Synergy and Symbiosis Analysis of Capacity-Contributing Polypyrrole and Carbon-Coated Lithium Iron Phosphate Nanostructures for High-Performance Cathode Materials

To address the existing problems of commercial inorganic cathodes, including relatively low capacity, poor rate performance, structural instability, and low conductivity, it is critical to introduce a conductive matrix accompanied with electrochemical activity. Conductive polymers have great potential as electrodes with good conductivity, high redox activity, and potential. In this study, carbon-coated lithium iron phosphate (C-LiFePO4) nanoparticles were effectively dispersed in a polypyrrole (PPy) matrix by in situ pulverization. PPy, as an active nanostructure, significantly improves conductivity and accelerates Li+ diffusion. To further explore the synergy and symbiosis mechanism of PPy and C-LiFePO4 (hereinafter called C-LFP in the composite), the nanoparticle dispersion, carburization dependence, and heat treatment preference were investigated. Therefore, a reasonable amount of PPy (25 wt %) hybridization, a moderately wrapped carbon buffer layer (5.3 wt %), and a suitable heat treatment (100 degrees C) were employed to prepare the (C-LFP)0.75(PPy)0.25 nanocomposite. With a smaller particle size, uniformly dispersed morphology, and good synergy effect between PPy and C-LiFePO4, (C-LFP)0.75(PPy)0.25 delivers a high discharge capacity (209.1 mAh g-1 at 0.1C), a superior rate capability (86.1 mAh g-1 at 10C), and an outstanding capacity retention (83.5% of the initial values after 500 cycles at 0.5C).