Catalytic performance of iron oxide loaded on electron-rich surfaces of carbon nitride

• Published in: Journal of energy chemistry Vol. 25; no. 6; pp. 1021 - 1026
• Main Authors: Dong, Zhen, Wang, Tao, Zhao, Jie, Fu, Teng, Wang, Li, Li, Jinlin, Ding, Weiping
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.11.2016
• Subjects: Electron-rich state; Fischer-Tropsch synthesis; H2-dissociation; Iron-based; Iron-based; Fischer-Tropsch synthesis; H2-dissociation; Electron-rich state
• ISSN: 2095-4956
• DOI: 10.1016/j.jechem.2016.10.005

Carbon nitride（CN） in CN encapsulated Ni/Al2O3（denoted as CN/Ni/Al2O3） catalyst was evidenced previously as a material in electron-rich state and possessed H2-dissociative adsorption activity due to the electron doping effect from underlying nickel. In this report, iron oxide loaded on the CN/Ni/Al2O3 was synthesized and investigated by Fischer-Tropsch（F-T） synthesis to test the special effect of electron-rich support on the catalytic activity of iron oxide. The Fe/CN/Al2O3 and CN/Ni/Al2O3 samples were accordingly synthesized for comparison. In Fe/CN/Ni/Al2O3, the iron oxide was reduced to magnetite by syngas as evidenced by the in-situ XPS measurements and XRD pattern of used catalyst. Compared with Fe/CN/Al2O3, more light hydrocarbons over Fe/CN/Ni/Al2O3 were observed. It should be understood by the interaction between iron oxide and support mainly due to the effect of electron-rich state and thus enhanced H2 adsorption ability. In addition, such a novel support facilitated the CO conversion and retarded the water-gas shift reaction and CO2 formation. The new type of adjustment on electronic state should be useful for novel catalyst design.