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Photodissociation of HNO3 at 193 nm: Near-infrared emission of NO detected by time-resolved Fourier transform spectroscopy
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Photodissociation of HNO3 at 193 nm: Near-infrared emission of NO detected by time-resolved Fourier transform spectroscopy

Pey-Shiun Yeh, Gen-Hou Leu, Yuan-Pern Lee and I-Chia Chen
The Journal of Chemical Physics, Vol.103(12), pp.4879-4886
1995

Abstract

Rotationally resolved emission of NO, produced from photolysis of HNO 3 at 193 nm, in the near infrared region (8900-9300 cm -1 ) was recorded with a step-scan Fourier-transform interferometer at a resolution of 0.1 cm -1 . The emission is assigned as NO D 2 Σ-A 2 Σ + (v′ ,v″) = (0,0) band with rotational states N′=17-42. Emission from selective rotational states of NO D 2 Σ + was observed when HNO 3 was photolyzed with an ArF excimer laser having a narrow bandwidth ≈0.01 nm. The experimental results indicate that the D 2 Σ + state of NO is formed via absorption of another 193 nm photon by NO (v″=1) in the ground electronic state. The measured distribution of intensity implies that NO is produced highly rotationally excited; the most likely mechanism for formation of NO is from the unstable NO 2 fragment undergoing secondary dissociation. © 1995 American Institute of Physics.
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PHOTODISSOCIATION_OF_HNO3_AT_193_NM_-_NEAR-INFRARED_EMISSION_OF_NO_DETECTED_BY_TIME-RESOLVED_FOURIER-TRANSFORM_SPECTROSCOPY.pdfDownloadView
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