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Regularities of cathodic hydrogen evolution at an electrolytic Co-V alloy and its components

机译:电解Co-V合金及其组分的阴极氢逸出规律。

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The regularities of cathodic hydrogen evolution from a 30 % K.OH solution at an electrolytic Co-V alloy, an electrolytic cobalt coating as well as at cobalt and vanadium with smooth surface in the temperature range 25-85 °C have been studied. The Co-V alloy and cobalt coating were deposited on stainless steel from a nonaqueous electrolyte. It has been found that at the least negative potentials and with the lowest overpotential hydrogen evolves at the Co-V alloy. The exchange currents and real activation energies of hydrogen evolution at the investigated electrodes as well as the Tafel coefficients have been determined. On the basis of an analysis of the angular Tafel coefficient values, it has been shown that the rate of cathodic hydrogen evolution at cobalt and cobalt coating is controlled by the rate of formation of adsorbed hydrogen atoms while at vanadium and electrolytic Co-V alloy by the rate of their electrochemical desorp-tion.
机译:研究了在30%K.OH溶液中在电解Co-V合金,电解钴涂层以及表面温度在25-85°C的钴和钒表面上产生的阴极氢的规律。用非水电解质将Co-V合金和钴涂层沉积在不锈钢上。已经发现在Co-V合金中至少产生负电势并且具有最低的超电势氢。已经确定了所研究电极处析氢的交换电流和实际活化能以及Tafel系数。根据对角Tafel系数值的分析,已表明,钴和钴涂层上阴极氢放出的速率受吸附氢原子的形成速率控制,而钒和电解Co-V合金则通过电化学脱附速率。

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