RESUMO
The problem of poisoning on the surface of catalysts used in CO oxidation reactions, such as Pt, needs to be solved. In this work, we constructed lattice-matched C2N/Pt(111) catalysts with different configurations (top/fcc/hcp) and found that, within the confined space between the cover and the substrate, the adsorption energy of CO is reduced by 0.35 eV to 0.43 eV, while the adsorption of other reactants O/O2 is strengthened and the adsorption energy of the product CO2 is positive, indicating that the constraint effect produced by C2N and Pt(111) is beneficial to CO oxidation, when compared to the pure Pt(111). Our work suggests that the C2N cover not only protects the Pt surface under harsh conditions but also allows gaseous molecules CO and O2 to approach the Pt surface through a facile intercalation process, with enhanced surface reactivity for CO oxidation and reduced catalyst poisoning.
RESUMO
Motivated by recent experimental developments of graphitic-CN (g-CN) sheets, we investigate the suitability of hydrogen storage on Li decorated g-CN via first-principles calculations. We find that the binding energies of Li atoms are very large, ranging from 2.70 to 4.73 eV, which are significantly higher than the cohesive energy of bulk Li. Lithium atoms therefore tend to form 2D rather than 3D patterns on g-CN, promoting reversible hydrogen adsorption and desorption. Remarkably, the average adsorption energy of H2 molecules falls in the 0.14-0.23 eV range, and the Li decorated CN shows a high theoretical gravimetric density of 10.81 wt%, which is favorable for massive hydrogen storage. Our results suggest that the Li decorated CN could be a promising hydrogen storage material under realistic conditions.
