All Publications


  • Photon catalysis of deuterium iodide photodissociation PHYSICAL CHEMISTRY CHEMICAL PHYSICS Hilsabeck, K., Meiser, J. L., Sneha, M., Balakrishnan, N., Zare, R. N. 2019; 21 (26): 14195–204

    View details for DOI 10.1039/c8cp06107f

    View details for Web of Science ID 000474136100030

  • Nonresonant photons catalyze photodissociation of phenol. Journal of the American Chemical Society Hilsabeck, K. I., Meiser, J. L., Sneha, M., Harrison, J. A., Zare, R. N. 2018

    Abstract

    Phenol represents an ideal polyatomic system for demonstrating photon catalysis because of its large polarizability, well-characterized excited-state potential energy surfaces, and nonadiabatic dissociation dynamics. A nonresonant IR pulse (1064 nm) supplies a strong electric field (εo = 4 x 107 V/cm) during the photolysis of isolated phenol (C6H5OH) molecules to yield C6H5O + H near two known energetic thresholds: the S1/S2 conical intersection and the S1 - S0 origin. H-atom speed distributions show marked changes in the relative contributions of dissociative pathways in both cases, compared to the absence of the nonresonant IR pulse. Results indicate that nonresonant photons lower the activation barrier for some pathways relative to others by dynamically Stark shifting the excited-state potential energy surfaces rather than aligning molecules in the strong electric field. Theoretical calculations offer support for the experimental interpretation.

    View details for PubMedID 30571915