A novel carbon supported LiMn2O4 nanocomposite framework has been explored to resolve multiple barriers associated with lithium manganese oxide cathodes for aqueous LIB systems. Here, we have successfully synthesized an architecturally stable AlF3-LiMn2O4/rGO composite with improved electron transfer kinetics and CV peak currents proportional to the square root of scan rate. The synergy between graphene and aluminium trifluoride enhances the intrinsic electrochemical properties of pristine LiMn2O4 (LMO) and reduced Mn+3 dissolution. The unique composite effectively reduced Li+ diffusion distances with less polarization as it effectively accommodates the structural transformation during Li+ ion charge and discharge. The electrochemical interrogation revealed faster charge transportation and decrease in charge transfer resistance due to inhibition of the pronounced pile-up of Li+ ions and undesired Mn3+ ions on the surfaces. The electrochemical performances were tested in LiNO3 aqueous electrolyte and the cell delivered a capacity of 90 mA h g(-1) based on the total weight of the active electrode materials. This aqueous LIB cathode system provides a promising alternative for safe, cost-effective and scalable energy storage with tolerance against misuse.
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