Communication: A new spectroscopic window on hydroxyl radicals using UV plus VUV resonant ionization

被引:23
作者
Beames, Joseph M. [1 ]
Liu, Fang [1 ]
Lester, Marsha I. [1 ]
Murray, Craig [2 ]
机构
[1] Univ Penn, Dept Chem, Philadelphia, PA 19104 USA
[2] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
关键词
free radicals; multiphoton spectra; nitrogen compounds; oxygen compounds; photoionisation; rotational states; Rydberg states; spectral line intensity; ultraviolet spectra; INDUCED FLUORESCENCE SPECTROSCOPY; PHOTOELECTRON-SPECTROSCOPY; NITRIC-ACID; TRANSITION-PROBABILITIES; SYNCHROTRON-RADIATION; QUANTUM YIELDS; OD RADICALS; 248; NM; OH; PHOTODISSOCIATION;
D O I
10.1063/1.3608061
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A 1 + 1' multiphoton ionization (MPI) detection scheme for OH radicals is presented. The spectroscopic approach combines initial excitation on the well-characterized A(2)Sigma(+)-X-2 Pi band system with vacuum ultraviolet (VUV) ionization via autoionizing Rydberg states that converge on the OH+ A(3)Pi ion state. Jet-cooled MPI spectra on the (1,0) and (2,0) bands show anomalous rotational line intensities, while initial excitation on the (0,0) band does not lead to detectable OH+ ions. The onset of ionization with the (1,0) band is attributed to an energetic threshold; the combined UV + VUV photon energies are above the first member of the autoionizing (A(3)Pi)nd Rydberg series. Comparison of the OH 1 + 1' MPI signal with that from single photon VUV ionization of NO indicates that the cross section for photoionization from OH A(2)Sigma(+), v' = 1 is on the order of 10(-17) cm(2). (C) 2011 American Institute of Physics. [doi: 10.1063/1.3608061]
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页数:4
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