Determining Reaction Pathways at Low Temperatures by Isotopic Substitution: The Case of BeD+ + H2O
Tiangang Yang, Bin Zhao, Gary K. Chen, Hua Guo, Wesley C. Campbell,, Eric R. Hudson

TL;DR
This study investigates low-temperature reactions of trapped BeD+ ions with H2O, revealing that BeOH+ is the primary product and elucidating the reaction pathways responsible for ion loss in quantum information experiments.
Contribution
The paper combines experimental observations with high-level theoretical calculations to identify the dominant reaction pathway producing BeOH+ at low temperatures.
Findings
BeOH+ is the main reaction product observed.
Direct abstraction pathways are energetically inaccessible at 150 K.
Double displacement via a submerged barrier explains the formation of BeOH+.
Abstract
Trapped Be+ ions are a leading platform for quantum information science [1], but reactions with background gas species, such as H2 and H2O, result in qubit loss. Our experiment reveals that the BeOH+ ion is the final trapped ion species when both H2 and H2O exist in a vacuum system with cold, trapped Be+. To understand the loss mechanism, low-temperature reactions between sympathetically cooled BeD+ ions and H2O molecules have been investigated using an integrated, laser-cooled Be+ ion trap and high-resolution Time-of-Flight (TOF) mass spectrometer (MS) [2]. Among all the possible products,BeH2O+, H2DO+, BeOD+, and BeOH+, only the BeOH+ molecular ion was observed experimentally, with the assumed co-product of HD. Theoretical analyses based on explicitly correlated restricted coupled cluster singles, doubles, and perturbative triples (RCCSD(T)-F12) method with the augmented…
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Taxonomy
TopicsMass Spectrometry Techniques and Applications · Advanced Chemical Physics Studies · Atomic and Molecular Physics
