the measured electron spin polarization when the samples are used as electron photo-emitters with a negative electron affinity surface preparation. The luminescence data is also analyzed in conjunction with the crystal structure data with the goal of understanding the strain dependent valence band structure, optical pumping characteristics and spin depolarization mechanisms of the photocathode structures. A simple model is used to describe the luminescence data, obtained for the set of samples. Within the assumptions of the model, the deformation potentials a, b and d for GaAs are determined. The measured values are a = -10.16{+-}.21 eV, b = -2.00{+-}.05 eV and d = -4.87{+-}.29 eV. Good agreement with published values of the deformation potentials provides support for the model used to describe the data.

  8. Experience at Fermilab with high quantum efficiency photo-cathodes for rf electron guns

    SciTech Connect

    A. Fry, E. Hahn, W. Hartung, M. Kuchnir, P. Michelato and D. Sertore

    1998-10-01

    As part of the A0 Photo-injector collaboration at Fermi-lab [1, 2] and the TeSLA collaboration [3], a high bright-ness, low emittance electron source has been developed. In the process, a system was constructed for coating molybde-num cathodes with a layer of csium telluride (Cs2 Te), a photo-emissive material of high quantum efficiency (QE). The use of Cs2 Te was first investigated at CERN [4] and LANL [5]. The development of the systems for the TeSLA Test Facility Linac and the Fermilab Photo-injector was done in Milano [6]. The system at Fermilab incorporates manipulator arms to transfer a cathode from the preparation chamber into a 1.3 GHz photo-electron RF gun while it re-mains in an ultra-high vacuum (UHV) environment, in or-der to avoid the deleterious effects of residual gases on the QE. A first prototype electron gun has been operated with a photo-cathode for several months [1]. This paper describes preliminary results obtained with the first 2 photo-cathodes and the first gun. Some of the desired parameters for the TeSLA Test Fa-cility beam are given in Table 1. The desired characteristics for the photo-cathodes include (i) high QE, (ii) high current density (>500 A/cm{sup 2} ), (iii) long lifetime, and (iv) low field emission. The choice of Cs2 Te is a compromise between long lifetime, rugged metal cathodes with low QE (typi-cally between 10{sup -6} and 10{sup -4} and semiconductor cathodes with high QE (>10%), which generally have a short life-time because of their sensitivity to contamination.

  9. Geopolymers and Related Alkali-Activated Materials

    NASA Astrophysics Data System (ADS)

    Provis, John L.; Bernal, Susan A.

    2014-07-01

    The development of new, sustainable, low-CO2 construction materials is essential if the global construction industry is to reduce the environmental footprint of its activities, which is incurred particularly through the production of Portland cement. One type of non-Portland cement that is attracting particular attention is based on alkali-aluminosilicate chemistry, including the class of binders that have become known as geopolymers. These materials offer technical properties comparable to those of Portland cement, but with a much lower CO2 footprint and with the potential for performance advantages over traditional cements in certain niche applications. This review discusses the synthesis of alkali-activated binders from blast furnace slag, calcined clay (metakaolin), and fly ash, including analysis of the chemical reaction mechanisms and binder phase assemblages that control the early-age and hardened properties of these materials, in particular initial setting and long-term durability. Perspectives for future research developments are also explored.

  10. Removal of Retired Alkali Metal Test Systems

    SciTech Connect

    Brehm, W. F.; Church, W. R.; Biglin, J. W.

    2003-02-26

    This paper describes the successful effort to remove alkali metals, alkali metal residues, and piping and structures from retired non-radioactive test systems on the Hanford Site. These test systems were used between 1965 and 1982 to support the Fast Flux Test Facility and the Liquid Metal Fast Breeder Reactor Program. A considerable volume of sodium and sodium-potassium alloy (NaK) was successfully recycled to the commercial sector; structural material and electrical material such as wiring was also recycled. Innovative techniques were used to safely remove NaK and its residues from a test system that could not be gravity-drained. The work was done safely, with no environmental issues or significant schedule delays.

  11. Structural characterization of alkali metal 3-nitrobenzoates

    NASA Astrophysics Data System (ADS)

    ?wis?ocka, R.; Oleksi?ski, E.; Regulska, E.; Kalinowska, M.; Lewandowski, W.

    2007-05-01

    In this paper, the influence of lithium, sodium, potassium, rubidium and cesium on the electronic system of the 3-nitrobenzoic acid was studied. The vibrational (FT-IR, FT-Raman) and NMR ( 1H and 13C) spectra for 3-nitrobenzoic acid and its alkali metal salts were recorded. The changes of chemical shifts of protons ( 1H NMR) and carbons ( 13C NMR) in the series of studied alkali metal 3-nitrobenzoates were observed too. Optimized geometrical structures of studied compounds were calculated by B3PW91 method using 6-311++G ?? and 6-311++G basis sets. Geometric aromaticity indices, dipole moments and energies were also calculated. The theoretical wavenumbers and intensities of IR spectra were obtained at B3PW91/6-311++G level. The calculated parameters were compared to experimental characteristic of studied compounds.

  12. A novel scaling law relating the geometrical dimensions of a photocathode radio frequency gun to its radio frequency properties.

    PubMed

    Lal, Shankar; Pant, K K; Krishnagopal, S

    2011-12-01

    Developing a photocathode RF gun with the desired RF properties of the ?-mode, such as field balance (e(b)) ~1, resonant frequency f(?) = 2856 MHz, and waveguide-to-cavity coupling coefficient ?(?) ~1, requires precise tuning of the resonant frequencies of the independent full- and half-cells (f(f) and f(h)), and of the waveguide-to-full-cell coupling coefficient (?(f)). While contemporary electromagnetic codes and precision machining capability have made it possible to design and tune independent cells of a photocathode RF gun for desired RF properties, thereby eliminating the need for tuning, access to such computational resources and quality of machining is not very widespread. Therefore, many such structures require tuning after machining by employing conventional tuning techniques that are iterative in nature. Any procedure that improves understanding of the tuning process and consequently reduces the number of iterations and the associated risks in tuning a photocathode gun would, therefore, be useful. In this paper, we discuss a method devised by us to tune a photocathode RF gun for desired RF properties under operating conditions. We develop and employ a simple scaling law that accounts for inter-dependence between frequency of independent cells and waveguide-to-cavity coupling coefficient, and the effect of brazing clearance for joining of the two cells. The method has been employed to successfully develop multiple 1.6 cell BNL?SLAC/UCLA type S-band photocathode RF guns with the desired RF properties, without the need to tune them by a tiresome cut-and-measure process. Our analysis also provides a physical insight into how the geometrical dimensions affect the RF properties of the photo-cathode RF gun. PMID:22225212

  13. Alkali metal protective garment and composite material

    DOEpatents

    Ballif, III, John L. (Salt Lake City, UT); Yuan, Wei W. (Seattle, WA)

    1980-01-01

    A protective garment and composite material providing satisfactory heat resistance and physical protection for articles and personnel exposed to hot molten alkali metals, such as sodium. Physical protection is provided by a continuous layer of nickel foil. Heat resistance is provided by an underlying backing layer of thermal insulation. Overlying outer layers of fireproof woven ceramic fibers are used to protect the foil during storage and handling.

