Pulsed fluorescence measurements of trapped molecular ions with zero background detection
Autor: | Joel H. Parks, Joseph T. Khoury, Sandra E. Rodriguez-Cruz |
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Rok vydání: | 2002 |
Předmět: | |
Zdroj: | Journal of the American Society for Mass Spectrometry. 13:696-708 |
ISSN: | 1879-1123 1044-0305 |
DOI: | 10.1016/s1044-0305(02)00364-1 |
Popis: | Sensitive methods have been developed to measure laser-induced fluorescence from trapped ions by reducing the detection of background scattering to zero levels during the laser excitation pulse. The laser beam diameter has been reduced to 150 m to eliminate scattering on trap apertures and the resulting laser–ion interaction is limited to a volume of 10 5 cm 3 which is 0.03– 0.15 of the total ion cloud volume depending on experimental conditions. The detection optics collected fluorescence only from within the solid angle defined by laser–ion interaction volume. Rhodamine 640 and Alexa Fluor 350 ions, commonly used as fluorescence resonance energy transfer (FRET) fluorophores, were generated in the gas phase by using electrospray ionization and injected into a radiofrequency Paul trap where they were stored and exposed to Nd:YAG laser pulses at 532 and 355 nm for times up to 10 m. Fluorescence emitted by these ions was investigated for several trap qz values and ion cloud temperatures. Analysis of photon statistics indicated an average of 10 photons were incident on the PMT detector per 15 ns pulse for 10 3 trapped ions in the interaction volume. Fluorescence measurements displayed a dependence on trapped ion number which were consistent with calculations of the space charge limited ion density. To investigate the quantitative capability of these fluorescence techniques, the laser-induced fragmentation of trapped Alexa Fluor 350 ions was measured and compared with a rate equation model of the dynamics. Decay of the fluorescence signal as well as the parent ion number compared closely with quantitative predictions of the photofragmentation model. (J Am Soc Mass Spectrom 2002, 13, 696 –708) © 2002 American Society for Mass Spectrometry |
Databáze: | OpenAIRE |
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