State Key Laboratory of Multiphase Complex Systems, Institute of Process Engineering, Chinese Academy of Sciences, Graduate University of Chinese Academy of Sciences, 100190 BeierSt. 1, Beijing, China.
Chemphyschem. 2011 Oct 24;12(15):2763-70. doi: 10.1002/cphc.201100346. Epub 2011 Aug 31.
We report on the preparation and characterization of CeO(2) nanofibers (CeO(2)-NFs) and nanocubes (CeO(2)-NCs), as well as Sm- and Gd-doped CeO(2) nanocubes (Sm-CeO(2)-NCs and Gd-CeO(2)-NCs), synthesized by a simple hydrothermal process for CO catalytic oxidation. The samples were characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), Raman spectroscopy, and photoluminescence spectroscopy. Their oxygen-storing capacity (OSC) was examined by means of hydrogen temperature-programmed reduction (H(2)-TPR) and oxygen pulse techniques. Their catalytic properties for CO catalytic oxidation were comparatively investigated. The results showed that the CeO(2)-NFs possessed a higher catalytic activity compared to the CeO(2)-NCs because of their smaller size and the greater number of oxygen vacancies. The activity of the Sm-CeO(2)-NCs was higher than that of the CeO(2)-NCs due to an increase in the number of oxygen vacancies, which results from the substitution of Ce(4+) species with Sm(3+) ions. In contrast, Gd doping had a negative effect on the CO catalytic oxidation due to the special electron configuration of Gd(3+) (4f(7)). Our work demonstrates that the oxygen vacancies in pure CeO(2) and the electron configuration of the dopants in doped CeO(2) play an important role in CO oxidation.
我们报告了 CeO(2)纳米纤维(CeO(2)-NFs)和纳米立方体(CeO(2)-NCs),以及 Sm 和 Gd 掺杂 CeO(2)纳米立方体(Sm-CeO(2)-NCs 和 Gd-CeO(2)-NCs)的制备和特性,这些材料是通过简单的水热法合成的,用于 CO 催化氧化。样品通过 X 射线衍射(XRD)、BET、X 射线光电子能谱(XPS)、透射电子显微镜(TEM)、拉曼光谱和光致发光光谱进行了表征。通过氢气程序升温还原(H(2)-TPR)和氧脉冲技术考察了它们的储氧能力(OSC)。比较研究了它们对 CO 催化氧化的催化性能。结果表明,CeO(2)-NFs 比 CeO(2)-NCs 具有更高的催化活性,因为它们的尺寸更小,氧空位更多。Sm-CeO(2)-NCs 的活性高于 CeO(2)-NCs,因为 Ce(4+)物种被 Sm(3+)离子取代导致氧空位增加。相比之下,Gd 掺杂对 CO 催化氧化有负面影响,这是由于 Gd(3+)(4f(7))的特殊电子构型所致。我们的工作表明,纯 CeO(2)中的氧空位和掺杂 CeO(2)中的掺杂剂的电子构型在 CO 氧化中起着重要作用。