催化作用
吡啶
钴
化学
酞菁
X射线光电子能谱
无机化学
氧还原反应
碳纤维
核化学
材料科学
有机化学
化学工程
物理化学
电化学
电极
复合材料
复合数
工程类
作者
Xianfeng Dai,Jinli Qiao,Xuejun Zhou,Jingjing Shi,Pan Xu,Lei Zhang,Jiujiun Zhang
标识
DOI:10.1016/s1452-3981(23)14381-1
摘要
Carbon-supported non-precious metal (cobalt) catalysts, namely Py-CoPc/C, where Py is the pyridine and Pc is the phthalocyanine, are synthesized for oxygen reduction reaction (ORR) using combined solvent-impregnation and high-temperature treatment process. The heat-treatment effect on the catalysts' activity toward ORR is examined using catalysts obtained at 600, 700, 800, and 900oC, respectively. The effect of pyridine addition on the ORR activity is also studied. It is found that the formed Py-CoPc/C catalysts all show the higher ORR activities than that of CoPc/C catalyst, and the catalyst obtained at 700oC treatment gives the best activity for the ORR in 0.1M KOH solution, which are tested using both CV and RDE techniques. XRD, TEM as well as XPS are employed to study the crystal structures, morphologies and surface structure changes of the synthesized Py-CoPc/C catalysts. Both XRD and TEM analysis indicate the formation of different amounts of Co-NX-C active site at different heat-treatment temperatures, which is well correlated with the catalysts' ORR activities. XPS results suggest that the pyridinic-N and graphitic-N groups are both responsible for the enhanced ORR activity, and the catalyst formed at 700oC treatment shows the most amount of these two groups, leading to the most active ORR catalyst.
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