Issue 26, 2019

The effect of CO rotation from shaped pulse polarization on reactions that form C2

Abstract

The effect of CO rotational energy on bimolecular reactions to form electronically excited C2 is reported here. The reactions are initiated by CO multiphoton absorption of 800 nm light in strong optical fields using two different polarization configurations based on shaped chirped pulses. The observation of Swan band emission indicates that C2(d3Πg) is a reaction product. The optical polarization is in the form of either an optical centrifuge or a dynamic polarization grating. In each case, the strong field aligns CO molecules and induces multiphoton absorption. Power-dependent measurements indicate at least seven photons are absorbed by CO; CO(a3Π) is a likely reactant candidate based on kinetic modeling. Relative reaction efficiencies are determined by measuring Swan band emission intensities. For a CO pressure of 100 Torr and an optical intensity of I = 2.0 × 1013 W cm−2, the relative C2(d3Πg) yield with the dynamic polarization grating is twice that with the optical centrifuge. The extent of CO rotational energy was determined for both optical polarizations using high-resolution transient IR absorption for a number of CO states with J = 62–73 and Erot up to 10 400 cm−1. Optical centrifuge excitation generates at least 2.5 times more rotationally excited CO molecules per quantum state than the dynamic polarization grating. The results indicate that the effect of large amounts of CO rotational energy is to reduce the yield of the C2 products.

Graphical abstract: The effect of CO rotation from shaped pulse polarization on reactions that form C2

Supplementary files

Article information

Article type
Paper
Submitted
07 Nov 2018
Accepted
30 Jan 2019
First published
30 Jan 2019

Phys. Chem. Chem. Phys., 2019,21, 14103-14110

Author version available

The effect of CO rotation from shaped pulse polarization on reactions that form C2

H. M. Ogden, T. J. Michael, M. J. Murray, Q. Liu, C. Toro and A. S. Mullin, Phys. Chem. Chem. Phys., 2019, 21, 14103 DOI: 10.1039/C8CP06917D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements