首页> 外文期刊>Collection of Czechoslovak Chemical Communications >ANODIC ELECTROCHEMICAL PRETREATMENT TIME AND POTENTIAL AFFECT THE ELECTROCHEMICAL CHARACTERISTICS OF MODERATELY BORON-DOPED DIAMOND ELECTRODE
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ANODIC ELECTROCHEMICAL PRETREATMENT TIME AND POTENTIAL AFFECT THE ELECTROCHEMICAL CHARACTERISTICS OF MODERATELY BORON-DOPED DIAMOND ELECTRODE

机译:阳极电化学预处理时间和中度掺杂硼的金刚石电极的电化学特性

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Boron-doped diamond (BDD) electrodes, both as-prepared and electrochemically oxidized were studied. The relation between the anodic oxidation treatment time, anodic potential and electrochemical characteristics has been discussed. Electron transfer processes in all BDD electrode surface were studied by cyclic voltammetry. The ferric/ferrous sulfate and ferri/ ferrocyanide redox systems were chosen respectively to act as the probe of one-electron transfer processes. The relation between ΔE and ψ, the dimensionless parameter, was obtained with a correlation coefficient greater than 0.9987 by mathematics fitting function. The rate constants of the electron transfer reaction, k~0, were evaluated using the ΔE_p values. The k~0 values for all BDD electrodes ranged from 3.33 x 10~(-5) to 4.72 x 10~(-5) cm s~(-1) in 0.1 m FeSO4/ 0.1 m H2SO4 and from 1.01 x 10~(-4) to 2.49 x 10~(-4) cm s~(-1) in 0.1 m K4[Fe(CN)6]/0.1 m H2SO4 system, which were in the standard range for a quasi-reversible system, respectively. The electrochemical properties of the BDD electrodes changed as a function of the surface anodic treatment time and potential. The anodic oxidation at low potential stripped mainly the impurities of BDD surface, sp~2-carbon, and had little effect on the modification of the surface. While increasing the anodic potential up to +2.0 V, the anodic oxidation stripped the impurities of the BDD surface at first and carried out the modification of the BDD surface from hydrogen-terminated hydrophobic to oxygen-terminated hydrophilic surface with increasing anodic treatment time.
机译:研究了已制备和电化学氧化的掺硼金刚石(BDD)电极。讨论了阳极氧化处理时间,阳极电位与电化学特性之间的关系。通过循环伏安法研究了所有BDD电极表面的电子转移过程。分别选择硫酸铁/硫酸亚铁和亚铁/亚铁氰化物的氧化还原体系作为单电子转移过程的探针。通过数学拟合函数,获得了相关系数大于0.9987的无量纲参数ΔE和ψ的关系。使用ΔE_p值评估电子转移反应的速率常数k〜0。在0.1 m FeSO4 / 0.1 m H2SO4中,所有BDD电极的k〜0值范围从3.33 x 10〜(-5)到4.72 x 10〜(-5)cm s〜(-1)和1.01 x 10〜(在0.1 m K4 [Fe(CN)6] /0.1 m H2SO4系统中为-4)至2.49 x 10〜(-4)cm s〜(-1),分别在准可逆系统的标准范围内。 BDD电极的电化学性能随表面阳极处理时间和电势的变化而变化。低电势下的阳极氧化主要去除了BDD表面的杂质sp〜2-碳,对表面改性的影响很小。在将阳极电势提高到+2.0 V的同时,阳极氧化首先去除了BDD表面的杂质,并随着阳极处理时间的增加将BDD表面从氢封端的疏水性表面改性为氧封端的亲水性表面。

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