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Electrochemical performance of porous Ni3Al electrodes for hydrogen evolution reaction

机译:Ni3Al多孔电极对析氢反应的电化学性能

摘要

Porous Ni3Al intermetallic material with a mean pore diameter of around 1 pm was prepared by step sintering Ni and Al powder pressed compacts in vacuum furnace at 900 degrees C. The electrocatalytic activity of the as-fabricated porous Ni3Al material as an electrode for hydrogen evolution reaction (HER) in alkaline solutions was investigated by cyclic voltammetry (CV), linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS) techniques. It is found that the onset potential of porous Ni3Al for HER shifted in the positive direction favoring hydrogen generation with lower overpotential, compared with foam Ni and dense Ni electrodes. Effects of electrolyte concentration and temperature on HER as well as the electrochemical stability in alkaline solution were investigated and the electrochemical activation energy was determined for the porous Ni3Al. The increased activity for HER was attributed to the high porosity, an increased electrochemical surface area and the nanostructure of porous Ni3Al electrode. The corrosion tests showed that the corrosion resistance of porous Ni3Al electrode changed during the immersion process due to the formation of passive film layers.
机译:通过在900℃的真空炉中分步烧结Ni和Al粉末压制坯,制备平均孔径为1 pm左右的多孔Ni3Al金属间化合物。制备的多孔Ni3Al材料作为析氢反应电极的电催化活性。通过循环伏安法(CV),线性扫描伏安法(LSV)和电化学阻抗谱(EIS)技术研究了碱性溶液中的(HER)。结果发现,与泡沫镍和致密镍电极相比,多孔Ni3Al的HER起始电位朝正方向移动,有利于氢气的产生,且过电位较低。研究了电解质浓度和温度对HER的影响以及在碱性溶液中的电化学稳定性,并确定了多孔Ni3Al的电化学活化能。 HER活性的提高归因于高孔隙率,电化学表面积的增加和多孔Ni3Al电极的纳米结构。腐蚀试验表明,由于钝化膜层的形成,多孔Ni3Al多孔电极的耐蚀性在浸渍过程中发生了变化。

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