  14. Alkali Metal Heat Pipe Life Issues

    NASA Technical Reports Server (NTRS)

    Reid, Robert S.

    2004-01-01

    One approach to space fission power system design is predicated on the use of alkali metal heat pipes, either as radiator elements, thermal management components, or as part of the core primary heat-transfer system. This synopsis characterizes long-life core heat pipes. References are included where more detailed information can be found. Specifics shown here are for demonstrational purposes and do not necessarily reflect current Project Prometheus point designs.

  15. Transcriptome Analysis of Alkali Shock and Alkali Adaptation in Listeria monocytogenes 10403S

    PubMed Central

    Giotis, Efstathios S.; Muthaiyan, Arunachalam; Natesan, Senthil; Wilkinson, Brian J.; Blair, Ian S.

    2010-01-01

    Abstract Alkali stress is an important means of inactivating undesirable pathogens in a wide range of situations. Unfortunately, Listeria monocytogenes can launch an alkaline tolerance response, significantly increasing persistence of the pathogen in such environments. This study compared transcriptome patterns of alkali and nonalkali-stressed L. monocytogenes 10403S cells, to elucidate the mechanisms by which Listeria adapts and/or grows during short- or long-term alkali stress. Transcription profiles associated with alkali shock (AS) were obtained by DNA microarray analysis of midexponential cells suspended in pH 9 media for 15, 30, or 60 min. Transcription profiles associated with alkali adaptation (AA) were obtained similarly from cells grown to midexponential phase at pH 9. Comparison of AS and AA transcription profiles with control cell profiles identified a high number of differentially regulated open-reading frames in all tested conditions. Rapid (15 min) changes in expression included upregulation of genes encoding for multiple metabolic pathways (including those associated with Na+/H+ antiporters), ATP-binding cassette transporters of functional compatible solutes, motility, and virulence-associated genes as well as the σB controlled stress resistance network. Slower (30 min and more) responses to AS and adaptation during growth in alkaline conditions (AA) involved a different pattern of changes in mRNA concentrations, and genes involved in proton export. PMID:20677981

  16. Analysis and experiments of a waveguide post's influence on photocathode RF gun

    NASA Astrophysics Data System (ADS)

    Qian, Houjun; Tang, Chuanxiang; Zheng, Shuxin; Tong, Dechun; Chen, Huaibi; Huang, Wenhui; Guan, Xin

    2008-12-01

    Several BNL/KEK/SHI type photocathode RF guns have been fabricated for high-quality electron beams in Accelerator Laboratory of Tsinghua University. This paper describes how the characteristics of a waveguide post can be chosen to correct for a mismatch in power coupling without affecting the pi-mode resonant frequency and the balance of fields between the two cells. Microwave circuit theories are used to analyze how to select the proper location and depth of the waveguide post. The tolerance on the post positioning is evaluated based on gun field quality requirements. MAFIA simulations and RF experiments have been done to confirm the theoretical analysis.

  17. The quantum efficiency of dispenser photocathodes: Comparison of theory to experiment

    NASA Astrophysics Data System (ADS)

    Jensen, Kevin L.; Feldman, Donald W.; O'Shea, Patrick G.

    2004-11-01

    The quantum efficiency (QE) characteristics of commercially available dispenser cathodes were measured, giving QEs of (for Scandate) 6.510-5, 2.010-4, and 8.010-4, and (for M-type) 3.010-4, 1.410-3, and 2.610-3, for wavelengths of 532, 355, and 266nm, respectively, corresponding to harmonics of an Nd:YAG laser. A time-dependent photoemission model was developed to analyze the data, as well as dispenser and metal photocathode data in the literature, and quantitatively good agreement is found, demonstrating the utility of the code as a predictive estimator of performance.

  18. Impact of transverse irregularities at the photocathode on the production of high-charge electron bunches

    SciTech Connect

    Rihaoui, M.; Bohn, C.L.; Piot, P.; Power, J.G.; /Argonne

    2007-06-01

    The properties of electron beams produced in a photoinjector are strongly dependent on the initial conditions, i.e. the photocathode drive laser shape and its uniformity. We explore the impact of well-defined transverse laser perturbations on the evolution of the electron beam both in configuration and velocity spaces and especially investigate how certain types of perturbations evolve as the beam propagates in the Argonne Wakefield Accelerator facility. Numerical simulations performed with IMPACT-T are presented. Finally preliminary experimental results aimed at validating our simulations are discussed.

  19. Quantum Efficiency and Topography of Heated and Plasma-Cleaned Copper Photocathode Surfaces

    SciTech Connect

    Palmer, Dennis T.; Kirby, R.E.; King, F.K.; /SLAC

    2005-08-04

    We present measurements of photoemission quantum efficiency (QE) for copper photocathodes heated and cleaned by low energy argon and hydrogen ion plasma. The QE and surface roughness parameters were measured before and after processing and surface chemical composition was tracked in-situ with x-ray photoelectron spectroscopy (XPS). Thermal annealing at 230 C was sufficient to improve the QE by 3-4 orders of magnitude, depending on the initial QE. Exposure to residual gas slowly reduced the QE but it was easily restored by argon ion cleaning for a few minutes. XPS showed that the annealing or ion bombardment removed surface water and hydrocarbons.

  20. Photoemission and optical constant measurements of a Cesium Iodide thin film photocathode

    NASA Astrophysics Data System (ADS)

    Triloki; Rai, R.; Gupta, Nikita; Jammal, Nabeel F. A.; Singh, B. K.

    2015-07-01

    The performance of cesium iodide as a reflective photocathode is presented. The absolute quantum efficiency of a 500 nm thick film of cesium iodide has been measured in the wavelength range 150 nm-200 nm. The optical absorbance has been analyzed in the wavelength range 190 nm-900 nm and the optical band gap energy has been calculated. The dispersion properties were determined from the refractive index using an envelope plot of the transmittance data. The morphological and elemental film composition have been investigated by atomic force microscopy and X-ray photo-electron spectroscopy techniques.

