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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Operando Time-Resolved X-ray Absorption Fine Structure Study for Pt Oxidation Kinetics on Pt/C and Pt3Co/C Cathode Catalysts by Polymer Electrolyte Fuel Cell Voltage Operation Synchronized with Rapid O-2 Exposure
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Operando Time-Resolved X-ray Absorption Fine Structure Study for Pt Oxidation Kinetics on Pt/C and Pt3Co/C Cathode Catalysts by Polymer Electrolyte Fuel Cell Voltage Operation Synchronized with Rapid O-2 Exposure

机译:Operando时间分辨的X射线吸收细结构研究Pt / C和Pt3Co / C阴极催化剂的PT氧化动力学通过聚合物电解质燃料电池电压操作与快速O-2曝光同步

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The oxidation of a cathode catalyst surface is one of the major factors for cathode catalyst degradation under polymer electrolyte fuel cell (PEFC) operating conditions; however, the oxidation kinetics of Pt cathode catalysts in a membrane electrode assembly with O-2 has not been investigated. We have investigated operando Pt L-III-edge time-resolved X-ray absorption fine structure analysis for the Pt oxidation processes on Pt/C and Pt3Co/C cathode catalysts controlled by transient PEFC voltage operation (0.4 V - 0.7-1.0V) synchronized with the rapid exchange of cathode gas (N-2 - 10% O-2 in N-2). We plotted Pt valence and the coordination numbers of Pt-Pt and Pt-O bonds every 20 ms, and the rate constants of the structural parameters for the Pt oxidation were successfully estimated. The structural kinetics of the Pt oxidation at the cathode suggested differences in the Pt oxidation kinetics between the Pt/C and Pt3Co/C cathode catalysts, showing the kinetic control of the Pt oxidation rate by the alloying with Co to Pt.
机译:阴极催化剂表面的氧化是用于阴极催化剂降解下高分子电解质型燃料电池(PEFC)的操作条件的一个主要因素;然而,铂阴极催化剂在膜中的氧化动力学与O-2还没有被研究电极组件。我们已经调查operando的Pt L-III-边缘时间分辨X射线吸收精细结构的分析对于通过瞬时电压PEFC操作来控制上的Pt / C和Pt3Co / C阴极催化剂铂的氧化过程(0.4 [V] - > 0.7-1.0 V)与阴极气体(N-2的快速交换同步 - →10%O-2在N-2)。我们绘制铂价和铂铂的配位数和Pt-O键每20毫秒,而对于铂氧化的结构参数的速率常数成功估计。在阴极处的Pt氧化的结构动力学建议在Pt / C和Pt3Co / C阴极催化剂之间在Pt氧化动力学的差异,示出了由用Co合金Pt的铂的氧化速率的动力学控制。

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