教授
博士生导师
硕士生导师
教师拼音名称:zhuxiaodong
电子邮箱:
职称:教授
毕业院校:哈尔滨工业大学
学术荣誉:2019 当选:省高端人才
邮箱:
2019-09-26 泰山学者青年专家
2009-01-06 “国防科技创新团队”核心成员
2007-05-15 黑龙江省优秀毕业生(博士)
2007-06-30 哈尔滨工业大学优秀毕业生
最后更新时间:..
关键字:ELECTROCATALYSIS; NANOSHEETS; CATALYSIS; ARRAYS; HOSTS
摘要:Lithium-sulfur (Li-S) batteries appear to be one of the most promising energy-storage devices owing to the unparalleled theoretical specific energy, relatively inexpensive price and abundant resources. Despite these attractive features, the practical performances of sulfur cathode still remain a lot of challenges, such as the electrical insulating nature of S and Li2S, huge volume change during cycling, notorious shuttle effect of lithium polysulfide intermediates (LiPSs), sluggish redox kinetics and construction of thick electrodes with high sulfur loading. Here, CoFe2O4 nanoparticles anchored on the carbon nanotube (CNT) paper is proposed as free-standing sulfur host to address the issues. The cross-linking CNT network can serve as conductive matrix and accommodate volume change upon cycling simultaneously. Meanwhile, the CoFe2O4 nano particles are capable of effectively anchoring LiPSs to suppress the shuttle effect and accelerating LiPSs conversion to boost redox kinetics. Moreover, the free-standing paper electrode without any binder is conducive to constructing stable cathode with high sulfur loading. In consequence, the well-designed S/ CoFe2O4/CNT paper cathodes deliver impressive electrochemical performance, demonstrating an initial discharge capacity of 755.3 mAh g(-1) and remaining a high reversible capacity of 642.6 mAh g(-1) after 400 cycles at 2 C with an inconspicuous decay of 0.04% per cycle. (C) 2022 Elsevier B.V. All rights reserved.
卷号:909
期号:
是否译文:否