The demand for today's material resources for energy storage is rapidly increasing and can result in both environmental and political conflicts that can affect the development of electronic devices due to high prices and limitations of raw materials for batteries. In this study, potential future composite electrodes were synthesised with an ex-situ approach by compositing redox-active 2,6-Diaminoanthraquinone and 1,3,5-Triformylphloroglucinol covalent organic framework (DAAQ-TFP COF) with conductive delaminated Ti3C2Tx MXene to maximise the number of redox-active moieties during cycling. In addition, solvothermal synthesis with the implementation of mechanical grinding as an exfoliation method was used to try to obtain DAAQ-TFP nanosheets to increase both the contact area between the two materials and the number of charge carriers. The sample was analysed with PXRD and BET surface analysis to characterise the crystallinity meanwhile SEM was utilised to study the morphology of the COF and the composite material. The specific capacitance of each electrode was estimated by cyclic voltammetry. The study showed a decrease in reduced specific capacitance with lower MXene content. Hence, this concludes pure Ti3C2Tx sheets have the highest capacitance contribution with a value of 48.79 Fg-1 meanwhile the composite electrode with a ratio of 1:1 was estimated to 32.26 Fg-1 with 0.0928 % of its moieties undergoing a redox reaction. A reduced capacitance with an increased COF-MXene ratio indicates that MXene contributes with more capacity relative to the COF, in combination with a non-successful exfoliation of DAAQ-TFP to single-layered nanosheets, reducing the interactions between the two materials.