New Energy Research Institute, College of Environment and Energy, South China University of Technology, Guangzhou, 510006, China.
Department of Chemistry and Biochemistry, University of California, 1156 High Street, Santa Cruz, CA, 95064, USA.
Small. 2016 Apr 13;12(14):1900-8. doi: 10.1002/smll.201503542. Epub 2016 Feb 19.
Graphene-supported mesoporous carbons with rich nitrogen self-doped active sites (N-MC/rGO) are prepared by direct pyrolysis of a graphene-oxide-supported polymer composite embedded with massive, evenly distributed amorphous FeOOH that serve as efficient thermally removable templates. The resulting N-MC/rGO catalysts exhibit high surface areas and apparent electrocatalytic activity for oxygen reduction reaction in alkaline media. Among the series, the sample prepared at 800 °C displays the best performance with a more positive onset potential, higher limiting currents, much higher stability, and stronger poison resistance than commercial Pt/C. This is ascribed to the synergetic functions of the highly conductive graphene support and the mesoporous N-doped carbons that effectively impede the restacking of the graphene sheets and enhance the exposure of the rich nitrogen self-doped active sites.
具有丰富氮自掺杂活性位的石墨烯负载中孔碳(N-MC/rGO)是通过直接热解负载在大量均匀分布无定形 FeOOH 上的聚合物复合材料制备的,FeOOH 作为高效的热去除模板。所得的 N-MC/rGO 催化剂在碱性介质中表现出高的比表面积和对氧还原反应的明显电催化活性。在该系列中,在 800°C 下制备的样品表现出最好的性能,具有更正的起始电位、更高的极限电流、更高的稳定性和更强的抗中毒能力,优于商业 Pt/C。这归因于高导电性石墨烯载体和中孔 N 掺杂碳的协同作用,有效地阻止了石墨烯片的堆积并增强了丰富氮自掺杂活性位的暴露。