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This thesis describes recent developments in multi-reflection time-of-flight mass spectrometry (MR-ToF MS) with ions exhibiting large masses and mass differences at an MR-ToF setup at the University of Greifswald. A series of in-trap manipulation techniques to selectively retain or eject ion bunches of multiple species with disparate mass-to-charge ratios is investigated. These highlight the possibility to correct long-term flight-time drifts using a reference ion species far away in mass from the species of interest and also the ability to use such a pair to perform single-reference precision mass determinations. In both cases, the results obtained with disparate-mass ion pairs are comparable to those known from operation with isobaric species.
In addition, an in-trap photoexcitation technique is developed and applied to study the dissociation behavior of atomic bismuth clusters (systems of some number of bismuth atoms). Compared to previous works by other groups, the probed cluster-size range is expanded for both ion polarities, resulting in a more comprehensive picture of the underlying dissociation pathways. The known significance of neutral-tetramer breakoff is confirmed, however, evidence is also found for the loss of larger neutral fragments.
Lastly, the principle of tandem high-resolution MR-ToF MS is introduced. This new method allows the study of the change in dissociation behavior of the cationic bismuth octamer resulting from substituting one of its atoms for lead. It is found that the lead-doping opens new preferential fragmentation pathways that outstrip the dominant tetramer breakoff for this specific precursor cluster size. As a first proof-of-principle experiment, the case of the cationic octamer shows that tandem MR-ToF MS is well-suited for the investigation of compound clusters.