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Journal articles on the topic 'Multi-Photon Ionization'

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Author: Grafiati

Published: 10 December 2022

Last updated: 28 January 2023

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1

Schuricke, Michael, Ganjun Zhu, Jochen Steinmann, Igor Ivanov, Anatoli Kheifets, Alexei Grum-Grzhimailo, Klaus Bartschat, Alexander Dorn, and Joachim Ullrich. "Multi-photon ionization of lithium." Journal of Physics: Conference Series 194, no. 3 (November 1, 2009): 032031. http://dx.doi.org/10.1088/1742-6596/194/3/032031.

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2

Gu, Zhen-Yu, and Pei-Yong Ji. "Multi-photon ionization in background of plasma." Journal of Shanghai University (English Edition) 6, no. 2 (June 2002): 141–44. http://dx.doi.org/10.1007/s11741-002-0022-3.

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3

Helle, Niklas, Tim Raeker, and Juergen Grotemeyer. "Studies of the First Electronically Excited State of 3-Fluoropyridine and Its Ionic Structure by Means of REMPI, Two-Photon MATI, One-Photon VUV-MATI Spectroscopy and Franck–Condon Analysis." Physical Chemistry Chemical Physics 24, no. 4 (2022): 2412–23. http://dx.doi.org/10.1039/d1cp04636e.

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3-Fluoropyridine has been investigated by means of resonance-enhanced multi photon ionization, mass-analyzed threshold ionization (MATI) and one-photon VUV-MATI spectroscopy to study the effect of m-fluorine substitution on the involved states.

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4

Kotelnikov, Igor A., and Aleksandr P. Shkurinov. "Multi-Photon Ionization by a Two-Color Laser Pulse." Siberian Journal of Physics 5, no. 4 (December 1, 2010): 108–12. http://dx.doi.org/10.54362/1818-7919-2010-5-4-108-112.

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A method of imaginary time [1] is used to calculate the probability of multi-photon ionization of atoms by a femtosecond laser field with an admixture of the second harmonic. The conditions for the second harmonic to dominate over the first harmonic in the course of ionization of atoms are found. It is shown that the average momentum of the photoelectrons ejected from an atom depends on the phase shift between the first and second harmonics, as well as on their mutual polarization. Asymptotic formulas for the ionization rate and the average momentum of photoelectrons are obtained. They generally confirm predictions of a phenomenological model based on the classical views [2]

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5

Köster, Claus, and Jürgen Grotemeyer. "Single-photon and multi-photon ionization of infrared laser-desorbed biomolecules." Organic Mass Spectrometry 27, no. 4 (April 1992): 463–71. http://dx.doi.org/10.1002/oms.1210270418.

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6

Inhester, Ludger, Kota Hanasaki, Koudai Toyota, Yajiang Hao, Oriol Vendrell, Sang-Kil Son, and Robin Santra. "Molecular ionization enhancement by charge rearrangement at high X-ray intensity." EPJ Web of Conferences 205 (2019): 06009. http://dx.doi.org/10.1051/epjconf/201920506009.

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We simulated the multi-photon multi-ionization dynamics of an iodomethane molecule, CH3I, exposed to ultraintense and ultrashort x-ray pulses. The strong ionization causes electronic charge rearrangement in the molecule that leads to an enhanced total charge.

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7

Ideböhn, Veronica, Alistair J. Sterling, Måns Wallner, Emelie Olsson, Richard J. Squibb, Ugne Miniotaite, Emma Forsmalm, et al. "Single photon double and triple ionization of allene." Physical Chemistry Chemical Physics 24, no. 2 (2022): 786–96. http://dx.doi.org/10.1039/d1cp04666g.

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Single photon double and triple ionization of allene is investigated using multi-particle coincidence spectroscopies. Key findings comprise supporting evidence for a previously proposed roaming mechanism in H3+ formation by double ionization.

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8

OGAWA, TEIICHIRO. "RECENT PROGRESS IN LASER MULTI-PHOTON IONIZATION SPECTROMETRY." Analytical Sciences 7, Supple (1991): 1475–78. http://dx.doi.org/10.2116/analsci.7.supple_1475.

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9

Schmitt, Michael, Frans Spiering, Vitali Zhaunerchyk, Rienk T. Jongma, Sander Jaeqx, Anouk M. Rijs, and Wim J. van der Zande. "Far-infrared spectra of the tryptamine A conformer by IR-UV ion gain spectroscopy." Physical Chemistry Chemical Physics 18, no. 47 (2016): 32116–24. http://dx.doi.org/10.1039/c6cp02358d.

