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原位多维 3D 化学成像技术在分级结构核壳催化剂中的应用

In Situ Multimodal 3D Chemical Imaging of a Hierarchically Structured Core@Shell Catalyst.

机构信息

Institute for Chemical Technology and Polymer Chemistry, Karlsruhe Institute of Technology , Engesserstraße 20, 76131 Karlsruhe, Germany.

Science Division, Diamond Light Source , Harwell Science and Innovation Campus, Didcot, Oxon OX11 0DE, United Kingdom.

出版信息

J Am Chem Soc. 2017 Jun 14;139(23):7855-7863. doi: 10.1021/jacs.7b02177. Epub 2017 May 26.

Abstract

A Cu/ZnO/AlO@ZSM-5 core@shell catalyst active for one-step conversion of synthesis gas to dimethyl ether (DME) was imaged simultaneously and in situ using synchrotron-based micro X-ray fluorescence (μ-XRF), X-ray diffraction (μ-XRD), and scanning transmission X-ray microscopy (STXM) computed tomography (CT) with micrometer spatial resolution. An identical sample volume was imaged stepwise, first under oxidizing and reducing atmospheres (imitating calcination and activation processes), and then under model reaction conditions for DME synthesis (H:CO:CO ratio of 16:8:1, up to 250 °C). The multimodal imaging methods offered insights into the active metal structure and speciation within the catalyst, and allowed imaging of both the catalyst core and zeolite shell in a single acquisition. Dispersion of nanosized Cu species was observed in the catalyst core during reduction, with formation of a metastable Cu phase at the core-shell interface. Under DME reaction conditions at 1 bar, the coexistence of Cu in the active catalyst core together with partially oxidized Cu species was unraveled. The zeolite shell and core-shell interface remained stable under all conditions, preserving the bifunctional nature of the catalyst. These observations are inaccessible using standard bulk techniques like X-ray absorption spectroscopy (XAS) and XRD, demonstrating the potential of multimodal in situ X-ray CT for characterization of hierarchically designed materials, which stand to benefit tremendously from such 3D spatially resolved measurements.

摘要

采用同步辐射微 X 射线荧光(μ-XRF)、X 射线衍射(μ-XRD)和扫描透射 X 射线显微镜(STXM)计算机断层扫描(CT),对用于一步法将合成气转化为二甲醚(DME)的 Cu/ZnO/AlO@ZSM-5 核壳催化剂进行了同步原位成像,空间分辨率可达微米级。对相同的样品体积进行分步成像,首先在氧化和还原气氛下(模拟煅烧和活化过程),然后在 DME 合成的模型反应条件下(H:CO:CO 比为 16:8:1,高达 250°C)。多模态成像方法深入了解了催化剂中活性金属结构和形态,并且可以在单次采集时对催化剂核和沸石壳进行成像。在还原过程中,在催化剂核中观察到纳米级 Cu 物种的分散,在核壳界面形成亚稳 Cu 相。在 1 巴的 DME 反应条件下,揭示了在活性催化剂核中 Cu 的共存以及部分氧化的 Cu 物种。在所有条件下,沸石壳和核壳界面都保持稳定,保持了催化剂的双功能性质。这些观察结果是使用标准的体相技术(如 X 射线吸收光谱(XAS)和 XRD)无法获得的,证明了多模态原位 X 射线 CT 对分级设计材料的表征具有潜力,这种 3D 空间分辨测量将使这些材料受益巨大。

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