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Sulfur-deficient MoS_(2-x) promoted lithium polysulfides conversion in lithium- sulfur battery: A first-principles study

机译:硫不足的MoS_(2-x)促进锂硫电池中多硫化锂的转化:一项第一性原理研究

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摘要

The lithium-sulfur batteries are becoming the promising next generation large-scale electrical energy storage, due to the high specific energy density and theoretical capacity. During the charge/discharge cycle, the shuttle effect reduces the Coulombic efficiency and cycle performance, greatly limiting the practical application of lithium-sulfur batteries. Two-dimensional materials metal sulfides are increasingly used in lithium-sulfur battery cathode materials due to their low lithiation voltage, good conductivity, strong adsorption and catalytic effects of lithium polysulfide. Recently, sulfur-deficient MoS2-x was creatively introduced into the cathode material, leading to better electrochemical performance than the perfect MoS2-x. The modification factor of "sulfur deficiencies" for metal sulfides is an innovative approach to further suppress the shuttle effect and improve the lithium-sulfur batteries performance. Understanding the specific working principle of sulfur-deficient MoS2-x would help to expand the application of defect metal sulfides. From experiment, the sulfur deficiencies are involved in the polysulfide conversion and enhance the conversion kinetics. However, the intuitive picture of how to enhance the conversion kinetics and the specific origins for the promotion effect are still unclear. A systematic theoretical study has been carried out on the molybdenum disulfide involved discharge process from S-8 to Li2S. According to the calculation results, both the discharge process on MoS2 (001) and MoS2-x, (001) surface undergo three consecutive "lithiation-cleavage" mechanism, with the last cleavage step Li4S2@MoS2 - Li2S@MoS2 as the rate-determining step. For MoS2-x (001), the product Li2S@MoS2-x is thermodynamically more stable, and the energy demands for the three cleavage steps are less than that of MoS2 (001) surface, which provide more thermodynamics and kinetic driving force for polysulfides conversion. Originally, the sulfur deficiency results in larger charge densities on MoS2-x (001) surface, enhance the interaction with the product and monomer molecules after cleavage, finally promotes the corresponding thermodynamic and kinetic processes.
机译:由于高的比能量密度和理论容量,锂硫电池正成为有前途的下一代大规模电能存储。在充电/放电循环期间,穿梭效应降低了库仑效率和循环性能,极大地限制了锂硫电池的实际应用。二维材料金属硫化物因其低锂化电压,良好的电导率,强的吸附力和多硫化锂的催化作用而越来越多地用于锂硫电池正极材料。最近,缺硫的MoS2-x被创造性地引入到阴极材料中,与理想的MoS2-x相比,具有更好的电化学性能。金属硫化物的“硫缺乏”修饰因子是一种创新的方法,可以进一步抑制穿梭效应并改善锂硫电池的性能。了解缺硫的MoS2-x的具体工作原理将有助于扩大有缺陷的金属硫化物的应用范围。从实验来看,硫缺乏与多硫化物的转化有关,并提高了转化动力学。但是,如何增强转化动力学的直观图景以及促进效果的具体来源仍然不清楚。对二硫化钼从S-8到Li2S的放电过程进行了系统的理论研究。根据计算结果,在MoS2(001)和MoS2-x,(001)表面上的放电过程都经历了三个连续的“锂化裂解”机理,最后的裂解步骤为Li4S2 @ MoS2-> Li2S @ MoS2速率确定步骤。对于MoS2-x(001),乘积Li2S @ MoS2-x在热力学上更稳定,三个解理步骤的能量需求比MoS2(001)表面的要少,这为多硫化物提供了更多的热力学和动力学驱动力转换。最初,硫缺乏会导致MoS2-x(001)表面的电荷密度更大,并在裂解后增强与产物和单体分子的相互作用,最终促进相应的热力学和动力学过程。

著录项

  • 来源
    《Applied Surface Science》 |2019年第1期|452-463|共12页
  • 作者单位

    Hefei Univ Technol, Inst Ind & Equipment Technol, Hefei 230009, Anhui, Peoples R China|Hefei Univ Technol, Sch Mat Sci & Engn, Hefei 230009, Anhui, Peoples R China|Key Lab Adv Funct Mat & Devices Anhui Prov, Hefei 230009, Anhui, Peoples R China;

    Hefei Univ Technol, Inst Ind & Equipment Technol, Hefei 230009, Anhui, Peoples R China;

    Hefei Univ Technol, Inst Ind & Equipment Technol, Hefei 230009, Anhui, Peoples R China;

    Hefei Univ Technol, Inst Ind & Equipment Technol, Hefei 230009, Anhui, Peoples R China|Hefei Univ Technol, Sch Mat Sci & Engn, Hefei 230009, Anhui, Peoples R China|Key Lab Adv Funct Mat & Devices Anhui Prov, Hefei 230009, Anhui, Peoples R China;

    Hefei Univ Technol, Sch Mat Sci & Engn, Hefei 230009, Anhui, Peoples R China|Key Lab Adv Funct Mat & Devices Anhui Prov, Hefei 230009, Anhui, Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    First-principles; Lithium-sulfur batteries; Metal sulfides; Sulfur deficiency; Shuttle effect;

    机译:第一性原理锂硫电池金属硫化物硫缺乏穿梭效应;

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