  1. Chemically induced fracturing in alkali feldspar

    NASA Astrophysics Data System (ADS)

    Scheidl, K. S.; Schaeffer, A.-K.; Petrishcheva, E.; Habler, G.; Fischer, F. D.; Schreuer, J.; Abart, R.

    2014-01-01

    Fracturing in alkali feldspar during Na+-K+ cation exchange with a NaCl-KCl salt melt was studied experimentally. Due to a marked composition dependence of the lattice parameters of alkali feldspar, any composition gradient arising from cation exchange causes coherency stress. If this stress exceeds a critical level fracturing occurs. Experiments were performed on potassium-rich gem-quality alkali feldspars with polished (010) and (001) surfaces. When the feldspar was shifted toward more sodium-rich compositions over more than about 10 mole %, a system of parallel cracks with regular crack spacing formed. The cracks have a general (h0l) orientation and do not correspond to any of the feldspar cleavages. The cracks are rather oriented (sub)-perpendicular to the direction of maximum tensile stress. The critical stress needed to initiate fracturing is about 325 MPa. The critical stress intensity factor for the propagation of mode I cracks, K Ic, is estimated as 2.30-2.72 MPa m1/2 (73-86 MPa mm1/2) from a systematic relation between characteristic crack spacing and coherency stress. An orientation mismatch of 18° between the crack normal and the direction of maximum tensile stress is ascribed to the anisotropy of the longitudinal elastic stiffness which has pronounced maxima in the crack plane and a minimum in the direction of the crack normal.

  2. Ion Pairing in Alkali Nitrate Electrolyte Solutions.

    PubMed

    Xie, Wen Jun; Zhang, Zhen; Gao, Yi Qin

    2016-03-10

    In this study, we investigate the thermodynamics of alkali nitrate salt solutions, especially the formation of contact ion pairs between alkali cation and nitrate anion. The ion-pairing propensity shows an order of LiNO3 < NaNO3 < KNO3. Such results explain the salt activity coefficients and suggest that the empirical "law of matching water affinity" is followed by these alkali nitrate salt solutions. The spatial patterns of contact ion pairs are different in the three salt solutions studied here: Li(+) forms the contact ion pair with only one oxygen of the nitrate while Na(+) and K(+) can also be shared by two oxygens of the nitrate. In reproducing the salt activity coefficient using Kirkwood-Buff theory, we find that it is essential to include electronic polarization for Li(+) which has a high charge density. The electronic continuum correction for nonpolarizable force field significantly improves the agreement between the calculated activity coefficients and their experimental values. This approach also improves the performance of the force field on salt solubility. From these two aspects, this study suggests that electronic continuum correction can be a promising approach to force-field development for ions with high charge densities. PMID:26901167

  3. Transport properties of alkali metal doped fullerides

    NASA Astrophysics Data System (ADS)

    Yadav, Daluram; Yadav, Nishchhal

    2015-07-01

    We have studied the intercage interactions between the adjacent C60 cages and expansion of lattice due to the intercalation of alkali atoms based on the spring model to estimate phonon frequencies from the dynamical matrix for the intermolecular alkali-C60 phonons. We considered a two-peak model for the phonon density of states to investigate the nature of electron pairing mechanism for superconducting state in fullerides. Coulomb repulsive parameter and the electron phonon coupling strength are obtained within the random phase approximation. Transition temperature, Tc, is obtained in a situation when the free electrons in lowest molecular orbital are coupled with alkali-C60 phonons as 5 K, which is much lower as compared to reported Tc (20 K). The superconducting pairing is mainly driven by the high frequency intramolecular phonons and their effects enhance it to 22 K. The importance of the present study, the pressure effect and normal state transport properties are calculated within the same model leading superconductivity.

  4. Alkali release from model coal compounds

    SciTech Connect

    Chakrabarti, A.

    1981-01-01

    Alkali materials exist in coal in both inorganic and organic forms. As a means of studying the release of alkali material from the organic phase, sodium and potassium benzoate have been chosen as model compounds. The decomposition of these two compounds, in terms of both gaseous species and residues, have been studied in argon, carbon dioxide, and air. Thermogravimetric methods were used to determine the different ranges where decomposition occurred and to obtain kinetic information. Pyrolysis-gas chromatography was used to identify the various organic products formed from the decomposition of the benzoates below 600/sup 0/C. Transpiration mass spectrometry at pressures up to 0.3 atm. of argon was used to identify and to measure the partial pressures of different gaseous products. At temperatures below 550/sup 0/C, the decomposition comprises of organic loss and is nearly independent of the atmosphere. At this temperature, the residue left from the decomposition is a mixture of carbonate and char. For the decomposition in argon atmosphere, activation energy was determined for the reaction leading to organic loss and for the reaction causing alkali release. Heat of the second reaction was also determined for both the model compounds.

  5. Alteration of alkali reactive aggregates autoclaved in different alkali solutions and application to alkali-aggregate reaction in concrete (II) expansion and microstructure of concrete microbar

    SciTech Connect

    Lu Duyou . E-mail: duyoulu@njut.edu.cn; Mei Laibao; Xu Zhongzi; Tang Mingshu; Mo Xiangyin; Fournier, Benoit

    2006-06-15

    The effect of the type of alkalis on the expansion behavior of concrete microbars containing typical aggregate with alkali-silica reactivity and alkali-carbonate reactivity was studied. The results verified that: (1) at the same molar concentration, sodium has the strongest contribution to expansion due to both ASR and ACR, followed by potassium and lithium; (2) sufficient LiOH can completely suppress expansion due to ASR whereas it can induce expansion due to ACR. It is possible to use the duplex effect of LiOH on ASR and ACR to clarify the ACR contribution when ASR and ACR may coexist. It has been shown that a small amount of dolomite in the fine-grained siliceous Spratt limestone, which has always been used as a reference aggregate for high alkali-silica reactivity, might dedolomitize in alkaline environment and contribute to the expansion. That is to say, Spratt limestone may exhibit both alkali-silica and alkali-carbonate reactivity, although alkali-silica reactivity is predominant. Microstructural study suggested that the mechanism in which lithium controls ASR expansion is mainly due to the favorable formation of lithium-containing less-expansive product around aggregate particles and the protection of the reactive aggregate from further attack by alkalis by the lithium-containing product layer.

