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A new electrocatalytic mechanism for the oxidation of phenols at platinum electrodes

机译:铂电极上苯酚氧化的新电催化机理

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Electrochemical oxidation of phenolic compounds generally produces unstable phenoxy radicals that readily polymerize to passivate the surface of solid electrodes. In this study, the electrocatalytic oxidation of phenol in the presence and absence of methanol was investigated by cyclic voltammetry on a platinum electrode. The cyclic voltammogram of phenol in a mixture of phosphate buffer/methanol solution showed well-defined peaks at ~600 mV vs. Ag/AgCl reference electrode, which surprising, gradually increased with repetitive scanning, stabilizing after 50 cycles. This unexpected behavior is in contrast to previous studies involving phenolic compounds, which always show a decrease in intensity during continuous potential scanning. Scanning electrochemical spectroscopy (SEM) was further used to investigate the changes in the surface morphology of the Pt electrode after electrodeposition. A new electrocatalytic mechanism for phenol oxidation on the surface of a Pt electrode is suggested in the presence of methanol. The proposed mechanism is based on the formation of a film of Pt oxide/hydroxides onto which the phenol and the products of its electrochemical oxidation are further deposited. The mechanism was also studied using more complex phenolic compounds including resveratrol, quercetin and bisphenol A. The results emphasized the effect of aryl substituents on the electrochemsitry of this particular class of compounds.
机译:酚类化合物的电化学氧化通常会产生不稳定的苯氧基,这些苯氧基容易聚合以钝化固体电极的表面。在这项研究中,通过循环伏安法在铂电极上研究了在有无甲醇存在下苯酚的电催化氧化。与Ag / AgCl参比电极相比,磷酸盐缓冲液/甲醇溶液混合物中苯酚的循环伏安图在〜600 mV处显示出明确定义的峰,这一峰出人意料,随着重复扫描而逐渐增加,在50个循环后稳定下来。这种出乎意料的行为与先前的涉及酚类化合物的研究相反,后者在连续电势扫描过程中总是显示出强度的降低。进一步使用扫描电化学光谱法(SEM)研究电沉积后Pt电极的表面形态变化。在甲醇存在下,提出了一种新的苯酚在Pt电极表面氧化的电催化机理。所提出的机理是基于形成Pt氧化物/氢氧化物的膜,苯酚及其电化学氧化产物进一步沉积在其上。还使用更复杂的酚类化合物(包括白藜芦醇,槲皮素和双酚A)研究了该机理。结果强调了芳基取代基对这类特殊化合物的电化学作用。

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