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Oxygen Evolution Reaction at Carbon Edge Sites: Investigation of Activity Evolution and Structure–Function Relationships with Polycyclic Aromatic Hydrocarbons

机译:碳边缘位点的放氧反应:与多环芳烃的活性演化及结构-功能关系的研究

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摘要

The abundance of available surface chemical information and edge structures of carbon materials have attracted tremendous interest in catalysis. For the oxygen evolution reaction (OER), the edge effects of carbon materials have rarely been studied in detail because of the complexity of various coexisting edge configurations and the controversy between carbon corrosion and carbon catalysis. Herein, the exact roles of common carbon active edge sites in the OER were interrogated using polycyclic aromatic hydrocarbons (PAHs) with designated configurations (zigzag and armchair) as model probe molecules, with a focus on structure–function relationships. Zigzag configurations of PAHs showed high activity for the OER while also showing a good stability at a reasonable potential. They show a TOF value of 0.276 s−1 in 0.1 m KOH. The catalytic activity of carbon edge sites was further effectively regulated by extending the π conjugation structure at a molecular level.
机译:大量可用的表面化学信息和碳材料的边缘结构引起了人们对催化的极大兴趣。对于氧气析出反应(OER),由于各种共存的边缘构型的复杂性以及碳腐蚀和碳催化之间的争议,很少对碳材料的边缘效应进行详细研究。在此,使用具有指定构型(锯齿形和扶手椅形)的多环芳烃(PAHs)作为模型探针分子,来研究OER中常见碳活性边缘位点的确切作用,重点是结构-功能关系。 PAH的Z字形构型显示出对OER的高活性,同时在合理的电位下也显示出良好的稳定性。它们在0.1 m KOH中的TOF值为0.276 s -1 。通过在分子水平上扩展π共轭结构,可以进一步有效地调节碳边缘位点的催化活性。

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