Year: 2018
Type: article
Abstract: Single-site catalysts (SSCs) have drawn considerable attention, because of their superior behaviors in catalysis. However, the origin of promoting the effect of a single site is not well understood. Here, we take the single-atom Ni 1 /Mg(100) and single-site Ni 4 /Mg(100) catalysts as a case study to elucidate their behaviors under the complex dry reforming of methane (DRM, CO 2 + CH 4 → 2CO + 2H 2 ) reaction by combining theoretical modeling (density functional theory and kinetic Monte Carlo simulation) and experimental studies. The synergy between single Ni atom and MgO is found to improve the binding property of MgO; yet, it is not enough to dissociate CO 2 and CH 4 . It can be achieved by the single-site Ni 4 /MgO(100) catalyst, enabling the formations of CO, H 2, and H 2 O under the DRM conditions. During this process, coking, as observed for bulklike Ni particles, is eliminated. By confining the reaction to occur at the isolated Ni sites in the SSC, the Ni 4 /MgO(100) catalyst is able to balance the CO 2 and CH 4 activations, which is identified as the key for tuning the DRM activity and selectivity of Ni/MgO catalysts. The theory-identified promotion introduced by increasing the size of MgO-supported Ni clusters from Ni 1 to Ni 4 and the MgO-introduced site confinement of single-site catalysts are verified by corresponding experimental studies, highlighting the essential roles of confined sites in tuning the performance of SSCs during complex catalytic processes.
Source: ACS Catalysis
Language: English
Subfield: Catalysis
Field: Chemical Engineering
Domain: Physical Sciences
Open Access status: green
Awards: G1285306620, Heterogeneous hydrophilic catalysts for green oxidation in bio-refining, G1847291448, G2203623476, G241279073, G3262563802, G3351671514, 合成气高效转化集成工艺及其关键科学与技术问题的研究, G357145406, G3850097093, Targeting nano-catalysts for sustainable biorefining and chemical processes, G473394231, G5765906131, G5958906545, G6965541988, G711835860, G7211337958, G7463374569, G945952457
OpenAlex ID: W2892024026
