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Electrodeposition-fabricated PtCu-alloy cathode catalysts for high-temperature proton exchange membrane fuel cells

机译:用于高温质子交换膜燃料电池的电沉积制备的PtCu合金阴极催化剂

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摘要

Pt electrocatalysts in high-temperature proton exchange membrane fuel cells (HT-PEMFCs) containing phosphoric acid (PA)-doped polymer membranes are prone to poisoning by leaked PA. We performed a preliminary density functional theory (DFT) study to investigate the relationship between the electronic structure of Pt surfaces and their adsorption of PA. Excess charge on Pt was found to weaken its bonding with the oxygen in PA, thus presenting a strategy for the fabrication of PA-resistant catalyst materials. Consequently, PtCu-alloy catalysts with various compositions were prepared by electrodeposition. The morphologies and crystalline structures of the alloys were strongly dependent on alloy composition. Moreover, the Pt atoms in the PtCu-alloy catalysts were found to be in an electron-rich state, similar to that of the excessively charged Pt simulated in the DFT study. As a result, the oxygen reduction reaction activities of the PtCu-alloy catalysts were superior to that of a Pt-only catalyst, regardless of the presence of PA. In the absence of PA, the higher activity of the PtCu-alloy catalysts was ascribable to conventional alloying effects, while the increased activity in the presence of PA was largely due to the enhanced resistance to PA poisoning. Therefore, PtCu-alloy catalysts easily prepared by electrodeposition were found to be strong candidate materials for HT-PEMFC electrodes.
机译:含有磷酸(PA)掺杂的聚合物膜的高温质子交换膜燃料电池(HT-PEMFC)中的Pt电催化剂容易因泄漏的PA而中毒。我们进行了初步的密度泛函理论(DFT)研究,以研究Pt表面的电子结构与其对PA的吸附之间的关系。发现Pt上的电荷过多会削弱其与PA中氧的键合,从而为制备耐PA的催化剂材料提供了一种策略。因此,通过电沉积制备了具有各种组成的PtCu合金催化剂。合金的形态和晶体结构在很大程度上取决于合金成分。此外,发现PtCu合金催化剂中的Pt原子处于富电子状态,这与DFT研究中模拟的过度充电的Pt相似。结果,无论PA的存在如何,PtCu合金催化剂的氧还原反应活性都优于仅Pt催化剂。在不存在PA的情况下,PtCu合金催化剂的较高活性归因于常规的合金作用,而在存在PA的情况下活性的提高主要是由于对PA中毒的抵抗力增强。因此,发现容易通过电沉积制备的PtCu合金催化剂是用于HT-PEMFC电极的强候选材料。

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