期刊
JOURNAL OF CATALYSIS
卷 399, 期 -, 页码 15-23出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2021.04.025
关键词
Doping engineering; Oxygen vacancies; Electron transfer; Pd nanoparticles; Suzuki coupling reaction
资金
- National Natural Science Foundation of China [51772158]
Doping engineering was used to improve the physical and chemical properties of CeO2, with rare earth ions La and Nd doped into Pd/CeO2 with a double-nanotube structure. Characterizations showed that oxygen vacancies on the CeO2 surface increased significantly with the radius of rare earth ions. The Pd/CeO2-La catalyst exhibited high catalytic performance for Suzuki coupling reaction without the need for phase-transfer reagents, toxic solvents, or inert atmospheres, demonstrating green catalysis.
Doping engineering is considered as a facile and effective method for improving the physical and chemical properties of CeO2. Herein, rare earth (RE) ions (La and Nd) doped Pd/CeO2 with the coaxial double-nanotube structure were manufactured by the electrospinning and high-temperature calcination. Through the doping engineering, the original morphologies of Pd/CeO2 were not destroyed and all the elements were uniformly distributed on the surface of nanotubes. XRD, Raman and UV-vis characterizations revealed that La3+ and Nd3+ ions were incorporated into the CeO2 lattice, while the cubic fluorite structure of CeO2 was maintained. Moreover, it has been proved that there were oxygen vacancies existed on the surface of CeO2 and the concentration of oxygen vacancies increased significantly as the radius of RE ions increases. In addition, an electron transfer pathway between CeO2 and Pd nanoparticles was proposed based on the experimental data and Density Functional Theory (DFT) calculations. The Pd/CeO2-La catalyst with abundant oxygen vacancies showed a high catalytic performance for Suzuki coupling reaction under mild conditions without any phase-transfer reagent, toxic solvent and inert protective atmosphere, which realizing the green catalysis. (C) 2021 Elsevier Inc. All rights reserved.
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