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Oxygen-Reconstituted Active Species of Single-Atom Cu Catalysts for Oxygen Reduction Reaction

机译:单原子Cu催化剂的氧重构活性物种用于氧还原反应

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摘要

Identification of an active center of catalysts under realistic working conditions of oxygen reduction reaction (ORR) still remains a great challenge and unclear. Herein, we synthesize the Cu single atom embedded on nitrogen-doped graphene-like matrix electrocatalyst (abbreviated as SA-Cu/NG). The results show that SA-Cu/NG possesses a higher ORR capability than 20% Pt/C at alkaline solution while the inferior activity to 20% Pt/C at acidic medium. Based on the experiment and simulation calculation, we identify the atomic structure of Cu-N2C2 in SA-Cu/NG and for the first time unravels that the oxygen-reconstituted Cu-N2C2-O structure is really the active species of alkaline ORR, while the oxygen reconstitution does not happen at acidic medium. The finding of oxygen-reconstituted active species of SA-Cu/NG at alkaline media successfully unveils the bottleneck puzzle of why the performance of ORR catalysts at alkaline solution is better than that at acidic media, which provides new physical insight into the development of new ORR catalysts.
机译:氧还原反应(ORR)的求真务实的工作条件下,催化剂活性中心的鉴定仍然是一个巨大的挑战和不明确的。在此,我们合成嵌入氮掺杂Cu的单个原子的石墨烯状矩阵电极催化剂(简称为SA-铜/ NG)。结果表明,SA-的Cu / NG在碱性溶液中具有大于20%的Pt / C高的ORR能力,而在酸性介质中的下活动至20%的Pt / C。基于实验和模拟计算中,我们确定的Cu-N2C2的在SA-铜/ NG和首次揭开,所述氧复原的Cu-N2C2-O结构确实是碱性ORR的活性种的原子结构,而氧气重组不会在酸性介质中发生。在碱性介质SA-铜/ NG的氧重组活性物种的发现成功地推出了为什么ORR催化剂在碱性溶液中的表现优于在酸性介质中的瓶颈的难题,它提供了新的物理洞察的新发展ORR催化剂。

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