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TiO-TiO 异质结构/聚吡咯的合理设计作为先进锂硫电池的多功能硫主体

Rational Design of TiO-TiO Heterostructure/Polypyrrole as a Multifunctional Sulfur Host for Advanced Lithium-Sulfur Batteries.

机构信息

School of Materials Science and Engineering , Georgia Institute of Technology , Atlanta , Georgia 30332-0245 , United States.

出版信息

ACS Appl Mater Interfaces. 2019 Feb 6;11(5):5055-5063. doi: 10.1021/acsami.8b19501. Epub 2019 Jan 28.

DOI:10.1021/acsami.8b19501
PMID:30656928
Abstract

Despite outstanding theoretical energy density (2600 Wh kg) and low cost of lithium-sulfur (Li-S) batteries, their practical application is seriously hindered by inferior cycle performance and low Coulombic efficiency due to the "shuttle effect" of lithium polysulfides (LiPSs). Herein, we proposed a strategy that combines TiO-TiO heterostructure materials (H-TiO , x = 1, 2) and conductive polypyrrole (PPy) to form a multifunctional sulfur host. Initially, the TiO-TiO heterostructure can enhance the redox reaction kinetics of sulfur species and improve the conductivity of sulfur cathode together with the PPy coating layer. Moreover, the defect-abundant H-TiO matrices can trap LiPSs by the formation of Ti-S bond via the Lewis acid-base interaction. Furthermore, the PPy coating can physically hinder the diffusion of LiPSs, as well as chemically adsorb LiPSs by the polar-polar mechanism. Benefiting from the synergistic effect of H-TiO and PPy layer, the novel cathode delivered high specific capacities at different current rates (1130, 990, 932, 862, and 726 mAh g at 0.1, 0.2, 0.3, 0.5, and 1C, respectively) and an ultralow capacity decay of 0.0406% per cycle after 1000 cycles at 1C. This work can not only indicate effectiveness of employing H-TiO materials to realize the LiPSs immobilization but also shed light on the feasibility of combining different materials to achieve the multifunctional sulfur hosts for advanced Li-S batteries.

摘要

尽管锂硫(Li-S)电池具有出色的理论能量密度(2600 Wh kg)和低廉的成本,但由于多硫化锂(LiPSs)的“穿梭效应”,其循环性能较差,库仑效率较低,严重限制了其实际应用。在此,我们提出了一种策略,即将 TiO-TiO 异质结构材料(H-TiO,x = 1,2)和导电聚吡咯(PPy)结合起来,形成一种多功能硫主体。首先,TiO-TiO 异质结构可以通过增强硫物种的氧化还原反应动力学并与 PPy 涂层一起提高硫阴极的导电性。此外,富含缺陷的 H-TiO 基体可以通过路易斯酸碱相互作用形成 Ti-S 键来捕获 LiPSs。此外,PPy 涂层可以通过物理方式阻碍 LiPSs 的扩散,并通过极性-极性机制化学吸附 LiPSs。得益于 H-TiO 和 PPy 层的协同效应,新型阴极在不同电流速率下表现出高比容量(0.1、0.2、0.3、0.5 和 1C 时分别为 1130、990、932、862 和 726 mAh g),在 1C 下循环 1000 次后容量衰减率极低(0.0406%/循环)。这项工作不仅可以表明利用 H-TiO 材料实现 LiPSs 固定的有效性,还可以为结合不同材料实现先进 Li-S 电池的多功能硫主体提供思路。

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