加氢脱氧
糠醛
催化作用
杂原子
纳米颗粒
X射线光电子能谱
化学工程
电子顺磁共振
化学
材料科学
有机化学
无机化学
光化学
纳米技术
选择性
工程类
物理
核磁共振
戒指(化学)
作者
Hui Yang,Hao Chen,Wenhua Zhou,Haoan Fan,Chao Chen,Yixuan Sun,Jiaji Zhang,Sifan Wang,Teng Guo,Jie Fu
标识
DOI:10.1016/j.jechem.2022.11.037
摘要
Hydrodeoxygenation of furfural (FF) into 2-methylfuran (MF) is a significant biomass utilization route. However, designing efficient and stable non-noble metal catalyst is still a huge challenge. Herein, we reported the N, O co-doped carbon anchored with Co nanoparticles (Co-SFB) synthesized by employing the organic ligands with the target heteroatoms. Raman, electron paramagnetic resonance (EPR), electrochemical impedance spectroscopy (EIS), and X-ray photoelectron spectroscopy (XPS) characterizations showed that the co-doping of N and O heteroatoms in the carbon support endows Co-SFB with enriched lone pair electrons, fast electron transfer ability, and strong metal-support interaction. These electronic properties resulted in strong FF adsorption as well as lower apparent reaction activation energy. At last, the obtained N, O co-doped Co/C catalyst showed excellent catalytic activity (nearly 100 mol% FF conversion and 94.6 mol% MF yield) and stability for in-situ dehydrogenation of FF into MF. This N, O co-doping strategy for the synthesis of highly efficient catalytic materials with controllable electronic state will provide an excellent opportunity to better understand the structure–function relationship.
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