4.7 Article

Enhanced performance of La1-xFeO3-6 oxygen carrier via A-site cation defect engineering for chemical looping dry reforming of methane

Journal

FUEL PROCESSING TECHNOLOGY
Volume 248, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.fuproc.2023.107820

Keywords

Perovskite; Defect; Chemical looping; Methane

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Chemical looping is a process-intensification tool that has wide applications in various energy-related and environmental-related areas. In this study, we developed a simple and efficient strategy to enhance the catalytic activity of LaFeO3 by tuning A-site cation defects via a sol-gel method. The results showed that the A-site cation defects significantly affect the physical and chemical properties of the material, and by adjusting the A-site cation defects, the catalytic performance for CH4 oxidation and CO2 splitting can be greatly improved.
Chemical looping is a process-intensification tool that focuses on the fields of fossil fuel combustion, CO2 capture, hydrocarbon valorization, energy storage, and other energy-related and environmental-related areas. Perovskitestructured LaFeO3, a typical oxygen storage material, shows great potential for chemical looping partial oxidation and H2O/CO2 splitting. Here, we report a simple and efficient strategy to enhance catalytic activity by tuning A-site cation defects in perovskites via a sol-gel method. Systematically studies show that A-site cation defects affect both the physical and chemical properties. With the A-site cation defect engineering, the crystallite size of the La1-xFeO3-6 perovskites is reduced. The catalytic performance for CH4 oxidation and CO2 splitting is enhanced with increasing oxygen vacancy concentration. The La0.93FeO3-6 oxygen carrier exhibits the highest catalytic performance with 88% CO selectivity and 90% methane conversion at 750 degrees C. In addition, the La0.93FeO3-6 shows higher stability in the successive CH4 partial oxidation/CO2 splitting redox cycles, with almost unchanged CH4 conversion and CO selectivity. All these results demonstrate that the strategy of adjustment of different molar ratios of A/B site in perovskite metal oxides can effectively regulate the oxygen vacancy concentration.

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