纳米材料基催化剂
催化作用
氧化还原
材料科学
化学工程
氧气
氧化铈
热液循环
纳米颗粒
比表面积
无机化学
纳米技术
化学
冶金
工程类
生物化学
有机化学
作者
Junjie Chen,Hien N. Pham,Tala Mon,Todd J. Toops,Abhaya K. Datye,Zhenglong Li,Eleni A. Kyriakidou
出处
期刊:ACS applied nano materials
[American Chemical Society]
日期:2023-03-07
卷期号:6 (6): 4544-4553
被引量:14
标识
DOI:10.1021/acsanm.2c05496
摘要
Catalytic oxidation of CH4 over nonprecious Ni/CeO2 catalysts has attracted wide attention. Controlling the morphology of a CeO2 support can enhance the CH4 oxidation activity without changing the catalyst composition. Herein, a series of 2 wt % Ni/CeO2 nanocatalysts with different CeO2 support morphologies (nanoparticles (P), rods (R), cubes (C)) and synthetic procedures (precipitation, sol-gel (SG)) were evaluated for their CH4 oxidation performance. The redox properties of CeO2 supports and corresponding Ni loaded catalysts were characterized by H2-temperature-programmed reduction and oxygen storage capacity (OSC) measurements. The relationship among the CeO2 morphologies, surface areas, redox properties, and CH4 oxidation activity for both CeO2 supports and Ni/CeO2 catalysts was established. The findings suggest that CeO2-R has a greater amount of surface oxygen vacancies as well as an improved OSC and CH4 oxidation activity compared to CeO2-P and CeO2-C supports. The same CH4 oxidation activity pattern was observed for the Ni containing catalysts (Ni/CeO2-R > Ni/CeO2-P > Ni/CeO2-C). Increasing the CeO2 surface area by using a sol-gel synthesis method (CeO2-SG) improved the amount of surface oxygen vacancies and CH4 oxidation performance of CeO2-SG and Ni/CeO2-SG compared to CeO2-R and Ni/CeO2-R, respectively. Finally, all studied Ni/CeO2 nanocatalysts showed improved hydrothermal stability compared to conventional Pd/Al2O3.
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