Fabrication of a polyaniline/MoS2 nanocomposite using self-stabilized dispersion polymerization for supercapacitors with high energy density

被引:71
|
作者
Kim, Minkyu [1 ]
Kim, Yun Ki [1 ]
Kim, Jihoo [1 ]
Cho, Sunghun [1 ,2 ,3 ]
Lee, Gyeongseop [1 ]
Jang, Jyongsik [1 ]
机构
[1] Seoul Natl Univ, Coll Engn, Sch Chem & Biol Engn, 599 Gwanangno, Seoul 151742, South Korea
[2] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Calif Nanosyst Inst, Los Angeles, CA 90095 USA
来源
RSC ADVANCES | 2016年 / 6卷 / 33期
关键词
GRAPHENE OXIDE; PERFORMANCE; CONDUCTIVITY; ELECTRODES; NANOFIBER; FILM;
D O I
10.1039/c6ra00797j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this report, a polyaniline/MoS2 nanocomposite has been firstly produced using a self-stabilized dispersion polymerization method. The synthesized polyaniline/MoS2 nanocomposite exhibited a remarkably high electrical conductivity of ca. 28.6 S cm(-1), which is higher than other previously reported MoS2-based composites. Additionally, the PANI/MoS2 nanocomposite exhibited substantially improved capacitance (ca. 400 F g(-1)) compared to pristine MoS2 nanosheets (ca. 3 F g(-1)) and PANI (ca. 232 F g(-1)) and enhanced cycling stability (retention rate of 84%) in comparison with pure PANI (retention rate of 62%). Furthermore, the PANI/MoS2 nanocomposite demonstrated a higher energy density (4.7 W h kg(-1) at 1000 W kg(-1)) than conventional electrochemical capacitors and other previously reported carbon and carbon/conducting polymer based electrochemical capacitors owing to its high utilizing of pseudocapacitance attributed to high electrical conductivity. What is more, the synthesized PANI/MoS2 nanocomposite demonstrated good rate capability and a good power characteristic as the supercapacitor electrode by keeping its high energy density (3.8 W h kg(-1)) at a high power density (2000 W kg(-1)) due to the existence of sufficient empty space between interconnected PANI nanofibers and high electrical conductivity of the PANI/MoS2 nanocomposite.
引用
收藏
页码:27460 / 27465
页数:6
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