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Modeling of Ultrathin Catalyst Layers in Polymer Electrolyte Fuel Cells: Proton Transport and Water Management

机译:聚合物电解质燃料电池中超薄催化剂层的建模:质子传输和水管理

摘要

Ultrathin catalyst layers (UTCLs) are emerging as a promising alternative to conventional catalyst layers in polymer electrolyte fuel cells. In comparison, UTCLs have dramatically reduced Pt loading and thicknesses and are ionomer–free. We explore two open questions in the theory of UTCLs (1) the proton transport mechanism within the ionomer–free layer and (2) water management in membrane electrode assemblies (MEAs) with UTCLs. To investigate (1), we present a UTCL model, which assumes the protons are drawn into the UTCL via their interaction with the metal surface charge. We consider a continuum model of a water–filled, cylindrical nanopore with charged walls. We derive the relation between metal potential and surface charge density from a Stern double layer model. The model suggests the proton concentration and reaction current density to be highly dependent on the charging properties of the metaljsolution interface, which are parameterized primarily by the potential of zero charge. Therefore, materials for UTCLs should be selected not only for their intrinsic mass activities and durability, but also for their charging properties. A systematic evaluation of the interplay of electrostatic, kinetic, and mass transport phenomena in UTCL demanded an impedance variant of the model. Based on the general set of transient equations, we have derived analytical impedance expressions and equivalent circuit representations in 4 limiting cases. While the UTCL model suggests the charging of the metaljsolution interface to be crucial to performance, theoretical studies on the charging behaviour of platinum are limited. We present a generalised computational hydrogen electrode that enables the ab initio simulation of metaljsolution interfaces as a function of pH and potential. To address (2), we present a water balance model to MEAs with UTCLs. The model relates the current densities, capillary pressure distributions, and fluxes of vapor and liquid water. Analysis of the model suggests that UTCLs require efficient liquid transport paths out of the MEA at low and moderate temperature. We discuss strategies for increasing the current density for the onset of GDL flooding, via enhanced liquid permeabilities, vaporization areas, and gas pressure differentials.
机译:超薄催化剂层(UTCL)正在出现,有望替代聚合物电解质燃料电池中的常规催化剂层。相比之下,UTCL大大降低了Pt的负载和厚度,并且不含离聚物。我们探讨了UTCL的理论中的两个悬而未决的问题:(1)无离聚物层内的质子传输机制;(2)含UTCL的膜电极组件(MEA)中的水管理。为了研究(1),我们提出了一个UTCL模型,该模型假设质子通过它们与金属表面电荷的相互作用而被吸入UTCL。我们考虑了一个充满水的圆柱形带电荷壁的纳米孔的连续模型。我们从斯特恩双层模型中得出金属势与表面电荷密度之间的关系。该模型表明,质子浓度和反应电流密度高度依赖于金属溶液界面的充电特性,该特性主要由零电荷的电势来参数化。因此,不仅应选择UTCL的材料,以考虑其固有的质量活度和耐用性,还应选择其充电性能。要对UTCL中的静电,动力学和质量传输现象之间的相互作用进行系统评估,就需要模型的阻抗变量。基于瞬态方程组的一般性,我们导出了4种极限情况下的分析阻抗表达式和等效电路表示。尽管UTCL模型表明金属溶液界面的充电对于性能至关重要,但有关铂的充电行为的理论研究却很有限。我们提出了一种通用的计算氢电极,该电极能够从头开始模拟金属溶液界面作为pH和电势的函数。为了解决(2),我们向具有UTCL的MEA提供水平衡模型。该模型将电流密度,毛细管压力分布以及蒸汽和液态水的通量联系起来。对模型的分析表明,UTCL需要在低温和中温下将有效的液体从MEA输送出MEA。我们讨论了通过提高液体渗透率,汽化面积和气压差来增加GDL驱油开始时的电流密度的策略。

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    Chan Karen Ka Wing;

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  • 年度 2013
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