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Single-far-infrared photon excited tryptamine has structured resonance enhanced multi-photon ionization UV spectra, revealing the mode composition of the S₁-state. Upon multiple-far-infrared photon absorption, the UV spectrum broadens allowing ion gain spectroscopy to be performed.

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10

OGAWA, Teiichiro. "Highly sensitive analysis by laser multi-photon ionization spectrometry." Bunseki kagaku 42, no. 4 (1993): 201–7. http://dx.doi.org/10.2116/bunsekikagaku.42.4_201.

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11

von Helden, G., I. Holleman, M. Putter, A. J. A. van Roij, and G. Meijer. "Infrared resonance enhanced multi-photon ionization spectroscopy of C84." Chemical Physics Letters 299, no. 2 (January 1999): 171–76. http://dx.doi.org/10.1016/s0009-2614(98)01259-7.

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12

Vinerot, Nataly, Yuheng Chen, Valery Bulatov, Vladimir V. Gridin, Victoria Fun-Young, and Israel Schechter. "Spectral characterization of surfaces using laser multi-photon ionization." Optical Materials 34, no. 2 (December 2011): 329–35. http://dx.doi.org/10.1016/j.optmat.2011.05.016.

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13

Kotochigova, S., and P. Lambropoulos. "Theory of multi-photon ionization and autoionization of SI." Zeitschrift f�r Physik D Atoms, Molecules and Clusters 31, no. 1-2 (March 1994): 41–48. http://dx.doi.org/10.1007/bf01426576.

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14

Arbó, Diego G., Kenichi L. Ishikawa, Klaus Schiessl, Emil Persson, and Joachim Burgdörfer. "Wavelength dependent channel-closing enhancements in multi-photon ionization." Journal of Physics: Conference Series 194, no. 2 (November 1, 2009): 022037. http://dx.doi.org/10.1088/1742-6596/194/2/022037.

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15

Fain, B., H. Kono, S. H. Lin, W. E. Henke, H. L. Selzle, and E. W. Schlag. "Theory of Multi-Photon Ionization of Atoms and Molecules." Journal of the Chinese Chemical Society 32, no. 3 (September 1985): 187–99. http://dx.doi.org/10.1002/jccs.198500032.

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16

Kastner, Alexander, Greta Koumarianou, Pavle Glodic, Peter C. Samartzis, Nicolas Ladda, Simon T. Ranecky, Tom Ring, et al. "High-resolution resonance-enhanced multiphoton photoelectron circular dichroism." Physical Chemistry Chemical Physics 22, no. 14 (2020): 7404–11. http://dx.doi.org/10.1039/d0cp00470g.

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By combining molecular beam techniques with high resolution resonance enhanced multi photon ionization followed by angular resolved photoelectron detection we pave the way for enantiomer specific molecular identification in multi-component mixtures.

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17

Laufer, Gabriel, and Anthony S. Lee. "Water assisted multi-photon ionization of N2 by KrF lasers." Chemical Physics Letters 266, no. 5-6 (March 1997): 584–90. http://dx.doi.org/10.1016/s0009-2614(97)00044-4.

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18

Du, D., X. Liu, and G. Mourou. "Reduction of multi-photon ionization in dielectrics due to collisions." Applied Physics B: Lasers and Optics 63, no. 6 (December 1, 1996): 617–21. http://dx.doi.org/10.1007/s003400050131.

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19

Neusser, H. J., H. Kühlewind, U. Boesl, and De E. W. Schlag. "Unimolecular Decay of Polyatomic Ions Prepared by Multi-Photon Ionization." Berichte der Bunsengesellschaft für physikalische Chemie 89, no. 3 (March 1985): 276–81. http://dx.doi.org/10.1002/bbpc.19850890318.

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20

Du, D., X. Liu, and G. Mourou. "Reduction of multi-photon ionization in dielectrics due to collisions." Applied Physics B Laser and Optics 63, no. 6 (December 1996): 617–21. http://dx.doi.org/10.1007/bf01831002.

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21

Ma, Kun, Lin-Fan Zhu, and Lu-You Xie. "Non-dipole effects on angular distribution of photoelectrons in sequential two-photon double ionization of Ar atom and K<sup>+</sup> ion." Acta Physica Sinica 71, no. 6 (2022): 063201. http://dx.doi.org/10.7498/aps.71.20211905.

