Yue Zhang , Rongrong Zhang , Guozhu Liu , Li Wang , Zhiyong Pan
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引用次数: 0
Abstract
Core-shell Ru@Pd/SBA-15 catalysts with various atomic layer numbers of Pd were prepared by changing the Pd/Ru ratio and Pd coating temperature. The results of characterizations show that the compressive strain of Pd atoms and electron transfer from Ru to Pd result in a downward shift in the d-band center of core–shell catalysts. Density functional theory calculations further reveal that the reduced d-band center of Pd via strain and electronic effects weakens the adsorption ability of Pd. A roughly volcano-shaped correlation between the d-band center and 2-ethyl-anthraquinone (EAQ) hydrogenation activity is experimentally observed. The catalyst with Pd shell of 2 atomic layers provides medium adsorption strength for EAQ and hydrogenated product, thereby exhibiting the highest activity of 0.37 molH2·gMet−1·min−1, with a selectivity of 97.3%. This work provides a facile strategy for optimizing hydrogenation performance by modulating the strain and electron effects between the Ru core and Pd shell through regulating the number of shell layers.
期刊介绍:
The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes.
The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods.
The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.