Department of Chemistry and Biochemistry, University of Delaware , Newark, Delaware 19716, United States.
Université Pierre et Marie Curie , Paris Cedex 05, France.
Langmuir. 2017 Feb 7;33(5):1121-1131. doi: 10.1021/acs.langmuir.6b02641. Epub 2016 Nov 22.
The covalent attachment of nonfunctionalized and carboxylic acid-functionalized carbon nanotubes to amine-terminated organic monolayers on gold and silicon surfaces is investigated. It is well established that the condensation reaction between a carboxylic acid and an amine is a viable method to anchor carbon nanotubes to solid substrates. The work presented here shows that the presence of the carboxylic group on the nanotube is not required for attachment to occur, as direct attachment via the substrate amine and the nanotube cage can take place. Scanning and transmission electron microscopy and atomic force microscopy confirm the presence of carbon nanotubes in intimate contact with the surface. X-ray photoelectron spectroscopy is utilized to compare the surface chemistry of the functionalized and nonfunctionalized carbon nanotubes and is supported by a computational investigation. Ion fragments attributed to the direct attachment between the surface and carbon nanotube cage are detected by time-of-flight secondary ion mass spectrometry. The overall attachment scheme is evaluated and can be further used on multiple carbonaceous materials attached to solid substrates.
非功能化和羧酸功能化的碳纳米管与金和硅表面上的胺端有机单层的共价附着进行了研究。羧酸和胺之间的缩合反应是将碳纳米管固定在固体基底上的一种可行方法,这一点已经得到了很好的证实。本文的研究表明,碳纳米管上存在羧酸基团对于附着的发生并不是必需的,因为可以通过基底胺和碳纳米管笼直接进行附着。扫描和透射电子显微镜以及原子力显微镜证实了碳纳米管与表面的紧密接触。X 射线光电子能谱用于比较功能化和非功能化碳纳米管的表面化学,并得到了计算研究的支持。飞行时间二次离子质谱检测到表面与碳纳米管笼之间直接附着产生的离子碎片。对整体附着方案进行了评估,并可进一步用于附着在固体基底上的多种含碳材料。