4.8 Article

Deep Eutectic Solvent-Assisted Synthesis of Ternary Heterojunctions for the Oxygen Evolution Reaction and Photocatalysis

期刊

CHEMSUSCHEM
卷 13, 期 10, 页码 2726-2738

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.202000177

关键词

deep eutectic solvents; dye degradation; oxygen evolution reaction; photocatalysis; ternary heterojunctions

资金

  1. Ministry of Science and Technology, Taiwan [MOST 109-2634-F-007-023, MOST 108-2218-E-007-045-MY3, MOST 108-2113-M-259 -004] Funding Source: Medline

向作者/读者索取更多资源

Hierarchical nano-/microstructured photocatalysts have drawn attention for enhanced photocatalytic performance. Deep eutectic solvents (DESs) have been used as a green sustainable media to act as both solvent and structure-inducing agent in the synthesis of hierarchical nanomaterials. In this work, the DESs-assisted synthesis of flower-structured BiOCl/BiVO4 (BOC/BVO) with g-C3N4 (BOC/BVO/g-CN) ternary heterojunctions was achieved by using a simple wet-chemical method, providing good acidic and alkaline oxygen evolution reaction (OER) catalysts. BOC/BVO/g-CN-15 achieved an enhanced photocatalytic activity for OER with an overpotential of 570 mV in 1 m H2SO4 and 220 mV in 1 m KOH electrolyte at a current density of 10 mA cm(-2) with excellent stability and extraordinary durability of the catalyst. The ternary heterojunctions displayed extended lifetimes for photogenerated charges and enhanced the separation efficiency of photogenerated electron-hole pairs, which is helpful to enhance the photocatalytic OER. Furthermore, the photocatalytic performance of the ternary heterojunctions in aqueous solution was demonstrated through photocatalytic dye degradation of methyl orange (MO) as a model pollutant, resulting in 95 % degradation of 20 ppm of MO in 210 min under the irradiation of a 35 W Xe arc lamp. This work not only provides new insight into the design of catalysts by using green solvents but also into the design of highly efficient metal-free OER photocatalysts for applications in acidic and alkaline media.

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