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Effects of Hydrogen and Stress on Anodic Dissolution of 304 Stainless Steel in Simulated Anode Environment of Polymer Electrolyte Membrane Fuel Cell

机译:氢和应力对高分子电解质膜燃料电池阳极环境中304不锈钢阳极溶解的影响

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The mechano-electrochemical effects of hydrogen and tensile stress on the anodic dissolution of type 304 stainless steel in simulated anode environment of polymer electrolyte membrane fuel cell (PEMFC) are investigated by potentiodynamical polarization tests, Mott-Schotky measurements and XPS characterization. The results reveal that hydrogen charging and tensile stress promote the anodic dissolution due to the increased donor density and difiusivity coefficient of vacancy in the passive film. Hydrogen dissolved in passive film decreases the ratio of O~2/OH~- in the passive film and also decreases the thickness of the passive film layer, resulting in increased film/solution interface potential and thus enhanced anodic dissolution rate of the passive film. The effect of hydrogen on the anodic dissolution rate in the active-passive transition region, which happens to be in the anode working potential range of metal bipolar plates of PEMFC, is more obvious than that in the steady passive potential region. The synergistic effect of hydrogen and stress on anodic dissolution is higher at the intermediate hydrogen charging current densities range than that at either lower or higher current densities range. These results indicate that dissolved hydrogen and applied stress on metal bipolar plates greatly promote its anodic dissolution rate in anode environment of PEMFC.
机译:通过电位动力学极化试验,Mott-Schotky测量和XPS表征研究了氢和拉伸应力对304型不锈钢在聚合物电解质膜燃料电池(PEMFC)模拟阳极环境中的阳极溶解的机械电化学效应。结果表明,由于钝化膜中供体密度和空位扩散系数的增加,氢的电荷和拉伸应力促进了阳极的溶解。溶解在钝化膜中的氢降低了钝化膜中O〜2 / OH_-的比率,并且还降低了钝化膜层的厚度,从而导致膜/溶液界面电势增加,从而提高了钝化膜的阳极溶解速率。氢对主动-被动过渡区中阳极溶解速率的影响(恰好在PEMFC的金属双极板的阳极工作电位范围内)比在稳定被动电位区中更为明显。在中等的氢充电电流密度范围内,氢和应力对阳极溶解的协同作用要高于在较低或较高的电流密度范围内。这些结果表明,在PEMFC的阳极环境中,溶解的氢和施加在金属双极板上的应力极大地促进了其阳极溶解速率。

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