Zhang Wendi, Liu Xiaoming, Gao Man, Shang Hong, Liu Xuanhe
School of Science, China University of Geosciences (Beijing), Beijing 100083, China.
Nanomaterials (Basel). 2021 Jan 20;11(2):261. doi: 10.3390/nano11020261.
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.
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催化剂储量低且成本高,有必要拓展高效非贵金属ORR电催化剂的范围。在此,我们通过在不同温度(t = 600、700、800、900°C)下用双氰胺对Co/Zn金属有机框架(MOF)进行简便碳化,合成了结晶态的钴嵌入氮掺杂碳纳米管(Co@CNTs-T)。Co@CNTs-800在碱性电解质中具有优异的ORR活性,相对于可逆氢电极(RHE)的半波电位为0.846 V,与Pt/C相当。由Co@CNTs-T形成的这种三维网络在ORR过程中促进了电子迁移和离子扩散。Co纳米颗粒周围的碳壳使Co@CNTs-800作为电催化剂具有稳定性。这项工作为设计高效且低成本的氧催化剂提供了一种新策略。