糠醇
糠醛
催化作用
钴
选择性
双功能
氢解
材料科学
化学工程
纳米颗粒
金属有机骨架
碳纤维
双功能催化剂
呋喃
碳纳米管
多相催化
协同催化
化学
炭黑
纳米技术
金属
有机化学
过渡金属
无机化学
镍
作者
Ying Quan Lu,Yi Du,Maya Marinova,Hazar Guesmi,Qing Wang,Sebastien Royer,Nisrine Hammi,Shuo Chen,Yunqi Liu
标识
DOI:10.1021/acssuschemeng.6c01785
摘要
We report a cobalt catalyst supported on spherical nitrogen-doped carbon (CoNC) prepared via a coordinated assembly of EDTA, melamine, and chitosan followed by pyrolysis. This strategy generates uniformly dispersed Co nanoparticles strongly anchored by N functionalities. The optimized CoNC2 catalyst (4 wt % Co) exhibits outstanding performance in liquid-phase furfural hydrogenation, achieving >99% conversion and >99% selectivity toward furfuryl alcohol under mild conditions (160 °C, 30 bar H2). In situ DRIFTS, XPS, catalytic controls, and DFT calculations support a bifunctional working model in which metallic Co promotes H2 activation while adjacent N-containing environments favor selective carbonyl adsorption. This synergistic interaction suppresses competing ring hydrogenation and hydrogenolysis pathways. The catalyst shows excellent stability and recyclability. Owing to the use of earth-abundant cobalt and renewable carbon precursors, this approach provides a scalable and sustainable platform for the selective upgrading of biomass-derived aldehydes.
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