4.8 Article

Single Co-Atoms as Electrocatalysts for Efficient Hydrazine Oxidation Reaction

期刊

SMALL
卷 17, 期 16, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202006477

关键词

electrocatalysis; hydrazine oxidation reaction; renewable energy; single atom catalyst; single Co atom catalyst

资金

  1. Operational Program Research, Development and Education-European Regional Development Fund (ERDF) of the Ministry of Education, Youth and Sports of the Czech Republic [CZ.02.1.01/0.0/0.0/16_019/0000754]
  2. ERDF project Development of pre-applied research in nanotechnology and biotechnology of the Ministry of Education, Youth and Sports of the Czech Republic [CZ.02.1.01/0.0/0.0/17_048/0007323]
  3. Czech Science Foundation [19-27454X]
  4. ERC project from the European Union's Horizon 2020 [683024]
  5. US National Science Foundation [NSF DMR1508611]
  6. U.S. Department of Energy Office of Basic Energy Sciences [DE-AC02-06CH11357]
  7. Department of Energy
  8. MRCAT member institutions

向作者/读者索取更多资源

A single-atom catalyst material named G(CN)-Co has been developed on functionalized graphene, demonstrating excellent catalytic activity for electrocatalytic hydrazine oxidation reaction (HzOR) with low overpotential and high current density, while remaining stable over long reaction times. This material shows promising potential as an alternative to conventional noble metal-based catalysts in HzOR-based fuel cells.
Single-atom catalysts (SACs) have aroused great attention due to their high atom efficiency and unprecedented catalytic properties. A remaining challenge is to anchor the single atoms individually on support materials via strong interactions. Herein, single atom Co sites have been developed on functionalized graphene by taking advantage of the strong interaction between Co2+ ions and the nitrile group of cyanographene. The potential of the material, which is named G(CN)-Co, as a SAC is demonstrated using the electrocatalytic hydrazine oxidation reaction (HzOR). The material exhibits excellent catalytic activity for HzOR, driving the reaction with low overpotential and high current density while remaining stable during long reaction times. Thus, this material can be a promising alternative to conventional noble metal-based catalysts that are currently widely used in HzOR-based fuel cells. Density functional theory calculations of the reaction mechanism over the material reveal that the Co(II) sites on G(CN)-Co can efficiently interact with hydrazine molecules and promote the N-H bond-dissociation steps involved in the HzOR.

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