共聚物
环氧乙烷
锂(药物)
电解质
材料科学
离子键合
氧化物
离子电导率
聚乙烯
高分子化学
离子液体
乙烯
化学工程
无机化学
离子
化学
聚合物
有机化学
催化作用
物理化学
电极
内分泌学
工程类
医学
冶金
复合材料
作者
Ernest Ahiavi,Jihen Talbi,Trang N. T. Phan,Priscillia Soudant,Fabrice Cousin,Renaud Bouchet,Didier Devaux
标识
DOI:10.1021/acs.chemmater.4c02594
摘要
Despite the high impact lithium–sulfur (Li–S) batteries can bring in terms of specific energy and battery lifetime, their full advantage has not yet been realized due to inherent issues associated with this technology. The intermediate polysulfide products produced in the positive electrode during discharge dissolve and diffuse in the electrolyte, leading to capacity fading and low Coulombic efficiency. A promising solution to this issue is the use of a solid polymer electrolyte that combines the advantages of an ion-conducting poly(ethylene oxide) (PEO) phase and a mechanically reinforced phase, such as polystyrene (PS), that can suppress the nonuniform electrodeposition of Li onto Li metal. In this work, the possibility of using PS–PEO–PS triblock copolymer as an electrolyte or binder in a Li–S battery was investigated by characterizing the thermodynamical, morphological, and ionic transport properties of lithium polysulfides species (Li2Sx, with x = 4 and 8). Thermodynamic results showed that the long-chain lithium polysulfide (Li2S8) is more soluble in the copolymers compared to the short-chain polysulfide (Li2S4). Meanwhile, the addition of Li2S4 and Li2S8 in the mesostructured block copolymer influences both the phase transition (lamellar or hexagonal) and the domain spacing in a fashion similar to the conventional LiTFSI salt. In terms of ionic transport, the mobility of the polysulfides (S42– and S82–) in the copolymers is reduced compared to the TFSI– anion, and the cationic transference number remains in the range of 0.5 compared to 0.15 for LiTFSI. To move toward the application, the introduction of Li2S4 into the block copolymer electrolyte is also used as an additive in the presence of LiTFSI salt, resulting in a very low interfacial resistance with the Li metal electrode. The results of these investigations would guide the design of solid polymer electrolytes for application in Li–S batteries.
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