An MXene-based aerogel with cobalt nanoparticles as an efficient sulfur host for room-temperature Na-S batteries

被引:48
|
作者
Yang, Qiuju [1 ,2 ]
Yang, Tingting [1 ,2 ]
Gao, Wei [1 ,2 ]
Qi, Yuruo [1 ,2 ]
Guo, Bingshu [1 ,2 ]
Zhong, Wei [1 ,2 ]
Jiang, Jian [1 ,2 ]
Xu, Maowen [1 ,2 ]
机构
[1] Southwest Univ, Key Lab Luminescent & Real Time Analyt Chem, Minist Educ, Sch Mat & Energy, Chongqing 400715, Peoples R China
[2] Southwest Univ, Sch Mat & Energy, Chongqing Key Lab Adv Mat & Clean Energies Techno, Chongqing 400715, Peoples R China
来源
INORGANIC CHEMISTRY FRONTIERS | 2020年 / 7卷 / 22期
基金
中国国家自然科学基金;
关键词
OXYGEN REDUCTION; GRAPHENE OXIDE; PERFORMANCE; ELECTROCATALYST; NITROGEN;
D O I
10.1039/d0qi00939c
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
High energy density room temperature sodium-sulfur (RT Na-S) batteries are receiving increasing attention as promising energy storage systems. However, the volume expansion of sulfur and the shuttle effect of polysulfides are the biggest obstacles to their development. In this study, a 3D porous aerogel (hybridized by Ti3C2Tx MXene and rGO) adhered with cobalt nanoparticles (MG-Co) is applied to RT Na-S batteries. The integration of highly conductive MXene and rGO into a crosslinked aerogel structure can alleviate the volume expansion of sulfur during (dis)charge. Moreover, the polar surface of Ti3C2Tx and the catalysis of cobalt particles can boost the strong chemical adsorption and conversion of soluble polysulfides. As a result, RT Na-S batteries assembled with MG-Co@S electrodes deliver a high specific capacity of 705 mA h g(-1) at 0.1 C and retain 428 mA h g(-1) at 5 C.
引用
收藏
页码:4396 / 4403
页数:8
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