双金属片
合金
催化作用
高分辨率透射电子显微镜
异构化
路易斯酸
材料科学
金属
X射线光电子能谱
氧化物
化学
单层
无机化学
化学工程
纳米技术
有机化学
透射电子显微镜
工程类
作者
Yan Wei,Weimin Shi,Maoyong Cao,Li Gong,Jifan Li,Chun‐Ling Liu,Wen‐Sheng Dong
标识
DOI:10.1002/cctc.202301112
摘要
Abstract In this work, a series of N‐doped carbon supported FeCo bimetallic catalysts with plentiful FeCo alloy‐FeO interfaces, which are derived from metal‐organic frameworks (MOFs) ZIF‐67, are designed for the one‐pot direct conversion of methyl levulinate to 1,4‐pentanediol. The FeCo alloy‐FeO interfaces are precisely controlled via tuning the reduction temperatures and Fe/Co ratios. The optimal catalyst gives a high 1,4‐pentanediol yield of 90.5 % along with complete conversion of methyl levulinate. These catalysts are carefully characterized by multiple techniques, such as HRTEM, XRD, XPS, NH 3 −TPD, and Py−IR. It is found that Co presents in electron deficiency caused by the electron transference from Co to Fe in FeCo alloy, which in turn enhances the heterolysis of H 2 . In addition, plentiful Lewis acid sites derived from interfacial FeO species favour the re‐adsorption and the ring‐opening reaction of γ‐valerolactone. With the synergy between FeCo alloy and Lewis acid, the FeCo alloy‐FeO interfaces exhibit excellent catalytic activity for selective hydrogenation of methyl levulinate to 1,4‐pentanediol.
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