Heterostructures have lately been recognized as a viable implement to achieve high-energy Li-ion batteries (LIBs) because the as-formed built-in electric field can greatly accelerate the charge transfer kinetics. Herein, we have constructed the Mott-Schottky heterostructured VS2/MoS2 hybrids with tailorable 1T/2H phase based on their matchable formation energy, which are made of metallic and few-layered VS2 vertically grown on MoS2 surface. The density functional theory (DFT) calculations unveil that such heterojunctions drive the rearrangement of energy band with a facilitated reaction kinetics and enhance the Li adsorption energy more than twice compared to the MoS2 surface. Furthermore, the VS2 catalytically expedites the Li-S bond fracture and meantime the enriched Mo6+ enables the sulfur anchoring toward the oriented reaction with Li+ to form Li2S, synergistically enhancing the reversibility of electrochemical redox. Consequently, the as-obtained VS2/MoS2 hybrids deliver a very large specific capacity of 1273 mAh g-1 at 0.1 A g-1 with 61% retention even at 5 A g-1. It can also stabilize 100 cycles at 0.5 A g-1 and 500 cycles at 1 A g-1. The findings provide in-depth insights into engineering heterojunctions towards the enhancement of reaction kinetics and reversibility for LIBs.
Keywords: Heterostructure; High-energy density; Interface effect; Li-ion batteries; VS(2)/MoS(2).
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