Direct versus hydrogen-assisted CO dissociation over stepped Ni and Ni3Fe surfaces: a computational investigation. Issue 44 (19th October 2015)

• Record Type: Journal Article
• Authors: Yang, Kuiwei; Zhang, Minhua; Yu, Yingzhe
• Is Part Of: Physical chemistry chemical physics. Volume 17:Issue 44(2015)
• Page Start: 29616
• Page End: 29627
• Publication Date: 2015-10-19
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c5cp04335b
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : We explored direct and H-assisted CO dissociation on pure and alloyed Ni(211) and highlighted the importance of Fe locating in the step edge. Abstract : The adsorption and dissociation of CO over stepped Ni and Ni3 Fe surfaces were systematically studied using density functional theory slab calculations. Both (211)-like surface structure terminations (NiNi step and NiFe step, denoted as Ni3 Fe(211)-AA and Ni3 Fe(211)-AB) are considered for Ni3 Fe. Direct scission of the C–O bond in CO is identified as the least likely one among the three proposed dissociation pathways and CO dissociation via a CHO intermediate appears to be most feasible at low CO coverage on pure and alloyed Ni(211) surfaces. The priority of H-assisted CO dissociation might originate from the more activated C–O bond in COH and CHO. Compared to Ni(211), the Ni3 Fe(211)-AB surface could facilitate CO activation especially for the most possible CHO intermediate mechanism, whose rate-limiting step is found to be altered. The d-band center theory and Mulliken charge analysis are also employed to explain the activity difference between Ni3 Fe(211)-AB and Ni3 Fe(211)-AA. The significant structural sensitivity of CO dissociation highlights the importance of Fe locating in the step edge and the high reactivity of Ni3 Fe(211)-AB is largely ascribed to the synergistic effect between Ni and Fe at the step edge.