期刊
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 23, 期 6, 页码 3826-3836出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cp05613h
关键词
-
资金
- Universidad de Buenos Aires [UBACyT-20020190100167BA]
- ANPCyT [PICT-2015-2135]
- FIUBA
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.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据