Journal
SMALL
Volume 18, Issue 24, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202201306
Keywords
bifunctional electrocatalysts; biomass electrooxidation; electrochemical coupling reaction; flow cells; hydrogen evolution reaction
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Funding
- Science and Technology Project of Shenzhen [JCYJ20190806155814624]
- Fundamental Research Funds for the Central Universities [3102017jc01001]
- China Postdoctoral Science Foundation [BX2021247, 2021M692635]
- Guangdong Basic and Applied Basic Research Foundation [2019A1515110507]
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A Ni3S2-MoS2 nanoheterojunction catalyst with strong electronic interactions was prepared in this study, showing high efficiency in both hydrogen evolution reaction (HER) and electrooxidation of 5-hydroxymethylfurfural (HMF). The findings are significant for developing efficient electrocatalysts and continuous production of high value-added products and H2.
The intrinsic sluggish kinetics of the oxygen evolution reaction (OER) limit the improvement of hydrogen evolution reaction (HER) performance, and substituting the anodic oxidation of biomass materials is an alternative approach, given its lower oxidation potential and higher added value compared to those of OER. In this study, a Ni3S2-MoS2 nanoheterojunction catalyst with strong electronic interactions is prepared. It exhibits high efficiency for both the HER and the electrooxidation of 5-hydroxymethylfurfural (HMF). In a two-electrode cell with Ni3S2-MoS2 serving as both the anode and cathode, the potential is only 1.44 V at a current density of 10 mA cm(-2), which is much lower than that of pure water splitting. Density functional theory calculations confirm that the strong chemisorption of H and HMF at the interface leads to outstanding electrocatalytic activity. The findings not only provide a strategy for developing efficient electrocatalysts, but also provide an approach for the continuous production of high value-added products and H-2.
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