Dissertation
Adsorption and catalysis on Pt and Pd monolayer-modified Pt single crystal electrodes
The focus throughout this thesis will be on gathering fundamental studies of the detailed structure and composition of the electrode/electrolyte interface effect on the rate and mechanism of key electrocatalytic reactions.
- Author
- Chen, X.
- Date
- 05 December 2019
- Links
- Thesis in Leiden Repository
The focus throughout this thesis will be on gathering fundamental studies of the detailed structure and composition of the electrode/electrolyte interface effect on the rate and mechanism of key electrocatalytic reactions. The first part (Chapter 2 and 3) of this PhD thesis is about the studies of the non-Nernstian dependence on pH of the step-related voltammetric peak on platinum surface. The combined experimental and computational studies prove the existence of the co-adsorbed alkaline metal cation (Li, Na, K, and Cs) and hydroxyl at step sites of a platinum electrode. The co-adsorbed alkaline metal cation weakens the hydroxyl adsorption which yielding the anomalous non-Nernstian dependence on pH of the step-related “hydrogen peaks”. The second part starts from Chapter 4 changes first to the study of adsorption processes on a Pd monolayer-modified Pt(111) surface. Chapter 5 deals with the mechanism of electrocatalytic oxidation of formic acid and reduction of carbon dioxide on this Pd monolayer-modified Pt(111) electrode. The work in Chapter 6 explores the effects of electrolyte composition and catalysts surface structure on formic acid oxidation reaction.