催化作用
石墨烯
多孔性
氮气
化学
磷
材料科学
贵金属
布朗斯特德-洛瑞酸碱理论
化学工程
无机化学
有机化学
纳米技术
工程类
作者
Chunlin Chen,Xingtao Li,Lingchen Wang,Ting Liang,Lei Wang,Yajie Zhang,Jian Zhang
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2017-11-01
卷期号:5 (12): 11300-11306
被引量:62
标识
DOI:10.1021/acssuschemeng.7b02049
摘要
The oxidation of 5-hydroxylmethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) is a sustainable and promising route to bioderived aromatic polyesters. So far, the design of catalyst has been restricted by the unclear working mechanism, and thus most of the supported noble metal catalysts cannot provide a remarkable reaction rate under atmospheric pressures and room temperature. Here we report a new mechanistic insight into the structure–performance correlation of graphene-supported Pd catalysts. It is demonstrated that a new kind of highly porous nitrogen- and phosphorus-codoped graphene sheets (HPGSs) will enhance the fraction of surface Pd2+ species, which plays a determining role to reduce the activation energies of both HMF conversion and FDCA formation. Such a support effect may assist in developing highly active catalysts for FDCA synthesis under mild conditions.
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