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阴极腐蚀对质子交换膜燃料电池面内水传输的影响。

Effects of Cathode Corrosion on Through-Plane Water Transport in Proton Exchange Membrane Fuel Cells.

作者信息

Fairweather Joseph D, Spernjak Dusan, Weber Adam Z, Harvey David, Wessel Silvia, Hussey Daniel S, Jacobson David L, Artyushkova Kateryna, Mukundan Rangachary, Borup Rodney L

机构信息

Los Alamos National Laboratory, Los Alamos, New Mexico 87545, USA.

Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.

出版信息

J Electrochem Soc. 2013;160(9). doi: 10.1149/2.024309jes.

Abstract

The corrosion of carbon in the cathodes of proton-exchange-membrane fuel cells leads to electrode collapse, reduced active catalyst area, and increased surface hydrophilicity. While these effects have been linked to performance degradation over cell lifetime, the role of corrosion in the evolving water balance has not been clear. In this study, neutron imaging was used to evaluate the through-plane water distribution within several cells over the course of accelerated stress testing using potential holds and square-wave cycling. A dramatic decrease in water retention was observed in each cell after the cathode was severely corroded. The increasing hydrophilic effect of carbon surface oxidation (quantified by ex situ X-ray photoelectron spectroscopy) was overwhelmed by the drying effect of increased internal heat generation. To evaluate this mechanism, the various observed electrode changes are included in a multiphase, non-isothermal one-dimensional cell model, and the simulated alterations to cell performance and water content are compared with those observed experimentally. Simulation results are consistent with the idea that collapse and compaction of the catalyst layer is the dominant limitation to cell performance and not the lower amounts of active Pt surface area, and that higher temperature gradients result in drying out of the cell.

摘要

质子交换膜燃料电池阴极中的碳腐蚀会导致电极坍塌、活性催化剂面积减小以及表面亲水性增加。虽然这些影响与电池寿命期间的性能退化有关,但腐蚀在不断变化的水平衡中的作用尚不清楚。在本研究中,利用中子成像技术在加速应力测试过程中,通过电位保持和方波循环来评估多个电池内部的面内水分布。在阴极严重腐蚀后,每个电池中的保水量都出现了显著下降。碳表面氧化增加的亲水性效应(通过非原位X射线光电子能谱定量)被内部产热增加的干燥效应所掩盖。为了评估这种机制,将观察到的各种电极变化纳入多相、非等温一维电池模型,并将模拟的电池性能和含水量变化与实验观察结果进行比较。模拟结果与以下观点一致:催化剂层的坍塌和压实是电池性能的主要限制因素,而非活性铂表面积的减少,并且较高的温度梯度会导致电池干涸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1382/8628568/8f603f2b2391/nihms-1753058-f0001.jpg

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