Interfacial and surface structures of CeO2-TiO2 mixed oxides

被引:76
作者
Fang, Jun [1 ]
Bao, Huizhi [1 ]
He, Bo [2 ]
Wang, Fang [1 ]
Si, Dejun [1 ]
Jiang, Zhiquan [1 ]
Pan, Zhiyun [2 ]
Wei, Shiqiang [2 ]
Huang, Weixin [1 ]
机构
[1] Fritz Haber Inst, Hefei Natl Lab Phys Sci Microscale, Dept Chem Phys, MPG CAS Partner Grp, Hefei 230026, Peoples R China
[2] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Peoples R China
关键词
D O I
10.1021/jp076627m
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
The interfacial and surface structures of CeO2-TiO2 mixed oxides prepared by the sol-gel method have been investigated in detail by means of X-ray diffraction (XRD), BET surface area measurement, X-ray absorption spectroscopy (XAS), high-resolution transmission electron microscope (HRTEM), and selective chemisorption of methyl orange. TiO2 and CeO2 are in the anatase phase and the cubic fluorite phase in CeO2-TiO2 mixed oxides, respectively. The mixed oxides exhibit much higher surface areas than the individual oxides and are with both mesopores and micropores. XAS results suggest that Ce atoms nucleate as cubic [CeO8] polyhedrons with the formation of a Ce-O-Ti interface in mixed oxides. With the increasing Ce/ TiO2 weight ratio, the cubic fluorite CeO2 crystallites gradually develop. TiO2 anatase forms ultrafine particles in mixed oxides, whose local structure is stabilized by the presence of CeO2. HRTEM results reveal that the exposed surfaces of mixed oxides depend on the Cc concentration. Chemisorption results of methyl orange that was found to adsorb profoundly on CeO2 but little on TiO2 demonstrate that CeO2 in mixed oxides exhibits much lower adsorption capacity toward methyl orange than pure CeO2. Our results demonstrate an approach to characterize interfacial and surface structures of complex mixed oxides, which are of great importance in understanding their properties.
引用
收藏
页码:19078 / 19085
页数:8
相关论文
共 39 条
[1]  
[Anonymous], CATALYSIS CERIA RELA
[2]   Photoinduced reactivity of titanium dioxide [J].
Carp, O ;
Huisman, CL ;
Reller, A .
PROGRESS IN SOLID STATE CHEMISTRY, 2004, 32 (1-2) :33-177
[3]   XAFS studies of surface structures of TiO2 nanoparticles and photocatalytic reduction of metal ions [J].
Chen, LX ;
Rajh, T ;
Wang, ZY ;
Thurnauer, MC .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (50) :10688-10697
[4]   INFLUENCE OF THE PREPARATION METHOD ON THE CHARACTERISTICS OF TIO2-CEO2 SUPPORTS [J].
DAUSCHER, A ;
WEHRER, P ;
HILAIRE, L .
CATALYSIS LETTERS, 1992, 14 (02) :171-183
[5]   Origin of enhanced reducibility/oxygen storage capacity of Ce1-xTixO2 compared to CeO2 or TiO2 [J].
Dutta, Gargi ;
Waghmare, Umesh V. ;
Baidya, Tinku ;
Hegde, M. S. ;
Priolkar, K. R. ;
Sarode, P. R. .
CHEMISTRY OF MATERIALS, 2006, 18 (14) :3249-3256
[6]   Spectroscopic studies of interfacial structures of CeO2-TiO2 mixed oxides [J].
Fang, Jun ;
Bi, Xinzhen ;
Si, Dejun ;
Jiang, Zhiquan ;
Huang, Weixin .
APPLIED SURFACE SCIENCE, 2007, 253 (22) :8952-8961
[7]   Structural study of copper oxide supported on a ceria-modified titanic catalyst system [J].
Francisco, MSP ;
Mastelaro, VR ;
Florentino, AO ;
Bazin, D .
TOPICS IN CATALYSIS, 2002, 18 (1-2) :105-111
[8]   Activity and characterization by XPS, HR-TEM, Raman spectroscopy, and BET surface area of CuO/CeO2-TiO2 catalysts [J].
Francisco, MSP ;
Mastelaro, VR ;
Nascente, PAP ;
Florentino, AO .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (43) :10515-10522
[9]   THE ATOMIC AND ELECTRONIC-STRUCTURE OF CERIUM SUBSTITUTIONAL DEFECTS IN ND2-XCEXCUO4+DELTA AN XAS STUDY [J].
GHIGNA, P ;
SPINOLO, G ;
SCAVINI, M ;
TAMBURINI, UA ;
CHADWICK, AV .
PHYSICA C, 1995, 253 (1-2) :147-155
[10]   STUDY OF THE K EDGES OF 3D TRANSITION-METALS IN PURE AND OXIDE FORM BY X-RAY-ABSORPTION SPECTROSCOPY [J].
GRUNES, LA .
PHYSICAL REVIEW B, 1983, 27 (04) :2111-2131