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Visualizing atomic-scale redox dynamics in vanadium oxide-based catalysts

机译:可视化氧化钒基催化剂中的原子级氧化还原动力学

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摘要

Surface redox processes involving oxygen atom exchange are fundamental in catalytic reactions mediated by metal oxides. These processes are often difficult to uncover due to changes in the surface stoichiometry and atomic arrangement. Here we employ high-resolution transmission electron microscopy to study vanadium oxide supported on titanium dioxide, which is of relevance as a catalyst in, e.g., nitrogen oxide emission abatement for environmental protection. The observations reveal a reversible transformation of the vanadium oxide surface between an ordered and disordered state, concomitant with a reversible change in the vanadium oxidation state, when alternating between oxidizing and reducing conditions. The transformation depends on the anatase titanium dioxide surface termination and the vanadium oxide layer thickness, suggesting that the properties of vanadium oxide are sensitive to the supporting oxide. These atomic-resolution observations offer a basis for rationalizing previous reports on shape-sensitive catalytic properties.
机译:涉及氧原子交换的表面氧化还原过程是金属氧化物介导的催化反应的基础。由于表面化学计量和原子排列的变化,通常很难发现这些过程。在这里,我们采用高分辨率透射电子显微镜研究了负载在二氧化钛上的氧化钒,该氧化钒在例如用于环保的减少氮氧化物排放中作为催化剂具有重要意义。这些观察结果揭示了当在氧化和还原条件之间交替时,钒氧化物表面在有序和无序状态之间可逆转变,同时伴随着钒氧化态的可逆变化。该转变取决于锐钛矿二氧化钛表面终止和氧化钒层的厚度,这表明氧化钒的性质对支持氧化物敏感。这些原子分辨率的观察结果为合理化先前有关形状敏感催化性能的报告提供了基础。

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