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<i>s</i>and<i>d</i>Rydberg series of NO probed by double resonance multiphoton ionization
170
Citations
35
References
1987
Year
EngineeringAtomic Emission SpectroscopyChemistryElectronic Excited StateRydberg Intermediate StateFringe FormationNuclear Quadrupole ResonanceQuantum MaterialsQuantum MatterPhotophysical PropertyBiophysicsPhotonicsQuantum SciencePhysicsQuantum Defect TheoryAtomic PhysicsQuantum ChemistryExcited State PropertyNatural SciencesSpectroscopyNo ProbedCondensed Matter PhysicsApplied PhysicsDouble ResonanceMultiphoton Process
The s and d Rydberg states of NO with v = 0 have been observed for 6 leqslant; n* leqslant; 40 by double resonance multiphoton ionization which was three-photon resonant with the 3pπC 2∏ (v = 0) Rydberg intermediate state. Strong parity selection is shown to occur in the intermediate level despite the fact that the Λ-doublets are not resolved. The OODR spectra are thereby considerably simplified. A unified description of the rotational-electronic structure of the s and d Rydberg states in terms of quantum defect theory is presented, extending from the low n* s, d supercomplexes up beyond the ionization threshold. Electronic radial dipole transition moments are calculated and included in the MQDT analysis, giving evidence for a Cooper minimum in the region of the supercomplex n* = 5. For 25 leqslant; n* leqslant; 40 fringes are observed in the OODR spectrum and are interpreted in terms of rotational l-uncoupling, electronic s ∼d mixing and energy dependent electronic dipole transition moments. The fringe formation is shown to have a different origin than the stroboscopic effect observed in Na2 by Labastie et al. Above n* = 35 the Stark induced p series appears and is also interpreted quantitatively.
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