Breaking the Thick Electrode Paradox With an in situ VS(2)@V(2)CTx MXene Heterostructure for High-Areal-Capacity Batteries

利用原位VS(2)@V(2)CTx MXene异质结构打破厚电极悖论,实现高面容量电池

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Abstract

Achieving high areal capacity is critical for advancing lithium-ion batteries (LIBs) toward high-energy-density applications. However, prevailing thick electrode architectures inevitably suffer from sluggish charge transport kinetics and mechanical degradation. Here, we pioneer an in situ gas-phase conversion strategy to directly grow metallic VS(2) nanosheets on V(2)CTx MXene within a multi-walled carbon nanotube (MWCNT) network. This integrated architecture simultaneously establishes interpenetrating electron/ion highways-enabling full lithiation in ultra-thick electrodes (12-fold higher Li(+) concentration compare to the traditional electrode)-and enhances mechanical toughness, thus achieving exceptional cycling stability under high current densities. Such TMDC-MXene heterostructure exhibit an impressive specific capacity of 1046 mAh g(-1) and areal capacity of 13.6 mAh cm(-2), with the thickness of 300 µm, representing only 12.8% gravimetric capacity decay despite 333% increased electrode thickness. Moreover, the resulting electrode maintains excellent cycling stability, retaining a capacity of 1.8 mAh cm(-2) even at high current density of 6.4 mA cm(-2), alongside 81% capacity retention over 600 cycles at 2C in LiFePO(4) full-cells.

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