Title
Electrochemical Reduction of CO at Functionalized Au Electrodes
Document Type
Article
Publication Date
3-8-2017
Abstract
Electrochemical reduction of CO provides an opportunity to store renewable energy as fuels with much greater energy densities than batteries. Product selectivity of the reduction reaction is known to be a function of the electrolyte and electrode; however, electrodes modified with functional ligands may offer new methods to control selectivity. Here, we report the electrochemical reduction of CO at functionalized Au surfaces with three thiol-tethered ligands: 2-mercaptopropionic acid, 4-pyridinylethanemercaptan, and cysteamine. Remarkably, Au electrodes modified with 4-pyridinylethanemercaptan show a 2-fold increase in Faradaic efficiency and 3-fold increase in formate production relative to Au foil. Conversely, electrodes with 2-mercaptopropionic acid ligands show nearly 100% Faradaic efficiency toward the hydrogen evolution reaction, while cystemine-modified electrodes show 2-fold increases in both CO and H production. We propose a proton-induced desorption mechanism associated with pK of the functionalized ligand as responsible for the dramatic selectivity changes.
Publication Source (Journal or Book title)
Journal of the American Chemical Society
First Page
3399
Last Page
3405
Recommended Citation
Fang, Y., & Flake, J. C. (2017). Electrochemical Reduction of CO at Functionalized Au Electrodes. Journal of the American Chemical Society, 139 (9), 3399-3405. https://doi.org/10.1021/jacs.6b11023