  6. Selective substitution of alkali cations in mixed alkali glass by solid-state electrochemistry

    NASA Astrophysics Data System (ADS)

    Kamada, Kai; Tsutsumi, Yuko; Yamashita, Shuichi; Matsumoto, Yasumichi

    2004-01-01

    Electrosubstitution of alkali cations in mixed-alkali glass containing both Na 2O and K 2O for other monovalent metal cations ( M+=Li +, Ag +, and Cs +) was investigated using a solid-state electrochemical method. The fundamental electrolysis system consists of anode/ M+-conducting microelectrode/glass/Na- ??-Al 2O 3/cathode, where M+ is substituted for the alkali metal ions in the glass under an applied electric field. Li + ions attacked only Na + sites, and Ag + ions replaced Na + sites more readily than K +. In contrast, Cs + ions simultaneously substituted for both Na + and K + sites. The substitution behavior appears to depend on the difference in ionic conductivity between K + and Na + and the radius of the dopant. This mechanism was discussed qualitatively.

  7. EPA (ENVIRONMENTAL PROTECTION AGENCY) METHOD STUDY 32: METHOD 450.1 - TOTAL ORGANIC HALIDES (TOX)

    EPA Science Inventory

    The report describes the interlaboratory method study that was performed to evaluate interim Method 450.1 for total organic halides (TOX). In the method, a measured volume of water is passed through two columns in series each containing 40 mg of activated charcoal. Organic halide...

  8. Aryl-triazole foldamers incorporating a pyridinium motif for halide anion binding in aqueous media.

    PubMed

    Shang, Jie; Zhao, Wei; Li, Xichen; Wang, Ying; Jiang, Hua

    2016-03-15

    Aryl-triazole oligomers incorporating a pyridinium motif have been synthesized from their pyridine precursors. Anion binding studies show that methylation of the pyridine units can significantly enhance the halide anion affinities of the folded oligomers so that the foldamers are capable of binding halide anions in aqueous solutions. PMID:26933696

  9. 10 CFR 431.322 - Definitions concerning metal halide lamp ballasts and fixtures.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... contains a third starting electrode (probe) in the arc tube, and does not generally contain an igniter but instead starts lamps with high ballast open circuit voltage. Pulse-start metal halide ballast means an electronic or electromagnetic ballast that starts a pulse-start metal halide lamp with high voltage...

  10. 10 CFR 431.322 - Definitions concerning metal halide lamp ballasts and fixtures.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... electrode (probe) in the arc tube, and does not generally contain an igniter but instead starts lamps with high ballast open circuit voltage. Pulse-start metal halide ballast means an electronic or electromagnetic ballast that starts a pulse-start metal halide lamp with high voltage pulses, where lamps shall...

  11. THE DETERMINATION OF TOTAL ORGANIC HALIDE IN WATER: A COMPARATIVE STUDY OF TWO INSTRUMENTS

    EPA Science Inventory

    Total organic halide (TOX) analyzers are commonly used to measure the amount of dissolved halogenated organic byproducts in disinfected waters. ecause of the lack of information on the identity of disinfection byproducts, rigorous testing of the dissolved organic halide (DOX) pro...

  12. An efficient transformation of primary halides into nitriles through palladium-catalyzed hydrogen transfer reaction.

    PubMed

    Zou, Tao; Yu, Xiaoqiang; Feng, Xiujuan; Bao, Ming

    2015-07-01

    Two-step one-pot transformation of primary halides into corresponding nitriles is successfully achieved. Nucleophilic substitution of primary halides with sodium azide and subsequent palladium-catalyzed hydrogen transfer proceeds smoothly in the presence of sterically bulky ligand dicyclohexyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (XPhos) in acetone to produce nitriles in satisfactory to good yields. PMID:26050994

  13. THE DETERMINATION OF TOTAL ORGANIC HALIDE IN WATER: AN INTERLABORATORY COMPARATIVE STUDY OF TWO METHODS

    EPA Science Inventory

    Total organic halide (TOX) analyzers are commonly used to measure the amount of dissolved halogenated organic byproducts in disinfected waters. Because of the lack of information on the identity of disinfection byproducts, rigorous testing of the dissolved organic halide (DOX) pr...

  14. CFTR-mediated halide transport in phagosomes of human neutrophils

    PubMed Central

    Painter, Richard G.; Marrero, Luis; Lombard, Gisele A.; Valentine, Vincent G.; Nauseef, William M.; Wang, Guoshun

    2010-01-01

    Chloride serves as a critical component of innate host defense against infection, providing the substrate for MPO-catalyzed production of HOCl in the phagosome of human neutrophils. Here, we used halide-specific fluorescent sensors covalently coupled to zymosan particles to investigate the kinetics of chloride and iodide transport in phagosomes of human neutrophils. Using the self-ratioable fluorescent probe specific for chloride anion, we measured chloride dynamics within phagosomes in response to extracellular chloride changes by quantitative fluorescence microscopy. Under the experimental conditions used, normal neutrophils showed rapid phagosomal chloride uptake with an initial influx rate of 0.31 0.04 mM/s (n=5). GlyH-101, a CFTRinh, decreased the rate of uptake in a dose-dependent manner. Neutrophils isolated from CF patients showed a significantly slower rate of chloride uptake by phagosomes, having an initial influx rate of 0.043 0.012 mM/s (n=5). Interestingly, the steady-state level of chloride in CF phagosomes was ?26 mM, significantly lower than that of the control (?68 mM). As CFTR transports chloride as well as other halides, we conjugated an iodide-sensitive probe as an independent approach to confirm the results. The dynamics of iodide uptake by neutrophil phagosomes were monitored by flow cytometry. CFTRinh172 blocked 4050% of the overall iodide uptake by phagosomes in normal neutrophils. In a parallel manner, the level of iodide uptake by CF phagosomes was only 2030% of that of the control. Taken together, these results implicate CFTR in transporting halides into the phagosomal lumen. PMID:20089668

  15. Calcium phosphate cements with strontium halides as radiopacifiers.

    PubMed

    López, Alejandro; Montazerolghaem, Maryam; Engqvist, Håkan; Ott, Marjam Karlsson; Persson, Cecilia

