Covalent-organic frameworks: potential host materials for sulfur impregnation in lithium-sulfur batteries

被引:250
作者
Liao, Huaping [1 ]
Ding, Huimin [1 ]
Li, Bijian [1 ]
Ai, Xinping [1 ]
Wang, Cheng [1 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Minist Educ, Key Lab Biomed Polymers, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
LI-S BATTERIES; ENERGY-STORAGE; GAS-STORAGE; CATHODE; PERFORMANCE; COMPOSITE; CRYSTALLINE; POLYPYRROLE; NANOTUBES; GRAPHENE;
D O I
10.1039/c4ta00523f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Commercial development of lithium-sulfur (Li-S) batteries is severely hindered by their insufficient cyclability, which is due to the loss of soluble lithium polysulfide intermediates generated during the discharge processes. To overcome this problem, considerable efforts have been devoted to designing novel micro-or nano-structured host materials, aiming to trap soluble polysulfide within the network. Herein, we report a new approach to construct a sulfur electrode by impregnating sulfur into the nanopores of covalent-organic frameworks (COFs). Our results clearly demonstrate that by using a 2D COF as a host material, e. g. CTF-1 (CTF: covalent triazine-based framework), the thus-prepared cathode can show a remarkable positive effect on the capacity retention of Li-S batteries. Considering the unique features of COFs, such as highly flexible molecular design and a controllable pore size, this proof-of-principle study provides new opportunities for materials scientists for tailoring cathode materials in Li-S batteries.
引用
收藏
页码:8854 / 8858
页数:5
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