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Electrocatalyst of two-dimensional CoP nanosheets embedded by carbon nanoparticles for hydrogen generation and urea oxidation in alkaline solution

机译:碳纳米粒子嵌入二维CoP纳米片的电催化剂在碱性溶液中产生氢和尿素氧化

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Hydrogen (H-2) producing from the electrolysis of water at cathode is limited by the sluggish kinetics of oxygen evolution reaction (OER) at anode. It is essential to search a facile anodic reaction to replace OER in the hydrogen generation process. Urea oxidation reaction (UOR) is an alternative strategy to instead of OER in the water splitting reaction. Based on this, we successfully prepare two-dimensional (2D) CoP nanosheets embedded by carbon nanoparticles (CoP/C) composites as bifunctional catalysts to achieve hydrogen evolution reaction (HER) at cathode and UOR at anode simultaneously. Benefiting from the presence of carbon particles and 2D sheet structure of CoP in the composites, the contact area of electrolyte/electrode is enlarged, the exposed active sites are increased, and charge transfer rate is improved. As the anode and cathode catalysts in a two-electrode system with continuous electrolyte supplementation by a flow reactor, the CoP/C-3 composite only need 1.40 V to reach the current density of 10 mA cm(-2) in the 1 M KOH electrolyte with 0.1 M urea. This study on hydrogen generation and urea oxidation at a low potential provides a promising method to prepare bifunctional catalysts for practical applications.
机译:阴极水电解产生的氢(H-2)受阳极氧释放反应(OER)缓慢的动力学限制。在氢生成过程中,寻找一种容易的阳极反应来代替OER至关重要。在水分解反应中,尿素氧化反应(UOR)是替代OER的替代策略。在此基础上,我们成功地制备了由碳纳米颗粒(CoP / C)复合物作为双功能催化剂嵌入的二维(2D)CoP纳米片,以同时实现阴极处的析氢反应(HER)和阳极处的UOR。受益于复合物中碳颗粒和CoP的2D片状结构的存在,电解质/电极的接触面积扩大,暴露的活性位点增加,电荷转移率提高。作为通过流动反应器连续补充电解质的双电极系统中的阳极和阴极催化剂,CoP / C-3复合材料仅需要1.40 V即可在1 M KOH中达到10 mA cm(-2)的电流密度含0.1 M尿素的电解液。在低电位下进行氢生成和尿素氧化的这项研究为制备用于实际应用的双功能催化剂提供了一种有前途的方法。

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