Insight into the mechanism of 5-hydroxymethylfurfural electroreduction to 2,5-bis(hydroxymethyl)furan over Cu anchored N-doped carbon nanosheets

被引:6
作者
Wu, Haoran [1 ]
Chen, Xinwei [2 ]
Xu, Haishan [2 ]
Yang, Runlu [1 ]
Wang, Xin [1 ]
Chen, Junying [1 ]
Xie, Zhenbing [3 ]
Wu, Liang [2 ]
Mai, Yiyong [2 ]
机构
[1] Zhengzhou Univ, Sch Chem Engn, Zhengzhou 450001, Peoples R China
[2] Shanghai Jiao Tong Univ, Frontiers Sci Ctr Transformat Mol, Sch Chem & Chem Engn, Shanghai Key Lab Elect Insulat & Thermal Ageing, Shanghai 200240, Peoples R China
[3] Tangshan Normal Univ, Dept Chem, Tangshan 063000, Peoples R China
基金
中国国家自然科学基金;
关键词
biomass; 5-hydroxymethylfurfural; electrochemical reduction; N-doped carbon materials; 2,5-bis(hydroxymethyl)furan; ELECTROCATALYTIC HYDROGENATION; OXIDATION; DESIGN;
D O I
10.1007/s12274-024-6816-x
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Design of non-noble metal electrocatalysts for biomass conversion to high-value chemicals and understanding the related catalytic mechanisms are of profound significance but have remained a major challenge. Here, we developed a novel biomass-derived electrocatalyst (denoted as Cu/NC), featuring with electron-deficient copper nanoparticles anchored on N-doped carbon nanosheets, for the electrochemical reduction of 5-hydroxymethylfurfural (HMF) to 2,5-bis(hydroxymethyl)furan (BHMF, a vital precursor of functional polymers). The optimized Cu/NC electrocatalyst exhibited an excellent performance with high Faradaic efficiency (89.5%) and selectivity (90.8%) of BHMF at a low concentration of HMF (18.1 mM). Even at a very high HMF concentration (108.6 mM), the Faraday efficiency and selectivity of BHMF could still reach 74.8% and 81.1%, respectively. This performance approached those of the reported noble metal-based electrocatalysts. Mechanism study revealed that the N doping in the Cu/NC catalyst could regulate the electronic structure of Cu, strengthening the adsorption of the HMF carbonyl group, and thus boosting the selectivity of BHMF. Additionally, strong electronic metal-support interactions of Cu and the N-doped carbon support optimized the charge transfer rate, thus promoting the dissociation of water to the active hydrogen (H*) species and boosting the reaction kinetic rate of H* and HMF.
引用
收藏
页码:7991 / 7999
页数:9
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