Carbon-coated SnO2 nanoparticles were synthesized by a simple one-pot hydrothermal treatment. During the hydrothermal process, SnO2 was formed by the hydrolysis of tin(II) dichloride dihydrate (SnCl2·2H2O) in alkali solution, while sucrose was used as the carbon source to form the coated polysaccharide shell on the SnO2 nanoparticles. In the obtained carbon-coated SnO2 nanoparticles, SnO2 nanocrystals with a diameter of 4 nm were observed to be homogeneously dispersed in the particles. After calcination, the product exhibited improved lithium storage properties, as compared to pure SnO2 nanoparticles. The carbon-coated SnO2 nanoparticles exhibit 430 mAh g−1 reversible capacities after 100 cycles and an average capacity fading of 0.2% per cycle after the 20th cycle. The good electrochemical performances of the carbon-coated SnO2 nanoparticles indicate that the obtained carbon shell can effectively increase the stability of the active materials and improve the cycling performance of oxide-based anode materials for lithium-ion batteries.
In this work, pure nanostructured Mg(2)FeH(6) is successfully synthesized by sintering of a mixture of 2Mg + Fe nanoparticles. The successful preparation of pure Mg(2)FeH(6) can be attributed to the small particle sizes of Mg and Fe nanoparticles prepared by hydrogen plasma-metal reaction (HPMR), which benefits the synthesis. The hydrogen storage properties of Mg(2)FeH(6) and the synthesis mechanism of the Mg-Fe-H system are studied. The sample desorbs 5.0 wt% of hydrogen rapidly in 6 min under an initial hydrogen pressure of approximately 100 Pa at 623 K. The enthalpy and entropy of the reaction are deduced from the equilibrium plateau pressures of the desorption isotherms. The obtained Mg(2)FeH(6) shows favorable hydrogen storage properties due to the specific nanostructure of the materials.
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