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Owing to the development of XUV and X ray of the free-electron lasers, the photoelectron angular distribution in the sequential two-photon double ionization has received increasing attention of theorists and experimentalists, because it provides the valuable information about the electronic structure of atom or molecule systems and allows the obtaining of additional information about mechanisms and pathways of the two-photon double ionization. In this paper, the expression of the sequential two-photon double ionization process of the photoelectron angular distributions, including the non-dipole effects, is obtained based on the multi-configuration Dirac-Fock method and the density matrix theory, and the corresponding calculation code is also developed. Based on the code, the sequential two-photon double ionization process of the 3p and 2p shells of Ar atom and K<sup>+</sup> ion are studied, in which, the dipole and the non-dipole parameters of photoelectron angular distribution are investigated systematically. It is found that the angular distributions of the first- and second-step electrons in sequential two-photon double ionization are similar and the two photoionization processes affect each other. Near the ionization threshold, the photoionization cross-sections and anisotropy parameters for the 3p shell and the 2p shell show a large difference. While away from the threshold, the cross-section and angular anisotropy parameters of the 3p and 2p shells show similar behaviors. At the position of Cooper minimum of the photoionization cross section, the contribution of the electric dipole is suppressed, and the non-dipole effect is obvious. The non-dipole effect leads to a forward-backward asymmetric distribution of photoelectrons relative to the direction of incident light. The results of this paper will be helpful in studying the nonlinear processes of photon and matter interaction in the XUV range.

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22

Zhang, Gui Yin, Yi Dong Jin, and Hai Ming Zheng. "Detection of Atmospheric Pollutant NO With the Method of Resonant-Enhanced Multiphoton Ionization." Applied Mechanics and Materials 209-211 (October 2012): 1596–99. http://dx.doi.org/10.4028/www.scientific.net/amm.209-211.1596.

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NO is one of the key substances of air pollution. This paper presents the use of the technique of resonant enhanced multi-photon ionization (REMPI) for NO ambient detection. NO is ionized by absorbing four photons and via A2Σ intermediate resonant state when use 452.4nm laser as radiation source. A physical model concerning the ionization process is presented. It is shown that the ion signal depends on laser character and the dynamic parameters of NO. Two-photon absorption and ionization cross section about the resonant state are obtained from the ion decay curve and the model. The detection limit of this work, which can reach 1.4 ppm, is determined by measuring the variation of the ion signal with the concentration of NO.

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23

Grotemeyer, Jürgen, Ulrich Boesl, Klaus Walter, and Edward W. Schlag. "A general soft ionization method for mass spectrometry: Resonance-enhanced multi-photon ionization of biomolecules." Organic Mass Spectrometry 21, no. 10 (October 1986): 645–53. http://dx.doi.org/10.1002/oms.1210211008.

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24

Tian, Yuan-Ye, Chun-Cheng Wang, Su-Yu Li, Fu-Ming Guo, Da-Jun Ding, Roeterdink Wim-G, Ji-Gen Chen, Si-Liang Zeng, Xue-Shen Liu, and Yu-Jun Yang. "Influence of multi-photon excitation on the atomic above-threshold ionization." Chinese Physics B 24, no. 4 (March 31, 2015): 043202. http://dx.doi.org/10.1088/1674-1056/24/4/043202.

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25

Ilchen, M., N. Douguet, T. Mazza, A. J. Rafipoor, C. Callegari, P. Finetti, O. Plekan, et al. "Circular Dichroism in the Multi-Photon Ionization of Oriented Helium Ions." Journal of Physics: Conference Series 875 (July 2017): 022029. http://dx.doi.org/10.1088/1742-6596/875/3/022029.

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26

Pomerantz, Andrew E., and Richard N. Zare. "Doppler-free multi-photon ionization: a proposal for enhancing ion images." Chemical Physics Letters 370, no. 3-4 (March 2003): 515–21. http://dx.doi.org/10.1016/s0009-2614(03)00158-1.

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27

Heaven, Michael C. "Probing actinide electronic structure using fluorescence and multi-photon ionization spectroscopy." Physical Chemistry Chemical Physics 8, no. 39 (2006): 4497. http://dx.doi.org/10.1039/b607486c.

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28

Ryszka, M., R. Pandey, C. Rizk, J. Tabet, B. Barc, M. Dampc, N. J. Mason, and S. Eden. "Dissociative multi-photon ionization of isolated uracil and uracil-adenine complexes." International Journal of Mass Spectrometry 396 (February 2016): 48–54. http://dx.doi.org/10.1016/j.ijms.2015.12.006.

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29

Zhang, Guiyin, Haiping Li, Weijia Jin, and Mengjun Li. "Theoretical investigation of 2+2 resonance enhanced multi-photon ionization probability." Optik - International Journal for Light and Electron Optics 124, no. 18 (September 2013): 3627–30. http://dx.doi.org/10.1016/j.ijleo.2012.11.069.

