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不溶性多硫化物Li2S(x)(x = 1, 2)在Li2S表面的吸附。

Adsorption of insoluble polysulfides Li2S(x) (x = 1, 2) on Li2S surfaces.

作者信息

Liu Zhixiao, Hubble Dion, Balbuena Perla B, Mukherjee Partha P

机构信息

Department of Mechanical Engineering, Texas A&M University, College Station, TX 77843, USA.

出版信息

Phys Chem Chem Phys. 2015 Apr 14;17(14):9032-9. doi: 10.1039/c4cp06118g. Epub 2015 Mar 10.

Abstract

In lithium-sulfur batteries, the growth of insulating discharge product Li2S film affects the cathode microstructure and the related electron as well as lithium ion transport properties. In this study, chemical reactions of insoluble lithium polysulfides Li2Sx (x = 1, 2) on crystal Li2S substrate are investigated by a first-principles approach. First-principles atomistic thermodynamics predicts that the stoichiometric (111) and (110) surfaces are stable around the operating cell voltage. Li2Sx adsorption is an exothermic reaction with the (110) surface being more active to react with the polysulfides than the stoichiometric (111) surface. There is no obvious charge transfer between the adsorbed molecule and the crystal Li2S substrate. Analysis of the charge density difference suggests that the adsorbate interacts with the substrate via a strong covalent bond. The growth mechanism of thermodynamically stable surfaces is investigated in the present study. It is found that direct Li2S deposition is energetically favored over Li2S2 deposition and reduction process.

摘要

在锂硫电池中,绝缘放电产物Li2S膜的生长会影响阴极微观结构以及相关的电子和锂离子传输特性。在本研究中,通过第一性原理方法研究了不溶性多硫化锂Li2Sx(x = 1, 2)在晶体Li2S衬底上的化学反应。第一性原理原子热力学预测,化学计量比的(111)和(110)表面在工作电池电压附近是稳定的。Li2Sx吸附是一个放热反应,(110)表面比化学计量比的(111)表面更易于与多硫化物发生反应。吸附分子与晶体Li2S衬底之间没有明显的电荷转移。电荷密度差分析表明,吸附质通过强共价键与衬底相互作用。本研究考察了热力学稳定表面的生长机制。研究发现,直接Li2S沉积在能量上比Li2S2沉积和还原过程更有利。

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