Boosting the catalytic performance of core-shell structured Ru@Pd/SBA-15 in 2-ethyl-anthraquinone hydrogenation by tuning d-band center

被引:5
作者
Zhang, Yue [1 ,3 ]
Zhang, Rongrong [1 ]
Liu, Guozhu [1 ]
Wang, Li [1 ]
Pan, Zhiyong [2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Minist Educ, Tianjin 300072, Peoples R China
[2] SINOPEC, Res Inst Petr Proc, Beijing 100083, Peoples R China
[3] China Wuzhou Engn Grp Corp Ltd, Beijing 100053, Peoples R China
关键词
Hydrogenation; Pd catalyst; Core-shell; d -band center; Bimetallic catalyst; H2O2; PD NANOPARTICLES; 2-ETHYLANTHRAQUINONE; RU; ANTHRAQUINONE; ELECTROCATALYST; FABRICATION; ETHANOL; ALUMINA; SBA-15; AU;
D O I
10.1016/j.jcat.2024.115793
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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 molH(2)center dot gMet(-1)center dot 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.
引用
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页数:13
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