Enhancing reactivity of SiO$^+$ ions by controlled excitation to extreme rotational states

Fuente: arXiv
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Main Authors: Venkataramanababu, Sruthi, Li, Anyang, Antonov, Ivan, Dragan, James, Stollenwerk, Patrick R., Guo, Hua, Odom, Brian C.
Format: Preprint
Published: 2022
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author Venkataramanababu, Sruthi
Li, Anyang
Antonov, Ivan
Dragan, James
Stollenwerk, Patrick R.
Guo, Hua
Odom, Brian C.
author_facet Venkataramanababu, Sruthi
Li, Anyang
Antonov, Ivan
Dragan, James
Stollenwerk, Patrick R.
Guo, Hua
Odom, Brian C.
contents Optical pumping of molecules provides unique opportunities for control of chemical reactions at a wide range of rotational energies. This work reports a chemical reaction with extreme rotational excitation of a reactant and its kinetic characterization. We investigate the chemical reactivity for the hydrogen abstraction reaction SiO$^+$ + H$_2$ $\rightarrow$ SiOH$^+$ + H in an ion trap. The SiO$^+$ cations are prepared in a narrow rotational state distribution, including super-rotor states with rotational quantum number $\it{(j)}$ as high as 170, using a broad-band optical pumping method. We show that the super-rotor states of SiO$^+$ substantially enhance the reaction rate, a trend reproduced by complementary theoretical studies. We reveal the mechanism for the rotational enhancement of the reactivity to be a strong coupling of the SiO$^+$ rotational mode with the reaction coordinate at the transition state on the dominant dynamical pathway.
format Preprint
id arxiv_https___arxiv_org_abs_2209_09129
institution arXiv
publishDate 2022
record_format arxiv
spellingShingle Enhancing reactivity of SiO$^+$ ions by controlled excitation to extreme rotational states
Venkataramanababu, Sruthi
Li, Anyang
Antonov, Ivan
Dragan, James
Stollenwerk, Patrick R.
Guo, Hua
Odom, Brian C.
Atomic Physics
Chemical Physics
Optical pumping of molecules provides unique opportunities for control of chemical reactions at a wide range of rotational energies. This work reports a chemical reaction with extreme rotational excitation of a reactant and its kinetic characterization. We investigate the chemical reactivity for the hydrogen abstraction reaction SiO$^+$ + H$_2$ $\rightarrow$ SiOH$^+$ + H in an ion trap. The SiO$^+$ cations are prepared in a narrow rotational state distribution, including super-rotor states with rotational quantum number $\it{(j)}$ as high as 170, using a broad-band optical pumping method. We show that the super-rotor states of SiO$^+$ substantially enhance the reaction rate, a trend reproduced by complementary theoretical studies. We reveal the mechanism for the rotational enhancement of the reactivity to be a strong coupling of the SiO$^+$ rotational mode with the reaction coordinate at the transition state on the dominant dynamical pathway.
title Enhancing reactivity of SiO$^+$ ions by controlled excitation to extreme rotational states
topic Atomic Physics
Chemical Physics
url https://arxiv.org/abs/2209.09129