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One-pot synthesis of triazine-framework derived catalysts with high performance for polymer electrolyte membrane fuel cells

机译:三嗪骨架衍生催化剂的单壶合成,具有高性能的聚合物电解质膜燃料电池

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摘要

The prohibitive cost and scarcity of the precious metals used for oxygen reduction reaction (ORR) catalysts limit the large-scale commercialization of proton exchange membrane fuel cells (PEMFCs). Great efforts have been made to improve the ORR activity of non-precious metal catalysts. Herein, we describe a one-pot synthesis process of preparing triazine-polymer–Fe–C catalysts using polyimide (PI), ferric chloride and melamine as the precursors with a pronounced electrocatalytic activity towards ORR in acid media. The ORR activity of catalysts and the performance of single cells strongly depend on the properties of the carbon supports, which affect the surface areas and microporosities of the final catalysts. The optimized PI–Fe–C catalyst exhibits an excellent performance (onset potential of 0.92 V and the half-wave potential 0.78 V) towards ORR activity in acid medium. A maximum power density of 310 mW cm ~(?2) is obtained with a loading of 2 mg cm ~(?2) in a single cell.
机译:用于氧还原反应(ORR)催化剂的贵金属的令人满意的成本和稀缺性限制了质子交换膜燃料电池(PEMFC)的大规模商业化。已经努力改善非贵金属催化剂的ORR活性。在此,我们描述了使用聚酰亚胺(PI),氯化铁和三聚氰胺作为前体制备三嗪聚合物-FE-C催化剂的单盆合成方法,以酸介质中的ORR具有明显的电催化活性。催化剂的ORR活性和单细胞的性能强烈地取决于碳载体的性质,这影响了最终催化剂的表面积和微孔。优化的PI-Fe-C催化剂表现出优异的性能(开始潜力为0.92V,半波电位0.78V),均为酸性介质的ORR活性。在单个细胞中载入2mg cm〜(Δ2)的载荷,获得310mM〜(α2)的最大功率密度。

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