Recently we presented a computational study on the conversion of ethylene to ethylidyne over Pd(111) via a plausible three-step mechanism, ethylene -> vinyl -> ethylidene -> ethylidyne. Here, using essentially the same periodic slab model density functional approach, we investigate two further possible routes, ethylene vinyl -> vinylidene -> ethylidyne and ethylene -> ethyl -> ethylidene -> ethylidyne. We systematically compared three coverages of the adsorbate, 1/3, 1/4, and 1/9. We show that the reaction pathway via vinylidene is also feasible on Pd(111). One is not able to judge solely from the potential energy landscape whether the route via ethylidene or that via vinylidene dominates the formation of ethylidyne; at low coverages, our results tend to favor slightly the latter mechanism. The mechanism via ethyl Could be operative when a sufficient concentration of surface hydrogen is present. It features the lowest activation barrier for the rate-limiting second step, 81-88 kJ mol(-1), but the activation energy for ethyl hydrogenation to ethane, 51 kJ mol(-1), is still much lowers this suggests that ethyl should preferentially convert to ethane rather than to ethylidene.     «

Recently we presented a computational study on the conversion of ethylene to ethylidyne over Pd(111) via a plausible three-step mechanism, ethylene -> vinyl -> ethylidene -> ethylidyne. Here, using essentially the same periodic slab model density functional approach, we investigate two further possible routes, ethylene vinyl -> vinylidene -> ethylidyne and ethylene -> ethyl -> ethylidene -> ethylidyne. We systematically compared three coverages of the adsorbate, 1/3, 1/4, and 1/9. We show that t...     »

ISI Document Delivery No.: 484BH Times Cited: 11 Cited Reference Count: 35 Moskaleva, Lyudmila V. Aleksandrov, Hristiyan A. Basaran, Duygu Zhao, Zhi-Jian Roesch, Notker Moskaleva, Lyudmila/D-1889-2012 Deutsche Forschungsgemeinsehaft; Fonds der Chemischen Industrie (Germany); National Center of Advanced Materials UNION; Bulgarian National Science Fund [VUH-17/05] This work was supported by Deutsche Forschungsgemeinsehaft and Fonds der Chemischen Industrie (Germany). H.A.A. is grateful for support by the National Center of Advanced Materials UNION and the Bulgarian National Science Fund (contract VUH-17/05). 11 Amer chemical soc Washington     «

ISI Document Delivery No.: 484BH Times Cited: 11 Cited Reference Count: 35 Moskaleva, Lyudmila V. Aleksandrov, Hristiyan A. Basaran, Duygu Zhao, Zhi-Jian Roesch, Notker Moskaleva, Lyudmila/D-1889-2012 Deutsche Forschungsgemeinsehaft; Fonds der Chemischen Industrie (Germany); National Center of Advanced Materials UNION; Bulgarian National Science Fund [VUH-17/05] This work was supported by Deutsche Forschungsgemeinsehaft and Fonds der Chemischen Industrie (Germany). H.A.A. is grateful for supp...     »