The electrocatalytic oxidation of 5-hydroxymethylfurfural (HMF) provides a feasible approach for the efficient utilization of biomass. Defect regulation is an effective strategy in the field of biomass upgrading to enhance the adsorption capacity of reactants and thus increase the activity. However, how to select appropriate strategies to regulate the over-enrichment of reactants induced by excessive oxygen vacancy is still a huge challenge. In this work, the defect-filling strategy to design and construct an element-filled oxygen vacancy site layered double hydroxide (S─Ov─LDH) is adopted, which achieves a significant reduction in the electrolysis potential of biomass platform molecule HMF oxidation reaction and a significant increase in current density. Physical characterizations, electrochemical measurements, and theoretical calculations prove that the formation of metal─S bond in the second shell effectively regulates the electronic structure of the material, thus weakening the over-strong adsorption of HMF and OH induced by excessive oxygen vacancy, promoting the formation of high-valence Co during the reaction, and forming new adsorption sites. This work discusses the catalytic enhancement mechanism of defect filling in detail, fills the gap of defect filling in the field of biomass upgrading, and provides favorable guidance for the further development of defect regulation strategies.
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http://dx.doi.org/10.1002/advs.202410725 | DOI Listing |
Int J Biol Macromol
December 2024
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China. Electronic address:
The conversion of abundant lignin was of great significance for the utilization of biomass resources. In this study, lignin sulfonate (LS) was selected as a carbon-based support, which was successfully introduced into the NiCo-MOF structure. A series of lignin and MOF hybrid catalysts (NiCo-MOF-LS) with varying metal ratios of Ni and Co were synthesized via the hydrothermal method.
View Article and Find Full Text PDFNanoscale
December 2024
Institute of Circular Economy, College of Materials Science and Engineering, Beijing University of Technology, Beijing 100124, P. R. China.
Renewable electricity-powered electrooxidation of 5-hydroxymethylfurfural (HMFOR) to FDCA offers a green and sustainable approach to producing an essential monomer for bio-polymers, provided that a highly efficient electrocatalyst is present. Herein, we show that the doping of scandium (Sc) into an NiFe-LDH electrocatalyst (Sc-NiFe-LDH) considerably promotes HMFOR by enhancing the formation of high-valence Ni-O active sites, facilitating electron transport and HMF adsorption and suppressing the oxygen evolution reaction. In the presence of the Sc-NiFe-LDH electrocatalyst, an FDCA faradaic efficiency and selectivity of 96.
View Article and Find Full Text PDFBiotechnol Biofuels Bioprod
December 2024
Norwegian Institute of Bioeconomy Research (NIBIO), Postbox 115, NO-1431, Ås, Norway.
Biofilm is a syntrophic community of microorganisms enveloped by extracellular polymeric substances and displays remarkable adaptability to dynamic environments. Implementing biofilm in anaerobic digestion has been widely investigated and applied as it promotes microbial retention time and enhances the efficiency. Previous studies on anaerobic biofilm primarily focused on application in wastewater treatment, while its role has been significantly extended to accelerate the degradation of lignocellulosic biomass, improve gas-liquid mass transfer for biogas upgrading, or enhance resistance to inhibitors or toxic pollutants.
View Article and Find Full Text PDFMolecules
December 2024
HUN-REN Research Centre for Natural Sciences, Institute of Materials and Environmental Chemistry, Magyar Tudósok Krt. 2, 1117 Budapest, Hungary.
Zeolites with different structures (P1, sodalite, and X) were synthesized from coal fly ash by applying ultrasonically assisted hydrothermal and fusion-hydrothermal synthesis. Bimetallic catalysts, containing 5 wt.% Ni and 2.
View Article and Find Full Text PDFChemSusChem
December 2024
Department of Energy, Environmental, and Chemical Engineering, McKelvey School of Engineering, Washington University in St. Louis, St Louis, MO 63130, USA.
Chemical depolymerization of lignin is a non-selective process that often generates a wide distribution of product compounds, denoted herein as lignin breakdown products (LBPs). To address this limitation, we developed a hybrid lignin conversion process that employs a lignin-first catalytic approach on biomass and subsequent microbial upgrading. A Pd/C catalyst was used for reductive catalytic fractionation (RCF) of poplar biomass, and Rhodococcus opacus PD630 (R.
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