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The development of catalysts with high activity and selectivity for the electrochemical nitrogen reduction reaction (NRR) remains crucial. Molybdenum carbide (MoC) shows promise as an electrocatalyst for NRR but faces challenges due to the difficulty of N adsorption and activation as well as the competitive hydrogen evolution reaction. In this study, we propose a strategy of combining TiO with MoC to form heterostructure catalysts.

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The mesopores and macropores within porous carbon materials help increase the surface for the depostion of solid-state products, reduce the LiS film thickness, enhance electron and mass transport, and accelerate the reaction kinetics. However, an excessive amount of mesopores and macropores can lead to increased electrolyte consumption, particularly at high sulfur loadings, where excessive electrolyte usage hampers the enhancement of practical energy density in lithium-sulfur (Li-S) batteries. A rational pore structure can minimize the amount of electrolyte to fill the pores, thereby reducing electrolyte consumption while achieving rapid reaction kinetics and a high gravimetric energy density.

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Exploring interfacial electrocatalysis for iodine redox conversion in zinc-iodine battery.

Sci Bull (Beijing)

November 2024

Key Laboratory for Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China. Electronic address:

The challenges posed by the non-conductive nature of iodine, coupled with the easy formation of soluble polyiodides in water, impede its integration with zinc for the development of advanced rechargeable batteries. Here we demonstrate the in-situ loading of molybdenum carbide nanoclusters (MoC) and zinc single atoms (Zn-SA) into porous carbon fibers to invoke electrocatalytic conversion of iodine at the interface. The electronic interactions between MoC and Zn-SA lead to an upshift in the d-band center of Mo relative to the Fermi level, thus promoting the interfacial interactions with iodine species to suppress shuttle effects.

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Zinc cadmium sulphide-based photoreforming of biomass-based monosaccharides to lactic acid and efficient hydrogen production.

J Colloid Interface Sci

December 2024

Key Laboratory of Bio-Based Material Science and Technology, Ministry of Education, Material Science and Engineering College, Northeast Forestry University, Harbin 150040, China. Electronic address:

Approaches that add value to biomass through the use of photoreforming reactions offer great opportunities for the efficient use of renewable resources. Here, we constructed a novel zinc cadmium sulphide/molybdenum dioxide-molybdenum carbide-carbon (ZnCdS-y/MoO-MoC-C) heterojunction which was applied to photoreforming of biomass-based monosaccharides for hydrogen and lactic acid production. Bandgap engineering effectively modulated the redox capacity of ZnCdS-y and exposed more (101) crystalline surfaces, which improved the lactic acid selectivity.

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A Highly Active Molybdenum Carbide Catalyst with Dynamic Carbon Flux for Reverse Water-Gas Shift Reaction.

Angew Chem Int Ed Engl

December 2024

Beijing National Laboratory for Molecular Sciences, New Cornerstone Laboratory, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, China.

Molybdenum carbide has been reported as an efficient and stable catalyst for reverse water-gas shift (RWGS) reaction. The conventional understanding of the mechanism suggests domination of the surface phenomena, with only surface or subsurface layers partaking in the catalytic cycle. In this study, we presented a highly active MoC catalyst from carburization process, which showed a mass-specific reaction rate over 260 μm with dynamic carbon flux in the bulk phase of the catalyst.

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