乙炔
铂金
氯乙烯
催化作用
Atom(片上系统)
氯化物
铂纳米粒子
材料科学
纳米颗粒
纳米技术
化学工程
无机化学
冶金
化学
有机化学
复合材料
计算机科学
工程类
嵌入式系统
共聚物
聚合物
作者
Selina K. Kaiser,Edvin Fako,Gabriele Manzocchi,Frank Krumeich,Roland Hauert,Adam H. Clark,Оlga V. Safonova,Núria Lopéz,Javier Pérez-Ramı́rez
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2020-03-02
卷期号:3 (4): 376-385
被引量:152
标识
DOI:10.1038/s41929-020-0431-3
摘要
The worldwide replacement of the toxic mercuric chloride catalyst in vinyl chloride manufacture via acetylene hydrochlorination is slowed by the limited durability of alternative catalytic systems at high space velocities. Here, we demonstrate that platinum single atoms on carbon carriers are substantially more stable (up to 1,073 K) than their gold counterparts (up to 473 K), enabling facile and scalable preparation and precise tuning of their coordination environment by simple temperature control. By combining kinetic analysis, advanced characterization, and density functional theory, we assess how the Pt species determines the catalytic performance and thereby identify Pt(ii)−Cl as the active site, being three times more active than Pt nanoparticles. We show that Pt single atoms exhibit outstanding stability in acetylene hydrochlorination and surpass the space–time yields of their gold-based analogues after 25 h time-on-stream, qualifying them as a candidate for sustainable vinyl chloride production. Platinum nanoparticles have been neglected as a catalyst for acetylene hydrochlorination due to their limited activity. Here, the authors show that nanostructuring to the single-atom level renders platinum on carbonaceous supports a superior catalyst for this important industrial process.
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