4.8 Article

Highly stable nitrogen-doped carbon nanotubes derived from carbon dots and metal-organic frameworks toward excellent efficient electrocatalyst for oxygen reduction reaction

期刊

NANO ENERGY
卷 63, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.nanoen.2019.05.074

关键词

Nitrogen-doped carbon nanotubes; Nitrogen-doped carbon dots; Metal-organic frameworks; Electrocatalyst; Oxygen reduction reaction

资金

  1. National Natural Science Foundation of China [21175114]
  2. Ministry of Science and Technology [107-2923-E-007-002-MY3, 107-2112-M-007-030-MY3, 106-2923-E-007-006- MY2, 107-2119-M-009-019, 107-3017-F-007-002]

向作者/读者索取更多资源

A highly efficient nitrogen-doped carbon nanotubes (N-CNTs) electrocatalyst derived from nitrogen-doped carbon dots (N-Cdots) and metal-organic frameworks (MOFs) for oxygen reduction reaction (ORR) was demonstrated successfully for the first time. The N-Cdots with plenty of hydroxyl and amine groups can favor the formation of N-CNTs through the catalytic decomposition of MOFs in a lower temperature. On the other hand, the N-Cdots serve as inducers of the graphitic structure and supply extra nitrogen, extending a potential electrocatalytic activity of N-CNTs. Results show that the N-CNTs provided an excellent ORR electrocatalytic performance, yielding a positive onset potential of 0.88 V vs. RHE and a high kinetic current density of up to 5.58 mA cm(-2) at 0.2 V. In addition, the slope of N-CNTs being similar to 81 mV/dec can be found to be much lower than that of the Pt/C catalyst (similar to 132 mV/dec). These superior performances are attributed to defects in the graphitic crystal structure and the synergistic coupling effects of N-Cdots and N-CNTs. In addition, a slight loss in activity for the N-CNTs catalyst can be found whereas the Pt/C catalyst decreases nearly 45% of its initial activity, which exhibit highly catalytic durability and tolerance to methanol in an alkaline media.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据