Awareness of the environmental pollution caused by fossil fuels and the ever-increasing demand for energy has driven research focussed on zero-carbon renewable energy sources. Conscious of this, direct absorption solar thermal collectors are gaining prominence, both for domestic heating and steam generation. Carbon nanotubes (CNTs) have been investigated as an additive to take advantage of the near blackbody absorption and high thermal conductivity to improve system efficiency. Critical to the success of the additive nanoparticles is the stability in the fluid, however, due to their high surface energy CNTs tend to agglomerate which can limit the efficacy of their integration into real-world products. Covalent functionalization of the CNT sidewalls with oxygen-based or nitrogen-based functional groups is one of the most popular techniques to modify the surface energy of the CNTs.1 As an alternative to the harsh chemicals used by traditional chemical functionalisation, plasma-based surface treatments can be used with great efficacy and reduced reaction times.In this work, macroscopic ribbon-like assemblies of carbon nanotubes are functionalized using a simple direct current-based plasma-liquid system. This system utilizes the plasma-generated species in a fluid of 10 %vol ethanol in water, with or without a nitrogen precursor, for the oxygen and/or nitrogen functionalisation of the carbon nanotube assembly. For this treatment, a ribbon-like piece of CNT was used as the anode and a helium plasma discharge triggered by applying 10 mA and 1 - 1.6 kV to act as the cathode. The plasma-generated species are then expected to migrate towards the CNTs and functionalisation the sidewalls.The oxygen content is shown to be increased by between 50 % and 200 % when the treatment solution of 10 %vol ethanol is used in the ribbon electrode configuration. When ethylenediamine is added as a nitrogen precursor, the atomic concentration of nitrogen reaches 23 % in the ribbon electrode configuration, with amine groups, pyrrolic groups and graphitic nitrogen observed in the x-ray photoelectron spectra. This nitrogen content is unmatched in quantity when compared to either a simple soaking procedure or an electrolysis process with a platinum foil replacing the plasma as the counter-electrode. This demonstrates that the plasma either directly or indirectly, by means of plasma-generated species, facilitates and enhances the availability of nitrogen from the ethylenediamine precursor. The potential plasma-induced chemical pathways which lead to the functionalization of the CNTs are also investigated and discussed.In the application of a DASC system, it is found that the covalent functionalisation provided by the plasma-liquid system enhances the stability of the CNT-EG nanofluid, with the oxygen-functionalized samples producing the most stable nanofluids. This functionalization method generates interest for a broader range of applications including mechanically superior advanced composites,2 more sensitive gas sensors,3 enhanced energy storage materials4 or ultra-conductive fibres.5 References (1) Mallakpour, S.; Soltanian, S. Surface Functionalization of Carbon Nanotubes: Fabrication and Applications. RSC Adv. 2016, 6 (111), 109916–109935.(2) Williams, J.; Broughton, W.; Koukoulas, T.; Rahatekar, S. S. Plasma Treatment as a Method for Functionalising and Improving Dispersion of Carbon Nanotubes in Epoxy Resins. J. Mater. Sci. 2013, 48 (3), 1005–1013.(3) Ham, S. W.; Hong, H. P.; Kim, J. H.; Min, S. J.; Min, N. K. Effect of Oxygen Plasma Treatment on Carbon Nanotube-Based Sensors. J. Nanosci. Nanotechnol. 2014, 14 (11), 8476–8481.(4) Hulicova-Jurcakova, D.; Seredych, M.; Lu, G. Q.; Bandosz, T. J. Combined Effect of Nitrogen- and Oxygen-Containing Functional Groups of Microporous Activated Carbon on Its Electrochemical Performance in Supercapacitors. Adv. Funct. Mater. 2009, 19 (3), 438–447.(5) Li, L.; Liu, E.; Shen, H.; Yang, Y.; Huang, Z.; Xiang, X.; Tian, Y. Charge Storage Performance of Doped Carbons Prepared from Polyaniline for Supercapacitors. J. Solid State Electrochem. 2011, 15 (1), 175–182. Figure 1