    2014-02-01

    High radiopacity is required to monitor the delivery and positioning of injectable implants. Inorganic nonsoluble radiopacifiers are typically used in nondegradable bone cements; however, their usefulness in resorbable cements is limited due to their low solubility. Strontium halides, except strontium fluoride, are ionic water-soluble compounds that possess potential as radiopacifiers. In this study, we compare the radiopacity, mechanical properties, composition, and cytotoxicity of radiopaque brushite cements prepared with strontium fluoride (SrF2 ), strontium chloride (SrCl2 ·6H2 O), strontium bromide (SrBr2 ), or strontium iodide (SrI2 ). Brushite cements containing 10 wt % SrCl2 ·6H2 O, SrBr2 , or SrI2 exhibited equal to or higher radiopacity than commercial radiopaque cements. Furthermore, the brushite crystal lattice in cements that contained the ionic radiopacifiers was larger than in unmodified cements and in cements that contained SrF2 , indicating strontium substitution. Despite the fact that the strontium halides increased the solubility of the cements and affected their mechanical properties, calcium phosphate cements containing SrCl2 ·6H2 O, SrBr2 , and SrI2 showed no significant differences in Saos-2 cell viability and proliferation with respect to the control. Strontium halides: SrCl2 ·6H2 O, SrBr2 , and SrI2 may be potential candidates as radiopacifiers in resorbable biomaterials although their in vivo biocompatibility, when incorporated into injectable implants, is yet to be assessed. PMID:23997030

  16. Method for the safe disposal of alkali metal

    DOEpatents

    Johnson, Terry R.

    1977-01-01

    Alkali metals such as those employed in liquid metal coolant systems can be safely reacted to form hydroxides by first dissolving the alkali metal in relatively inert metals such as lead or bismuth. The alloy thus formed is contacted with a molten salt including the alkali metal hydroxide and possibly the alkali metal carbonate in the presence of oxygen. This oxidizes the alkali metal to an oxide which is soluble within the molten salt. The salt is separated and contacted with steam or steam-CO.sub.2 mixture to convert the alkali metal oxide to the hydroxide. These reactions can be conducted with minimal hydrogen evolution and with the heat of reaction distributed between the several reaction steps.

  17. Lithium halide primary cell having end of life indicator means

    SciTech Connect

    O'boyle, M.

    1981-01-27

    The present invention relates to a lithium halide primary cell having means to indicate its end of life. The cell includes at least one lithium anode and a cathode in contact with a major surface of the anode wherein the indicating means comprises a stepped portion on the major surface of said anode which is not in contact with the cathode. The stepped portion of the anode comprises a surface area of from about 40 to 60% of the area of the major surface in contact with the cathode and about 15 to 5% of the total thickness of said anode.

  18. Transport phenomena of aluminium oxide in metal halide lamps

    NASA Astrophysics Data System (ADS)

    Fischer, S.; Niemann, U.; Markus, T.

    2008-07-01

    A better understanding of the transport phenomena observed in metal halide lamps can be achieved using computer-based model calculations. The chemical transport of aluminium oxide in advanced high-pressure discharge vessels was calculated as a function of temperature and composition of the salt mixture relevant to the lamp. Below 1773 K chemical transport is the prevailing process; above this temperature the vaporization and condensation of the envelope materialaluminium oxidebecome more important. The results of the calculations show that the amount of transported alumina increases linearly with the number of iteration cycles and exponentially with the temperature gradient.

  19. Volatile species in halide-activated-diffusion coating packs

    NASA Technical Reports Server (NTRS)

    Bianco, Robert; Rapp, Robert A.; Jacobson, Nathan S.

    1992-01-01

    An atmospheric pressure sampling mass spectrometer was used to identify the vapor species generated in a halide-activated cementation pack. Pack powder mixtures containing a Cr-Al binary masteralloy powder, an NH4Cl activator salt, and either ZrO2 or Y2O3 (or neither) were analyzed at 1000 C. Both the equilibrium calculations for the pack and mass spectrometer results indicated that volatile AlCl(x) and CrCl(y) species were generated by the pack powder mixture; in packs containing the reactive element oxide, volatile ZrCl(z) and YCl(w) species were formed by the conversion of their oxide sources.

  20. Heavy ion passive dosimetry with silver halide single crystals

    NASA Technical Reports Server (NTRS)

    Childs, C. B.; Parnell, T. A.

    1972-01-01

    A method of detecting radiation damage tracks due to heavy particles in large single crystals of the silver halides is described. The tracks, when made visible with a simple electrical apparatus, appear similar to tracks in emulsions. The properties of the crystals, the technique of printing out the tracks, and evidence concerning the threshold energy for registering particles indicates that this method may find application in heavy ion dosimetry. The method has been found to be sensitive to stopping He nuclei and relativistic M group cosmic rays. Some impurities strongly influence the printout of the tracks, and the effects of these impurities are discussed.

  1. Thermal conductivity of halide solid solutions: Measurement and prediction

    NASA Astrophysics Data System (ADS)

    Gheribi, Amen E.; Poncsk, Sndor; St-Pierre, Rmi; Kiss, Lszl I.; Chartrand, Patrice

    2014-09-01

    The composition dependence of the lattice thermal conductivity in NaCl-KCl solid solutions has been measured as a function of composition and temperature. Samples with systematically varied compositions were prepared and the laser flash technique was used to determine the thermal diffusivity from 373 K to 823 K. A theoretical model, based on the Debye approximation of phonon density of state (which contains no adjustable parameters) was used to predict the thermal conductivity of both stoichiometric compounds and fully disordered solid solutions. The predictions obtained with the model agree very well with our measurement. A general method for predicting the thermal conductivity of different halide systems is discussed.

  2. Thermal conductivity of halide solid solutions: measurement and prediction.

    PubMed

    Gheribi, Amen E; Poncsk, Sndor; St-Pierre, Rmi; Kiss, Lszl I; Chartrand, Patrice

    2014-09-14

    The composition dependence of the lattice thermal conductivity in NaCl-KCl solid solutions has been measured as a function of composition and temperature. Samples with systematically varied compositions were prepared and the laser flash technique was used to determine the thermal diffusivity from 373 K to 823 K. A theoretical model, based on the Debye approximation of phonon density of state (which contains no adjustable parameters) was used to predict the thermal conductivity of both stoichiometric compounds and fully disordered solid solutions. The predictions obtained with the model agree very well with our measurement. A general method for predicting the thermal conductivity of different halide systems is discussed. PMID:25217938

