4.6 Article

DFT insights into structural effects of Ni-Cu/CeO2 catalysts for CO selective reaction towards water-gas shift

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PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 23, 期 6, 页码 3826-3836

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cp05613h

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  1. Universidad de Buenos Aires [UBACyT-20020190100167BA]
  2. ANPCyT [PICT-2015-2135]
  3. FIUBA

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The water-gas shift reaction is crucial for hydrogen production, especially for meeting the high-purity H2 requirement of PEM fuel cells. Current catalysts in large-scale WGS plants require a two-step process, while Ni-Cu/CeO2 solids show promise for a one-step process in small-scale applications. By studying Ni4-xCux/CeO2(111) systems, it was found that the presence of Cu strengthens the C-O bond and increases the CO dissociation energy, leading to improved selectivity towards WGS.
The water-gas shift (WGS) reaction is a key step in hydrogen production, particularly to meet the high-purity H-2 requirement of PEM fuel cells. The catalysts currently employed in large-scale WGS plants require a two-step process to overcome thermodynamic and kinetic limitations. Ni-Cu/CeO2 solids are promising catalysts for the one-step process required for small-scale applications, as the addition of Cu hinders undesired methanation reactions occurring on Ni/CeO2. In this work, we performed calculations on Ni4-xCux/CeO2(111) systems to evaluate the influence of cluster conformation on the selectivity towards water-gas shift. The structure and miscibility of CeO2-supported Ni4-xCux clusters were investigated and compared with those of gas-phase clusters to understand the effect of metal-support interactions. The adsorption of CO onto apical Ni and Cu atoms of Ni4-xCux/CeO2(111) systems was studied, and changes in the C-O bond strength were confirmed at the electronic level by investigating shifts in the 3 sigma and 1 pi orbitals. The selectivity towards WGS was evaluated using Bronsted-Evans-Polanyi relations for the C-O activation energy. Overall, a strengthening of the C-O bond and an increase in CO dissociation energy were verified on Cu-containing clusters, explaining the improvement in selectivity of Ni4-xCux/CeO2(111) systems.

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