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Iron-nitrogen co-doped hollow carbon sphere with mesoporous structure for enhanced oxygen reduction reaction

机译:具有中孔结构的铁氮共掺杂空心碳球,用于增强氧还原反应

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An iron-nitrogen co-doped hollow carbon sphere (FeN-HCS) with a mesoporous structure is designed and prepared via simple pyrolysis of melamine on the surface of Fe3O4 nanospheres. In the reaction, Fe3O4 nanospheres are used both as templates for catalyzing the growth of carbon shells and iron sources to form ORR active sites. The FeN-HCS catalyst obtained exhibits extremely high oxygen reduction activity in an alkaline medium with a half-wave potential of 0.834 V (vs. RHE), which is 5 mV more positive than a Pt/ C catalyst, and shifts negatively by only 6 mV after accelerated degradation tests (ADT). Moreover, the FeN-HCS catalyst shows a clear 4-electron reduction pathway and a high methanol tolerance. The outstanding performance of FeN-HCS can be attributed to its unique hierarchical porous hollow shell structure, which maximizes exposure of active sites and enhances mass transfer. Such a synthetic strategy offers a novel route to prepare functional hollow carbon spheres for energy storage and conversion applications.
机译:通过简单地将三聚氰胺在Fe3O4纳米球表面热解,设计并制备了具有介孔结构的铁氮共掺杂空心碳球(FeN-HCS)。在反应中,Fe3O4纳米球既用作模板,用于催化碳壳和铁源的生长,以形成ORR活性位点。所获得的FeN-HCS催化剂在碱性介质中显示出极高的氧还原活性,其半波电势为0.834 V(vs. RHE),比Pt / C催化剂正电高5 mV,而负移仅6加速降解测试(ADT)后的mV。而且,FeN-HCS催化剂显示出清晰的4电子还原途径和高甲醇耐受性。 FeN-HCS的出色性能可归因于其独特的分级多孔中空壳结构,该结构可使活性部位的暴露最大化并增强质量传递。这种合成策略为制备功能性空心碳球用于能量存储和转化应用提供了一条新颖的途径。

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