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Evaluation of the stability and durability of Pt and Pt-Co/C catalysts for polymer electrolyte membrane fuel cells

机译:用于聚合物电解质膜燃料电池的Pt和Pt-Co / C催化剂的稳定性和耐久性评估

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Carbon supported Pt and Pt-Co nanoparticles were prepared by reduction of the metal precursors with NaBH_4. The activity for the oxygen reduction reaction (ORR) of the as-prepared Co-containing catalyst was higher than that of pure Pt. 30 h of constant potential operation at 0.8 V, repetitive potential cycling in the range 0.5-1.0 V and thermal treatments were carried out to evaluate their electrochemical stability. Loss of non-alloyed and, to a less extent, alloyed cobalt was observed after the durability tests with the Pt-Co/C catalyst. The loss in ORR activity following durability tests was higher in Pt-Co/C than in Pt/C, i.e. pure Pt showed higher electrochemical stability than the binary catalyst. The lower stability of the Pt-Co catalyst during repetitive potential cycling was not ascribed to Co loss, but to the dissolution-re-deposition of Pt, forming a surface layer of non-alloyed pure Pt. The lower activity of the Pt-Co catalyst than Pt following the thermal treatment, instead, was due to the presence of non-alloyed Co and its oxides on the catalyst surface, hindering the molecular oxygen to reach the Pt sites.
机译:通过用NaBH_4还原金属前驱物来制备碳载Pt和Pt-Co纳米颗粒。所制备的含Co催化剂的氧还原反应(ORR)活性高于纯Pt。在0.8 V的恒定电势下运行30 h,重复电势在0.5-1.0 V范围内循环,并进行热处理以评估其电化学稳定性。在使用Pt-Co / C催化剂进行耐久性测试后,观察到了非合金和合金钴的损失。耐久性试验后,Pt-Co / C中ORR活性的损失高于Pt / C,即纯Pt的电化学稳定性高于二元催化剂。 Pt-Co催化剂在重复电位循环过程中较低的稳定性并非归因于Co的损失,而是归因于Pt的溶解-再沉积,形成了非合金纯Pt的表面层。相反,Pt-Co催化剂的活性比热处理后的Pt低,这是由于催化剂表面上存在非合金化的Co及其氧化物,从而阻碍了分子氧到达Pt位置。

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