UV cavity enhanced absorption spectroscopy of the hydroxyl radical |
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Authors: | G?Hancock Email author" target="_blank">VL?KasyutichEmail author |
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Institution: | (1) Physical and Theoretical Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, OX1 3QZ, UK |
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Abstract: | We present the application of a continuous-wave ultra-violet tuneable light source for detection of the hydroxyl radical (OH) using cavity-enhanced absorption spectroscopy of the Q11(2) and Q21(2) absorption lines in the A2+(v=0)23/2(v=0) band at ca. 308 nm. A tuneable infra-red diode laser operating at 835 nm and either an Ar+ laser or a single frequency continuous-wave intracavity frequency-doubled diode laser, both operating at ca. 488 nm, were used to produce 0.1–0.5 W of tuneable radiation at ca. 308 nm by sum frequency generation in a BaB2O4 crystal. Cavity enhanced absorption spectroscopy was used to detect OH generated by UV photolysis of water vapour in argon, nitrogen, neon and helium at atmospheric pressure. A noise-equivalent (1) absorption sensitivity of 2.1×10-7 cm-1Hz-1/2 measured over 128 scans in a time of 1.16 s was demonstrated with mirrors of reflectivity 0.9963 in a cavity of length 58.5 cm for a 2 cm-1 scanning range at a UV power of 0.5 W. An OH detection limit (1) of 3.84×109 moleculecm-3 was estimated in argon at atmospheric pressure. OH collisional broadening in humidified N2, Ar, Ne and He was determined at atmospheric pressure . PACS 39.30.+w; 42.55.Px; 42.62.Fi; 42.68.Ca |
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