| Autor: |
Lake WR; Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States., Meng J; Department of Chemistry, Emory University, Atlanta, Georgia 30322, United States., Dawlaty JM; Department of Chemistry, University of Southern California, Los Angeles, California 90089, United States., Lian T; Department of Chemistry, Emory University, Atlanta, Georgia 30322, United States., Hammes-Schiffer S; Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States.; Department of Chemistry, Princeton University, Princeton, New Jersey 08544, United States. |
| Abstrakt: |
A microscopic understanding of electric fields and molecular polarization at interfaces will aid in the design of electrocatalytic systems. Herein, variants of 4-mercaptobenzonitrile are designed to test different schemes for breaking the continuous conjugation between a gold electrode surface and a nitrile group. Periodic density functional theory calculations predict applied potential dependencies of the CN vibrational frequencies similar to those observed experimentally. The CN frequency response decreased more when the conjugation was broken between the benzene ring and the nitrile group than between the electrode and the benzene ring, highlighting molecular polarizability effects. The systems with continuous or broken conjugation are dominated by electro-inductive effects or through-space electrostatic effects, respectively. Analysis of the fractional charge transfer between the electrode and the molecule as well as the occupancy of the CN antibonding orbital provides further insights. Balancing the effects of molecular polarizability, electro-induction, and through-space electrostatics has broad implications for electrocatalyst design. |
