Digital oscillography of proton-conductive polymer membranes

I. Prokhorov
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Abstract

Polyvinyl alcohol-based cast membranes have promising application in creating commonly available fuel cells and fuel synthesizers, as well as inexpensive water sources and microelectromechanical systems. In order to control the properties of such membranes a deep understanding of the charge transfer mechanisms and their relationship with the structure formed at a certain composition and manufacturing technology is required. A method for studying the structure of the proton-conductive polymer membranes using digital oscillography of ion currents excited by the low-frequency rectangular pulses with the amplitudes below the threshold voltage of the ionic conductivity in a dehydrated membrane, and for the analysis of the resulting ion current pulses (spikes) in the frames of the model of a proton pump acting in each layer of the membrane is proposed in this paper. Fast Fourier transform of these oscillograms reveals from 2 to 4 branches or spike sequences corresponding to the phases with different ionic conductivity and makes it possible to determine the thicknesses of both high-conductivity phase layers (7–30 µm) and low-conductivity phase interlayers (1–7 µm) formed in the process of polymerization. The reason of spike merging into bursts is described in terms of successively induced increase in the excited proton density over a threshold value in highly conductive layers. The resonance observed in dry proton membranes at the frequencies of about 2.2 to 3.0 kHz is interpreted as the burst merge point with the further increase in impedance due to proton lagging and respective decrease in the effective thickness of active layers. The effective charge carrier concentrations (as small as 1012 to 1013 cm−3) and the velocity (from 5 to 18 cm/s for the highly conductive phases which turned out to be much higher than those observed in solutions) are estimated. The asymmetry of the cast membranes, which becomes apparent at low frequencies and causes the generation of a direct ion current in response to excitation by a purely alternating current, is studied. It is found that the apparent conductivity determining contribution to the total ohmic resistance is made by a thin interlayer with a very low ion velocity, presumably surface layer, rather than the main layers. The conclusion on the optimization of the production technology and the composition of the proton membranes for various applications is made.
质子导电聚合物膜的数字示波器
聚乙烯醇基铸膜在制造常见的燃料电池和燃料合成装置以及廉价的水源和微机电系统方面具有很好的应用前景。为了控制这种膜的性质,需要深入了解电荷转移机制及其与在特定组成和制造技术下形成的结构的关系。一种使用由振幅低于脱水膜中离子导电性阈值电压的低频矩形脉冲激发的离子电流的数字示波器来研究质子导电聚合物膜的结构的方法,并且为了分析在质子泵模型的框架中产生的离子电流脉冲(尖峰),本文提出了作用在膜的每一层中的质子泵模型。这些波形图的快速傅立叶变换揭示了与具有不同离子电导率的相对应的2-4个分支或尖峰序列,并使确定聚合过程中形成的高电导率相层(7-30µm)和低电导率相夹层(1-7µm)的厚度成为可能。尖峰合并为爆发的原因是根据高导电层中激发的质子密度连续增加超过阈值来描述的。在约2.2至3.0kHz的频率下在干质子膜中观察到的共振被解释为突发合并点,其中由于质子滞后和活性层的有效厚度的相应减小而导致阻抗的进一步增加。估计了有效载流子浓度(小至1012至1013 cm−3)和速度(高导电相的速度为5至18 cm/s,结果证明远高于溶液中观察到的速度)。研究了铸膜的不对称性,这种不对称性在低频下变得明显,并导致响应于纯交流电的激励而产生直接离子电流。研究发现,表观电导率对总欧姆电阻的决定作用是由离子速度非常低的薄中间层(可能是表层)而不是主要层造成的。对各种应用的质子膜的生产工艺和组成进行了优化,得出了结论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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