4.8 Article

Solvent Engineering of Oxygen-Enriched Carbon Dots for Efficient Electrochemical Hydrogen Peroxide Production

Journal

SMALL
Volume -, Issue -, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202303156

Keywords

electrochemical generations; flow cells; hydrogen peroxide; metal-free carbon materials; selectivity

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A scalable solvent engineering strategy was used to fabricate oxygen-doped carbon dots (O-CDs) with excellent performance as electrocatalysts. The surface electronic structure of the O-CDs was systematically tunable by adjusting the ratio of ethanol and acetone solvents during synthesis. The optimal O-CDs-3 exhibited high H2O2 selectivity of 96.55% at 0.65 V (vs RHE) and low Tafel plot of 64.8 mV dec(-1). The realistic H2O2 productivity yield of flow cell was measured to be as high as 111.18 mg h(-1) cm(-2) for a duration of 10 h. These findings highlight the potential of universal solvent engineering approach for improving carbon-based electrocatalytic materials.
The development of cost-effective and reliable metal-free carbon-based electrocatalysts has gained significant attention for electrochemical hydrogen peroxide (H2O2) generation through a two-electron oxygen reduction reaction. In this study, a scalable solvent engineering strategy is employed to fabricate oxygen-doped carbon dots (O-CDs) that exhibit excellent performance as electrocatalysts. By adjusting the ratio of ethanol and acetone solvents during the synthesis, the surface electronic structure of the resulting O-CDs can be systematically tuned. The amount of edge active C-O group was strongly correlated with the selectivity and activity of the O-CDs. The optimum O-CDs-3 exhibited extraordinary H2O2 selectivity of up to 96.55% (n = 2.06) at 0.65 V (vs RHE) and achieved a remarkably low Tafel plot of 64.8 mV dec(-1). Furthermore, the realistic H2O2 productivity yield of flow cell is measured to be as high as 111.18 mg h(-1) cm(-2) for a duration of 10 h. The findings highlight the potential of universal solvent engineering approach for enabling the development of carbon-based electrocatalytic materials with improved performance. Further studies will be undertaken to explore the practical implications of the findings for advancing the field of carbon-based electrocatalysis.

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