Driving chemical reactions with polariton condensates

Abstract

When molecular transitions strongly couple to photon modes, they form hybrid light-matter modes called polaritons. Collective vibrational strong coupling is a promising avenue for control of chemistry, but this can be deterred by the large number of quasi-degenerate dark modes. The macroscopic occupation of a single polariton mode by excitations, as observed in Bose-Einstein condensation, offers promise for overcoming this issue. Here we theoretically investigate the effect of vibrational polariton condensation on the kinetics of electron transfer processes. Compared with excitation with infrared laser sources, the vibrational polariton condensate changes the reaction yield significantly at room temperature due to additional channels with reduced activation barriers resulting from the large accumulation of energy in the lower polariton, and the many modes available for energy redistribution during the reaction. Our results offer tantalizing opportunities to use condensates for driving chemical reactions, kinetically bypassing usual constraints of fast intramolecular vibrational redistribution in condensed phase.

Document Details

Document Type
Pub Defense Publication
Publication Date
Mar 28, 2022
Source ID
10.1038/s41467-022-29290-9

Entities

People

  • Joel Yuen-Zhou
  • Jorge A Campos-Gonzalez-Angulo
  • Luis A. Martínez-martínez
  • Shubham Sinha
  • Sindhana Selvi Pannir Sivajothi

Organizations

  • Air Force Office of Scientific Research
  • National Science Foundation
  • United States Department of Energy

Tags

Fields of Study

  • Physics

Readers

  • Quantum Chemistry
  • Quantum Dot Semiconductor Device Photonics and Graphene Optoelectronic Materials and THz Physics.

Technology Areas

  • Directed Energy
  • Microelectronics