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Co-Zn-MOFs Derived N-Doped Carbon Nanotubes with Crystalline Co Nanoparticles Embedded as Effective Oxygen Electrocatalysts

机译:Co-Zn-Mofs通过嵌入为有效氧气催化剂的结晶CO纳米颗粒衍生N-掺杂的碳纳米管

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摘要

The oxygen reduction reaction (ORR) is a crucial step in fuel cells and metal-air batteries. It is necessary to expand the range of efficient non-precious ORR electrocatalysts on account of the low abundance and high cost of Pt/C catalysts. Herein, we synthesized crystalline cobalt-embedded N-doped carbon nanotubes (Co@CNTs-T) via facile carbonization of Co/Zn metal-organic frameworks (MOFs) with dicyandiamide at different temperatures (t = 600, 700, 800, 900 °C). Co@CNTs- 800 possessed excellent ORR activities in alkaline electrolytes with a half wave potential of 0.846 V vs. RHE (Reversible Hydrogen Electrode), which was comparable to Pt/C. This three-dimensional network, formed by Co@CNTs-T, facilitated electron migration and ion diffusion during the ORR process. The carbon shell surrounding the Co nanoparticles resulted in Co@CNTs-800 being stable as an electrocatalyst. This work provides a new strategy to design efficient and low-cost oxygen catalysts.
机译:氧还原反应(ORR)是燃料电池和金属 - 空气电池中的关键步骤。由于PT / C催化剂的低丰度和高成本,有必要扩展有效的非珍贵ORR电催化剂的范围。在此,我们在不同温度下用双氰胺的Co / Zn金属 - 有机框架(MOF)的碳化合成结晶钴嵌入的N掺杂的碳纳米管(CO @ CNTS-T)(MOF)(T = 600,700,800,900° C)。 CO @ CNTS-800在碱性电解质中具有优异的ORR活性,其半波电位为0.846V与RHE(可逆氢电极),其与PT / C相当。该三维网络由CO @ CNTS-T形成,促进电子迁移和ORR过程中的离子扩散。围绕CO纳米颗粒的碳壳导致CO @ CNTS-800作为电催化剂稳定。这项工作提供了一种设计高效和低成本氧气催化剂的新策略。

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