Enhancing Infrared Laser Dissociation of Molecules with the Electromagnetic Vacuum

TL;DR

This study demonstrates that infrared laser dissociation of a molecule is significantly enhanced inside an electromagnetic vacuum cavity, reducing energy requirements and revealing quantum mechanical effects that alter molecular vibrational dynamics.

Contribution

It provides the first detailed quantum mechanical analysis of molecule dissociation in an infrared vacuum cavity, showing enhanced dissociation efficiency and modified vibrational ladder climbing.

Findings

Lower laser intensities needed for dissociation inside the cavity

Photon injection into the cavity causes dissociation with less energy

Vacuum-induced vibrational state mixing alters molecular dynamics

Abstract

Controlling bond breaking is a long-standing goal in molecular physics. Infrared nanocavities are currently being developed for reaching exotic coupling regimes of cavity QED with a few molecules, but it is not well understood how chemical reactions would proceed in such systems. To address this, we study infrared laser photodissociation of a single CS$_{2}$ molecule with a stretching mode that strongly interacts with a resonant infrared vacuum, subject to a strong laser field that either resonantly drives the molecule at its fundamental vibration frequency or injects photons at the cavity resonance. We show that the intensities required for photodissociation are significantly lower inside the cavity than in free space, with a strong dependence on the type of driving condition. By directly injecting photons into the cavity, the molecule dissociates with two orders of magnitude less laser energy than by directly driving the vibrational mode. This photodissociation enhancement is a purely quantum mechanical effect that cannot be captured semi-classically. The intracavity ladder climbing dynamics is substantially modified relative to free space due to vacuum-induced admixing a large number of vibrational quantum numbers and the cavity field acting as a surrogate molecular mode that strongly interacts with the dissociative vibrational motion. Our work provides fundamental mechanistic understanding of chemical dynamics that can be used for designing new types of nanophotonics experiments that probe single-molecule chemistry.