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Surface chemistry and catalysis on well-defined oxide surfaces: nanoscale design bases for single-site heterogeneous catalysts

机译:明确定义的氧化物表面上的表面化学和催化作用:单中心非均相催化剂的纳米级设计基础

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As the surface science of metal oxides has developed over the past two decades, it has made increasing contributions to the understanding of the site requirements for catalysis by oxides. Metal oxide single crystals and thin films represent the systems most often studied by surface science techniques as models of oxide catalysts. We explore an alternative approach-molecular functionalization of surfaces with ordered arrays of discrete, reactive oxide molecules. Heteropolyanions (polyoxometalates) can be deposited to form ordered monolayers that permit site-by-site mapping of chemical functions on the surface, as well as characterization of redox properties of individual molecules by tunneling spectroscopy with the scanning tunneling microscope. These nanoscale oxide clusters exhibit negative differential resistance in their tunneling spectra at potentials that track their reduction potentials. Thus tunneling spectroscopy measurements may provide correlation and prediction tools for catalyst performance in selective oxidation processes. Because polyoxometalate monolayers present uniform catalytic sites whose redox properties can be defined by single molecule spectroscopy, they may serve as a prototype of single site heterogeneous catalysts designed and fabricated on the nanoscale. (C) 2003 Elsevier Science (USA). All rights reserved. [References: 63]
机译:在过去的二十年中,随着金属氧化物表面科学的发展,它对理解氧化物催化的位点要求做出了越来越大的贡献。金属氧化物单晶和薄膜代表最常通过表面科学技术研究的系统,作为氧化物催化剂的模型。我们探索了一种替代方法-用离散的反应性氧化物分子的有序阵列对表面进行分子功能化。杂多阴离子(多金属氧酸盐)可以沉积形成有序的单分子层,从而可以在表面上逐点绘制化学功能,并利用扫描隧道显微镜通过隧道光谱法表征单个分子的氧化还原特性。这些纳米级氧化物簇在其隧穿谱中在追踪其还原电位的电位处显示负的差分电阻。因此,隧道光谱测量可以为选择性氧化过程中的催化剂性能提供相关和预测工具。因为多金属氧酸盐单分子层具有均匀的催化位点,其氧化还原特性可以通过单分子光谱法确定,所以它们可以用作在纳米级设计和制造的单位点非均相催化剂的原型。 (C)2003 Elsevier Science(美国)。版权所有。 [参考:63]

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