Low-energy electron scattering cross section for the production of CO within condensed acetone

Journal of Chemical Physics

Volumn 113, Issue 9, 2000, Pages 3602-3608

  Lepage, M ^a,b   Michaud, M ^a   Sanche, L ^a  

^a UNIVERSITY OF SHERBROOKE   (Canada)

^b QUEENSLAND UNIVERSITY OF TECHNOLOGY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ACETONE; ARGON; CARBON MONOXIDE; CONDENSATION; DECOMPOSITION; DISSOCIATION; ELECTRON ENERGY LEVELS; ELECTRON ENERGY LOSS SPECTROSCOPY; ELECTRON RESONANCE; ELECTRON TRAPS; THICKNESS MEASUREMENT; THIN FILMS;

CORE EXCITED ELECTRON RESONANCE; ELECTRON DOSE; FILM THICKNESS; HIGH RESOLUTION ELECTRON ENERGY LOSS SPECTROSCOPY; LOW ENERGY ELECTRON SCATTERING; THIN SOLID FILMS;

ELECTRON SCATTERING;

EID: 0034270471     PISSN: 00219606     EISSN: None     Source Type: Journal    
DOI: 10.1063/1.1287400     Document Type: Article

References (98)

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30. H. Zuckerman, B. Schmitz, and Y. Haas, J. Phys. Chem. 93, 4083 (1989).
31. G. E. Hall, D. Vanden Bout, and T. J. Sears, J. Chem. Phys. 94, 4182 (1991).
32. F. Mohammad, V. R. Morris, A. C. Jones, and W. M. Jackson, J. Phys. Chem. 97, 6974 (1993).
33. J. Pola and R. Taylor, Tetrahedron Lett. 35, 2799 (1994).
34. G. E. Hall, H. W. Metzler, J. T. Muckerman, J. M. Preses, and R. E. Weston, Jr., J. Chem. Phys. 102, 6660 (1995).
35. S. K. Kim, S. Pedersen, and A. H. Zewail, J. Chem. Phys. 103, 477 (1995).
36. S. A. Buzza, E. M. Snyder, and A. W. Castleman, Jr., J. Chem. Phys. 104, 5040 (1996).
37. J. C. Owrutsky and A. P. Baronavski, J. Chem. Phys. 108, 6652 (1998).
38. I. Kusunoki, M. Sakashita, T. Takaoka, and H. Range, Surf. Sci. 357-358, 693 (1996).
39. R. McDiarmid and X. Xing, J. Chem. Phys. 107, 675 (1997).
40. F. H. Dorman, J. Chem. Phys. 44, 3856 (1966).
41. W. M. Trott, N. C. Biais, and E. A. Walters, J. Chem. Phys. 69, 3150 (1978).
42. E. Murad and M. G. Inghram, J. Chem. Phys. 40, 3263 (1964).
43. F. H. Dorman, J. Chem. Phys. 42, 65 (1964).
44. The energies are obtained as follows: Process (8b), from Ref. 19. Process (8c), energy for process (8b) plus the energy barrier for acetyl decomposition taken as 0.87 eV from Ref. 21. Process (8d), energy for process (8c) minus the recombination energy of 3.82 eV of the two methyl radicals from Ref. 44. Process (8e), from Ref. 35. Process (8f), energy for process (8e) plus acetyl decomposition barrier of 0.87 eV. Process (8g), from Ref. 36. Process (8h), calculated thermodynamic threshold in Ref. 42. Process (8i), from Ref. 38. Process (8j), energy for process (8i) plus acetyl decomposition barrier of 0.87 eV.
45. L. G. Christophorou, Electron-Molecule Interactions and Their Applications (Academic, New York, 1984), Vol. 1, p. 174.
46. M. Ben Arfa and M. Tronc J. Electron Spectrosc. Relat. Phenom. 50, 117 (1990), and references therein.
47. C. S. T. Cant, C. J. Danby, and J. H. D. Eland, J. Chem. Soc., Faraday Trans. 2 71, 1015 (1975).
48. D. B. Thomson, D. Ji, K. Lee, C. I. Ma, and D. M. Hanson, J. Phys. B 32, 2649 (1999).
49. J. A. Kerr, Chem. Rev. 66, 465 (1966).
50. See, for example, A. D. Bass and L. Sanche, Radiat. Environ. Biophys. 37, 243 (1998).
51. L. Sanche, IEEE Trans. Dielectr. Electr. Insul. 4, 507 (1997).
52. R. Martel, A. Rochefort, and P. H. McBreen, J. Am. Chem. Soc. 116, 5965 (1994).
53. B. Rowland and W. P. Hess, Chem. Phys. Lett. 263, 574 (1996).
54. Desortion Induced by Electronic Transitions (DIET) I, edited by N. H. Tolk, M. M. Traum, J. C. Tully, and T. E. Madey (Springer, Berlin, 1983);
55. DIET II, edited by W. Brenig and D. Menzel (Springer. Berlin, 1985);
56. DIET III, edited by R. H. Stulen and M. L. Knotek (Springer, Berlin, 1988);
57. DIET IV, edited by G. Betz and P. Varga (Springer, Berlin, 1990);
