ELECTROCATALYTIC COBALT-VANADIUM COATINGS FOR THE HYDROGEN EVOLUTION REACTION

M. Sakhnenko, Yu. Zhelavska, Svitlana Zyubanova, Valeriia Proskurina
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Abstract

The study of existing energy-saving materials and obtaining the new ones for reducing the cost of the hydrogen production, is relevant for modern hydrogen energy industry. Such properties can be predicted for materials containing vanadium, molybdenum, tungsten and exhibiting catalytic activity for the hydrogen evolution reaction Aforementioned metals can be co-deposited from aqueous solutions with iron subgroup metal-catalysts through the formation of cluster intermetallic compounds with Me-V bond adsorbed on the cathode surface.  The induced co-deposition of cobalt with vanadium from the complex citrate electrolyte was investigated in the current work. As a result of the research, it was found that the uniform microcrystalline light-gray high-quality cobalt-vanadium alloy coating is possible to precipitate from a citrate electrolyte with content of 20 g/dm3 vanadium (in terms of metal) as a citrate complex The process was carried out at a current density of 5–10 A/dm2, at a temperature of 30–40°С, pH = 2,8–3,2. The content of vanadium in the coating is 0,37–0,53 % by weight. The maximum vanadium content in the coating is observed at current densities 8–9 А/dm2. The catalytic activity study of the coating that was obtained using cobalt-vanadium alloy in the reaction of hydrogen reduction at the cathode was performed in solution of 2,5М NaOH + 0,02 M NaCl. By increasing the vanadium content in the coating from 0,37 to 0,53% the hydrogen evolution overvoltage is reduced by 0,5 V. It was found that the overvoltage of the hydrogen ion evolution reaction on cathodes from steel 20 with cobalt-vanadium coating is 0.08–0,1 V lower, and the exchange current is higher than on electrodes made of steel 20, which are used in industrial water-alkali electrolysis. This indicates the electrocatalytic activity of the investigated materials for the hydrogen evolution reaction. Electrodes with coating, obtained by cobalt-vanadium alloy can be recommended as a cathode material for the hydrogen electrochemical production. Hydrogen evolution overvoltage reduction also decrease the energy consumption for this process by 15–20 %.
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用于析氢反应的电催化钴钒涂层
研究现有的节能材料,开发新的节能材料,降低制氢成本,对现代氢能工业具有重要意义。这种性质可以预测为含有钒、钼、钨的材料,并表现出析氢反应的催化活性。上述金属可以通过在阴极表面吸附Me-V键形成簇状金属间化合物,与铁亚族金属催化剂在水溶液中共沉积。本文研究了复合柠檬酸电解质中诱导钴与钒共沉积的过程。研究结果表明,在钒(以金属计)含量为20 g/dm3的柠檬酸电解质中,可以以柠檬酸配合物的形式析出均匀的微晶浅灰色优质钴钒合金涂层。该工艺在电流密度为5-10 a /dm2,温度为30-40°С, pH = 2,8 - 3,2的条件下进行。镀层中钒的重量含量为0.37 ~ 0.53%。在电流密度为8-9 А/dm2时,涂层中钒含量最高。在2,5М NaOH + 0.02 M NaCl溶液中,对钴钒合金镀层在阴极氢还原反应中的催化活性进行了研究。将镀层中钒含量从0.37%提高到0.53%,析氢过电压降低0.5 V。结果表明,与工业水碱电解用的20钢电极相比,涂有钴钒涂层的20钢阴极上的析氢过电压低0.08 ~ 0.1 V,交换电流大。这表明了所研究材料对析氢反应的电催化活性。钴钒合金镀层电极可作为氢电化学生产的正极材料。析氢过电压的降低也使这一过程的能耗降低了15 - 20%。
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