Journal
ANALYTICAL CHEMISTRY
Volume 94, Issue 28, Pages 9960-9969Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.2c00955
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Funding
- Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [263334553]
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This paper introduces a new ion source that combines X-ray and UV ionization to improve the sensitivity of ion mobility spectrometers, and conducts a comparison between chemical and direct ionization.
Efficient ionization of analyte molecules is a crucial step for the outstanding sensitivity of ion mobility spectrometers (IMS) used for trace gas detection. Here, we present a new ion source that combines the previously published extended field switching ion shutter with two switchable ionization sources and an optimized sample gas flow that leads to a focused laminar stream through the reaction region of the ion source. The X-ray ionization source allows for chemical gas phase ionization of analyte molecules, while the UV ionization source allows for direct ionization of analyte molecules. The optimized sample gas flow not only allows for quickly washing out analyte molecules from the reaction region but also has improved sensitivity by a factor of about 5 for protonated monomers, 20 for proton-bound dimers, and over 100 for the proton-bound trimer of 1-octanol. The resulting limits of detection using chemical X-ray ionization are in the subpptv-range for protonated monomers and in the low pptv-range for proton-bound dimers, while the limits of detection using direct UV ionization are in the subppbv-range. Especially, a direct comparison between chemical and direct ionization of ketones using this ultrasensitive ion source reveals a stepwise conversion from directly ionized monomers to proton-bound dimers via protonated monomers during direct UV ionization.
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