电解质
电化学
电池(电)
化学工程
阴极
材料科学
锂(药物)
储能
锂硫电池
硫黄
准固态
离子电导率
化学
无机化学
电极
物理化学
冶金
内分泌学
功率(物理)
工程类
物理
医学
量子力学
色素敏化染料
作者
Canghai Long,Libo Li,Mo Zhai,Yuhang Shan
标识
DOI:10.1016/j.jpcs.2019.06.017
摘要
Abstract With a higher theoretical energy density relative to Li ion batteries (LIBs) and abundance of elemental sulfur, the lithium sulfur (L-S) batteries were regarded as the promising next-generation high energy density storage devices for the protable electronics and electric vehicles. However, there were some main challenges stemming from the polysulphide dissolution and the high flammability of the sulfur which limited the further application of the lithium sulfur Li–S batteries. Here, we reported a facile method to prepare the quasi solid-state Li–S batteries (LSBs) with sulfur nanoparticles electrode and PVDF-based solid polymer electrolyte (SPE), which had less flammability, electrochemical stability and ionic conductivity. The prepared PVDF-based solid polymer electrolyte possessed the conductivity ∼10−4 S cm−1 at 25 °C and the lithium ions transference number of 0.49. GITT demonstrated the Li+ transport diffusion mechanism in the active S@nano-TiO2 cathode of the quasi solid-state lithium–sulfur battery. It was important to get the smooth diffusion path for the lower resistance in the charging process. Because of the high content and the sulfur uniform distribution on the nanoscale titanium dioxide (TiO2), the S@nano-TiO2 cathode exhibited its performance. The first cycle discahrge specific capacity was 1160 mAh g−1 at 0.15C at room temperature.
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