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Mechanism for Electrochemical Oxidation of Highly Oriented Pyrolytic Graphite during Potential Cycling in Sulfuric Acid Solution

机译:硫酸溶液中循环循环期间高温热解石墨电化学氧化机理

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We investigated the electrochemical oxidation of highly oriented pyrolytic graphite (HOPG) during potential cycling in sulfuric acid solution to clarify the oxidation mechanism of carbon materials under dynamic operation conditions in polymer electrolyte fuel cells (PEFCs). The redox current peaks corresponding to hydroquinone-quinone reaction appeared on CVs following cycling between 0.6 and 0.8 V vs. NHE, suggesting that HOPG was partially oxidized to form surface functional groups, while it was hardly oxidized below 0.6 V. Ex-situ SEM observations show that the surface of HOPG became roughened with cycling between 0.6 and 0.8 V with formation an oxidized layer, whereas this oxidized layer became less stable in the course of gasification reaction involving CO{sub}2 and/or CO evolution in the potential ranges above 0.8 V. We discuss oxidation mechanism for HOPG corresponding to various potential ranges.
机译:我们研究了在硫酸溶液中的潜在循环期间高温热解石墨(HOPG)的电化学氧化,以阐明聚合物电解质燃料电池(PEFC)的动态操作条件下碳材料的氧化机理。对应于氢醌 - 醌反应的氧化还原电流峰在循环后的CVS上出现在0.6和0.8V与NHE之间的CV之后,表明跳跃部分氧化以形成表面官能团,而在0.6V的情况下难以氧化。出原位SEM观察表明,跳跃的表面在0.6至0.8V之间形成粗糙的氧化层,而形成氧化层在涉及上述潜在范围内的Co {} 2和/或CO进化的气化反应过程中变得较小。 0.8 V.我们讨论对应于各种潜在范围的HOPG的氧化机制。

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