催化作用
糠醛
呋喃
键裂
选择性
X射线光电子能谱
吸附
化学
纳米颗粒
氧烷
无机化学
材料科学
化学工程
纳米技术
有机化学
光谱学
工程类
物理
量子力学
作者
Shenyu Wang,Junjie Zhang,Ying Zhang
出处
期刊:Chemsuschem
[Wiley]
日期:2024-11-05
卷期号:18 (6): e202401938-e202401938
被引量:7
标识
DOI:10.1002/cssc.202401938
摘要
In the conversion of furfural using non-noble metal catalysts, preferential cleavage of the C2-O bond followed by hydrogenation of the C=C bond facilitates selective access to valuable 1,5-pentanediol (1,5-PeD). Herein, we developed CeO₂ loaded core-shell CoO@Co nanoparticle catalysts. Adjusting Co loading, Fe doping, and reduction temperature improved reaction efficiency. 7Co-0.2Fe/CeO₂ catalysts reduced at 500 °C demonstrated optimal performance. 1,5-PeD produced at 54.76 mmol/gCo/h, representing the top activity levels among the reported catalysts. H₂-TPR, XRD, HAADF-STEM, FT-IR, XPS, and XANES were employed to investigate the catalyst structure-activity relationship. Co2+ cleaves furan ring C-O bond, Co⁰ promotes double-bond hydrogenation. The CoO@Co structure favors the desired 1,5-PeD production route. Trace Fe species optimize the Co2+/Co⁰ ratio, enhance the substrate adsorption, and inhibit the furan ring saturation. These findings emphasize the importance of fine-tuning catalyst structure and composition for selectivity improvement.
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