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首页> 外文期刊>Topics in Catalysis >Model catalysts fabricated by electron beam lithography: AFM and TPD surface studies and hydrogenation/dehydrogenation of cyclohexene + H_2 on a Pt nanoparticle array supported by silica
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Model catalysts fabricated by electron beam lithography: AFM and TPD surface studies and hydrogenation/dehydrogenation of cyclohexene + H_2 on a Pt nanoparticle array supported by silica

机译:电子束光刻法制备的模型催化剂:AFM和TPD表面研究以及在二氧化硅支撑的Pt纳米颗粒阵列上环己烯+ H_2的加氢/脱氢

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Pt nanoparticle model catalysts with 28 +- 2 nm diameters and 100 +- 2 nm square periodicity have been fabricated with electron beam lithography on silica substrates. The reactivity of the Pt/SiO_2 arrays was compared to a Pt foil for cyclohexene + H_2 at 100 deg C. The overall reactivity of the Pt particle arrays was higher by a factor of two, the selectivity towards dehydrogenation was three times higher, and the rate of deactivation was about the same as for the Pt foil. Since the primary difference between the nanoparticle array and the Pt foil was the interface between the Pt and the SiO_2, the interfacial region was most likely responsible for the changes in reactivity on the arrays. Using AFM, SEM, and TPD, the arrays were characterized before and after being exposed to reaction conditions. AFM images of a sample cleaned by ion sputtering showed that the pattern of the Pt nanoparticle array was replicated in the silica during the sputtering process.
机译:已经通过电子束光刻在二氧化硅衬底上制备了具有28±2nm直径和100±2nm正方形周期性的Pt纳米颗粒模型催化剂。将Pt / SiO_2阵列的反应性与Pt箔在100℃下对环己烯+ H_2的反应性进行了比较。Pt颗粒阵列的总体反应性高出两倍,对脱氢的选择性高出三倍,并且失活速率与Pt箔大致相同。由于纳米颗粒阵列和Pt箔之间的主要区别是Pt和SiO_2之间的界面,因此界面区域最有可能负责阵列上反应性的变化。使用AFM,SEM和TPD,在暴露于反应条件之前和之后对阵列进行表征。通过离子溅射清洁的样品的AFM图像显示,在溅射过程中,Pt纳米颗粒阵列的图案在二氧化硅中复制。

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