  3. Optical Properties of Photovoltaic Organic-Inorganic Lead Halide Perovskites.

    PubMed

    Green, Martin A; Jiang, Yajie; Soufiani, Arman Mahboubi; Ho-Baillie, Anita

    2015-12-01

    Over the last several years, organic-inorganic lead halide perovskites have rapidly emerged as a new photovoltaic contender. Although energy conversion efficiency above 20% has now been certified, improved understanding of the material properties contributing to these high performance levels may allow the progression to even higher efficiency, stable cells. The optical properties of these new materials are important not only to device design but also because of the insight they provide into less directly accessible properties, including energy-band structures, binding energies, and likely impact of excitons, as well as into absorption and inverse radiative recombination processes. PMID:26560862

  4. Impact of the organic halide salt on final perovskite composition for photovoltaic applications

    SciTech Connect

    Moore, David T.; Sai, Hiroaki; Wee Tan, Kwan; Estroff, Lara A.; Wiesner, Ulrich

    2014-08-01

    The methylammonium lead halide perovskites have shown significant promise as a low-cost, second generation, photovoltaic material. Despite recent advances, however, there are still a number of fundamental aspects of their formation as well as their physical and electronic behavior that are not well understood. In this letter we explore the mechanism by which these materials crystallize by testing the outcome of each of the reagent halide salts. We find that components of both salts, lead halide and methylammonium halide, are relatively mobile and can be readily exchanged during the crystallization process when the reaction is carried out in solution or in the solid state. We exploit this fact by showing that the perovskite structure is formed even when the lead salt's anion is a non-halide, leading to lower annealing temperature and time requirements for film formation. Studies into these behaviors may ultimately lead to improved processing conditions for photovoltaic films.

  5. New generation of medium wattage metal halide lamps and spectroscopic tools for their diagnostics

    NASA Astrophysics Data System (ADS)

    Dunaevsky, A.; Tu, J.; Gibson, R.; Steere, T.; Graham, K.; van der Eyden, J.

    2010-11-01

    A new generation of ceramic metal halide high intensity discharge (HID) lamps has achieved high efficiencies by implementing new design concepts. The shape of the ceramic burner is optimized to withstand high temperatures with minimal thermal stress. Corrosion processes with the ceramic walls are slowed down via adoption of non-aggressive metal halide chemistry. Light losses over life due to tungsten deposition on the walls are minimized by maintaining a self-cleaning chemical process, known as tungsten cycle. All these advancements have made the new ceramic metal halide lamps comparable to high pressure sodium lamps for luminous efficacy, life, and maintenance while providing white light with high color rendering. Direct replacement of quartz metal halide lamps and systems results in the energy saving from 18 up to 50%. High resolution spectroscopy remains the major non-destructive tool for the ceramic metal halide lamps. Approaches to reliable measurements of relative partial pressures of the arc species are discussed.

  6. Organic-Inorganic Hybrid Solution-Processed H?-Evolving Photocathodes.

    PubMed

    Lai, Lai-Hung; Gomulya, Widianta; Berghuis, Matthijs; Protesescu, Loredana; Detz, Remko J; Reek, Joost N H; Kovalenko, Maksym V; Loi, Maria A

    2015-09-01

    Here we report for the first time an H2-evolving photocathode fabricated by a solution-processed organic-inorganic hybrid composed of CdSe and P3HT. The CdSe:P3HT (10:1 (w/w)) hybrid bulk heterojunction treated with 1,2-ethanedithiol (EDT) showed efficient water reduction and hydrogen generation. A photocurrent of -1.24 mA/cm(2) at 0 V versus reversible hydrogen electrode (V(RHE)), EQE of 15%, and an unprecedented Voc of 0.85 V(RHE) under illumination of AM1.5G (100 mW/cm(2)) in mild electrolyte were observed. Time-resolved photoluminescence (TRPL), internal quantum efficiency (IQE), and transient photocurrent measurements were carried out to clarify the carrier dynamics of the hybrids. The exciton lifetime of CdSe was reduced by one order of magnitude in the hybrid blend, which is a sign of the fast charge separation upon illumination. By comparing the current magnitude of the solid-state devices and water-splitting devices made with identical active layers, we found that the interfaces of the water-splitting devices limit the device performance. The electron/hole transport properties investigated by comparing IQE spectra upon front- and back-side illumination evidenced balanced electron/hole transport. The Faradaic efficiency is 80-100% for the hybrid photocathodes with Pt catalysts and ?70% for the one without Pt catalysts. PMID:26261996

  7. Improved Ion Resistance for III-V Photocathodes in High Current Guns

    SciTech Connect

    Mulhollan, Gregory, A.

    2012-11-16

    The two photocathode test systems were modified, baked and recommissioned. The first system was dedicated to ion studies and the second to electron stimulated recovery (ESR) work. The demonstration system for the electron beam rejuvenation was set up, tested and demonstrated to one of the SSRL team (Dr. Kirby) during a site visit. The requisite subsystems were transferred to SSRL, installed and photoemission studies conducted on activated surfaces following electron beam exposure. Little surface chemistry change was detected in the photoemission spectra following the ESR process. The yield mapping system for the ion (and later, the electron beam rejuvenation) studies was implemented and use made routine. Ion species and flux measurements were performed for H, He, Ne, Ar, Kr and Xe ions at energies of 0.5, 1.0 and 2.0 kV. Gas induced photoyield measurements followed each ion exposure measurement. These data permit the extraction of photoyield induced change per ion (by species) at the measured energies. Electron beam induced rejuvenation was first demonstrated in the second chamber with primary electron beam energy and dependency investigations following. A Hiden quadrupole mass spectrometer for the electron stimulated desorption (ESD) measurements was procured. The UHV test systems needed for subsequent measurements were configured, baked, commissioned and utilized for their intended purposes. Measurements characterizing the desorption products from the ESD process and secondary electron (SE) yield at the surfaces of negative electron affinity GaAs photocathodes have been performed. One US Utility Patent was granted covering the ESR process.

