催化作用
材料科学
电池(电)
碳纤维
化学工程
氮气
阴极
耐久性
无机化学
氧还原反应
甲醇
化学
电极
电化学
物理化学
有机化学
复合材料
复合数
工程类
功率(物理)
物理
量子力学
作者
Xiao Liu,Chi Chen,Qing‐Qing Cheng,Liangliang Zou,Zhiqing Zou,Hui Yang
出处
期刊:Catalysts
[Multidisciplinary Digital Publishing Institute]
日期:2018-04-13
卷期号:8 (4): 158-158
被引量:10
摘要
It is still a challenge to synthesize non-precious-metal catalysts with high activity and stability for the oxygen reduction reaction (ORR) to replace the state-of-the art Pt/C catalyst. Herein, a Fe, N, S co-doped porous carbon (Fe-NS/PC) is developed by using g-C3N4 and 2,4,6-tri(2-pyridyl)-1,3,5-triazine (TPTZ) as binary nitrogen precursors. The interaction of binary nitrogen precursors not only leads to the formation of more micropores, but also increases the doping amount of both iron and nitrogen dispersed in the carbon matrix. After a second heat-treatment, the best Fe/NS/C-g-C3N4/TPTZ-1000 catalyst exhibits excellent ORR performance with an onset potential of 1.0 V vs. reversible hydrogen electrode (RHE) and a half-wave potential of 0.868 V (RHE) in alkaline medium. The long-term durability is even superior to the commercial Pt/C catalyst. In the meantime, an assembled Zn-air battery with Fe/NS/C-g-C3N4/TPTZ-1000 as the cathode shows a maximal power density of 225 mW·cm−2 and excellent durability, demonstrating the great potential of practical applications in energy conversion devices.
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