纳米棒
X射线光电子能谱
材料科学
高分辨率透射电子显微镜
透射电子显微镜
拉曼光谱
傅里叶变换红外光谱
甲醛
扫描透射电子显微镜
化学工程
分析化学(期刊)
催化作用
化学
纳米材料
核化学
纳米技术
热液循环
扫描电子显微镜
生物化学
物理
光学
色谱法
工程类
复合材料
作者
Quanlong Xu,Wanying Lei,Xinyang Li,Xiaoying Qi,Jiaguo Yu,Gang Liu,Jinlong Wang,Pengyi Zhang
摘要
Gold (Au) nanoparticles (NPs) supported on well-defined ceria (CeO2) nanorods with exposed {110} and {100} facets were prepared by a deposition-precipitation method and characterized by powder X-ray diffraction, micro-Raman spectroscopy, X-ray photoelectron spectroscopy, nitrogen adsorption-desorption, transmission electron microscopy, high-resolution transmission electron microscopy, and high-angle annular dark-field scanning transmission electron microscopy. Both nanometer and subnanometer gold particles were found to coexist on ceria supports with various Au contents (0.01-5.4 wt %). The catalytic performance of Au/CeO2 catalysts was examined for formaldehyde (HCHO) oxidation into CO2 and H2O at room temperature and shown to be Au content dependent, with 1.8 wt % Au/CeO2 displaying the best performance. On the basis of the results from hydrogen temperature-programmed reduction and in situ Fourier transform infrared spectroscopy observations, the high reactivity and stability of Au/CeO2 catalysts is mainly attributed to the well-defined ceria nanorods with {110} and {100} facets which present a relatively low energy for oxygen vacancy formation. Furthermore, gold NPs could induce the weakened Ce-O bond which in turn promotes HCHO oxidation.
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