双金属片
催化作用
乙炔
王水
氯乙烯
铂金
氯
材料科学
反应性(心理学)
色散(光学)
碳纤维
化学工程
金属
化学
纳米技术
无机化学
组合化学
有机化学
共聚物
替代医学
医学
复合数
聚合物
光学
物理
病理
工程类
复合材料
作者
Selina K. Kaiser,Adam H. Clark,Lucrezia Cartocci,Frank Krumeich,Javier Pérez‐Ramírez
出处
期刊:Small
[Wiley]
日期:2021-01-12
卷期号:17 (16)
被引量:38
标识
DOI:10.1002/smll.202004599
摘要
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 2 PtCl 6 . 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.
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