碳纳米纤维
多硫化物
硫黄
锂(药物)
纳米颗粒
材料科学
纳米纤维
阴极
纳米技术
化学工程
碳纤维
储能
锂硫电池
复合数
化学
电极
复合材料
碳纳米管
电化学
冶金
电解质
物理化学
内分泌学
工程类
功率(物理)
物理
量子力学
医学
作者
Zheng Li,Congyu Qi,Qiang Chang,Jun Jin,Yan Lü,Zhaoyin Wen
标识
DOI:10.1016/j.compositesb.2023.110679
摘要
Lithium–sulfur (Li–S) batteries hold great promise for substituting current energy-storage technologies owing to their exceptional advantage in energy density. The main challenge in developing practical Li–S batteries is the lack of efficient sulfur host which can simultaneously suppress the shuttle effect and improve the redox kinetics. Polar host materials manifest chemisorptive properties for localizing the mobile polysulfide intermediates, being promising in inhibiting the shuttle effect; however, their poor intrinsic conductivity hinders their role in enhancing the redox kinetics of subsequent conversion reactions. In this regard, a conductive polar host material is highly desirable for efficient and long-life Li–S batteries. Herein, we design and develop a free-standing sulfur host consisted of carbon nanofibers decorated with titanium carbides nanoparticles (TiC/CNFs) for high performance Li–S batteries. Benefiting from the intrinsic chemical polarity and high electric conductivity of TiC, the chemisorption and conversion kinetics of lithium polysulfides are simultaneously promoted, leading to the greatly enhanced battery performance. For example, the S@TiC/CNFs composite cathode retains a high capacity of 672 mA h g−1 after 1000 cycles and an excellent rate performance of 938 mA h g−1 at 5 C. Impressively, even at a super high sulfur loading of 7 mg cm−2, the TiC/CNFs can retain a capacity of 5 mA h (630 mA h g−1) after 100 cycles, highlighting the advantages of the polar conductive sulfur host design for efficient conversion of lithium polysulfides.
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