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首页> 外文期刊>Physical chemistry chemical physics: PCCP >Synthesis of silica supported AuCu nanoparticle catalysts and the effects of pretreatment conditions for the CO oxidation reaction
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Synthesis of silica supported AuCu nanoparticle catalysts and the effects of pretreatment conditions for the CO oxidation reaction

机译:二氧化硅负载的AuCu纳米粒子催化剂的合成及CO氧化反应的预处理条件的影响

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Supported gold nanoparticles have generated an immense interest in the field of catalysis due to their extremely high reactivity and selectivity. Recently, alloy nanoparticles of gold have received a lot of attention due to their enhanced catalytic properties. Here we report the synthesis of silica supported AuCu nanoparticles through the conversion of supported Au nanoparticles in a solution of Cu(C2H3O2)2 at 300 °C. The AuCu alloy structure was confirmed through powder XRD (which indicated a weakly ordered alloy phase), XANES, and EXAFS. It was also shown that heating the AuCu/SiO2 in an O2 atmosphere segregated the catalyst into a Au-CuO_x heterostructure between 150 °C to 240 °C. Heating the catalyst in H2 at 300 °C reduced the CuO_x back to Cu° to reform the AuCu alloy phase. It was found that the AuCu/SiO2 catalysts were inactive for CO oxidation. However, various pretreatment conditions were required to form a highly active and stable Au-CuO_x/SiO2 catalyst to achieve 100% CO conversion below room-temperature. This is explained by the in situ FTIR result, which shows that CO molecules can be chemisorbed and activated only on the Au-CuO_x/SiO2 catalyst but not on the AuCu/SiO2 catalyst.
机译:负载的金纳米颗粒由于其极高的反应性和选择性而在催化领域引起了极大的兴趣。近来,金的合金纳米颗粒由于其增强的催化性能而受到了广泛的关注。在这里,我们报告了在300°C的Cu(C2H3O2)2溶液中负载的Au纳米颗粒的转化,从而合成了二氧化硅负载的AuCu纳米颗粒。通过粉末XRD(表明合金相较弱),XANES和EXAFS证实了AuCu合金的结构。还显示了在O 2气氛中加热AuCu / SiO 2将催化剂分离成150℃至240℃之间的Au-CuO x异质结构。将催化剂在H2中于300°C加热,将CuO_x还原为Cu°,以重整AuCu合金相。发现AuCu / SiO 2催化剂对于CO氧化是惰性的。但是,需要各种预处理条件以形成高活性和稳定的Au-CuO_x / SiO2催化剂,以在室温以下实现100%的CO转化率。这由原位FTIR结果解释,该结果表明CO分子只能在Au-CuO_x / SiO2催化剂上而不是在AuCu / SiO2催化剂上被化学吸附和活化。

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