催化作用
中心(范畴论)
生物量(生态学)
化学
5-羟甲基糠醛
对偶(语法数字)
核化学
结晶学
有机化学
生物
生态学
文学类
艺术
作者
Haoran Wu,Haishan Xu,Zhenbing Xie,Runlu Yang,Xin Wang,Xinwei Chen,Liang Wu,Chongyin Zhang,Weixia Zhu,Yiyong Mai
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2024-12-16
卷期号:18 (2): 94907089-94907089
被引量:4
标识
DOI:10.26599/nr.2025.94907089
摘要
Using natural resources to construct electrocatalysts for biomass conversion and elucidating their catalytic mechanisms are of great significance, but have remained challenging. Here, a series of two-dimensional (2D) biomass-based Pb/PbO@C catalysts with Pb/PbO nanoparticles anchored on carbon nanosheets were synthesized using natural-derived humate as the precursor. By adjusting the carbonization temperature, an electron-deficient Pb0/Pb2+ dual-center-site catalyst can be achieved. The optimized Pb/PbO@C catalyst showed an excellent performance for the electrochemical hydrogenation of 5-hydroxymethylfurfural (HMF) to high value-added 2,5-bis(hydroxymethyl)furan (BHMF), with high Faradaic efficiency (FE: 91.9%) and selectivity (Sel: 89.7%), achieving comparable performance to those of the reported noble metal-based electrocatalysts. Mechanism study revealed that the electron-deficient Pb0/Pb2+ dual-center-site provided abundant Lewis acidic sites and promoted the dissociation of water to the active hydrogen (H*) species, thus enhancing the adsorption of HMF on Pb2+ sites and the coverage of H* species on Pb0 sites. The high coverage of H* species and the synergistic effect of dual-center sites substantially promoted the binding of H* and HMF to form H-HMF* and inhibited the recombination of H* species, thereby accelerating the reaction kinetics of HMF reduction.
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