| Literature DB >> 27445106 |
Peng Zhai1, Cong Xu2, Rui Gao3,4, Xi Liu3,4, Mengzhu Li1, Weizhen Li1, Xinpu Fu5, Chunjiang Jia5, Jinglin Xie1, Ming Zhao2, Xiaoping Wang3,4, Yong-Wang Li3,4, Qianwen Zhang6, Xiao-Dong Wen7,8, Ding Ma9.
Abstract
Zn- and Na-modulated Fe catalysts were fabricated by a simple coprecipitation/washing method. Zn greatly changed the size of iron species, serving as the structural promoter, while the existence of Na on the surface of the Fe catalyst alters the electronic structure, making the catalyst very active for CO activation. Most importantly, the electronic structure of the catalyst surface suppresses the hydrogenation of double bonds and promotes desorption of products, which renders the catalyst unexpectedly reactive toward alkenes-especially C5+ alkenes (with more than 50% selectivity in hydrocarbons)-while lowering the selectivity for undesired products. This study enriches C1 chemistry and the design of highly selective new catalysts for high-value chemicals.Entities:
Keywords: CO hydrogenation; heterogeneous catalysis; iron catalysts; olefins; sodium dopant
Year: 2016 PMID: 27445106 DOI: 10.1002/anie.201603556
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336