Electrochemical Effects of the Hollow Structure Co3O4/MWCNT Interlayer Derived through ZIF-67 in Lithium-Sulfur Batteries

Abstract

The self-standing ZIF-67 derived Co3O4@MWCNT interlayer is prepared without a binder and conductor. The hollow structure of ZIF-67 derived Co3O4 is confirmed through SEM and TEM analysis. XRD analysis confirms the synthesis of ZIF-67 and the subsequent formation of ligand-free Co3O4 after thermal decomposition. BET analysis also confirms a specific surface area of approximately 139.72 m2 g−2. Through polarization measurements, Co3O4 effectively reduces polarization by more than 22% compared to when it is not used. After 10 cycles, the capacity of the Co3O4@MWCNT cell is 1120.65 mAh g−1, which is 315 mAh g−1 higher than that of an MWCNT cell (805 mAh g−1). The Co3O4 promotes the conversion from Li2S4 to Li2S2 and Li2S, which leads to higher capacity. Moreover, the cycle stability improves by more than 28% by adsorbing more polysulfide through the hollow structure. Furthermore, it is confirmed that Co3O4@MWCNT exhibits approximately 33% less polarization compared to MWCNT even under high C-rate conditions (2 C rate). Various electrochemical characteristics and X-ray photoelectron spectroscopy (XPS) reveal that the hollow Co3O4 physically and chemically suppresses the shuttling phenomenon.