Abstract

Carbon nanotubes (CNTs) are good candidates to construct nanostructured, implantable micro-electrodes since they are conductive materials and may increase the overall electrode surface area, and thus the signal/noise ratio. However, the adsorption of biomolecules on CNTs is well-known to lead to a surface passivation. In this context, a surface modification appears essential to overcome these limitations. In this paper, the non-covalent functionalisation of multi-walled carbon nanotubes (MWNTs) by pyrene–PEG molecules through π–π stacking is presented. We describe in the first part the functionalisation of MWNT powders in aqueous solution for which we obtained a stable dispersion of functionalised MWNTs. The stability of the non-covalently functionalised MWNT dispersion during 7 cycles of dialysis in H2O was studied by UV spectroscopy. The density of pyrene–PEG on the MWNT surface stabilised at about 4 × 1011 molecules mm−2 after 4 cycles of dialysis (all the free pyrene–PEG molecules were removed by dialysis). Next, this non-covalent functionalisation of MWNT arrays on a substrate was examined. After the functionalisation, the increase of the MWNT wettability led to a 50-fold increase of the capacitance of the MWNT nanostructured electrode. Finally, we chose streptavidin, a well-known adhesive protein, as an example to test the efficiency of functionalised MWNTs towards preventing non-specific adsorption. The result shows that the presence of pyrene–PEG on the MWNT surface is indeed efficient.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.