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arXiv:1004.4797 · The European Physical Journal D

Slowing polar molecules using a wire Stark decelerator

Adela Marian, Henrik Haak, P. Geng, Gerard Meijer

Published May 24, 2010• 10 citations
arXivHTMLPDF
DOI
10.1140/epjd/e2010-00143-3

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A Stark decelerator can slow down polar molecules to very low velocities. When the velocities are very low, the number of cold molecules obtained is very small. In order to obtain a higher quantity of cold molecules, inspired by the work of Reens et al. [Phys. Rev. Res. 2 (2020) 033 095], we propose an alternative method of operating a Stark decelerator. Through the trajectory simulation of OH molecules in the decelerator, we find that the number of cold molecules can be greatly increased by one order of magnitude at both low and high final velocities on a Stark decelerator consisting of around 150 electrodes. This development is due to the improved longitudinal and the transverse focusing property provided by the new switching schemes and the high-voltage configurations on the decelerator unit.
We propose a modified Stark-chirped rapid adiabatic passage technique for a robust rovibrational population transfer in the gas phase molecules in the presence of certain inhomogeneous electric fields. As an example application, the new state switching scheme is shown to greatly enhance the process of slowing polar ammonia molecules in the Stark decelerator. High-level quantum mechanical simulations show that a virtually complete population inversion between a selected pair of weak-field and strong-field seeking states of NH3_33​ can be achieved. Strong dc electric fields within the Stark decelerator are used as part of the rovibrational population transfer protocol. Classical-dynamics simulations for ammonia demonstrate notable improvements in the longitudinal phase space acceptance of the Stark decelerator upgraded with the state switching and an increased deceleration efficiency with respect to the standard Stark deceleration technique.