A generic π* shape resonance observed in energy-dependent photoelectron angular distributions from two-colour, resonant multiphoton ionization of difluorobenzene isomers
Author(s) -
Michael Staniforth,
Steven Daly,
Katharine L. Reid,
Ivan Powis
Publication year - 2013
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.4817324
Subject(s) - photoionization , ionization , shape resonance , atomic physics , resonance enhanced multiphoton ionization , resonance (particle physics) , photon energy , scattering , chemistry , excited state , photon , physics , ion , optics , organic chemistry
We present new evidence for the existence of a near threshold π* shape resonance as a common feature in the photoionization of each isomer of difluorobenzene. Experimentally this is revealed by significant changes in the anisotropy of the photoelectron angular distributions (PADs) following the ionization of the optically aligned S1 state of these molecules at varying photon energies. Continuum multiple scattering Xα calculations reproduce this behaviour well and allow the visualisation of the continuum shape resonances. The resonances are unusually narrow in energy (<1 eV) but nevertheless appear to extend right down to the ionization thresholds—exactly the low energy range typically accessed in laser-based resonance enhanced multiphoton ionization (REMPI) schemes. The anticipation of such pronounced energy dependence in the PADs and cross-sections sought for other molecules and an ability to accurately predict such features should be important for the reliable application and interpretation of experiments involving REMPI probing of those molecules
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