4.8 Article

Oxidative Unzipping of Stacked Nitrogen-Doped Carbon Nanotube Cups

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 7, 期 20, 页码 10734-10741

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.5b00447

关键词

nitrogen doped; carbon nanotubes; unzipping; graphene-carbon nanotube hybrid structure; optimized morphology

资金

  1. NIEHS [R01ES019304]
  2. NSF CAREER [0954345]
  3. Bayer MaterialScience Fellowship
  4. Direct For Mathematical & Physical Scien
  5. Division Of Chemistry [0954345] Funding Source: National Science Foundation

向作者/读者索取更多资源

We demonstrate a facile synthesis of different nanostructures, by Oxidative unzipping of stacked nitrogen doped carbon nanotube cups (NCNCs). Depending on the initial number of stacked-cup segments, this method can yield graphene nanosheets (GNSs) or hybrid nanostructures comprised, of graphene nanoribbons partially unzipped from a Central nanotube core. Due to the stacked-cup structure of as-synthesized NCNCs, preventing complete exposure of graphitic planes, the unzipping Mechanism, is hindered, resulting in incomplete unzipping, however, individual, separated NCNCs are completely unzipped; yielding individual nitrogen-doped GNSs. Graphene-based materials have been employed as electrocatalysts for Many important chemical reactions, and it has been proposed that increasing the reactive edges results in more efficient, electrocatalysis. In this paper, we apply these graphene conjugates as electrocatalysts for the oxygen reduction reaction (ORR) to determine how the increase in reactive edges affects the electrocatalytic activity. This investigation introduces a new method for the improvement of ORR, electrocatalysts by using nitrogen dopants mote effectively, allowing for enhanced ORR performance with lower overall nitrogen content. Additionally, the GNSs were functionalized with gold nanoparticles (GNPs), resulting in a GNS/GNP hybrid, which shows efficient surface-enhanced Raman scattering and expands. the scope of its application in advanced device fabrication and biosensing.

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