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

被引:19
|
作者
Jaihindh, Dhayanantha Prabu [1 ]
Manikandan, Arumugam [2 ]
Chueh, Yu-Lun [2 ,3 ,4 ]
Fu, Yen-Pei [1 ]
机构
[1] Natl Dong Hwa Univ, Dept Mat Sci & Engn, Shoufeng 97401, Hualien, Taiwan
[2] Natl Tsing Hwa Univ, Dept Mat Sci & Engn, Hsinchu 30013, Taiwan
[3] Natl Sun Yat Sen Univ, Dept Phys, Kaohsiung 80424, Taiwan
[4] Natl Tsing Hwa Univ, Frontier Res Ctr Fundamental & Appl Sci Matter, Hsinchu 30013, Taiwan
关键词
deep eutectic solvents; dye degradation; oxygen evolution reaction; photocatalysis; ternary heterojunctions; FACILE SYNTHESIS; COMPOSITE PHOTOCATALYST; EFFICIENT PHOTOCATALYST; SOLVOTHERMAL SYNTHESIS; G-C3N4; NANOSHEETS; BIVO4; PHOTOANODES; PERFORMANCE; NITRIDE; OXIDE; ELECTROCATALYST;
D O I
10.1002/cssc.202000177
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:2726 / 2738
页数:13
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