详细信息
A Synergistic Strategy with 3D Highly Conductive Carbon Matrix-Decorated with Low Loading of CdS Quantum Dots as a Sulfur Host for Advanced Li-S Batteries ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:A Synergistic Strategy with 3D Highly Conductive Carbon Matrix-Decorated with Low Loading of CdS Quantum Dots as a Sulfur Host for Advanced Li-S Batteries
作者:Li, Yangping[1];Xu, Jie[1];Xu, Da[1];He, Yun[1];Sun, Xinyi[1];Niu, Dongfang[1];Zhang, Xinsheng[1]
机构:[1]East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
年份:2021
卷号:8
期号:9
起止页码:1642
外文期刊名:CHEMELECTROCHEM
收录:;EI(收录号:20212510543754);WOS:【SCI-EXPANDED(收录号:WOS:000664219100013)】;
语种:英文
外文关键词:synergistic combination; high conductivity; porous structure; electrocatalysis; lithium-sulfur batteries
摘要:Lithium-sulfur batteries (LSBs) have become one of the most competitive candidates for next generation energy storage systems due to the high theoretical energy density, nevertheless, the severe shuttle effect, volume expansion, and poor electrical conductivity restrict their practical application. Herein, we report a synergistic combination of 3D carbon matrix (CdS@NG-CNT) composed of low-defect carbon nanotubes (CNTs) and nitrogen-doped graphene (NG) decorated with low loading of cadmium sulfide quantum dots as sulfur host and carbon black (CB) as separator layer to collectively solve these issues. Specifically, the developed host material possesses abundant macropores and mesopores and high electrical conductivity, which endow the carbon matrix multifaceted structural properties for polysulfides immobilization, electrons/Li+ transfer, and Li2S formation, as well as buffering the volume expansion during cycling. The CB-modified separator can help to enhance the interconversion of intercepted polysulfides. Benefiting from these aspects, the cell equipped with CdS@NG-CNT/S//CB-PP exhibits a superior rate capacity of 1493.6 mA h/g at 0.2 C (1(st)), and maintains a capacity of 479.7 mA h/g after 1050 cycles with an ultralow capacity decay rate of 0.051 % at 1.0 C. This work provides a useful strategy to solve issues of the current LSBs, which may practically be used in the high-energy density.
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