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一种用于热催化 CO 加氢的碳化钼纳米粒子的超温和可扩展的溶液相合成方法。

An Exceptionally Mild and Scalable Solution-Phase Synthesis of Molybdenum Carbide Nanoparticles for Thermocatalytic CO Hydrogenation.

机构信息

National Bioenergy Center , National Renewable Energy Laboratory , 15013 Denver West Parkway , Golden , Colorado 80401-3305 , United States.

Department of Chemistry , University of Southern California , 840 Downey Way , Los Angeles , California 90089-0744 , United States.

出版信息

J Am Chem Soc. 2020 Jan 15;142(2):1010-1019. doi: 10.1021/jacs.9b11238. Epub 2020 Jan 2.

DOI:10.1021/jacs.9b11238
PMID:31894975
Abstract

Transition metal carbides (TMCs) have demonstrated outstanding potential for utilization in a wide range of catalytic applications because of their inherent multifunctionality and tunable composition. However, the harsh conditions required to prepare these materials have limited the scope of synthetic control over their physical properties. The development of low-temperature, carburization-free routes to prepare TMCs would unlock the versatility of this class of materials, enhance our understanding of their physical properties, and enable their cost-effective production at industrial scales. Here, we report an exceptionally mild and scalable solution-phase synthesis route to phase-pure molybdenum carbide (α-MoC) nanoparticles (NPs) in a continuous flow millifluidic reactor. We exploit the thermolytic decomposition of Mo(CO) in the presence of a surface-stabilizing ligand and a high boiling point solvent to yield MoC NPs that are colloidally stable and resistant to bulk oxidation in air. To demonstrate the utility of this synthetic route to prepare catalytically active TMC NPs, we evaluated the thermochemical CO hydrogenation performance of α-MoC NPs dispersed on an inert carbon support. The α-MoC/C catalyst exhibited a 2-fold increase in both activity on a per-site basis and selectivity to C products as compared to the bulk α-MoC analogue.

摘要

过渡金属碳化物 (TMCs) 由于其固有的多功能性和可调的组成,在广泛的催化应用中表现出了卓越的潜力。然而,制备这些材料所需的苛刻条件限制了对其物理性质进行合成控制的范围。开发低温、无碳化的方法来制备 TMCs 将释放这类材料的多功能性,增强我们对其物理性质的理解,并能够以经济有效的方式在工业规模上生产。在这里,我们报告了一种在连续流微流控反应器中用异常温和且可扩展的溶液相合成路线制备纯相碳化钼 (α-MoC) 纳米颗粒 (NPs) 的方法。我们利用 Mo(CO) 在表面稳定配体和高沸点溶剂存在下的热解分解来生成胶体稳定且在空气中不易被体相氧化的 MoC NPs。为了展示这种合成路线在制备催化活性 TMC NPs 方面的实用性,我们评估了分散在惰性碳载体上的 α-MoC NPs 的热化学 CO 加氢性能。与块状 α-MoC 类似物相比,α-MoC/C 催化剂在单位活性位基础上的活性和 C 产物选择性均提高了一倍。

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