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Interface-modulated nanojunction and microfluidic platform for photoelectrocatalytic chemicals upgrading

机译:用于光电催化化学品升级的接口调制纳米功能和微流体平台

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摘要

Photoelectrocatalytic oxidation provides a technically applicable way for solar-chemical synthesis, but its efficiency and selectivity are moderate. Herein, a microfluidic photoelectrochemical architecture with 3-D micro flow channels is constructed by interfacial engineering of defective WO3/TiO2 heterostructures on porous carbon fibers. Kelvin probe force microscopy and photoluminescence imaging visually evidence the charge accumulation sites on the nanojunction. This efficient charge separation contributes to a 3-fold enhancement in the yield of glyceraldehyde and 1,3-dihydroxyacetone during glycerol upgrading, together with nearly doubled production of high value-added KA oil and S2O82- oxidant through cyclohexane and HSO4- oxidization, respectively. More importantly, the microfluidic platform with enhanced mass transfer exhibits a typical reaction selectivity of 85 %, which is much higher than the conventional planar protocol. Integrating this microfluidic photoanode with an oxygen reduction cathode leads to a self-sustained photocatalytic fuel cell with remarkably high open circuit voltage (0.9 V) and short-circuit current (1.2 mA cm(-2)).
机译:光电催化氧化为太阳能化学合成提供了一种技术上可行的方法,但其效率和选择性适中。在此,通过多孔碳纤维上缺陷WO3/TiO2异质结构的界面工程,构建了具有三维微流道的微流控光电化学体系结构。开尔文探针力显微镜和光致发光成像从视觉上证明了纳米结上的电荷积累位置。这种有效的电荷分离有助于在甘油升级期间将甘油醛和1,3-二羟基丙酮的产率提高3倍,同时通过环己烷和HSO4-氧化,高附加值KA油和S2O82-氧化剂的产量分别增加近一倍。更重要的是,具有强化传质的微流控平台显示出85%的典型反应选择性,这远高于传统的平面协议。将这种微流控光阳极与氧还原阴极相结合,可以产生具有极高开路电压(0.9 V)和短路电流(1.2 mA-cm(-2))的自持光催化燃料电池。

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