化学
对苯二酚
儿茶酚
电子转移
动力学
玻璃碳
电极
光化学
无机化学
有机化学
电化学
循环伏安法
物理化学
物理
量子力学
作者
Stacy Hunt DuVall and,Richard L. McCreery
摘要
The electrochemical oxidation of dopamine, 4-methylcatechol, dihydroxyphenylacetic acid, dihydroxyphenyl ethylene glycol, and hydroquinone was examined on several native and modified glassy carbon (GC) surfaces. Treatment of polished GC with pyridine yielded small ΔEp values for cyclic voltammetry of all systems studied, implying fast electron-transfer kinetics. Changes in surface oxide coverage had little effect on kinetics, nor did the charge of the catechol species or the solution pH. Small ΔEp values correlated with catechol adsorption, and surface pretreatments that decreased adsorption also increased ΔEp. Electron transfer from catechols was profoundly inhibited by a monolayer of nitrophenyl or (trifluoromethyl)phenyl (TFMP) groups on the GC surface, so that voltammetric waves were not observed. The ΔEp increased monotonically with surface coverage of TFMP groups. The results indicate that catechol adsorption to GC is required for fast electron transfer for the redox systems studied. Unlike Ru(NH3)6...
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