Details

Autor(en) / Beteiligte

• Herburger, H.
• Hollenstein, U.
• Agner, J. A.
• Merkt, F.

Titel

PFI-ZEKE-photoelectron spectroscopy of N2O using narrow-band VUV laser radiation generated by four-wave mixing in Ar using a KBBF crystal

Ist Teil von

• The Journal of chemical physics, 2019-10, Vol.151 (14), p.144302-144302

Ort / Verlag

Melville: American Institute of Physics

Erscheinungsjahr

2019

Quelle

American Institute of Physics

Beschreibungen/Notizen

• A new nonlinear optical scheme relying on sum-frequency mixing in a KBe2BO3F2 crystal has been used to generate intense, broadly tunable, narrow-bandwidth, coherent vacuum-ultraviolet (VUV) radiation beyond 16 eV by resonance-enhanced four-wave mixing in Ar. The VUV radiation was used to record high-resolution pulsed-field-ionization zero-kinetic-energy photoelectron spectra of the N2O+ A+ ← N2O X photoionizing transition in the wave-number range from 132 000 cm−1 to 135 000 cm−1. The rotational structure of almost all vibrational levels of the A+ state with vibrational term values up to 2700 cm−1 could be resolved, and improved values of the first two adiabatic ionization energies of N2O, corresponding to the formation of the X+ 2Π3/2(000) J+ = 3/2 and A+ 2Σ+(000) N+ = 0 levels of N2O+ from the X 1Σ+(000) J″ = 0 ground state [103 969.30(12) cm−1 and 132 197.70(12) cm−1, respectively], were derived. The rotational intensity distributions of the bands were found to depend strongly on the value of the vibrational angular momentum of the ionic levels. The vibrational structure is discussed in terms of previously reported effective-Hamiltonian analyses.