异质结
动力学
电化学
氧化还原
密度泛函理论
锂(药物)
材料科学
肖特基势垒
吸附
化学工程
化学物理
纳米技术
光电子学
电极
计算化学
化学
物理化学
冶金
医学
物理
量子力学
内分泌学
二极管
工程类
作者
Yuru Dong,Yu Liu,Yanjie Hu,Kun Ma,Hao Jiang,Chunzhong Li
出处
期刊:Science Bulletin
[Elsevier BV]
日期:2020-05-15
卷期号:65 (17): 1470-1478
被引量:86
标识
DOI:10.1016/j.scib.2020.05.007
摘要
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.
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