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Effect of hydrothermal reaction time and calcination temperature on properties of Au@CeO2 core-shell catalyst for CO oxidation at low temperature

机译:水热反应时间和煅烧温度对Au @ CeO2核壳催化剂低温CO氧化性能的影响

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摘要

Au@CeO2 core-shell nanostructure catalysts were synthesized by hydrothermal reaction method. The effect of hydrothermal reaction time and calcination temperature on the textural and morphological characteristics of the catalyst was investigated by TEM, SEM, XRD, XPS, ICP, UV-Vis, and N-2 adsorption-desorption techniques. The results proved that gold core and CeO2 shell formed simultaneously at the beginning of the reaction. By extending the hydrothermal reaction time, both the grain size of Au core and CeO2 shell increased. The crystallization degree of CeO2 and the interaction between Au and CeO2 were also enhanced. The 90 % CO conversion temperature (T-90 %) of Au@CeO2 declined from 187 to 142 degrees C with the hydrothermal reaction time extended from 6 to 20 h. After 70-h reaction, the catalytic activity was still maintained without any loss. The effect of the calcination temperature on the catalytic performance was also investigated and it turned out that high calcination temperature has a positive influence on the catalytic activity. The likely active sites are the interface between Au core and CeO2 shell. Gold content, metal-support interaction (MSI), and oxygen vacancy are all related to the activity. The excellent performance of 20 h-600 degrees C-Au@CeO2 in catalytic activity and stability results from the joint effects of these triple factors.
机译:采用水热反应法合成了Au @ CeO2核壳纳米结构催化剂。通过TEM,SEM,XRD,XPS,ICP,UV-Vis和N-2吸附-脱附技术研究了水热反应时间和煅烧温度对催化剂结构和形貌特征的影响。结果证明,在反应开始时金核和CeO2壳同时形成。通过延长水热反应时间,金核和CeO2壳的晶粒尺寸均增加。 CeO2的结晶度以及Au和CeO2之间的相互作用也得到了增强。 Au @ CeO2的90%CO转化温度(T-90%)从187降低到142℃,水热反应时间从6延长到20 h。反应70小时后,仍保持催化活性而没有任何损失。还研究了煅烧温度对催化性能的影响,结果表明高煅烧温度对催化活性具有积极的影响。可能的活性部位是Au核与CeO2壳之间的界面。金含量,金属-载体相互作用(MSI)和氧空位均与活性有关。这些三因素的共同作用导致20 h-600摄氏度C-Au @ CeO2的出色催化活性和稳定性。

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