We describe a prototype designed for in situ detection ofthe nitrate radical (NO
3) by laser-induced fluorescence(LIF) and of N
2O
5 by thermal dissociation followed by LIFdetection of NO
3. An inexpensive 36 mW continuous wavemulti-mode diode laser at 662 nm is used to excite NO
3in the
2E'(0000)
journals/esthag/37/i24/eqn/es034507we10001.gif"> band. Fluorescence iscollected from 700 to 750 nm. The prototype has a sensitivityto NO
3 of 76 ppt for a 60 s integration with an accuracyof 8%. Although this sensitivity is adequate for studies ofN
2O
5 in many environments, it is much less sensitive (about300 times) than expected based on a comparison ofpreviously measured photophysical properties of NO
2 andNO
3. This implies much stronger nonradiative couplingof electronic states in NO
3 than in NO
2.