文献类型：期刊文献

英文题名：Selective hydrogenation of 5-(hydroxymethyl)furfural to 5-methylfurfural over single atomic metals anchored on Nb2O5

作者：Li, Shaopeng[1,2];Dong, Minghua[1,2];Yang, Junjuan[1];Cheng, Xiaomeng[1,2];Shen, Xiaojun[1,2];Liu, Shulin[1,2];Wang, Zhi-Qiang[3];Gong, Xue-Qing[3];Liu, Huizhen[1,2,4];Han, Buxing[1,2,4]

机构：[1]Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, CAS Key Lab Colloid & Interface & Thermodynam, Beijing 100190, Peoples R China;[2]Univ Chinese Acad Sci, Sch Chem & Chem Engn, Beijing 100190, Peoples R China;[3]East China Univ Sci & Technol, Sch Chem & Mol Engn, Ctr Computat Chem & Res Inst Ind Catalysis, Key Lab Adv Mat, Shanghai 200237, Peoples R China;[4]Huairou Natl Comprehens Sci Ctr, Phys Sci Lab, Beijing 101407, Peoples R China

年份：2021

卷号：12

期号：1

外文期刊名：NATURE COMMUNICATIONS

收录：;WOS:【SCI-EXPANDED(收录号:WOS:000614030100001)】；

基金：This work was supported by the National Key Research and Development Program of China (2018YFB0605801, 2017YFA0403003), Beijing Municipal Science & Technology Commission (Z191100007219009, Z181100004218004), and National Natural Science Foundation of China (21871277). Chinese Academy of Sciences (QYZDY-SSW-SLH013). The EXAFS experiment was conducted at Beijing Synchrotron Radiation Facility.

语种：英文

摘要：5-Methylfurfural (MF) is a very useful chemical. Selective hydrogenation of biomass platform molecule 5-(hydroxymethyl)furfural (HMF) to MF using H-2 as the reducing agent is very attractive, but challenging because hydrogenation of C=O bond in HMF is more favourable than C-OH both kinetically and thermodynamically, and this route has not been realized. In this work, we prepare isolated single atomic catalysts (SACs) Pt-1/Nb2O5-Ov, Pd-1/Nb2O5-Ov, and Au-1/Nb2O5-Ov, in which single metal atoms are supported on oxygen defective Nb2O5 (Nb2O5-Ov). It is discovered that the SACs can efficiently catalyze the hydrogenation of HMF to MF using H-2 as the reducing agent with MF selectivity of >99% at complete conversion, while the selectivities of the metal nanocatalysts supported on Nb2O5 are very poor. A combination of experimental and density function theory (DFT) studies show that the unique features of the SACs for the reaction result from the cooperation of the Nb and Pt sites near the interface in the Pt-1/Nb2O5-Ov. The Pt atoms are responsible for the activation of H-2 and the Nb sites activate C-OH in the reaction. This work opens the way for producing MF by direct hydrogenation of biomass-derived HMF using H-2 as the reductant. Selective hydrogenation of 5-(hydroxymethyl)furfural (HMF) to 5-Methylfurfural using H2 as reductant is very attractive, but remains challenging. Here, the authors report that isolated single atomic catalysts can catalyze the reaction efficiently with selectivity >99% at complete conversion of HMF.