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Ordered mesoporous porphyrinic carbons with very high electrocatalytic activity for the oxygen reduction reaction

机译:有序介孔卟啉碳对氧还原反应具有很高的电催化活性

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摘要

The high cost of the platinum-based cathode catalysts for the oxygen reduction reaction (ORR) has impeded the widespread application of polymer electrolyte fuel cells. We report on a new family of non-precious metal catalysts based on ordered mesoporous porphyrinic carbons (M-OMPC; M = Fe, Co, or FeCo) with high surface areas and tunable pore structures, which were prepared by nanocasting mesoporous silica templates with metalloporphyrin precursors. The FeCo-OMPC catalyst exhibited an excellent ORR activity in an acidic medium, higher than other non-precious metal catalysts. It showed higher kinetic current at 0.9 V than Pt/C catalysts, as well as superior long-term durability and MeOH-tolerance. Density functional theory calculations in combination with extended X-ray absorption fine structure analysis revealed a weakening of the interaction between oxygen atom and FeCo-OMPC compared to Pt/C. This effect and high surface area of FeCo-OMPC appear responsible for its significantly high ORR activity.
机译:用于氧还原反应(ORR)的铂基阴极催化剂的高成本阻碍了聚合物电解质燃料电池的广泛应用。我们报告了一种新的非贵金属催化剂家族,该催化剂基于具有高表面积和可调节孔结构的有序介孔卟啉碳(M-OMPC; M = Fe,Co或FeCo),这些催化剂是通过将介孔二氧化硅模板与金属卟啉前体。 FeCo-OMPC催化剂在酸性介质中表现出优异的ORR活性,高于其他非贵金属催化剂。它在0.9 V处显示出比Pt / C催化剂更高的动电流,以及出色的长期耐久性和MeOH耐受性。密度泛函理论计算结合扩展的X射线吸收精细结构分析显示,与Pt / C相比,氧原子与FeCo-OMPC之间的相互作用减弱。 FeCo-OMPC的这种作用和高表面积似乎是其明显较高的ORR活性的原因。

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