Owing to the unique and significant properties of the layered twodimensional (2D) structure of MXenes, they are being widely employed for various electrochemical device applications such as Li-ion batteries (LIBs), supercapacitors (SC), and hydrogen storage. Less attention has been paid toward their catalytic applications (energy conversion), perhaps due to the non-ideal electrochemical performance. Therefore, in the present study, we are reporting the preparation and electrocatalytic ability of MXene (Ti 3 C 2 T x ) and metal organic framework (Cobalt-MOF)-derived composites (Co-NC/Ti 3 C 2 -T). Interestingly, the optimized composite Co-NC/Ti 3 C 2 -800 reveals improved electrocatalytic oxygen reduction reaction (ORR) activity with a reasonably higher onset potential (E onset ) of 1.04 V versus reversible hydrogen electrode (RHE), a current density (J L ) of 4.8 mA/cm 2 , and a half wave potential (E 1/2 ) of 0.93 V versus RHE. Furthermore, the first order kinetics mechanism of ORR and percentage peroxide yield (HO 2 − ) were investigated using RRDE measurement. Finally, an optimized catalyst Co-NC/Ti 3 C 2 -800 demonstrates robust potential cycling performance (after 10k) over Pt/C under similar experimental conditions. Superior electrochemical performance of as-prepared nanocomposite materials is attributed to the redox centers of Co and the direct growth of a N-doped carbon network around a skeleton of Ti 3 C 2 T x that act as efficient charge transfer channel after redox reactions. Moreover, the formation of TiO 2 on the surface of MXene flakes may decrease the mass transport limitation and help to boost the electrocatalytic activity. Thus, the hybrid of MXene and Co-MOF (Co-NC/ Ti 3 C 2 -800) could be hopefully be a substitute for state-of-the-art catalysts, especially under alkaline conditions.