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30

Goto, M., and K. Hansen. "Competitive ionization processes of anthracene excited with a femtosecond pulse in the multi-photon ionization regime." Journal of Chemical Physics 135, no. 21 (December 7, 2011): 214310. http://dx.doi.org/10.1063/1.3663618.

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31

Liu, Hang, Wenliang Li, and Liqiang Feng. "Chirp control of multi-photon resonance ionization and charge-resonance enhanced ionization on molecular harmonic generation." Chemical Physics Letters 676 (May 2017): 118–23. http://dx.doi.org/10.1016/j.cplett.2017.03.049.

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32

Chiu, Ying-Nan, and Lue-Yung Chow Chiu. "An alternative mechanism for spin-forbidden photo-ionization of diatomic molecules and its rotation–electronic selection rules." Canadian Journal of Physics 68, no. 2 (February 1, 1990): 177–83. http://dx.doi.org/10.1139/p90-025.

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The spin-forbidden photo-ionization of diatomic molecules is proposed. Spin orbit interaction is invoked resulting in the correction and mixing of the wave functions of different multiplicities. The rotation–electronic selection rules given, but not proven, by Dixit and McKoy for Hund's case a based on the conventional mechanism of electric dipole transition (see Chem. Phys. Lett. 128, 49 (1986) are rederived and expressed in a different format. This new format permits the generalization of the selection rules to other photo-ionization transitions caused by the magnetic dipole, the electric quadrupole, and the two- and three-photon operators. These selection rules, which are for transitions from one specific rotational level of a given Kronig reflection symmetry to another, will help understand rotational branching and the dynamics of interaction in the excited state. They will also help in the selective preparation of well-defined rovibronic states in resonant-enhanced multi-photon ionization processes.

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33

Mauritsson, J., P. Johnsson, R. López-Martens, K. Varjú, A. L'Huillier, M. B. Gaarde, and K. J. Schafer. "Probing temporal aspects of high-order harmonic pulses via multi-colour, multi-photon ionization processes." Journal of Physics B: Atomic, Molecular and Optical Physics 38, no. 13 (June 15, 2005): 2265–78. http://dx.doi.org/10.1088/0953-4075/38/13/018.

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34

Näher, U., H. Göhlich, T. Lange, and T. P. Martin. "Observation of Highly Charged Sodium Clusters." International Journal of Modern Physics B 06, no. 23n24 (December 1992): 3721–30. http://dx.doi.org/10.1142/s021797929200178x.

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Singly charged sodium clusters have been multiply ionized in the drift tube of a TOF-mass-spectrometer. By this method multi-step photoionization of clusters can be examined mass selectively. Up to fourteenfold positively charged clusters have been observed in the mass spectra. The upper limit for multiple ionization is found to be exclusively a function of cluster size and photon energy. The energy required for each stage of ionization varies with cluster size in a manner well described by a purely classical electrostatic model.

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35

KAWAZUMI, Hirofumi, To-oru YASUDA, and Teiichiro OGAWA. "Application of Laser Multi-Photon Ionization Detection to Thin-Layer Chromatographic Plates." Analytical Sciences 9, no. 2 (1993): 309–10. http://dx.doi.org/10.2116/analsci.9.309.

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36

YAMADA, Sunao, Nariaki SATO, Hirofumi KAWAZUMI, and Teiichiro OGAWA. "Laser multi-photon ionization of PAHs in solution. Analysis of photocurrent signal." Journal of the Spectroscopical Society of Japan 37, no. 1 (1988): 18–23. http://dx.doi.org/10.5111/bunkou.37.18.

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37

Bartelt, A., A. Lindinger, C. Lupulescu, Š. Vajda, and L. Wöste. "Optimal control of multi-photon dissociation and ionization processes in small NamKnclusters." Phys. Chem. Chem. Phys. 6, no. 8 (2004): 1679–86. http://dx.doi.org/10.1039/b317107h.

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38

Weber, Th, M. Weckenbrock, A. Staudte, M. Hattass, L. Spielberger, O. Jagutzki, V. Mergel, et al. "Atomic dynamics in single and multi-photon double ionization: An experimental comparison." Optics Express 8, no. 7 (March 26, 2001): 368. http://dx.doi.org/10.1364/oe.8.000368.

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39

Secor, Ethan, Xiaoxu Guan, Klaus Bartschat, and Barry I. Schneider. "Multi-photon ionization of the H+2molecule by an xuv laser pulse." Journal of Physics: Conference Series 388, no. 3 (November 5, 2012): 032076. http://dx.doi.org/10.1088/1742-6596/388/3/032076.

