Valence state and redox property of Fe-CNTs added CeO2/TiO2 catalyst

被引:0
|
作者
Lee, Minseo [1 ]
Park, Gwanhee [2 ]
Kim, Myungju [2 ]
Lee, Jaekwang [2 ]
Jo, Ilguk [3 ]
Lee, Heesoo [2 ]
机构
[1] Pusan Natl Univ, Grad Sch Convergence Sci, Busan, South Korea
[2] Pusan Natl Univ, Dept Mat Sci & Engn, Busandaehak Ro 63beon Gil2, Busan 609705, South Korea
[3] Dong Eui Univ, Ctr Brain Busan 21 Plus Program, Busan 47340, South Korea
关键词
ceria-based catalyst; Fe-CNTs; oxygen vacancy; reactive oxygen species (ROS); redox property; MIXED-OXIDE CATALYST; REDUCTION; PERFORMANCE; NOX;
D O I
10.1111/ijac.14919
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The investigation focused on examining the impact of incorporating Fe-carbon nanotubes (CNTs) on the valence state and oxygen vacancies, and the physicochemical parameters of the catalytic system. For the CeO2/TiO2 catalyst with Fe-CNTs, no distinct X-ray diffraction (XRD) peaks corresponding to Fe-CNTs were observed. This indicated their uniform dispersion, supported by transmission electron microscopy (TEM) and scanning electron microscopy (SEM) imaging. X-ray photoelectron spectroscopy (XPS) analysis was conducted to observe the changes in the valence state due to the addition of Fe-CNTs. The concentration of Ce3+ on catalyst surface increased from 19.90% to 29.48% with an increased concentration of the chemisorbed oxygen species (O-alpha). This suggests that the addition of Fe-CNTs into CeO2/TiO2 catalyst reduced Ce4+ on the catalyst surface, resulting in the formation of oxygen vacancies. Oxygen temperature-programmed desorption (O-2-TPD) and hydrogen temperature-programmed reduction (H-2-TPR) analyses showed both the adsorbed oxygen species and H-2 consumption increased with adding Fe-CNTs. Furthermore, the onset temperatures for O-2 desorption and H-2 consumption became lower, confirming the enhancement of catalytic redox properties.
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页数:7
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