Junhao Wu, Xiao Zhang, Sijia Ren, Xinhui Lu, Jiaxin Yang and Kui Li
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引用次数: 0
Abstract
The electrochemical manipulation of organic compounds offers a promising alternative for the synthesis of valuable organic materials under mild conditions. In this study, the MoO2@NiO heterostructure was successfully synthesized as an efficient thin-film electrode material for electrochemical ethanol oxidation, using amorphous Ni(OH)x nanosheets as the precursor. During electrocatalytic ethanol oxidation, this electrode exhibited a significantly reduced overpotential, achieving a value of only 1.41 V at a current density of 50 mA cm−2. Additionally, product analysis revealed that the heterojunction electrode demonstrated high faradaic efficiency (70%) and selectivity (80%) for acetaldehyde. The outstanding performance of this electrode can be attributed to the in situ transformation of MoO2 species during the catalytic process. In the electrolyte, MoO2 exists as MoO42− and undergoes a series of processes including precipitation, dissolution, and redeposition on the electrode surface. These processes lead to the formation of a novel molecular outer layer, significantly enhancing the activity and stability of the electrode material. This study provides valuable insights into the potential replacement of anodes in the electrocatalytic oxidation of ethanol in aqueous solutions, thereby contributing to the development of more efficient and sustainable electrochemical systems.
有机化合物的电化学处理为在温和条件下合成有价值的有机材料提供了一个有前途的选择。本研究以无定形Ni(OH)x纳米片为前驱体,成功合成了MoO2@NiO异质结构作为乙醇电化学氧化的高效薄膜电极材料。在电催化乙醇氧化过程中,该电极的过电位显著降低,在电流密度为50 mA cm−2时,过电位仅为1.41 V。此外,产品分析表明,异质结电极对乙醛具有很高的法拉第效率(70%)和选择性(80%)。该电极的优异性能可归因于在催化过程中MoO2物质的原位转化。在电解质中,MoO2以MoO42−的形式存在,并在电极表面经历了沉淀、溶解、再沉积等一系列过程。这些过程导致了一种新的分子外层的形成,显著提高了电极材料的活性和稳定性。这项研究为在水溶液中乙醇的电催化氧化中潜在的阳极替代提供了有价值的见解,从而有助于开发更有效和可持续的电化学系统。