电催化剂
催化作用
热解
材料科学
甲醇
金属有机骨架
化学
兴奋剂
无机化学
多孔性
贵金属
碳纤维
化学工程
电化学
金属
电极
物理化学
冶金
有机化学
复合材料
吸附
工程类
复合数
光电子学
作者
Pengfei Zhang,Chen Chen,Xiaohua Zhang,Zhigang Jiang,Junlin Huang,Jinhua Chen
标识
DOI:10.1016/j.electacta.2018.12.119
摘要
N-enriched porous carbon materials represent a kind of effective electrocatalysts for oxygen reduction reaction (ORR), which have received extensive attention owing to their low-cost, advantageous catalytic activity and stability. However, exploring non-noble-metal catalysts for replacing high-cost notable metal catalysts remains a major challenge. Herein, iron and sulfur co-doped N-enriched hierarchical porous carbon polyhedron (NC) derived from metal-organic framework (Fe/S-NC) was successfully prepared by a facile strategy, including a direct pyrolyzation of zeolitic imidazolium framework (ZIF-8) and a further pyrolysis of the impregnated NC with Fe(SCN)3 solution. Electron microscopic studies showed that Fe/S co-doping has not changed the polyhedron morphology of NC. The resulted Fe/S-NC demonstrated obviously enhanced ORR activity, excellent durability and methanol tolerance in both alkaline and acidic media. The half-wave potential of the Fe/S-NC exhibited 32 mV positive shift in 0.1 M KOH, and only 25 mV negative shift in 0.5 M H2SO4, respectively, as compared to that of the commercial Pt/C (20% Pt loading) catalyst. The superior performance is attributable to the combined roles of the unique hierarchical porous structure of NC and the Fe/S co-doping by endowing Fe/S-NC with great specific surface area, rich active sites, excellent conductivity and synergistic effect between Fe-Nx-C active sites and a thiophene-like structure (C-S-C).
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