Biomass-derived 2D Pb <sup>0</sup>/Pb <sup>2+</sup> dual-center-site catalysts for efficient 5-hydroxymethylfurfural electroreduction

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 Pb<sup>0</sup>/Pb<sup>2+</sup> 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 Pb<sup>0</sup>/Pb<sup>2+</sup> 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 Pb<sup>2+</sup> sites and the coverage of H* species on Pb<sup>0</sup> 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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Publication Details

Journal
Nano Research
Published
2024-12-16
DOI
https://doi.org/10.26599/nr.2025.94907089
Citations
4
Primary Topic
Catalysis for Biomass Conversion
Type
article
Field-Weighted Citation Impact
0.74

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article

Biomass-derived 2D Pb 0/Pb 2+ dual-center-site catalysts for efficient 5-hydroxymethylfurfural electroreduction

Chongyin Zhang, Weixia Zhu, Yiyong Mai, Haoran Wu et al.
4 citations
Nano Research
Catalysis for Biomass Conversion
0.74
article

Biomass-derived 2D Pb 0/Pb 2+ dual-center-site catalysts for efficient 5-hydroxymethylfurfural electroreduction

Chongyin Zhang, Weixia Zhu, Yiyong Mai, Haoran Wu, Xinwei Chen, Xin Wang, Zhenbing Xie, Haishan Xu, Liang Wu, Runlu Yang
article en
4 citations

Abstract

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 Pb<sup>0</sup>/Pb<sup>2+</sup> 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 Pb<sup>0</sup>/Pb<sup>2+</sup> 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 Pb<sup>2+</sup> sites and the coverage of H* species on Pb<sup>0</sup> 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.

Nano ResearchVol. 18(2)
PLA Information Engineering University (CN), Shanghai Jiao Tong University (CN), Zhengzhou University (CN), Henan University of Engineering (CN), Shanghai Power Equipment Research Institute (CN), Tangshan Normal University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 31%
Catalysis for Biomass Conversion
0.74
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