  8. Covalent Immobilization of a Molecular Catalyst on Cu2O Photocathodes for CO2 Reduction.

    PubMed

    Schreier, Marcel; Luo, Jingshan; Gao, Peng; Moehl, Thomas; Mayer, Matthew T; Grätzel, Michael

    2016-02-17

    Sunlight-driven CO2 reduction is a promising way to close the anthropogenic carbon cycle. Integrating light harvester and electrocatalyst functions into a single photoelectrode, which converts solar energy and CO2 directly into reduced carbon species, is under extensive investigation. The immobilization of rhenium-containing CO2 reduction catalysts on the surface of a protected Cu2O-based photocathode allows for the design of a photofunctional unit combining the advantages of molecular catalysts with inorganic photoabsorbers. To achieve large current densities, a nanostructured TiO2 scaffold, processed at low temperature, was deposited on the surface of protected Cu2O photocathodes. This led to a 40-fold enhancement of the catalytic photocurrent as compared to planar devices, resulting in the sunlight-driven evolution of CO at large current densities and with high selectivity. Potentiodynamic and spectroelectrochemical measurements point toward a similar mechanism for the catalyst in the bound and unbound form, whereas no significant production of CO was observed from the scaffold in the absence of a molecular catalyst. PMID:26804626

  9. Performance Study of K2CsSb Photocathode Inside a DC High Voltage Gun

    SciTech Connect

    McCarter J. L.; Rao T.; Smedley, J.; Grames, J.; Mammei, R.; Poelker, M.; Suleiman, R.

    2011-09-01

    In the past decade, there has been considerable interest in the generation of tens of mA average current in a photoinjector. Until recently, GaAs:Cs cathodes and K{sub 2}CsSb cathodes have been tested successfully in DC and RF injectors respectively for this application. Our goal is to test the K{sub 2}CsSb photocathode inside a DC gun. Since the multialkali cathode is a compound with constant characteristics over its entire thickness, we anticipate that the lifetime issues seen in GaAs:Cs due to surface damage by ion bombardment would be minimized. Hence successful operation of the K{sub 2}CsSb cathode in a DC gun could lead to a relatively robust electron source capable of delivering ampere level currents. In order to test the performance of a K{sub 2}CsSb cathode in a DC gun, we have designed and built a load lock system that allows the fabrication of the cathode at Brookhaven National Lab (BNL) and its testing at Jefferson Lab (JLab). In this paper, we will present the performance of the K{sub 2}CsSb photocathode in the preparation chamber and in the DC gun.

  10. Use of non evaporable getter pumps to ensure long term performances of high quantum efficiency photocathodes

    SciTech Connect

    Sertore, Daniele Michelato, Paolo; Monaco, Laura; Manini, Paolo; Siviero, Fabrizio

    2014-05-15

    High quantum efficiency photocathodes are routinely used as laser triggered emitters in the advanced high brightness electron sources based on radio frequency guns. The sensitivity of “semiconductor” type photocathodes to vacuum levels and gas composition requires special care during preparation and handling. This paper will discuss the results obtained using a novel pumping approach based on coupling a 20 l s{sup −1} sputter ion getter pump with a CapaciTorr® D100 non evaporable getter (NEG) pump. A pressure of 8⋅10{sup −8} Pa was achieved using only a sputter ion pump after a 6 day bake-out. With the addition of a NEG pump, a pressure of 2⋅10{sup −9} Pa was achieved after a 2 day bake-out. These pressure values were maintained without power due to the ability of the NEG to pump gases by chemical reaction. Long term monitoring of cathodes quantum efficiencies was also carried out at different photon wavelengths for more than two years, showing no degradation of the photoemissive film properties.

  11. Nanostructured Ternary FeCrAl Oxide Photocathodes for Water Photoelectrolysis.

    PubMed

    Kondofersky, Ilina; Müller, Alexander; Dunn, Halina K; Ivanova, Alesja; Štefanić, Goran; Ehrensperger, Martin; Scheu, Christina; Parkinson, Bruce A; Fattakhova-Rohlfing, Dina; Bein, Thomas

    2016-02-17

    A sol-gel method for the synthesis of semiconducting FeCrAl oxide photocathodes for solar-driven hydrogen production was developed and applied for the production of meso- and macroporous layers with the overall stoichiometry Fe0.84Cr1.0Al0.16O3. Using transmission electron microscopy and energy-dispersive X-ray spectroscopy, phase separation into Fe- and Cr-rich phases was observed for both morphologies. Compared to prior work and to the mesoporous layer, the macroporous FeCrAl oxide photocathode had a significantly enhanced photoelectrolysis performance, even at a very early onset potential of 1.1 V vs RHE. By optimizing the macroporous electrodes, the device reached current densities of up to 0.68 mA cm(-2) at 0.5 V vs RHE under AM 1.5 with an incident photon-to-current efficiency (IPCE) of 28% at 400 nm without the use of catalysts. Based on transient measurements, this performance increase could be attributed to an improved collection efficiency. At a potential of 0.75 V vs RHE, an electron transfer efficiency of 48.5% was determined. PMID:26743183

  12. Transmission photocathodes based on stainless steel mesh coated with deuterated diamond like carbon films

    NASA Astrophysics Data System (ADS)

    Huran, J.; Balalykin, N. I.; Feshchenko, A. A.; Kobzev, A. P.; Kleinová, A.; Sasinková, V.; Hrubčín, L.

    2014-07-01

    In this study we report on the dependence of electron emission properties on the transmission photocathodes DC gun based on stainless steel mesh coated with diamond like carbon films prepared at various technological conditions. Diamond like carbon films were deposited on the stainless steel mesh and silicon substrate by plasma enhanced chemical vapor deposition from gas mixtures CH4+D2+Ar, CH4+H2+Ar and reactive magnetron sputtering using a carbon target and gas mixtures Ar+D2, Ar+H2. The concentration of elements in films was determined by Rutherford backscattering spectrometry (RBS) and elastic recoil detection (ERD) analytical methods simultaneously. Chemical compositions were analyzed by Fourier transform infrared spectroscopy (FT-IR). Raman spectroscopy at visible excitation wavelength was used for the intensity ratio determination of Gaussian fit D-peak and G-peak of Raman spectra. The quantum efficiency was calculated from the measured laser energy and the measured cathode charge. The quantum efficiency of a prepared transmission photocathode was increased with increasing intensity ratio of D-peak and G-peak, which was increased by adding deuterium to the gas mixture and using technology reactive magnetron sputtering.

  13. Cold Photocathode Electron Sources and Perspectives for Low-Energy Magnetically Guided Electron Beams

    SciTech Connect

    Orlov, D. A.; Fadil, H.; Grieser, M.; Wolf, A.

    2006-10-18

    Cold electron beams from a cryogenic GaAs photocathode source, developed for the electron target of the Heidelberg TSR, will serve as a major tool to cool the ions and to study electron-ion interactions at the low-energy electrostatic Cryogenic Storage Ring which will be built in the institute. The photocathode source delivers electrons within emission energy spreads of about 10 meV allowing to reach low longitudinal and transverse temperatures of magnetized electron beams of eV energies and finally to improve cooling rates and the energy resolution in merged beam experiments. We propose a new electron-ion merging scheme for a low-energy cooler which improves magnetic field homogeneity in the beam merging area and, in contrast to standard schemes, does not deteriorate the dynamics of the low-energy ions in the ring through non-linear coupling. Even for 20 keV protons, magnetic guiding fields of about 50 G, as is required to suppress electron temperature heating, can be used this way. The electric and magnetic fields of the individual elements of the ring and cooler were calculated with the TOSCA code and models of the entire ring were simulated by particle tracking.

