贵金属
催化作用
密度泛函理论
化学吸附
化学
物理吸附
空位缺陷
氧化还原
电子转移
铑
金属
烟灰
材料科学
X射线光电子能谱
氧气
无机化学
物理化学
化学工程
计算化学
结晶学
有机化学
工程类
燃烧
作者
Jae‐Hwan Lee,Deok Yeon Jo,Jin Woo Choung,Chang Hwan Kim,Hyung Chul Ham,Kwan Young Lee
标识
DOI:10.1016/j.jhazmat.2020.124085
摘要
The effects of noble metal (M = Ag, Au, Pd, Pt, and Rh) on CeO2 in enhancing the activity toward soot oxidation were studied through experimental methods and density functional theory (DFT) calculations. Each noble metal (3 mol.%) was supported on CeO2 (M/CeO2) and the properties of the catalysts were verified by XRD, HRTEM, N2 physisorption, CO chemisorption, XPS, and H2-TPR results. The noble metal was highly dispersed over CeO2, except for Au due to the sintering of Au, and the reducibility of the catalysts was greatly improved according to degree of the interaction between each noble metal and CeO2. The activities of M/CeO2 catalysts for soot oxidation were better than that of CeO2, and followed the order Rh/CeO2 > Ag/CeO2 > Pt/CeO2 > Au/CeO2 > Pd/CeO2 > CeO2. Moreover, our DFT calculations showed that vacancy formation energy was gradually lowered in the following order: CeO2 > Pd4/CeO2 > Pt4/CeO2 > Au4/CeO2 = Ag4/CeO2 > Rh4/CeO2, which was similar order with experimental activity. In addition, the electronic states of the p and f orbitals of CeO2 were studied to compare with the occupied Ce 4f electrons, which affect the redox property. Rh/CeO2 and Ag/CeO2 showed the improved soot oxidation activity, with an enhanced ability to generate oxygen vacancy formation and oxygen adsorption and increased electron transfer. Consequently, the experimental and DFT calculation results revealed the roles of noble metals on ceria with respect to catalytic activity.
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