The 1T-phase MoS2 is a highly attractive cathode candidate for aqueous aluminum-ion batteries (AAIBs) due to its metallic conductivity, impressive theoretical specific capacity, and tunable interlayer spacing. However, its thermodynamic instability under ambient conditions hinders direct synthesis and limits practical applications. In this study, 1T-phase-rich MoS2 nanoflowers were successfully fabricated via an intercalation strategy, resulting in a structure of alternating monolayer carbon and 1T-phase MoS2. This architecture significantly increases the interlayer spacing, reduces the ion diffusion barrier, and enhances the ion transport kinetics. The incorporation of monolayer carbon further improves the electrical conductivity and structural stability. Electrochemical measurements reveal that, after 150 cycles under a current density of 0.4 A g-1, the electrode retains a discharge capacity of 209.12 mAh g-1 alongside a Coulombic efficiency exceeding 90%, indicating excellent Al-ion storage performance. Ex situ characterization elucidates the reaction mechanism and phase evolution of MoS2 during battery operation, while density functional theory (DFT) calculations confirm that monolayer carbon promotes rapid reaction kinetics and reduces the ion diffusion energy barrier. The study provides valuable guidance for the design of MoS2-based cathodes, advancing their development and application in AAIBs.
Chen et al. (2026) studied this question.