Mobility Selective Ion Soft-Landing and Characterization Enabled Using Structures for Lossless Ion Manipulation.

Autor: Lee JY; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99354, United States., Li A; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99354, United States., Prabhakaran V; Physical Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99354, United States., Zhang X; Physical Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99354, United States., Harrilal CPP; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99354, United States., Kovarik L; Physical Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99354, United States., Ibrahim YM; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99354, United States., Smith RD; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99354, United States., Garimella SVB; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99354, United States.
Jazyk: angličtina
Zdroj: Analytical chemistry [Anal Chem] 2024 Feb 27; Vol. 96 (8), pp. 3373-3381. Date of Electronic Publication: 2024 Feb 12.
DOI: 10.1021/acs.analchem.3c04328
Abstrakt: While conventional ion-soft landing uses the mass-to-charge ( m / z ) ratio to achieve molecular selection for deposition, here we demonstrate the use of Structures for Lossless Ion Manipulation (SLIM) for mobility-based ion selection and deposition. The dynamic rerouting capabilities of SLIM were leveraged to enable the rerouting of a selected range of mobilities to a different SLIM path (rather than MS) that terminated at a deposition surface. A selected mobility range from a phosphazene ion mixture was rerouted and deposited with a current pulse (∼150 pA) resembling its mobility peak. In addition, from a mixture of tetra-alkyl ammonium (TAA) ions containing chain lengths of C5-C8, selected chains (C6, C7) were collected on a surface, reconstituted into solution-phase, and subsequently analyzed with a SLIM-qToF to obtain an IMS/MS spectrum, confirming the identity of the selected species. Further, this method was used to characterize triply charged tungsten-polyoxometalate anions, PW 12 O 40 3- (WPOM). The arrival time distribution of the IMS/MS showed multiple peaks associated with the triply charged anion (PW 12 O 40 3- ), of which a selected ATD was deposited and imaged using TEM. Additionally, the identity of the deposited WPOM was ascertained using energy-dispersive (EDS) spectroscopy. Further, we present theory and computations that reveal ion landing energies, the ability to modulate the energies, and deposition spot sizes.
Databáze: MEDLINE