Methanol oxidation on the PtPd(111) alloy surface: A density functional theory study

International Journal of Quantum Chemistry

3 years ago

Methanol oxidation on the PtPd(111) alloy surface: A density functional theory study

Sheng Guo, Fei Hou, Jing Xu, Jing Li, Lianming Zhao

The mechanisms of methanol (CH3OH) oxidation on the PtPd(111) alloy surface were systematically investigated by using density functional theory calculations. The energies of all the involved species were analyzed. The results indicated that with the removal of H atoms from adsorbates on PtPd(111) surface, the adsorption energies of (i) CH3OH, CH2OH, CHOH, and COH increased linearly, while those of (ii) CH3OH, CH3O, CH2O, CHO, and CO exhibited odd-even oscillation. On PtPd(111) surface, CH3OH underwent the preferred initial CH bond scission followed by successive dehydrogenation and then CHO oxidation, that is, CH3OH CH2OH CHOH CHO CHOOH COOH CO2. Importantly, the rate-determining step of CH3OH oxidation was found to switch from CO CO2 on Pt(111) to COOH CO2 + H on PtPd(111) with a lower energy barrier of 0.96 eV. Moreover, water also decomposed into OH more easily on PtPd(111) than on Pt(111). The calculated results indicate that alloying Pt with Pd could efficiently improve its catalytic performance for CH3OH oxidation through altering the primary pathways from the CO path on pure Pt to the non-CO path on PtPd(111). The mechanisms of methanol oxidation on the PtPd(111) alloy surface are systematically evaluated by means of density functional theory calculations. The reaction prefers a path in which the initial CH bond scission step is followed by successive dehydrogenation and CHO oxidation. The simulation results suggest that alloying Pt with Pd efficiently improves catalytic performances for CH3OH oxidation through altering the primary pathways from the CO path on pure Pt to a non-CO path.

Publisher URL: http://onlinelibrary.wiley.com/resolve/doi

DOI: 10.1002/qua.25491