Direct synthesis of N, S co-doped graphynes via copolymerization strategy for electrocatalytic application

Yuxin Hou, Haotian Sun, Fanan Kong, Mengyang Wang, Longyu Li, Shijie Ren
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Abstract

Graphynes (GYs) are a novel set of carbon allotropes with high potential as future catalytic electrodes for oxygen reduction reactions because of their unique physical and chemical properties. In recent years, a number of heteroatom-doped graphdiyne (GDYs) based electrocatalysts have been developed. However, the development of GYs has made slow progress due to their limited synthetic strategies. Here, the first case of nitrogen and sulfur co-doped graphynes (NS-GYs) synthesized through the copolymerization between hydrogen-deficient heterocyclic aromatic monomers via the Sonogashira–Hagihara cross-coupling reaction is reported. The NS-GYs exhibit abundant porosity after heat treatment with large specific area and high heteroatom content for use as potential electrocatalysts. In addition, NS-GY-3-800 with the best electrocatalytic performance shows excellent power density and stability in Zn-air batteries.

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共聚策略直接合成N, S共掺杂石墨烯的电催化应用
石墨炔(GYs)是一种新型的碳同素异形体,由于其独特的物理和化学性质,在未来的氧还原反应中具有很高的催化潜力。近年来,研究人员开发了许多杂原子掺杂石墨烯基电催化剂。然而,由于合成策略的限制,GYs的发展进展缓慢。本文报道了首个通过Sonogashira-Hagihara交叉偶联反应,在缺氢杂环芳香单体之间共聚合成氮硫共掺杂石墨炔(NS-GYs)的案例。NS-GYs经热处理后孔隙度丰富,比表面积大,杂原子含量高,可作为潜在的电催化剂。此外,电催化性能最好的NS-GY-3-800在锌空气电池中表现出优异的功率密度和稳定性。
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