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Complex structural dynamics of nanocatalysts revealed in Operando conditions by correlated imaging and spectroscopy probes

机译:相关成像和光谱探针在Operando条件下揭示纳米催化剂的复杂结构动力学

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Understanding how heterogeneous catalysts change size, shape and structure during chemical reactions is limited by the paucity of methods for studying catalytic ensembles in working state, that is, in operando conditions. Here by a correlated use of synchrotron X-ray absorption spectroscopy and scanning transmission electron microscopy in operando conditions, we quantitatively describe the complex structural dynamics of supported Pt catalysts exhibited during an exemplary catalytic reaction-ethylene hydrogenation. This work exploits a microfabricated catalytic reactor compatible with both probes. The results demonstrate dynamic transformations of the ensemble of Pt clusters that spans a broad size range throughout changing reaction conditions. This method is generalizable to quantitative operando studies of complex systems using a wide variety of X-ray and electron-based experimental probes.
机译:缺乏了解在化学反应过程中非均相催化剂如何改变尺寸,形状和结构的方法受到研究工作状态(即在操作条件下)催化团簇的方法匮乏的限制。在此,通过在操作条件下同步使用加速器X射线吸收光谱法和扫描透射电子显微镜,我们定量地描述了在示例性催化反应-乙烯加氢过程中表现出的负载Pt催化剂的复杂结构动力学。这项工作开发了与两个探针兼容的微型催化反应器。结果表明,在不断变化的反应条件下,Pt团簇的动态转变跨越了很大的尺寸范围。该方法可推广到使用各种基于X射线和电子的实验探针对复杂系统进行定量操作研究。

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