The catalytic activity of Ni-Fe oxide embedded in CNTs was investigated in terms of valence states and active oxygen species. Ni-Fe oxides were prepared by the sol-gel combustion process, and Ni-Fe oxides embedded in CNT catalysts were synthesized by the catalytic chemical vapor deposition (CCVD) method. The lattice structure of the Ni-Fe oxide catalysts was analyzed, and the lattice distortion was increased with the addition of Fe. The specific surface areas and pore structures of the Ni-Fe oxides embedded in CNTs were determined through the BET method. The nano-sized Ni-Fe oxides embedded in CNTs were observed using morphology analysis. The crystallinity and defects of CNTs were analyzed by Raman spectroscopy, and the ID/IG ratio of Ni1.25Fe0.75O/CNT was the lowest at 0.36, representing the high graphitization and low structural defects of the CNT surface. The valence states of Fe and Ni were changed by the interaction between catalysts and CNTs. The redox property of the catalysts was evaluated by H2-TPR analysis, and the H2 consumption of Ni1.25Fe0.75O/CNT was the highest at 2.764 mmol/g. The catalytic activity of Ni-Fe oxide embedded in CNT exhibited much higher activity than Ni-Fe oxide for the selective catalytic reduction of NOx with NH3 in the temperature range of 100 °C to 450 °C.
Keywords: CNT synthesis; active oxygen species; catalytic activity; charge transfer; redox property.