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提高Mott-Schottky VS/MoS异质结中的反应动力学和可逆性以增强锂存储性能。

Boosting reaction kinetics and reversibility in Mott-Schottky VS/MoS heterojunctions for enhanced lithium storage.

作者信息

Dong Yuru, Liu Yu, Hu Yanjie, Ma Kun, Jiang Hao, Li Chunzhong

机构信息

Key Laboratory for Ultrafine Materials of Ministry of Education, Shanghai Engineering Research Center of Hierarchical Nanomaterials, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.

School of Chemical Engineering and Technology, Sun Yat-sen University, Guangzhou 510275, China.

出版信息

Sci Bull (Beijing). 2020 Sep 15;65(17):1470-1478. doi: 10.1016/j.scib.2020.05.007. Epub 2020 May 15.

DOI:10.1016/j.scib.2020.05.007
PMID:36747404
Abstract

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 VS/MoS hybrids with tailorable 1T/2H phase based on their matchable formation energy, which are made of metallic and few-layered VS vertically grown on MoS 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 MoS surface. Furthermore, the VS catalytically expedites the Li-S bond fracture and meantime the enriched Mo enables the sulfur anchoring toward the oriented reaction with Li to form LiS, synergistically enhancing the reversibility of electrochemical redox. Consequently, the as-obtained VS/MoS hybrids deliver a very large specific capacity of 1273 mAh g at 0.1 A g with 61% retention even at 5 A g. It can also stabilize 100 cycles at 0.5 A g and 500 cycles at 1 A g. The findings provide in-depth insights into engineering heterojunctions towards the enhancement of reaction kinetics and reversibility for LIBs.

摘要

异质结构最近被认为是实现高能量锂离子电池(LIBs)的一种可行手段,因为形成的内建电场可以极大地加速电荷转移动力学。在此,我们基于可匹配的形成能构建了具有可定制1T/2H相的Mott-Schottky异质结构VS/MoS杂化物,其由垂直生长在MoS表面的金属性和少层VS组成。密度泛函理论(DFT)计算表明,这种异质结驱动能带重排,反应动力学得到促进,与MoS表面相比,Li吸附能提高了两倍多。此外,VS催化加速Li-S键断裂,同时富集的Mo使硫锚定,有利于与Li发生定向反应形成LiS,协同增强了电化学氧化还原的可逆性。因此,所制备的VS/MoS杂化物在0.1 A g下具有1273 mAh g的非常大的比容量,即使在5 A g下仍有61%的容量保持率。它还能在0.5 A g下稳定循环100次,在1 A g下稳定循环500次。这些发现为通过工程设计异质结来增强LIBs的反应动力学和可逆性提供了深入的见解。

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