Signatures of ChargedDroplets from ESI: A StatisticalAnalysis of Non-summed Mass Spectra Compared to APCI

Electrospray ionization (ESI) is the most widely used technique for the ionization of liquid samples, for example, from liquid chromatography (LC) coupled to mass spectrometry. Recent experiments demonstrate the penetration of charged droplets or at least large clusters into the high-vacuum region of different ESI mass spectrometers. Using a Bruker micrOTOF equipped with a standard Bruker Apollo ESI source, we demonstrated that time-of-flight (TOF) MS can detect signatures of these droplets by analyzing the statistics of individual TOF spectra, resulting from a single orthogonal acceleration (oa) stage pulse. A custom experimental setup allows additional online monitoring of the ion current in the oa-stage by coupling an oscilloscope to an auxiliary secondary electron multiplier (SEM). The results obtained with ESI are compared to mass spectra recorded under similar conditions using atmospheric pressure chemical ionization (APCI). Our findings reveal that the observation of droplet signatures is unique to the ESI process, with their frequency and intensity strongly determined by the ion source settings. We also report that the majority of the individual spectra obtained do not contain ion signals. The observed intensity in the summed spectra stems from a few very intense spectra, which result from single droplet fragment bursts. In contrast, APCI provides an almost continuous and stable ion current, without intense signal bursts characteristic for ESI. Additional optical monitoring strongly suggests that these signatures are not a result of spray instability, but are common even for undisturbed, continuous spray operation. The variation of ion source parameters shows that specific capillary voltages, nebulizer pressures, and dry gas flows lead to an increase in the frequency of droplet occurrence. Since these parameters are fundamental and frequently altered in analytical measurements, the results reported in this contribution underscore the significance of understanding droplet dynamics in ESI-MS and provide insights regarding droplets affecting the ESI signal intensity recorded in analytical runs.

Publication Details

Journal
Figshare
Published
2025-03-21
DOI
https://doi.org/10.1021/jasms.4c00508.s001
Primary Topic
Mass Spectrometry Techniques and Applications
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article
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article

Signatures of ChargedDroplets from ESI: A StatisticalAnalysis of Non-summed Mass Spectra Compared to APCI

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Mass Spectrometry Techniques and Applications
article

Signatures of ChargedDroplets from ESI: A StatisticalAnalysis of Non-summed Mass Spectra Compared to APCI

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Abstract

Electrospray ionization (ESI) is the most widely used technique for the ionization of liquid samples, for example, from liquid chromatography (LC) coupled to mass spectrometry. Recent experiments demonstrate the penetration of charged droplets or at least large clusters into the high-vacuum region of different ESI mass spectrometers. Using a Bruker micrOTOF equipped with a standard Bruker Apollo ESI source, we demonstrated that time-of-flight (TOF) MS can detect signatures of these droplets by analyzing the statistics of individual TOF spectra, resulting from a single orthogonal acceleration (oa) stage pulse. A custom experimental setup allows additional online monitoring of the ion current in the oa-stage by coupling an oscilloscope to an auxiliary secondary electron multiplier (SEM). The results obtained with ESI are compared to mass spectra recorded under similar conditions using atmospheric pressure chemical ionization (APCI). Our findings reveal that the observation of droplet signatures is unique to the ESI process, with their frequency and intensity strongly determined by the ion source settings. We also report that the majority of the individual spectra obtained do not contain ion signals. The observed intensity in the summed spectra stems from a few very intense spectra, which result from single droplet fragment bursts. In contrast, APCI provides an almost continuous and stable ion current, without intense signal bursts characteristic for ESI. Additional optical monitoring strongly suggests that these signatures are not a result of spray instability, but are common even for undisturbed, continuous spray operation. The variation of ion source parameters shows that specific capillary voltages, nebulizer pressures, and dry gas flows lead to an increase in the frequency of droplet occurrence. Since these parameters are fundamental and frequently altered in analytical measurements, the results reported in this contribution underscore the significance of understanding droplet dynamics in ESI-MS and provide insights regarding droplets affecting the ESI signal intensity recorded in analytical runs.

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Mass Spectrometry Techniques and Applications
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