  14. Solar Hydrogen Production from Zinc Telluride Photocathode Modified with Carbon and Molybdenum Sulfide.

    PubMed

    Jang, Youn Jeong; Lee, Jaehyuk; Lee, Jinwoo; Lee, Jae Sung

    2016-03-30

    A zinc telluride (ZnTe) film modified with MoS2 and carbon has been studied as a new photocathode for solar hydrogen production from photoelectrochemical (PEC) water splitting. The modification enhances PEC activity and stability of the photocathode. Thus, the MoS2/C/ZnTe/ZnO electrode exhibits highly improved activity of -1.48 mA cm(-2) at 0 VRHE with a positively shifted onset potential up to 0.3 VRHE relative to bare ZnO/ZnTe electrode (-0.19 mA cm(-2), 0.18 VRHE) under the simulated 1 sun illumination. This represents the highest value ever reported for ZnTe-based electrodes in PEC water splitting. The carbon densely covers the surface of ZnTe to protect it against photocorrosion in aqueous electrolyte and improves charge separation. In addition, MoS2 further enhances the PEC performance as a hydrogen evolution co-catalyst. PMID:26909873

  15. Hydrogen evolution from a copper(I) oxide photocathode coated with an amorphous molybdenum sulphide catalyst

    NASA Astrophysics Data System (ADS)

    Morales-Guio, Carlos G.; Tilley, S. David; Vrubel, Heron; Grtzel, Michael; Hu, Xile

    2014-01-01

    Concerns over climate change resulting from accumulation of anthropogenic carbon dioxide in the atmosphere and the uncertainty in the amount of recoverable fossil fuel reserves are driving forces for the development of renewable, carbon-neutral energy technologies. A promising clean solution is photoelectrochemical water splitting to produce hydrogen using abundant solar energy. Here we present a simple and scalable technique for the deposition of amorphous molybdenum sulphide films as hydrogen evolution catalyst onto protected copper(I) oxide films. The efficient extraction of excited electrons by the conformal catalyst film leads to photocurrents of up to -5.7mAcm-2 at 0V versus the reversible hydrogen electrode (pH 1.0) under simulated AM 1.5 solar illumination. Furthermore, the photocathode exhibits enhanced stability under acidic environments, whereas photocathodes with platinum nanoparticles as catalyst deactivate more rapidly under identical conditions. The work demonstrates the potential of earth-abundant light-harvesting material and catalysts for solar hydrogen production.

  16. Heat load of a P-doped GaAs photocathode in SRF electron gun

    SciTech Connect

    Wang, E.; Ben-Zvi, I.; Kewisch, J.; Burrill, A.; Rao, T.; Wu, Q.; Jain, A.; Gupta, R.; Holmes, D.

    2010-05-23

    Many efforts were made over the last decades to develop a better polarized electron source for the high energy physics. Several laboratories operate DC guns with the Gallium-Arsenide photo-cathode, which yield a highly polarized electron beam. However, the beam's emittance might well be improved using a Superconducting RF electron gun, which delivers beams of higher brightness than DC guns does, because the field gradient at the cathode is higher. SRF guns with metal cathodes and CsTe cathodes have been tested successfully. To produce polarized electrons, a Gallium-Arsenide photo-cathode must be used: an experiment to do so in a superconducting RF gun is under way at BNL. Since the cathode will be normal conducting, the problem about the heat load stemming from the cathode arises. We present our measurements of the electrical resistance of GaAs at cryogenic temperatures, a prediction of the heat load and the verification by measuring the quality factor of the gun with and without cathode.

  17. Environmental mercury contamination around a chlor-alkali plant

    SciTech Connect

    Lodenius, M.; Tulisalo, E.

    1984-04-01

    The chlor-alkali industry is one of the most important emitters of mercury. This metal is effectively spread from chlor-alkali plants into the atmosphere and it has been reported that only a few percent of the mercury emissions are deposited locally the major part spreading over very large areas. The purpose of this investigation was to study the spreading of mercury up to 100 km from a chlor-alkali plant using three different biological indicators.

  18. Determination of the common and rare alkalies in mineral analysis

    USGS Publications Warehouse

    Wells, R.C.; Stevens, R.E.

    1934-01-01

    Methods are described which afford a determination of each member of the alkali group and are successful in dealing with the quantities of the rare alkalies found in rocks and minerals. The procedures are relatively rapid and based chiefly on the use of chloroplatinic acid, absolute alcohol and ether, and ammonium sulfate. The percentages of all the alkalies found in a number of minerals are given.

  19. Electrochemical devices utilizing molten alkali metal electrode-reactant

    DOEpatents

    Hitchcock, D.C.; Mailhe, C.C.; De Jonghe, L.C.

    1985-07-10

    Electrochemical cells are provided with a reactive metal to reduce the oxide of the alkali metal electrode-reactant. Cells employing a molten alkali metal electrode, e.g., sodium, in contact with a ceramic electrolyte, which is a conductor of the ions of the alkali metal forming the electrode, exhibit a lower resistance when a reactive metal, e.g., vanadium, is allowed to react with and reduce the alkali metal oxide. Such cells exhibit less degradation of the electrolyte and of the glass seals often used to joining the electrolyte to the other components of the cell under cycling conditions.

  20. Electrochemical devices utilizing molten alkali metal electrode-reactant

    DOEpatents

    Hitchcock, David C. (Omaha, NE); Mailhe, Catherine C. (Berkeley, CA); De Jonghe, Lutgard C. (Oakland, CA)

    1986-01-01

    Electrochemical cells are provided with a reactive metal to reduce the oxide of the alkali metal electrode-reactant. Cells employing a molten alkali metal electrode, e.g., sodium, in contact with a ceramic electrolyte, which is a conductor of the ions of the alkali metal forming the electrode, exhibit a lower resistance when a reactive metal, e.g., vanadium, is allowed to react with and reduce the alkali metal oxide. Such cells exhibit less degradation of the electrolyte and of the glass seals often used to joining the electrolyte to the other components of the cell under cycling conditions.