At present, the development of novel catalysts with high activity Selective Catalytic Reduction (SCR) reaction at the low temperature is still a challenge. In this work, the authors prepare CeO2/quasi-MIL-101 catalysts with various amounts of deposited ceria by a double-solvent method, which are characterized by X-ray diffraction (XRD), Fourier Transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and so on. The results show that the increase of Ce content has a great influence on the catalytic property of the catalyst. The introduction of Ce can promote the conversion between Cr3+ and Cr5+ and increase the proportion of lattice oxygen, which improves the activity of the catalyst. However, the catalyst will be peroxidized when the content of Ce is too high, resulting in the decline of the catalytic activity. This experiment indicates that CeO2/quasi-MIL-101 plays a significant role in the NH3-SCR process at the low temperature when the loading of Ce is 0.5%. This work has proved the potential of this kind of material in NH3-SCR process at the low temperature, providing help for subsequent studies.
Two-component composites consisting of transition metal copper oxide (CuO) and graphite carbon nitride (g-C3N4) were successfully synthesized. This CuO/g-C3N4 displays a high reversible specific capacity (1530.4 F g−1, 2 A g−1) as an anode material.
This paper reports on the preparation, characterization, and catalytic properties of the Pd@UIO-66 for toluene oxidation. The samples are prepared by the double-solvent method to form catalysts with large specific surface area, highly dispersed Pd0 (Elemental palladium) and abundant adsorbed oxygen, which are characterized by X-ray Photoelectron Spectroscopy (XPS), Brunauer-Emmett-Teller (BET) and Transmission Electron Microscopy (TEM). The results show that as the Pd content increases, the adsorbed oxygen content further increases, but at the same time Pd0 will agglomerate and lose some active sites, which will affect its catalytic performance. While 0.2%Pd@UIO-66 has the highest concentration of Pd0, the result shows it has the best catalytic activity and the T90 temperature is 210 °C.
Metal organic frameworks (MOFs) have been rapidly developed in the application of electrode materials due to their controllable morphology and ultra-high porosity. In this research, flower-like layered nickel-based bimetallic MOFs microspheres with different metal central ions were synthesized by solvothermal method. Compared with Ni-MOFs, the optimization of the specific capacitance of NiCo-MOFs and NiMn-MOFs was been confirmed. For example, the specific capacitance of NiCo-MOFs can reach 882 F·g−1 at 0.5 A·g−1 while maintaining satisfactory cycle life (the specific capacity remains 90.1% of the initial value after 3000 charge-discharge cycles at 5 A·g−1). In addition, the NiCo-MOFs//AC HSCs, which are composed of NiCo-MOFs and activated carbon (AC), achieved a maximum energy density of 18.33 Wh·kg−1 at a power density of 400 W·kg−1, and showed satisfactory cycle life (82.4% after 3000 cycles). These outstanding electrochemical properties can be ascribed to the synergistic effect between metal ions, the optimized conductivity, and the unique layered stacked flower structure, which provides a smooth transmission channel for electrons/ions. In addition, this research gives a general method for the application of MOFs in the field of supercapacitors.
Hybrid supercapacitors (HSCs) have aroused considerable concern in virtue of high ionic conductivity and operation voltage. In this study, three-dimensional (3D) flower-like hierarchical NiCo layered double hydroxide (LDH) microspheres are...
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