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Analysis of stresses generated during hydrogen transport through a Pd foil electrode under potential sweep conditions

机译:分析在电位扫描条件下氢气通过Pd箔电极传输过程中产生的应力

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In the present work, the stresses generated during cyclic voltammetric measurements on a Pd foil electrode in 0.1 M NaOH solution have been analysed by using a laser beam deflection technique combined with cyclic voltammetry. From the linear relationship between the anodic peak current density and the scan rate on a logarithmic scale, it is recognised that the hydrogen concentration at the electrode surface is determined by the applied potential above the transition scan rate, whereas the change in the hydrogen concentration at the electrode surface with time is specified by the Butler- Volmer equation below the transition scan rate. The deflection transient measured simultaneously with the cyclic voltammogram shows that in the high scan rate range, the compressive deflection increases to a maximum value and then is completely relaxed. In the low scan rate range, however, the deflection transient is characterised by the occurrence of a maximum compressive deflection, a transition of compressive to tensile deflection, a maximum tensile deflection and finally a complete decay of the tensile deflection in sequence. From the hydrogen concentration profile transient simulated under the two constraints at the electrode surface, we simulated the deflection transients as a function of the scan rate. From the coincidence of the calculated deflection transient with that measured, the movement of the deflection in the compressive and tensile directions can be accounted for in terms of the difference in the molar volume of rx-PdH, across the whole electrode, developed during hydrogen diffusion.
机译:在目前的工作中,已经通过使用激光束偏转技术结合循环伏安法分析了在0.1 M NaOH溶液中Pd箔电极上的循环伏安法测量期间产生的应力。从阳极峰值电流密度与扫描速率的对数尺度上的线性关系可以看出,电极表面的氢浓度由过渡扫描速率以上的施加电势确定,而在电极表面随时间的变化由低于转换扫描速率的Butler-Volmer方程指定。与循环伏安图同时测量的挠度瞬变表明,在高扫描速率范围内,压缩挠度增大到最大值,然后完全放松。然而,在低扫描速率范围内,挠曲瞬变的特征在于出现最大压缩挠曲,从压缩挠曲到拉伸挠曲的过渡,最大拉伸挠曲以及最终顺序地拉伸挠曲的完全衰减。根据在电极表面的两个约束条件下模拟的氢浓度分布瞬态,我们模拟了偏转瞬态作为扫描速率的函数。从计算出的挠度瞬态与测得的挠度瞬态一致,可以用氢扩散过程中在整个电极上形成的rx-PdH摩尔体积之差来解释在压缩和拉伸方向上的挠度运动。 。

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