选择性
镍
催化作用
乙烯
化学
无机化学
亲核细胞
吸附
解吸
钼
掺杂剂
铼
氧气
材料科学
有机化学
兴奋剂
光电子学
作者
Anika Jalil,Elizabeth E. Happel,Laura A. Cramer,Adrian Hunt,Adam S. Hoffman,Iradwikanari Waluyo,M. M. Montemore,Phillip Christopher,E. Charles H. Sykes
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-02-20
卷期号:387 (6736): 869-873
标识
DOI:10.1126/science.adt1213
摘要
Over the last 80 years, chlorine (Cl) has been the primary promoter of the ethylene epoxidation reaction valued at ~40 billion USD per year, providing a ~25% selectivity increase over unpromoted silver (Ag) (~55%). Promoters such as cesium, rhenium, and molybdenum each add a few percent of selectivity enhancements to achieve 90% overall, but their codependence on Cl makes optimizing and understanding their function complex. We took a theory-guided, single-atom alloy approach to identify nickel (Ni) as a dopant in Ag that can facilitate selective oxidation by activating molecular oxygen (O 2 ) without binding oxygen (O) too strongly. Surface science experiments confirmed the facile adsorption/desorption of O 2 on NiAg, as well as demonstrating that Ni serves to stabilize unselective nucleophilic oxygen. Supported Ag catalyst studies revealed that the addition of Ni in a 1:200 Ni to Ag atomic ratio provides a ~25% selectivity increase without the need for Cl co-flow and acts cooperatively with Cl, resulting in a further 10% initial increase in selectivity.
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