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具有增强乙炔氢氯化耐久性的双金属单原子金基催化剂的可持续合成

Sustainable Synthesis of Bimetallic Single Atom Gold-Based Catalysts with Enhanced Durability in Acetylene Hydrochlorination.

作者信息

Kaiser Selina K, Clark Adam H, Cartocci Lucrezia, Krumeich Frank, Pérez-Ramírez Javier

机构信息

Institute for Chemical and Bioengineering, Department of Chemistry and Applied Biosciences, ETH Zurich, Vladimir-Prelog-Weg 1, Zürich, 8093, Switzerland.

Paul Scherrer Institut, Villigen PSI, 5232, Switzerland.

出版信息

Small. 2021 Apr;17(16):e2004599. doi: 10.1002/smll.202004599. Epub 2021 Jan 12.

Abstract

Gold single-atom catalysts (SACs) exhibit outstanding reactivity in acetylene hydrochlorination to vinyl chloride, but their practical applicability is compromised by current synthesis protocols, using aqua regia as chlorine-based dispersing agent, and their high susceptibility to sintering on non-functionalized carbon supports at >500 K and/or under reaction conditions. Herein, a sustainable synthesis route to carbon-supported gold nanostructures in bimetallic catalysts is developed by employing salts as alternative chlorine source, allowing for tailored gold dispersion, ultimately reaching atomic level when using H PtCl . To rationalize these observations, several synthesis parameters (i.e., pH, Cl-content) as well as the choice of metal chlorides are evaluated, hinting at the key role of platinum in promoting a chlorine-mediated dispersion mechanism. This can be further extrapolated to redisperse large gold agglomerates (>70 nm) on carbon carriers into isolated atoms, which has important implications for catalyst regeneration. Another key role of platinum single atoms is to inhibit the sintering of their spatially isolated gold-based analogs up to 800 K and during acetylene hydrochlorination, without compromising the intrinsic activity of Au(I)-Cl active sites. Accordingly, exploiting cooperativity effects of a second metal is a promising strategy towards practical applicability of gold SACs, opening up exciting opportunities for multifunctional single-atom catalysis.

摘要

金单原子催化剂(SACs)在乙炔氢氯化制氯乙烯反应中表现出出色的反应活性,但其实际应用受到当前合成方法的限制,这些方法使用王水作为氯基分散剂,并且它们在高于500 K和/或反应条件下对非功能化碳载体上的烧结高度敏感。在此,通过使用盐作为替代氯源,开发了一种可持续的合成路线,用于制备双金属催化剂中碳负载的金纳米结构,从而实现了定制的金分散,当使用H₂PtCl₆时最终达到原子水平。为了合理解释这些观察结果,评估了几个合成参数(即pH值、Cl含量)以及金属氯化物的选择,这暗示了铂在促进氯介导的分散机制中的关键作用。这可以进一步推断为将碳载体上的大金团聚体(>70 nm)重新分散成孤立原子,这对催化剂再生具有重要意义。铂单原子的另一个关键作用是在高达800 K的温度下以及在乙炔氢氯化过程中抑制其空间隔离的金基类似物的烧结,而不会损害Au(I)-Cl活性位点的固有活性。因此,利用第二种金属的协同效应是实现金SACs实际应用的一种有前途的策略,为多功能单原子催化开辟了令人兴奋的机会。

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