Influence of H2/O2 redox treatments at different temperatures on Pd-CeO2 catalyst: Structure and oxygen storage capacity

被引:20
作者
Wang, Bin [1 ]
Weng, Duan [1 ]
Wu, Xiaodong [1 ]
Fan, Jun [1 ]
机构
[1] Tsinghua Univ, State Key Lab New Ceram & Fine Proc, Dept Mat Sci & Engn, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Palladium; Ceria; Redox treatment; Oxygen storage capacity; Structure reorgnaization; CEO2-ZRO2 MIXED OXIDES; SOLID-SOLUTION; OXIDATIVE/REDUCTIVE TREATMENTS; PD/CEO2; CATALYST; 3-WAY CATALYSTS; CARBON-MONOXIDE; SURFACE-AREA; CERIA; OXIDATION; PLATINUM;
D O I
10.1016/j.cattod.2010.02.013
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In order to investigate the metal-support interaction in PM-CeO2 system, a Pd-doped CeO2 catalyst prepared by the sol-gel method and was treated in the H-2-O-2 redox atmosphere at 300,500 and 800 degrees C. respectively The Brunauer-Emmett-Teller (BET). X-ray diffraction (XRD) and temperature-programmed reduction (TPR) results indicate that the redox treatment at 300 degrees C mainly affect the surface properties of the catalyst, while those at higher temperatures have an influence on the bulk pi pet ties The step-scanning XRD and Raman results prove that Pd species on the surface of the sample mainly exist in the form of bulk Pd and pdO crystallites after the redox treatment at 500 degrees C, which are encapsulated by CeO2 particles after the treatment at 800 degrees C The CO oxidation activity. dynamic oxygen storage capacity (DOSC) and oxygen storage complete capacity (OSCC) of the catalyst vary with the treating temperature The 300 degrees C-treated sample presents the highest activity for CO oxidation and oxygen storage capacity The reduction-ratio dependent activation energy (E-a) is extremely low for the surface reduction of this sample. suggesting the participation of highly active oxygen The active oxygen are suggested to originate from the enlarged Pd-Ce interface. which depends on the avaibility of surface Pd sites and contact between metal and support (C) 2010 Elsevier B V. All rights reserved
引用
收藏
页码:111 / 117
页数:7
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