催化作用
钴
氨生产
氨
吸附
化学
镧
活动站点
合理设计
无机化学
化学工程
组合化学
材料科学
纳米技术
物理化学
有机化学
工程类
作者
Ke Zhang,Ang Cao,Lau Halkier Wandall,Jerome Vernieres,Jakob Kibsgaard,Jens K. Nørskov,Ib Chorkendorff
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2024-03-21
卷期号:383 (6689): 1357-1363
被引量:20
标识
DOI:10.1126/science.adn0558
摘要
Over the past two decades, there has been growing interest in developing catalysts to enable Haber-Bosch ammonia synthesis under milder conditions than currently pertain. Rational catalyst design requires theoretical guidance and clear mechanistic understanding. Recently, a spin-mediated promotion mechanism was proposed to activate traditionally unreactive magnetic materials such as cobalt (Co) for ammonia synthesis by introducing hetero metal atoms bound to the active site of the catalyst surface. We combined theory and experiment to validate this promotion mechanism on a lanthanum (La)/Co system. By conducting model catalyst studies on Co single crystals and mass-selected Co nanoparticles at ambient pressure, we identified the active site for ammonia synthesis as the B 5 site of Co steps with La adsorption. The turnover frequency of 0.47 ± 0.03 per second achieved on the La/Co system at 350°C and 1 bar surpasses those of other model catalysts tested under identical conditions.
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