文献类型：期刊文献

英文题名：Promoting Effects of In2O3 on Co3O4 for CO Oxidation: Tuning O2 Activation and CO Adsorption Strength Simultaneously

作者：Lou, Yang[1];Ma, Jian[1];Cao, Xiaoming[1];Wang, Li[1];Dai, Qiguang[1];Zhao, Zhenyang[1];Cai, Yafeng[1];Zhan, Wangcheng[1];Guo, Yanglong[1];Hu, P.[1];Lu, Guanzhong[1];Guo, Yun[1]

机构：[1]E China Univ Sci & Technol, Res Inst Ind Catalysis, Key Labs Adv Mat, Shanghai 200237, Peoples R China

年份：2014

卷号：4

期号：11

起止页码：4143

外文期刊名：ACS CATALYSIS

收录：;EI(收录号：20144600208793);WOS:【SCI-EXPANDED(收录号:WOS:000344639300041)】；

基金：This project was supported financially by the National Basic Research Program of China (2010CB732300, 2013CB933201), the National High Technology Research and Development Program of China (2012AA062703, 2012AA111717), NSFC of China (21171055, 21273150, 21333003, 21303051), and the "Shu Guang" Project of the Shanghai Municipal Education Commission. The authors thank the National Supercomputer Center in Jinan for computing time. P.H. thanks the Chinese Government for the "Thousands Talents" program.

语种：英文

外文关键词：Co3O4; In2O3; CO oxidation; CO adsorption strength; redox ability; surface carbonate species

摘要：The doping of In2O3 significantly promoted the catalytic performance of Co3O4 for CO oxidation. The activities of In2O3Co3O4 increased with an increase in In2O3 content, in the form of a volcano curve. Twenty-five wt % In2O3Co3O4 (25 InCo) showed the highest CO oxidation activity, which could completely convert CO to CO2 at a temperature as low as -105 degrees C, whereas it was only -40 degrees C over pure Co3O4. The doping of In2O3 induced the expansion of the unit cell and structural distortion of Co3O4, which was confirmed by the slight elongation of the CoO bond obtained from EXAFS data. The red shift of the UVvis absorption illustrated that the electron transfer from O-2 to Co3+/Co2+ became easier and implied that the bond strength of CoO was weakened, which promoted the activation of oxygen. Low-temperature H-2-TPR and O-2-TPD results also revealed that In2O3Co3O4 behaved with excellent redox ability. The XANES, XPS, XPS valence band, and FT-IR data exhibited that the CO adsorption strength became weaker due to the downshiftof the d-band center, which correspondingly weakened the adsorption of CO2 and obviously inhibited the accumulation of surface carbonate species. In short, the doping of In2O3 induced the structural defects, modified the surface electronic structure, and promoted the redox ability of Co3O4, which tuned the adsorption strength of CO and oxygen activation simultaneously.