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Triply differential photoelectron studies of non-Franck–Condon behavior in the photoionization of acetylene

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.443568· OSTI ID:5456157
 [1];  [1];  [2];  [3];  [4]
  1. National Bureau of Standards, Washingtion D.C., (United States)
  2. Daresbury Lab. (United Kingdom). Cockcroft Inst. of Accelerator Science and Technology (AST)
  3. Univ. of Maryland, College Park, MD (United States)
  4. Argonne National Lab. (ANL), Argonne, IL (United States)
Vibrational branching ratios and photoelectron angular distributions for alternative vibrational levels of C2H+2 X² Πu have been measured in the range 13 eV≤hv≤25 eV using synchrotron radiation. Below hv≈16 eV, these data exhibit strong non-Franck--Condon effects, namely, wavelength-dependent vibrational branching ratios and vibrational-state-dependent photoelectron asymmetry parameters. Moreover, enhanced excitation of bending modes of the ion is observed below hv≈16 eV, in addition to the C--C stretch mode, which is the only mode readily observed in photoelectron spectra of C2H2 at shorter wavelengths, e.g., at the He I (21.2 eV) resonance line. The non-Franck--Condon behavior is attributed to resonant photoionization processes, whose identification is discussed in the framework of several recent theoretical and experimental studies on acetylene and related molecules.
Research Organization:
Synchrotron Ultraviolet Radiation Facility, National Bureau of Standards, Washington, D.C. 20234
Sponsoring Organization:
USDOE; Office of Naval Research (ONR)
OSTI ID:
5456157
Journal Information:
Journal of Chemical Physics, Journal Name: Journal of Chemical Physics Journal Issue: 9 Vol. 76; ISSN JCPSA6; ISSN 0021-9606
Publisher:
American Institute of Physics (AIP)
Country of Publication:
United States
Language:
English