Carboxyl group enhanced CO tolerant GO supported Pt catalysts: DFT and electrochemical analysis
Research output: Contribution to journal › Article › peer-review
- Aarhus Universitet
- Department of Chemistry, College of Chemistry and Chemical Engineering, and MOE Key Laboratory of Analytical Sciences, Xiamen University, Xiamen 361005, China.
- Department of Physics and Astronomy
- Aarhus University
- Royal Military College of Canada
- Institute for Renewable Energy and Environmental Technologies (IREET)
- Knowledge Centre for Materials Chemistry (KCMC)
- University of Bolton
The effect of residual oxygen species in as-prepared Pt nanoparticle on partially reduced graphene oxide (Pt/PRGO) and partially reduced carboxylated-GO (Pt/PR(GO-COOH)) supports was investigated using electrochemical CO stripping and density functional theory (DFT) analysis. Pt/PRGO and Pt/PR(GO-COOH) revealed a clear negative shift in CO-stripping onset potential compared to commercial Pt/carbon black. DFT analysis confirmed that the presence of a -COOH group provides the most resistance for CO adsorption. This CO-Pt binding energy is significantly lower than that observed in the presence of an OH group, which is the most abundant oxygen group in carbon supports. The Pt-CO dissociation energies (on a 42-atom graphene sheet) in the presence of various oxygen groups, in descending order, were OH > C=O ≈ C-O-C > COOH. Although single-bonded carbon-oxygen groups (-OH and C-O-C) are more abundant on the GO basal plane and play an important role in Pt nanoparticle nucleation and distribution on graphene sheets, the double-bonded carbon-oxygen (C=O and COOH) groups are more abundant residual species post Pt nanoparticle growth and play a vital role in enhancing CO tolerance.
|Number of pages||10|
|Journal||Chemistry of Materials|
|Publication status||Published - 11 Nov 2014|