Effect of the Presence of Carbon in Ti4O7 Electrodes on Anodic Oxidation of Contaminants

电化学 电极 阳极 材料科学 电子转移 碳纤维 亚氧化物 化学工程 析氧 无机化学 化学 冶金 复合材料 氧化物 光化学 工程类 复合数 物理化学
作者
Jiangzhou Xie,Jinxing Ma,Changyong Zhang,Xiangtong Kong,Zhiwei Wang,T. David Waite
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:54 (8): 5227-5236 被引量:85
标识
DOI:10.1021/acs.est.9b07398
摘要

Magnéli phase titanium suboxide, Ti4O7, has attracted increasing attention as a potential electrode material in anodic oxidation as a result of its high efficiency and (electro)chemical stability. Although carbon materials have been amended to Ti4O7 electrodes to enhance the electrochemical performance or are present as an unwanted residual during the electrode fabrication, there has been no comprehensive investigation of how these carbon materials affect the electrochemical performance of the resultant Ti4O7 electrodes. As such, we investigated the electrochemical properties of Ti4O7 electrodes impregnated with carbon materials at different contents (and chemical states). Results of this study showed that while pure Ti4O7 electrodes exhibited an extremely low rate of interfacial electron transfer, the introduction of minor amounts of carbon materials (at values as low as 0.1 wt %) significantly facilitated the electron transfer process and decreased the oxygen evolution reaction potential. The oxygen-containing functional groups have been shown to play an important role in interfacial electron transfer with moderate oxidation of the carbon groups aiding electron uptake at the electrode surface (and consequently organic oxidation) while the generation of carboxyl groups—a process that is likely to occur in long-term operation—increased the interfacial resistance and thus retarded the oxidation process. Results of this study provide a better understanding of the relationship between the nature of the electrode surface and anodic oxidation performance with these insights likely to facilitate improved electrode design and optimization of operation of anodic oxidation reactors.
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