Line strength factors for E,F1Σ+g(v′=0, J′=J")-X1Σ+g (v", J") (2+1) REMPI transitions in molecular hydrogen

被引:20
作者
Pomerantz, AE
Ausfelder, F
Zare, RN [1 ]
Huo, WM
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[2] NASA, Ames Res Ctr, Moffett Field, CA 94035 USA
关键词
hydrogen; spectroscopy; REMPI; line strength; multiphoton;
D O I
10.1139/V04-074
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Experimentally and theoretically determined line strengths are presented for E,F(1)Sigma(g)(+)(v' = 0, J' = J'') - X(1)Sigma(g)(+) (v'', J'') (2 + 1) REMPI transitions in H-2, HD, and D-2. The experimental technique employs a hot filament source of internally excited hydrogen that allows experimental determination of line strengths for the low rotational states of highly excited vibrational manifolds (v'' less than or equal to 4). The line strengths are found to depend only weakly on J'' for the states measured here, and theoretical results indicate that the line strengths depend strongly on v''. These values are combined with previously measured and calculated line strengths for these transitions (K.-D. Rinnen, M.A. Buntine, D.A.V. Kliner, R.N. Zare, and W.M. Huo. J. Chem. Phys. 95, 214 (1991)), resulting in a more complete compilation of REMPI line strengths for molecular hydrogen.
引用
收藏
页码:723 / 729
页数:7
相关论文
共 25 条
[1]   Collision energy dependence of the HD(ν′=2) product rotational distribution of the H+D2 reaction in the range 1.30-1.89 eV [J].
Ausfelder, F ;
Pomerantz, AE ;
Zare, RN ;
Althorpe, SC ;
Aoiz, FJ ;
Bañares, L ;
Castillo, JF .
JOURNAL OF CHEMICAL PHYSICS, 2004, 120 (07) :3255-3264
[2]   OBSERVATION OF EXCEPTIONALLY HIGH VIBRATIONAL-EXCITATION OF HYDROGEN MOLECULES FORMED BY WALL RECOMBINATION [J].
EENSHUISTRA, PJ ;
BONNIE, JHM ;
LOS, J ;
HOPMAN, HJ .
PHYSICAL REVIEW LETTERS, 1988, 60 (04) :341-344
[3]   Rovibrational state distribution of deuterium molecules resulting from D-atom interaction with Ni(110) [J].
Eilmsteiner, G ;
Winkler, A .
SURFACE SCIENCE, 1996, 366 (03) :L750-L754
[4]   New scheme for measuring the angular momentum spatial anisotropy of vibrationally excited H2 via the I 1Πg state [J].
Fernández-Alonso, F ;
Bean, BD ;
Ayers, JD ;
Pomerantz, AE ;
Zare, RN .
ZEITSCHRIFT FUR PHYSIKALISCHE CHEMIE-INTERNATIONAL JOURNAL OF RESEARCH IN PHYSICAL CHEMISTRY & CHEMICAL PHYSICS, 2000, 214 :1167-1186
[5]   VIBRATIONAL-EXCITATION OF HYDROGEN VIA RECOMBINATIVE DESORPTION OF ATOMIC-HYDROGEN GAS ON A METAL-SURFACE [J].
HALL, RI ;
CADEZ, I ;
LANDAU, M ;
PICHOU, F ;
SCHERMANN, C .
PHYSICAL REVIEW LETTERS, 1988, 60 (04) :337-340
[6]   D(2)E,F-1-SIGMA(+)(G)(V'=0 AND 1)-X(1)SIGMA(+)(G)(V''=0-5) TRANSITION ENERGIES FOR J'=J''=0-26 - COMPARISON OF EXPERIMENT AND THEORY [J].
HECK, AJR ;
HUO, WM ;
ZARE, RN ;
CHANDLER, DW .
JOURNAL OF MOLECULAR SPECTROSCOPY, 1995, 173 (02) :452-462
[7]   THE LYMAN BANDS OF MOLECULAR HYDROGEN [J].
HERZBERG, G ;
HOWE, LL .
CANADIAN JOURNAL OF PHYSICS, 1959, 37 (05) :636-&
[8]   ROTATIONAL AND VIBRATIONAL EFFECTS IN THE E 1-SIGMA-G+-X 1-SIGMA-G+ 2-PHOTON TRANSITIONS OF H2, HD, AND D2 [J].
HUO, WM ;
RINNEN, KD ;
ZARE, RN .
JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (01) :205-213
[9]   ABINITIO CALCULATION OF THE 2-PHOTON ABSORPTION CROSS-SECTION OF THE X1 SIGMA-G+-](E,F)1 SIGMA-G+ IN H-2 [J].
HUO, WM ;
JAFFE, RL .
CHEMICAL PHYSICS LETTERS, 1983, 101 (4-5) :463-471
[10]   PRODUCT INTERNAL-STATE DISTRIBUTION FOR THE REACTION H+HI-]H2+I [J].
KLINER, DAV ;
RINNEN, KD ;
BUNTINE, MA ;
ADELMAN, DE ;
ZARE, RN .
JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (03) :1663-1670