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Development and characterization of membrane electrode assembly of direct methanol fuel cells using hydrocarbon membranes and supported catalysts .

机译:直接甲醇燃料电池用碳氢膜和负载催化剂的膜电极组件的研制与表征。

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摘要

Direct methanol fuel cell (DMFC) is an attractive power source for portable applications in the near future, due to the high energy density of liquid methanol. Towards commercialization of the DMFC, several technical and economic challenges need to be addressed though. The present study aims at developing and characterizing high performance membrane electrode assemblies (MEAs) for the DMFCs by using a hydrocarbon type membrane (PolyFuel 62) and supported catalysts (PtRu/C).;First, methanol and water transport properties in the PolyFuel 62 membrane were examined by various material characterization methods. Compared with the currently used perflurosulfonated Nafion 212 membrane, the PolyFuel membrane has lower methanol crossover, especially at high testing temperature. In addition, based on results of water diffusivity test, water diffusion through the PolyFuel membrane was also lower compared with the Nafion membrane.;In order to check the possible impacts of the low methanol and water diffusivities in the PolyFuel membrane, a MEA with this new type of membrane was developed and its performance was compared with a Nafion MEA with otherwise identical electrodes and GDLs. The results showed anode performance was identical, while cathode performance of the PolyFuel MEA was lower. More experiments combined with a transmission line model revealed that low water transport through the PolyFuel membrane resulted in a higher proton resistance in the cathode electrode and thus, leading to a low cathode performance. Thus increasing the water content in the cathode electrode is critical for using the PolyFuel membrane in the DMFC MEA.;Then, a low loading carbon supported catalyst, PtRu/C, was prepared and tested as the anode electrode in a MEA of the DMFC. Compared with performance of an unsupported MEA, we could find that lower performance in the supported MEA was due to methanol transport limitation because of the denser and thicker supported catalyst layer. Accordingly, an addition of a pore former, Li 2CO3, was proposed during the catalyst ink preparation. This was proved to be very effective, largely improving anode performance with only 1/3 of catalyst loading.;Finally, the PolyFuel membrane and supported catalysts were ready to be applied in the new MEA for the DMFCs. The new made MEA, with the catalyst loading of 2.6-time lower than a reference MEA, showed a very promising result, about only 10mV performance loss under the current density of 150mA/cm² compared with the reference MEA. Moreover, a short-term decay test indicated that the new MEA may have better durability and life because of its low methanol crossover on the cathode electrode due the PolyFuel membrane.
机译:由于液态甲醇的高能量密度,直接甲醇燃料电池(DMFC)在不久的将来是便携式应用中有吸引力的电源。为了使DMFC商业化,需要解决一些技术和经济上的挑战。本研究旨在通过使用烃类膜(PolyFuel 62)和负载型催化剂(PtRu / C)开发和表征DMFC的高性能膜电极组件(MEA)。首先,PolyFuel 62中的甲醇和水传输性能通过各种材料表征方法检查膜。与目前使用的全氟磺化Nafion 212膜相比,PolyFuel膜的甲醇穿透率更低,尤其是在较高的测试温度下。此外,根据水扩散性测试的结果,通过PolyFuel膜的水扩散也比Nafion膜低。;为了检查低甲醇和水扩散性在PolyFuel膜中的可能影响,MEA开发了新型膜,并将其性能与带有相同电极和GDL的Nafion MEA进行了比较。结果表明,阳极性能相同,而PolyFuel MEA的阴极性能较低。更多的实验与传输线模型相结合,揭示了通过PolyFuel膜的低水传输导致阴极电极中较高的质子电阻,从而导致阴极性能低下。因此,增加阴极电极中的水分含量对于在DMFC MEA中使用PolyFuel膜至关重要。然后,制备了低负载碳负载催化剂PtRu / C并作为DMFC MEA中的阳极电极进行了测试。与未负载的MEA的性能相比,我们可以发现负载的MEA中较低的性能是由于甲醇的运输限制所致,因为负载的催化剂层更致密,更厚。因此,提出了在催化剂油墨制备过程中加入成孔剂Li 2 CO 3的方法。事实证明,这是非常有效的,仅用催化剂负载的1/3即可大大提高阳极性能。新型MEA的催化剂负载量比参考MEA低2.6倍,显示出非常有希望的结果,与参考MEA相比,在电流密度为150mA /cm²时,性能损失仅为10mV。此外,短期衰减测试表明,由于MEA由于PolyFuel膜在阴极电极上的甲醇穿透率低,因此新的MEA可能具有更好的耐久性和寿命。

著录项

  • 作者

    Huang, Xiaoming.;

  • 作者单位

    The Pennsylvania State University.;

  • 授予单位 The Pennsylvania State University.;
  • 学科 Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 181 p.
  • 总页数 181
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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