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Samson, J. A. R.

Publications and source records attributed to Samson, J. A. R..

At least 19 records
All sourcesNASA NTRSDOE OSTI
NASA NTRS1994

A photoionization study of OH and OD from 680A to 950A: An analysis of the Rydberg series

The photoionization spectra of OH(+) and OD(+) have been reported from 680 to 950 A (18.23 to 13.05 eV) at a wavelength resolution of 0.07 A. Through interpretation of both spectra, the Rydberg series and their higher vibrational members have been reported for three of the excited ionic states, a(sup 1)Delta, A(sup 3)Pi(i), and b(sup 1) Sigma(sup +). A vibrational progression has also been observed in both OH(+) and OD(+) which is apparently related to a fourth excited ionic state, c(sup 1)Pi. Finally, the dissociative ionization limits, corrected to 0 K,for H2O AND D2O have been measured to be 18.11+/-0.01 and 18.21+/-0.01 eV, respectively, and shown to be in good agreement with previously reported results.

Cutler, J. N.↗
NASA NTRS1994

An Optics Free Spectrometer for the Extreme Ultraviolet

The optics-free spectrometer is a photon spectrometer. It provides the photon spectrum of a broadband source by converting photons of energy E into electrons of energy E', according to the Einstein relation, E' = E - Ei. E, is the ionization threshold of the gas target of interest (any of the rare gases are suitable) and E is the incoming photon energy. As is evident from the above equation, only a single order spectrum is produced throughout the energy range between the first and second ionization potentials of the rare gas used. Photons with energy above the second ionization potential produce two groups of electrons, but they are readily distinguished from each other. This feature makes this device extremely useful for determining the true spectrum of a continuum source or a many line source. The principle of operation and the laboratory results obtained with a representative configuration of the optics-free spectrometer are presented.

Judge, D. L.↗
NASA NTRS1992

A rare gas optics-free absolute EUV photon spectrometer for solar system studies

We have developed a prototype spectrometer for space applications which require long term absolute EUV photon flux measurements. In this recently developed spectrometer, the energy spectrum of the incoming photons is transformed directly into an electron energy spectrum by taking advantage of the photoelectric effect in one of several rare gases at low pressures. Using an electron energy spectrometer operating at a few eV, and followed by an electron multiplying detector, pulses due to individual electrons are counted. The overall efficiency of this process is essentially independent of gain drifts in the signal path, and the secular degradation of optical components which is often a problem in other techniques is avoided.

Daybell, M. D.↗
NASA NTRS1986

Relative fluorescent efficiency of sodium salicylate between 90 and 800 eV

The relative fluorescent quantum efficiency of sodium salicylate was measured between 90 and 800 eV (138-15 A) by the use of synchrotron radiation. A general increase in efficiency was observed in this spectral range except for abrupt decreases in efficiency at the carbon and oxygen K-edges. Beyond the oxygen K-edge (532 eV) the efficiency increased linearly with the incident photon energy to the limit of the present observations.

Angel, G. C.↗
NASA NTRS1986

Total absorption and photoionization cross sections of water vapor between 100 and 1000 A

Absolute photoabsorption and photoionization cross sections of water vapor are reported at a large number of discrete wavelengths between 100 and 1000 A with an estimate error of + or - 3 percent in regions free from any discrete structure. The double ionization chamber technique utilized is described. Recent calculations are shown to be in reasonable agreement with the present data.

Haddad, G. N.↗
NASA NTRS1986

The relative fluorescent efficiency of sodium salicylate between 90 and 800 eV

The relative fluorescent quantum efficiency of sodium salicylate was measured between 90 and 800 eV (138 -15 A) by the use of synchrotron radiation. A general increase in efficiency was observed in this spectral range except for abrupt decreases in efficiency at the carbon and oxygen K-edges. Beyond the oxygen K-edge (532 eV) the efficiency increased linearly with the incident photon energy to the limit of the present observations.

Angel, G. C.↗
NASA NTRS1985

Dissociative and double photoionization cross sections of NO from threshold to 120 A

The partial photoionization cross sections for producing the NO(+) parent ion and the O(+), N(+), and NO(2+) fragmentations from neutral NO are presented from 120 to 614 A. The results indicate predissociation of the 3 pi (21.72 eV) and B-prime 1Sigma(+) (22.73 eV) electronic states of NO(+). The photoionization threshold for double ionization was found to be 39.4 + or - 0.12 eV.

Samson, J. A. R.↗
NASA NTRS1985

Kinetic energies of fragment ions produced by dissociative photoionization of NO

The kinetic energies of ions produced by dissociative photoionization of NO have been measured at the discrete resonance lines of He (584A) and Ne (736A), and with undispersed synchrotron radiation. O sup + ions were identified with energies from 0 to approximately 0.5 eV and two groups of N sup + ions one with energy of 0.36 eV and another with energies between 0.9 and 1.5 eV, apparently produced by predissociation of the C sup 3 P 1 and B'1 sigma states respectively.

