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Full-Text Articles in Physical Sciences and Mathematics
Auger Analysis Of Si–H Bonding And Hydrogen Concentration In Hydrogenated Amorphous Silicon, Nancy Burnham, Aj Nelson, Ab Schwartzlander, Se Asher, Ll Kazmerski
Auger Analysis Of Si–H Bonding And Hydrogen Concentration In Hydrogenated Amorphous Silicon, Nancy Burnham, Aj Nelson, Ab Schwartzlander, Se Asher, Ll Kazmerski
Nancy A. Burnham
Auger electron spectroscopy line‐shape analysis of the Si‐L 2 3 V V peak has been performed on hydrogenated amorphous silicon (a‐Si:H). Both a‐Si:H produced by hydrogen implantation of siliconsingle crystals (for analytical standards) and thin films (fabricated for solar cell applications) were examined in these studies. Hydrogen concentrations were confirmed by secondary ion mass spectrometry, and samples having hydrogen content over the range 101 6–102 2 cm− 3 were evaluated. Correlations between the area under the deconvoluted L 2 3 V V transition peak and the known hydrogen content have resulted in a semiquantitative method of determining hydrogen concentration using …
Scanning Auger Microprobe Studies Of Ball Cratered Cds/Cuinse2 Solar Cells, Nancy Burnham, Ll Levenson, Rj Matson, R Noufi, Ll Kazmerski
Scanning Auger Microprobe Studies Of Ball Cratered Cds/Cuinse2 Solar Cells, Nancy Burnham, Ll Levenson, Rj Matson, R Noufi, Ll Kazmerski
Nancy A. Burnham
CdS/CuInSe2solar cell films are typically several micrometers thick. Composition profiles of these films are usually carried out on fracture cross sections by scanning Auger microscopy or by recording Auger spectra during ion milling. For fracture cross sections, the depth resolution depends on the electron beam diameter and the roughness of the fracture surface. Ion milling is time consuming, and artifacts are caused by ion beam faceting. Ball cratering requires only a fraction of an hour and provides significant magnification of the film cross section. There is sufficient contrast, both in optical and electron microscopy, to distinguish between CdS and CuInSe2 …
Improvement Of Trace Aluminum Determination By Electrothermal Atomic Absorption Spectrophotometry Using Phosphoric Acid, Chris Craney, Kurt Swartout, F. Smith, C. West
Improvement Of Trace Aluminum Determination By Electrothermal Atomic Absorption Spectrophotometry Using Phosphoric Acid, Chris Craney, Kurt Swartout, F. Smith, C. West
Chris L. Craney
No abstract provided.
Electrochemical Reduction Of Alkyl Halides At Vitreous Carbon Cathodes In Dimethylformamide, James Cleary, Mohammed Mubarak, Kenneth Viera, Mark Anderson, Dennis Peters
Electrochemical Reduction Of Alkyl Halides At Vitreous Carbon Cathodes In Dimethylformamide, James Cleary, Mohammed Mubarak, Kenneth Viera, Mark Anderson, Dennis Peters
Mark R. Anderson
At vitreous carbon electrodes in dimethylformamide which contains tetramethylammonium perchlorate, cyclic voltammograms for 1-iododecane, 1-bromodecane, and 2-bromooctane consist of one irreversible reduction wave signaling formation of the alkyl carbanion, whereas voltammograms for 2-iodooctane, t-butyl bromide, and t-butyl iodide reveal stepwise generation of the alkyl radical and carbanion. Large-scale electrolysis of 1-iododecane at reticulated vitreous carbon yields decane, eicosane, 1-decene, and 1-decanol; the first two compounds arise, respectively, from reaction of decyl carbanions with a proton donor and with unreduced alkyl iodide, whereas the last two species are produced via chemical attack of hydroxide ion on 1-iododecane. Reduction of 1-bromodecane results …
Electrochemistry Of 1,1,4,4-Tetraphenyl-1,3-Butadiene, 1,1,4,4-Tetraphenyl-1,2-Butadiene, And 1,1,4,4-Tetraphenyl-1-Butene In Dimethylformamide, Tsu-Yu Chen, Mark Anderson, Dennis Peters
Electrochemistry Of 1,1,4,4-Tetraphenyl-1,3-Butadiene, 1,1,4,4-Tetraphenyl-1,2-Butadiene, And 1,1,4,4-Tetraphenyl-1-Butene In Dimethylformamide, Tsu-Yu Chen, Mark Anderson, Dennis Peters
Mark R. Anderson
In dimethylformamide containing tetra-n-butylammonium perchlorate, 1,1,4,4-tetraphenyl-1-butene exhibits a single polarographic wave; preparative-scale reduction of the starting material produces 1,1,4,4-tetraphenylbutane.A polarogram for 1,1,4,4-tetraphenyl-1,3-butadiene consists of three waves. Large-scale electrolysis of 1,1,4,4-tetraphenyl-1,3-butadiene at potentials corresponding to either the first or second wave yields 1,1,4,4-tetraphenyl-1-butene in the absence of a proton donor and a mixture of 1,1,4,4-tetraphenyl-2-butene and 1,1,4,4-tetraphenyl-1-butene in the presence of excess glacial acetic acid. If 1,1,4,4-tetraphenyl-1,3-butadiene is electrolyzed at a potential on the third polarographic wave, one obtains 1,1,4,4-tetraphenylbutane in the absence of a proton donor but a mixture of 1,1,4,4-tetraphenyl-2-butene and 1,1,4,4-tetraphenylbutane in the presence of glacial acetic acid. …
A Highly Enantioselective Hydrolysis Of -3,5-Diacetoxycyclopent-1-Ene, Donald Deardorff, A. Matthews, D. Mcmeekin, Chris Craney
A Highly Enantioselective Hydrolysis Of -3,5-Diacetoxycyclopent-1-Ene, Donald Deardorff, A. Matthews, D. Mcmeekin, Chris Craney
Chris L. Craney
Exposure of -3,5-diacetoxycyclopent-1-ene () to the hydrolase enzyme acetylcholinesterase (from electric eel) affords In 94% yield 3()-acetoxy-5()-hydroxycyclopent-1-ene () with an e.e. of 96% (greater than 99% e.e. after one recrystallization).
Solution Of Systems With Toeplitz Matrices Generated By Rational Functions, William F. Trench
Solution Of Systems With Toeplitz Matrices Generated By Rational Functions, William F. Trench
William F. Trench
No abstract provided.
Extensions Of A Theorem Of Wintner On Systems With Asymptotically Constant Solutions, William F. Trench
Extensions Of A Theorem Of Wintner On Systems With Asymptotically Constant Solutions, William F. Trench
William F. Trench
No abstract provided.