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Selectively nitrogen-doped carbon materials as superior metal-free catalysts for oxygen reduction

机译:选择性掺杂氮的碳材料可作为卓越的无金属催化剂用于氧还原

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摘要

Doping with pyridinic nitrogen atoms is known as an effective strategy to improve the activity of carbon-based catalysts for the oxygen reduction reaction. However, pyridinic nitrogen atoms prefer to occupy at the edge or defect sites of carbon materials. Here, a carbon framework named as hydrogen-substituted graphdiyne provides a suitable carbon matrix for pyridinic nitrogen doping. In hydrogen-substituted graphdiyne, three of the carbon atoms in a benzene ring are bonded to hydrogen and serve as active sites, like the edge or defect positions of conventional carbon materials, on which pyridinic nitrogen can be selectively doped. The as-synthesized pyridinic nitrogen-doped hydrogen-substituted graphdiyne shows much better electrocatalytic performance for the oxygen reduction reaction than that of the commercial platinum-based catalyst in alkaline media and comparable activity in acidic media. Density functional theory calculations demonstrate that the pyridinic nitrogen-doped hydrogen-substituted graphdiyne is more effective than pyridinic nitrogen-doped graphene for oxygen reduction.
机译:掺杂吡啶氮原子是提高碳基催化剂用于氧还原反应活性的有效策略。但是,吡啶二氮原子更倾向于占据碳材料的边缘或缺陷位置。在此,被称为氢取代的石墨二炔的碳骨架为吡啶氮的掺杂提供了合适的碳基质。在氢取代的石墨二炔中,苯环中的三个碳原子与氢键合并用作活性位点,就像常规碳材料的边缘或缺陷位置一样,可以选择性地掺杂吡啶氮。所合成的吡啶二酮氮掺杂的氢取代的石墨二炔在氧还原反应中的电催化性能比在碱性介质中的市售铂基催化剂好,并且在酸性介质中具有可比的活性。密度泛函理论计算表明,吡啶氮掺杂的氢取代的石墨二炔在氧还原方面比吡啶氮掺杂的石墨烯更有效。

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