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Differences in the electrochemical behavior of ruthenium and iridium oxide in electrocatalytic coatings of activated titanium anodes prepared by the sol-gel procedure

机译:溶胶-凝胶法制备的活化钛阳极电催化涂层中钌和氧化铱的电化学行为差异

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摘要

The electrochemical characteristics of Ti0.6Ir0.4O2/Ti and Ti0.6Ru0.4O2/Ti anodes prepared by the sol-gel procedure from the corresponding oxide sols, obtained by force hydrolysis of the corresponding metal chlorides, were compared. The voltammetric properties in H2SO4 solution indicate that Ti0.6Ir0.4O2/Ti has more pronounced pseudocapacitive characteristics, caused by proton-assisted, solid state surface redox transitions of the oxide. At potentials negative to 0.0 VSCE, this electrode is of poor conductivity and activity, while the voltammetric behavior of the Ti0.6Ru0.4O2/Ti electrode is governed by proton injection/ejection into the oxide structure. The Ti0.6Ir0.4O2/Ti electrode had a higher electrocatalytical activity for oxygen evolution, while the investigated anodes were of similar activity for chlorine evolution. The potential dependence of the impedance characteristics showed that the Ti0.6Ru0.4O2/Ti electrode behaved like a capacitor over a wider potential range than the Ti0.6Ir0.4O2/Ti electrode, with fully-developed pseudocapacitive properties at potentials positive to 0.60 VSCE. However, the impedance characteristics of the Ti0.6Ir0.4O2/Ti electrode changed with increasing potential from resistor-like to capacitor-like behavior.
机译:比较了通过溶胶-凝胶法从相应的氧化物溶胶(通过强制水解相应的金属氯化物获得)制备的Ti0.6Ir0.4O2 / Ti和Ti0.6Ru0.4O2 / Ti阳极的电化学特性。 H2SO4溶液中的伏安特性表明,Ti0.6Ir0.4O2 / Ti具有更明显的拟电容特性,这是由氧化物的质子辅助的固态表面氧化还原转变引起的。在负电势为0.0 VSCE时,该电极的电导率和活性较差,而Ti0.6Ru0.4O2 / Ti电极的伏安行为受质子注入/注入氧化物结构控制。 Ti0.6Ir0.4O2 / Ti电极对氧的释放具有较高的电催化活性,而所研究的阳极对氯的释放具有相似的活性。阻抗特性的电势依赖性表明,Ti0.6Ru0.4O2 / Ti电极在比Ti0.6Ir0.4O2 / Ti电极更宽的电势范围内表现得像电容器,在正电势为0.60 VSCE时具有充分开发的伪电容特性。 。但是,Ti0.6Ir0.4O2 / Ti电极的阻抗特性随着电势的增加而从电阻态变为电容态。

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