A modified SCRAP technique using the decelerator's time-varying dc electric field as the chirp can achieve >99.5% population inversion between weak-field- and strong-field-seeking states of ammonia, improving Stark deceleration efficiency.
Alternating gradient focusing and deceleration of large molecules
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abstract
We have focused and decelerated benzonitrile (C$_7$H$_5$N) molecules from a molecular beam, using an array of time-varying inhomogeneous electric fields in alternating gradient configuration. Benzonitrile is prototypical for large asymmetric top molecules that exhibit rich rotational structure and a high density of states. At the rotational temperature of 3.5 K in the pulsed molecular beam, many rotational states are populated. Benzonitrile molecules in their absolute ground state are decelerated from 320 m/s to 289 m/s, and similar changes in velocity are obtained for excited rotational states. All measurements agree well with the outcome of trajectory calculations. These experiments demonstrate that such large polyatomic molecules are amenable to the powerful method of Stark deceleration.
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Controlling rovibrational state populations of polar molecules in inhomogeneous electric fields of the Stark deceleration: molecular dynamics and quantum chemistry simulations
A modified SCRAP technique using the decelerator's time-varying dc electric field as the chirp can achieve >99.5% population inversion between weak-field- and strong-field-seeking states of ammonia, improving Stark deceleration efficiency.