非化学计量纳米氧化铈基催化剂的合成与性能研究

Jackie Y. Ying, Andreas Tschöpe
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引用次数: 15

摘要

纳米晶材料具有高表面积和高反应性。气体冷凝技术已经发展到合成这样的系统具有独特的控制化学计量和分散。在CeO2−x纳米晶中,高浓度的氧空位和表面吸附物质大大增强了SO2还原和CO氧化的催化活性。通过在纳米晶CeO2−x上实现Cu的超高分散,我们进一步证明了在纳米复合材料中不同组分之间定制密切协同效应的可能性。所得到的支撑母金属体系具有异常高的热稳定性,可以在显著较低的温度(分别为420°C和80°C)下选择性催化SO2还原和CO氧化。纳米晶CeO2−x基体系的高氧化还原活性与这种先进催化剂的微观结构、表面化学和电导率有关。
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Synthesis and characteristics of non-stoichiometric nanocrystalline cerium oxide-based catalysts

Nanocrystalline materials are associated with high surface area and reactivity. Gas condensation techniques have been developed to synthesize such systems with a unique control of stoichiometry and dispersion. The high concentrations of oxygen vacancies and surface adsorbed species in nanocrystalline CeO2−x were found to greatly enhance catalytic activity in SO2 reduction and CO oxidation. By having an ultrahigh dispersion of Cu on nanocrystalline CeO2−x, we have further demonstrated the possibility of tailoring intimate synergistic effects between different components in a nanocomposite material. The resulting supported base metal system has an unusually high thermal stability and could selectively catalyze SO2 reduction and CO oxidation at significantly lower temperatures (420 °C and 80 °C, respectively). The high redox activity of the nanocrystalline CeO2−x-based system is tied to the microstructure, surface chemistry, and electrical conductivity of this advanced catalyst.

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