Genz Nina S, Kallio Antti-Jussi, Oord Ramon, Krumeich Frank, Pokle Anuj, Prytz Øystein, Olsbye Unni, Meirer Florian, Huotari Simo, Weckhuysen Bert M
Inorganic Chemistry and Catalysis group, Department of Chemistry, Utrecht University, Universiteitsweg 99, 3584 CG, Utrecht, The Netherlands.
Department of Physics, University of Helsinki, P. O. Box 64, 00014, Helsinki, Finland.
Angew Chem Int Ed Engl. 2022 Nov 25;61(48):e202209334. doi: 10.1002/anie.202209334. Epub 2022 Oct 26.
Laboratory-based X-ray absorption spectroscopy (XAS) and especially X-ray absorption near-edge structure (XANES) offers new opportunities in catalyst characterization and presents not only an alternative, but also a complementary approach to precious beamtime at synchrotron facilities. We successfully designed a laboratory-based setup for performing operando, quasi-simultaneous XANES analysis at multiple K-edges, more specifically, operando XANES of mono-, bi-, and trimetallic CO hydrogenation catalysts containing Ni, Fe, and Cu. Detailed operando XANES studies of the multielement solid catalysts revealed metal-dependent differences in the reducibility and re-oxidation behavior and their influence on the catalytic performance in CO hydrogenation. The applicability of operando laboratory-based XANES at multiple K-edges paves the way for advanced multielement catalyst characterization complementing detailed studies at synchrotron facilities.
基于实验室的X射线吸收光谱(XAS),尤其是X射线吸收近边结构(XANES),为催化剂表征提供了新的机会,不仅提供了一种替代方法,也是同步加速器设施宝贵束流时间的补充方法。我们成功设计了一种基于实验室的装置,用于在多个K边进行原位、准同步的XANES分析,更具体地说,是对含镍、铁和铜的单金属、双金属和三金属CO加氢催化剂进行原位XANES分析。对多元素固体催化剂进行的详细原位XANES研究揭示了还原度和再氧化行为中与金属相关的差异及其对CO加氢催化性能的影响。基于实验室的多K边原位XANES的适用性为先进的多元素催化剂表征铺平了道路,对同步加速器设施的详细研究起到了补充作用。