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40

Abeln, Brant, Daniel Weflen, Klaus Bartschat, and Alexei N. Grum-Grzhimailo. "Angular distribution in multi-photon ionization of hydrogen in intense laser fields." Journal of Physics: Conference Series 194, no. 3 (November 1, 2009): 032034. http://dx.doi.org/10.1088/1742-6596/194/3/032034.

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41

Sakamoto, Tetsuo, Jyunji Kawasaki, and Masaomi Koizumi. "Instrumental factors in resonance enhanced multi-photon ionization of FIB-sputtered atoms." Applied Surface Science 255, no. 4 (December 2008): 1580–83. http://dx.doi.org/10.1016/j.apsusc.2008.05.006.

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42

Koizumi, M., and T. Sakamoto. "Resonance enhanced multi-photon ionization of neutral atoms sputtered with Ga-FIB." Applied Surface Science 255, no. 4 (December 2008): 901–4. http://dx.doi.org/10.1016/j.apsusc.2008.05.061.

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43

Arimondo, E., C. E. Burkhardt, F. Giammanco, L. J. Qin, and A. Vellante. "Multi-photon laser ionization of sodium in the 540–600 nm range." Optics Communications 71, no. 1-2 (May 1989): 52–58. http://dx.doi.org/10.1016/0030-4018(89)90303-9.

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44

Koga, Masafumi, Yusuke Yoneda, Hikaru Sotome, and Hiroshi Miyasaka. "Ionization dynamics of a phenylenediamine derivative in solutions as revealed by femtosecond simultaneous and stepwise two-photon excitation." Physical Chemistry Chemical Physics 21, no. 6 (2019): 2889–98. http://dx.doi.org/10.1039/c8cp06530f.

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45

Kudryashov, S. I., P. A. Danilov, E. D. Startseva, and A. A. Ionin. "Multi-zone single-shot femtosecond laser ablation of silica glass at variable multi-photon ionization paths." Journal of the Optical Society of America B 35, no. 10 (August 31, 2018): B38. http://dx.doi.org/10.1364/josab.35.000b38.

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46

Ivanov, I. A., and A. S. Kheifets. "On the use of the Kramers–Henneberger Hamiltonian in multi-photon ionization calculations." Journal of Physics B: Atomic, Molecular and Optical Physics 38, no. 13 (June 15, 2005): 2245–55. http://dx.doi.org/10.1088/0953-4075/38/13/016.

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47

Sorokin, A. A., S. V. Bobashev, K. Tiedtke, and M. Richter. "Multi-photon ionization of molecular nitrogen by femtosecond soft x-ray FEL pulses." Journal of Physics B: Atomic, Molecular and Optical Physics 39, no. 14 (June 30, 2006): L299—L304. http://dx.doi.org/10.1088/0953-4075/39/14/l04.

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48

Welkie, David G. "Non-resonant multi- and single-photon ionization for the chemical characterization of surfaces." Proceedings, annual meeting, Electron Microscopy Society of America 50, no. 2 (August 1992): 1554–55. http://dx.doi.org/10.1017/s0424820100132406.

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The chemical analysis of surfaces, where the ‘surface’ of a sample refers to the top few monolayers, is most commonly performed using the techniques of Auger electron spectroscopy (AES), secondary ion mass spectrometry (SIMS), and/or electron spectroscopy for chemical analysis (ESCA). For inorganic materials, AES is especially advantageous for quantitative elemental surface analysis at high spatial resolution. At lower spatial resolutions, SIMS generally provides the highest sensitivity, although quantitative interpretation of the results is often difficult or impossible. The primary reason for such difficulties is that the SIMS signal often depends more strongly on the nature of the local chemical environment at the analysis site than on the concentration of the species that is generating the signal. This is commonly referred to as the SIMS ‘matrix effect’.For organic materials, both ESCA and SIMS are used to obtain information on the chemical structure at surfaces. While ESCA can provide unique information on the nature of the chemical bonds between species at a surface, SIMS can provide complementary information on the molecular structures that are present.

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49

Du, Chuanmei, Xianwen Zhang, and Xilong Cheng. "Study on the resonance enhanced multi-photon ionization and photodissociation of CS2 molecules." Optik 225 (January 2021): 165869. http://dx.doi.org/10.1016/j.ijleo.2020.165869.

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50

Stellpflug, M., M. Johnsson, I. D. Petrov, and T. Halfmann. "Investigation of auto-ionizing states in xenon by resonantly enhanced multi-photon ionization." European Physical Journal D - Atomic, Molecular and Optical Physics 23, no. 1 (April 1, 2003): 35–42. http://dx.doi.org/10.1140/epjd/e2003-00021-1.

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