RESUMEN
We have studied the reactivity of hydrogen on the Pt(211) stepped surface using supersonic molecular beam techniques. We observe an energy dependence that is indicative of indirect adsorption below 9 kJ mol(-1) and direct adsorption between 0 and 37 kJ mol(-1). Comparison of our results to predictions based on six-dimensional quantum dynamics calculations for Pt(211) [R. A. Olsen et al., J. Chem. Phys. 128, 194715 (2008)] yields reasonable agreement. Discrepancies between theory and our experiments at low kinetic energy strongly indicate that the wells in the used potential energy surface are too shallow. Discrepancies at high kinetic energy point toward neglect of degrees of freedom vital to capture the full dynamics.
RESUMEN
We examined reactivity of H(2) on Ru(0001) using molecular beam techniques and we compared our results to experimental results for similar systems. The dissociative adsorption of H(2) on Ru(0001) is similar to that on Pt(111) and Ni(111), although on ruthenium nonactivated adsorption is strongly suggested. However, we find no clear signature of a steering- or precursor-based mechanism that favors nonactivated reaction paths at low kinetic energy. In comparison to Pd(111) and Rh(111) our results indicate that a universal mechanism enhancing reactivity at low energy does not have a mass dependence. In addition, we have compared our results to predictions of reactivity for H(2) on Ru(0001) from six-dimensional dynamical calculations using two different generalized gradient approximation functionals. It leads us to conclude that the PW91 functional yields a more accurate value for the minimum energy path but does not impose enough corrugation in the potential. The revised-Perdew-Burke-Ernzerhof (RPBE) functional appears to behave slightly better at higher energies, but we find significant quantitative disagreement. We show that the difference is not due to different energy resolutions between experiment and theory. However, it may be due to a dependence of the reactivity on rotational state or on omission of relevant dimensions in the theoretical description.
RESUMEN
State-resolved measurements on clean Ni(100) and Ni(111) surfaces quantify the reactivity of CH4 excited to v = 3 of the nu4 bend vibration. A comparison with prior data reveals that 3nu4 is significantly less effective than the nu3 C-H stretch at promoting dissociative chemisorption, even though 3nu4 contains 30% more energy. These results contradict statistical theories of gas-surface reactivity, provide clear evidence for vibrational mode specificity in a gas-surface reaction, and point to a central role for C-H stretching motion along the reaction path to dissociative chemisorption.