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Influence of the Synthesis Parameters in Carbon Nanotubes Doped with Nitrogen for Oxygen Electroreduction
Nitrogen doped carbon nanotubes (N-CNTs) were synthesized by modified chemical vapor deposition method using a novel two steps thermal technique. Pyridine was used as carbon and nitrogen source and ferrocene as catalyst for nanotubes growth. The effects of reactor temperature and carrier gas flow we...
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Published in: | ECS journal of solid state science and technology 2017, Vol.6 (6), p.M3135-M3139 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Nitrogen doped carbon nanotubes (N-CNTs) were synthesized by modified chemical vapor deposition method using a novel two steps thermal technique. Pyridine was used as carbon and nitrogen source and ferrocene as catalyst for nanotubes growth. The effects of reactor temperature and carrier gas flow were investigated using scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, X-ray photoelectron spectroscopy and linear scan voltammetry. Results show that the synthesis temperature and gas flow rate have influence on the physical, chemical and electrochemical properties of the nanostructures. Microscopy studies exhibit that synthesis temperature modify the length, yield and diameter of the N-CNTs. Transmission microscopy electron images show multiwalled carbon nanotubes with the typical bamboo like structures. High temperature and low flow rate generate more defects, as revealed by Raman analyses. N-CNTs synthesized at the highest temperature and flow rate show better electrocatalytic activity toward oxygen reduction reaction with promising lower onset potential and current densities up to 80% when compared to traditional Pt/C. The favorable performance is attributed to the higher nitrogen content and the type of nitrogen species, mainly pyrrolic and pyridinic incorporated in the carbon lattice. |
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ISSN: | 2162-8769 2162-8769 2162-8777 |
DOI: | 10.1149/2.0251706jss |