Abstract 2D layered MXene‐based materials are applied as cation‐intercalation electrode materials for sodium‐ion batteries (SIBs) due to their layered structures but suffer from spontaneous restacking during Na + insertion and deintercalation processes, resulting in sluggish reaction kinetics and poor cycling stability. Herein, fullerene C 60 is intercalated covalently into the interlayer of Ti 3 C 2 T x MXene nanosheets by using a low‐temperature hydrothermal reaction between a water‐soluble C 60 derivative and hydrophilic MXene nanosheets, resulting in enlarged interlayer spacing of MXene nanosheets from 12.8 to 14.1 Å and consequently retarded self‐restacking. Moreover, the strong electron extraction ability of C 60 facilitates electron transfer from MXene to C 60 , enabling faster charge transport during Na + transportation. The as‐prepared C 60 @MXene hybrid is applied as a novel anode of SIBs, exhibiting outstanding electrochemical performance and super‐long cycling stability. C 60 @MXene‐based SIB delivers a specific capacity of 226.8 mAh g −1 at 0.1 A g −1 after 300 cycles, which surpasses that obtained from the pristine MXene anode, and retains 94.5% capacity at 1 A g −1 after 10 000 cycles. DFT simulations confirm that C 60 ‐induced enlarged interlayer spacing benefits Na + migrations, which is responsible for improved electrochemical performance and cycling stability.
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Wang et al. (2024) studied this question.
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