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Study of Degradation of Membrane-Electrode Assemblies of Hydrogen-Oxygen (Air) Fuel Cell under the Conditions of Life Tests and Voltage Cycling

机译:寿命试验和电压循环条件下氢氧(空气)燃料电池膜电极组件的降解研究

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The degradation processes of HiSPEC 9100 (60% Pt/C) and 13100 (70% Pt/C) cathodic monoplatinum catalysts, which were tested under the model conditions and in the composition of membraneelectrode assemblies (MEA) of hydrogen-air and hydrogen-oxygen fuel cells, are studied. It is shown that, in all cases, the main reason for a decrease in the catalyst activity was a decrease in its surface area, which was caused by the coarsening of platinum nanoparticles, irreversible oxidation of a fraction of active centers, and the destruction of the catalyst due to the carbon support oxidation. The results of electrochemical measurements are supplemented with the structural investigations by the methods of transmission electron microscopy (TEM), X-ray diffraction analysis (XRD), and X-ray photoelectron spectroscopy (XPS). It is found that the degradation processes of MEA in the accelerated stress tests (AST) are similar to those in the long-term life tests. With respect to a decrease in the catalyst active surface area, the application of 2500 cycles in the voltage range of 0.6 to 1.2 V in the AST is equivalent to the life tests for 1010 h. During the fuel cell operation, the destruction of polymer electrolyte proceeds along with the catalyst degradation. This leads to a decrease in the ion-exchange capacity of the membrane and ionomer in the composition of cathode active layer.
机译:HiSPEC 9100(60%Pt / C)和13100(70%Pt / C)阴极单铂催化剂的降解过程在模型条件下以及在氢气,空气和氢气的膜电极组件(MEA)的组成中进行了测试研究了氧气燃料电池。结果表明,在所有情况下,催化剂活性降低的主要原因是其表面积的降低,这是由于铂纳米粒子的粗化,活性中心部分的不可逆氧化以及甲氧基的破坏引起的。催化剂由于碳载体的氧化。电化学测量的结果通过透射电子显微镜(TEM),X射线衍射分析(XRD)和X射线光电子能谱(XPS)的方法得到结构研究的补充。发现加速应力测试(AST)中MEA的降解过程与长期寿命测试中的相似。关于催化剂活性表面积的减少,在AST的0.6至1.2 V的电压范围内施加2500个循环相当于1010小时的寿命测试。在燃料电池运行期间,聚合物电解质的破坏与催化剂的降解一起进行。这导致阴极活性层的组成中膜和离聚物的离子交换能力降低。

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