Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology (HUST), 1037 Luoyu Road, Wuhan 430074, P. R. China.
Nanoscale. 2017 Oct 19;9(40):15534-15541. doi: 10.1039/c7nr05208a.
The design and synthesis of a promising porous carbon-based electrocatalyst with an ordered and uninterrupted porous structure for oxygen reduction reaction (ORR) is still a significant challenge. Herein, an efficient catalyst based on cobalt-embedded nitrogen-doped ordered mesoporous carbon nanosheets (Co/N-OMCNS) is successfully prepared through a two-step procedure (cobalt ion-coordinated self-assembly and carbonization process) using 3-aminophenol as a nitrogen source, cobalt acetate as a cobalt source and Pluronic F127 as a mesoporous template. This work indicates that the formation of a two dimensional nanosheet structure is directly related to the extent of the cobalt ion coordination interaction. Moreover, the critical roles of pyrolysis temperature in nitrogen doping and ORR catalytic activity are also investigated. Benefiting from the high surface area and graphitic degree, high contents of graphitic N and pyridinic N, ordered interconnected mesoporous carbon framework, as well as synergetic interaction between the cobalt nanoparticles and protective nitrogen doped graphitic carbon layer, the resultant optimal catalyst Co/N-OMCNS-800 (pyrolyzed at 800 °C) exhibits comparable ORR catalytic activity to Pt/C, superior tolerance to methanol crossover and stability.
设计和合成具有有序且连续多孔结构的、用于氧还原反应(ORR)的有前景的多孔碳基电催化剂仍然是一个重大挑战。本文通过两步法(钴离子配位自组装和碳化过程),以 3-氨基酚作为氮源、醋酸钴作为钴源、Pluronic F127 作为介孔模板,成功制备了一种基于嵌入氮掺杂有序介孔碳纳米片的高效催化剂(Co/N-OMCNS)。这项工作表明,二维纳米片结构的形成与钴离子配位相互作用的程度直接相关。此外,还研究了热解温度对氮掺杂和 ORR 催化活性的关键作用。得益于高比表面积和石墨化程度、高含量的石墨 N 和吡啶 N、有序互联的介孔碳骨架以及钴纳米粒子与保护性氮掺杂石墨碳层之间的协同相互作用,所得最佳催化剂 Co/N-OMCNS-800(在 800°C 下热解)表现出与 Pt/C 相当的 ORR 催化活性、对甲醇交叉的更高耐受性和稳定性。