58. DIET V, edited by A. R. Bums, E. B. Stechel, and D. R. Jennison (Springer, Berlin, 1993).
59. C. O. Olsen and P. A. Rowntree, J. Chem. Phys. 108, 3750 (1998).
60. M. Lepage, M. Michaud, and L. Sanche, J. Chem. Phys. 107, 3478 (1997).
61. L. Sanche and M. Michaud, Phys. Rev. B 30, 6078 (1984).
62. M. Michaud, P. Cloutier, and L. Sanche, Rev. Sci. Instrum. 66, 2661 (1995).
63. H. Kuhlenbeck, M. Lepage, M. Michaud, L. Sanche, H. Sambe, and D. E. Ramaker, Chem. Phys. Lett. 238, 93 (1995).
64. L. Sanche, J. Chem. Phys. 71, 4860 (1979).
65. M. Michaud, M. Lepage, and L. Sanche, Phys. Rev. Lett. 81, 2807 (1998).
66. M. Lepage, M. Michaud, and L. Sanche, J. Chem. Phys. 112, 6707 (2000).
67. D. C. Cartwright, A. Chutjan, S. Trajmar, and W. Williams, Phys. Rev. A 16, 1013 (1977).
68. R. M. Marsolais, M. Michaud, and L. Sanche, Phys. Rev. A 35, 607 (1987);
69. M. Michaud and L. Sanche (unpublished results).
70. R. B. Cundall and A. S. Davies, Proc. R. Soc. London Ser. A 290, 563 (1966).
71. H. Shaw and S. Toby, J. Phys. Chem. 72, 2337 (1968).
72. L. D. Waits, R. J. Horwitz, and J. A. Guest, Chem. Phys. 155, 149 (1991).
73. S. W. North, D. A. Blank, J. Daniel Gezelter, C. A. Longfellow, and Y. T. Lee, J. Chem. Phys. 102, 4447 (1995).
74. H. Zuckermann, B. Schmitz, and Y. Haas, J. Phys. Chem. 92, 4835 (1988).
75. A. Gandini and P. A. Hackett, J. Am. Chem. Soc. 99, 6195 (1977).
76. L. J.-T. Lin and P. Ausloos, Photochem. 1, 453 (1972/73).
77. A. G. Leiga and H. A. Taylor, J. Chem. Phys. 41, 1247 (1964).
78. M. Baba, I. Hanazaki, and U. Nagashima, J. Chem. Phys. 82, 3938 (1985).
79. H. Zuckerman, B. Schmitz, and Y. Haas, J. Phys. Chem. 93, 4083 (1989).
80. G. E. Hall, D. Vanden Bout, and T. J. Sears, J. Chem. Phys. 94, 4182 (1991).
81. F. Mohammad, V. R. Morris, A. C. Jones, and W. M. Jackson, J. Phys. Chem. 97, 6974 (1993).
82. J. Pola and R. Taylor, Tetrahedron Lett. 35, 2799 (1994).
83. G. E. Hall, H. W. Metzler, J. T. Muckerman, J. M. Preses, and R. E. Weston, Jr., J. Chem. Phys. 102, 6660 (1995).
84. S. K. Kim, S. Pedersen, and A. H. Zewail, J. Chem. Phys. 103, 477 (1995).
85. S. A. Buzza, E. M. Snyder, and A. W. Castleman, Jr., J. Chem. Phys. 104, 5040 (1996).
86. J. C. Owrutsky and A. P. Baronavski, J. Chem. Phys. 108, 6652 (1998).
87. I. Kusunoki, M. Sakashita, T. Takaoka, and H. Range, Surf. Sci. 357-358, 693 (1996).
88. R. McDiarmid and X. Xing, J. Chem. Phys. 107, 675 (1997).
89. F. H. Dorman, J. Chem. Phys. 44, 3856 (1966).
90. W. M. Trott, N. C. Biais, and E. A. Walters, J. Chem. Phys. 69, 3150 (1978).
91. E. Murad and M. G. Inghram, J. Chem. Phys. 40, 3263 (1964).
92. F. H. Dorman, J. Chem. Phys. 42, 65 (1964).
93. The energies are obtained as follows: Process (8b), from Ref. 19. Process (8c), energy for process (8b) plus the energy barrier for acetyl decomposition taken as 0.87 eV from Ref. 21. Process (8d), energy for process (8c) minus the recombination energy of 3.82 eV of the two methyl radicals from Ref. 44. Process (8e), from Ref. 35. Process (8f), energy for process (8e) plus acetyl decomposition barrier of 0.87 eV. Process (8g), from Ref. 36. Process (8h), calculated thermodynamic threshold in Ref. 42. Process (8i), from Ref. 38. Process (8j), energy for process (8i) plus acetyl decomposition barrier of 0.87 eV.
94. L. G. Christophorou, Electron-Molecule Interactions and Their Applications (Academic, New York, 1984), Vol. 1, p. 174.
95. M. Ben Arfa and M. Tronc J. Electron Spectrosc. Relat. Phenom. 50, 117 (1990), and references therein.
96. C. S. T. Cant, C. J. Danby, and J. H. D. Eland, J. Chem. Soc., Faraday Trans. 2 71, 1015 (1975).
97. D. B. Thomson, D. Ji, K. Lee, C. I. Ma, and D. M. Hanson, J. Phys. B 32, 2649 (1999).
98. J. A. Kerr, Chem. Rev. 66, 465 (1966).