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Electrochemical oxygen transfer reactions: electrode materials, surface processes, kinetic models, linear free energy correlations, and perspectives

机译:电化学氧转移反应:电极材料,表面过程,动力学模型,线性自由能相关性和观点

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摘要

This work summarizes progresses achieved in electrochemical oxygen transfer reactions from water to organic pollutant molecules on metal oxide electrodes during the past two decades. Fundamental understanding of the dynamics of the electrochemical oxygen transfer reaction is of crucial importance for the development of key concepts of electrocatalytic processes, leading to the implementation of environmental electrochemistry wastewater treatment schemes with rational design of the suitable electrocatalytic systems. We discuss the current knowledge on the electrochemical oxygen transfer reaction, emphasizing the importance of surface processes in order to generalize mechanistically the experimental results obtained on different electrode materials, describing also the practical kinetic models developed and their implications. From the information gathered in this review, it is apparent that explanations for the kinetics of the reactions in relation to the structure of the organic compounds involved is lacking, hence that new information about structure-reactivity relationships is needed. We show in particular that the open circuit decay of the concentration of radical cations, obtained from spectroelectrochemical data, allows correlating the structure of adsorbed states with reactivity during oxygen transfer reactions, pointing as well to research efforts required to understand the catalytic performance of metal oxide electrodes in decomposing organic compounds strongly adsorbed on their surfaces. Finally, some perspectives for future research in this area are briefly commented.
机译:这项工作总结了在过去的二十年中,从水到金属氧化物电极上有机污染物分子的电化学氧转移反应取得的进展。对电化学氧转移反应动力学的基本了解对于开发电催化过程的关键概念至关重要,从而通过合理设计合适的电催化系统来实施环境电化学废水处理方案。我们讨论了有关电化学氧转移反应的当前知识,强调了表面过程的重要性,以便以机械方式概括在不同电极材料上获得的实验结果,还描述了开发的实际动力学模型及其含义。从本综述中收集到的信息中,很明显,对于与所涉及的有机化合物的结构有关的反应动力学缺乏解释,因此需要有关结构-反应性关系的新信息。我们特别表明,从光谱电化学数据获得的自由基阳离子浓度的开路衰减,可以使吸附态的结构与氧转移反应过程中的反应性相关联,还指出了了解金属氧化物催化性能所需的研究工作分解有机化合物的电极强烈吸附在其表面上。最后,简要评论了该领域未来研究的一些观点。

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