催化作用
氮气
氧还原反应
无机化学
金属
还原(数学)
材料科学
碳纤维
兴奋剂
氧还原
氧气
化学
纳米技术
有机化学
冶金
物理化学
电化学
电极
复合数
复合材料
光电子学
数学
几何学
作者
Qing Lv,Wenyan Si,Jianjiang He,Lei Sun,Chunfang Zhang,Ning Wang,Ze Yang,Xiaodong Li,Xin Wang,Wei Deng,Yun‐Ze Long,Changshui Huang,Yuliang Li
标识
DOI:10.1038/s41467-018-05878-y
摘要
Doping with pyridinic nitrogen atoms is known as an effective strategy to improve the activity of carbon-based catalysts for the oxygen reduction reaction. However, pyridinic nitrogen atoms prefer to occupy at the edge or defect sites of carbon materials. Here, a carbon framework named as hydrogen-substituted graphdiyne provides a suitable carbon matrix for pyridinic nitrogen doping. In hydrogen-substituted graphdiyne, three of the carbon atoms in a benzene ring are bonded to hydrogen and serve as active sites, like the edge or defect positions of conventional carbon materials, on which pyridinic nitrogen can be selectively doped. The as-synthesized pyridinic nitrogen-doped hydrogen-substituted graphdiyne shows much better electrocatalytic performance for the oxygen reduction reaction than that of the commercial platinum-based catalyst in alkaline media and comparable activity in acidic media. Density functional theory calculations demonstrate that the pyridinic nitrogen-doped hydrogen-substituted graphdiyne is more effective than pyridinic nitrogen-doped graphene for oxygen reduction.
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