摘要

Hierarchically nanoporous N-doped carbon nanowires (N-CWs) were prepared by a novel space-confinement-induced assembly strategy, for which nitrogen-enriched pyrimidine and anodic aluminium oxide (AAO) template bearing metal oxides are employed as precursor and nanoscale channels, respectively, and the Fe/Co metal oxide not only blocks the AAO surface from the original surface-templating carbonization, but also introduces nanoporosity with acid etching. Thus-obtained carbon nanowires composed of N-doped graphene-like carbon nanosheets not only contain a high N content (up to similar to 12%), but also possess a hierarchically meso/microporous structure (similar to 1.3 cm(3) g(-1)) with high specific surface area (similar to 455 m(2) g(-1)). This protocol allows for the simultaneous optimization of graphitization, porous structure and surface functionalization. As a result, the prepared N-CWs demonstrate an attractive electrocatalytic capability towards oxygen reduction reaction (ORR). Specifically, in addition to the improved kinetic current density and overpotential, the N-CWs prepared at 700 degrees C show the optimized ORR performance with an electron-transfer number of similar to 4.0, which very close to that of a commercial Pt/C catalyst.