The effect of temperature on the morphology and chemical surface properties of nitrogen-doped carbon nanotubes

被引:108
作者
Chizari, Kambiz [1 ]
Vena, Alexander [1 ]
Laureritius, Lars [2 ]
Sundararaj, Uttandaraman [1 ]
机构
[1] Univ Calgary, Dept Chem & Petr Engn, Calgary, AB T2N 1N4, Canada
[2] Univ Alberta, Dept Chem, Natl Inst Nanotechnol, Edmonton, AB, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
HIGH ELECTROCATALYTIC ACTIVITY; C-N NANOTUBES; EMISSION PROPERTIES; GROWTH TEMPERATURE; PYROLYSIS; NITRIDE; OXYGEN; BORON; NANOMATERIALS; CHEMISTRY;
D O I
10.1016/j.carbon.2013.11.013
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
One of the most effective ways to tune the physical and Chemical properties of CNTs is to dope them with a foreign element, such as nitrogen. Nitrogen atoms that are incorporated into the CNT structure can drastically change the properties of CNTs. The properties of nitrogen-doped carbon nanotubes (N-CNTs) originate from their structure; thus, it is practical to create a desired structure during synthesis. We have investigated the effects of synthesis parameters, mainly temperature, on various characterizations of N-CNTs, such as their morphologies, dimensions (diameter and length), defects, nitrogen inclusions and thermal stability. The results revealed strong correlations between the synthesis parameters and the properties of the synthesized N-CNTs. XPS characterization indicated that the percentage of nitrogen inclusion decreased with increasing synthesis temperature up to 850 degrees C and then increased at 950 degrees C. Raman spectroscopy showed a decrease in the number of defects in the N-CNT structure with increasing synthesis temperature. Finally TGA demonstrated a trend of increasing thermal stability of N-CNTs with increasing synthesis temperature, up to 850 degrees C then a reduced thermal stability at 950 degrees C. Based on these results, one can control the properties of N-CNTs and obtain materials with the desired characteristics by choosing the appropriate synthesis conditions. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:369 / 379
页数:11
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