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首页> 外文期刊>Electroanalysis >Electrocatalytic reduction of Dioxygen at carbon paste electrode modified with a novel cobalt(III) schiffs base complex
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Electrocatalytic reduction of Dioxygen at carbon paste electrode modified with a novel cobalt(III) schiffs base complex

机译:新型钴(III)席夫斯碱配合物修饰的碳糊电极上双氧的电催化还原

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摘要

A carbon paste modified electrode with a new cobalt(III) Schiff's base complex (CPME) and its application to electrocatalytic activity for dioxygen reduction is developed. The electrochemical behavior and stability of the CPME as well as the two-electron reduction of O-2 at the electrode, were investigated using cyclic voltammetry, chronoamperometry and rotating disk electrode methods. At the CPME, the reduction of dioxygen to hydrogen peroxide occurs at potentials where it is not observed at a bare carbon paste electrode. The CPME exhibited potent and persistent electrocatalysis for O-2 reduction in acetate buffer solutions of pH 4.0 with an overpotential of about 800 mV lower than unmodified CPE and drastic increase in the peak current. ne heterogeneous rate constant for the reduction of O-2 at the surface of CPME was determined by hydrodynamic voltammetry using the Koutecky-Levich plot. A possible catalytic mechanism is proposed and discussed.
机译:开发了一种具有新型钴(III)席夫碱配合物(CPME)的碳糊修饰电极,并将其应用于电催化还原双氧的活性。使用循环伏安法,计时电流法和转盘电极法研究了CPME的电化学行为和稳定性以及O-2在电极上的两电子还原。在CPME,在裸碳糊电极上未观察到的电势下,双氧会还原为过氧化氢。 CPME对pH 4.0的乙酸盐缓冲溶液中的O-2还原具有强而持久的电催化作用,其超电势比未修饰的CPE低约800 mV,并且峰值电流急剧增加。使用Koutecky-Levich图通过流体动力学伏安法测定CPME表面O-2还原的异质速率常数。提出并讨论了一种可能的催化机理。

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