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Adsorption of Macrocyclic Cobalt Complex on a Glassy Carbon Electrode for the Electrocatalytic Reduction of O2

机译:玻碳电极上大环钴配合物的吸附对O2的电催化还原

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It was found that the adsorption of a cobalt(III) complex with a macrocyclic ligand, C-meso-5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane (hmc), was induced on a glassy carbon electrode by heavily oxidizing the electrode surface. Adsorption properties are discussed. The glassy carbon electrode with the adsorbed complex was employed to see the catalytic activities for the electro-reduction of O2. In the presence of oxygen, reduction of (hmc)Co3+ showed two cathodic waves in cyclic voltammetry. Compared to the edge plane graphite electrode at which two cathodic waves were also observed in a previous study, catalytic reduction of O2 occurred in the potential region of the first wave while it happened in the second wave region with the other electrode. A rotating disk electrode after the same treatment was employed to study the mechanism of the O2 reduction and two-electron reduction of O2 was observed. The difference from the previous results was explained by the different reactivity of the (hmc)CoOOH2+ intermediate, which is produced after the two electron reduction of (hmc)Co3+ in the presence of O2.
机译:发现具有大环配体C-meso-5,7,7,12,14,14-六甲基-1,4,8,11-四氮杂环十四烷(hmc)的钴(III)配合物的吸附为通过严重氧化电极表面而在玻璃碳电极上产生感应。吸附性能进行了讨论。使用具有吸附的复合物的玻璃碳电极观察O2电还原的催化活性。在氧气的存在下,(hmc)Co3 +的还原在循环伏安法中显示出两个阴极波。与先前研究中还观察到两个阴极波的边缘平面石墨电极相比,O 2的催化还原发生在第一波的电势区域中,而在第二波区域与另一电极发生了催化还原。用相同处理后的旋转盘电极研究O 2还原的机理,观察到O 2的二电子还原。与先前结果的差异是由(hmc)CoOOH2 +中间体的不同反应性所解释的,该中间体是在(hmc)Co3 +在氧气存在下两次电子还原后产生的。

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