Samson, J. A. R.↗
NASA NTRS1985

Absolute photoionization cross sections of atomic oxygen

The absolute values of photoionization cross sections of atomic oxygen were measured from the ionization threshold to 120 A. An auto-ionizing resonance belonging to the 2S2P4(4P)3P(3Do, 3So) transition was observed at 479.43 A and another line at 389.97 A. The experimental data is in excellent agreement with rigorous close-coupling calculations that include electron correlations in both the initial and final states.

Samson, J. A. R.↗
NASA NTRS1985

Kinetic energies of fragment ions produced by dissociative photoionization of NO

The kinetic energies of ions produced by dissociative photoionization of NO have been measured at the discrete resonance lines of He (584A) and Ne (736A), and with undispersed synchrotron radiation. O sup + ions were identified with energies from 0 to approximately 0.5 eV and two groups of N sup + ions one with energy of 0.36 eV and another with energies between 0.9 and 1.5 eV, apparently produced by predissociation of the C sup 3 P 1 and B'1 sigma states respectively.

Samson, J. A. R.↗
NASA NTRS1985

Dissociative and double photoionization cross sections of NO from threshold to 120 A

The partial photoionization cross sections for producing the NO(+) parent ion and the O(+), N(+), and NO2(+) fragment ions from neutral NO are presented from 120 to 614 A. The results indicate predissociation of the c(sup3) pi (21.72 eV) and B prime (sup 1) sigma (+) (22.73 eV) electronic states of NO(+). The photoionization threshold for double ionization was found to be 39.4 + or 0.12 eV.

Samson, J. A. R.↗
NASA NTRS1982

Atomic photoionization

After a brief historical review, this work discusses in detail the experimental techniques available for the investigation of photoionization processes, presents results on typical atoms, and examines some of the problems yet unsolved; in general, the discussion is concerned primarily with the photoionization of atoms in the spectral range from ionization threshold to about 100 A. The examination of experimental techniques treats such topics as light sources, monochromators and spectrographs, absorption and photoionization cells, branching-ratio studies, and electron-impact 'photoionization'. Photoionization measurements are discussed with reference to total and partial photoionization cross sections.

Samson, J. A. R.↗
NASA NTRS1982

Absolute photoionization cross sections of atomic oxygen

The absolute values of photoionization cross sections of atomic oxygen were measured from the ionization threshold to 120 A. An auto-ionizing resonance belonging to the 2S2P4(4P)3P(3Do, 3So) transition was observed at 479.43 A and another line at 389.97 A. The experimental data is in excellent agreement with rigorous close-coupling calculations that include electron correlations in both the initial and final states.

Samson, J. A. R.↗
NASA NTRS1981

The production rate of C/+/ from the photoionization of CO and CO2

The dissociative photoionization cross sections for the production of C(+) ions are presented for the spectral region from the dissociative ionization threshold to 90 A. The cross sections are considerably larger than previously published data and should therefore influence the calculations of the C(+) concentrations in the Mars and Venus ionospheres. It is suggested that the released energy in the C(+) fragment ion could reduce the loss rate of the ions in collisional processes, thereby accounting for the apparent discrepancies between the observed and calculated C(+) ion density in the Venus ionosphere.

Samson, J. A. R.↗
NASA NTRS1981

Dissociative and double photoionization of CO from threshold to 90 A

Partial cross sections for molecular photoionization (CO(+)), dissociative photoionization (C(+) and O(+)), and dissociative double photoionization (C(2+)) in CO have been measured from their thresholds to 90 A using techniques of mass spectrometry. The results are compared with data reported previously. Several peaks observed in the cross section curves for dissociated fragments are tentatively assigned by comparing with those in the photoelectron spectra reported for CO. It is concluded that the shoulder in the total absorption cross section curve between 400 and 90 A results solely from the dissociative ionization processes.

Masuoka, T.↗
NASA NTRS1979

Dissociative and double photoionization of CO2 from threshold to 90 A

The molecular photoionization, dissociative photoionization and double photoionization cross sections for CO2 were measured from their onsets down to 90 A by using various combinations of mass spectrometers (a coincidence time-of-flight mass spectrometer and a magnetic mass spectrometer) and light sources (synchrotron radiation, and glow and spark discharge). It is concluded that the one broad peak and the three shoulders in the total adsorption cross section curve between 640 and 90 A are caused completely by dissociative ionization processes. Several peaks observed in the cross section curve for the total fragmentation CO(+)3, O(+) and C(+) are compared with those in the photoelectron spectrum reported for CO2.

Masuoka, T.↗