Three-dimensional crisscross porous manganese oxide/carbon composite networks for high performance supercapacitor electrodes

被引:16
|
作者
Li, Chunying [1 ,2 ]
Wang, Shuyuan [3 ]
Zhang, Guowei [2 ]
Du, Zhiling [2 ]
Wang, Guiling [2 ]
Yang, Jing [2 ]
Qin, Xiujuan [1 ,2 ]
Shao, Guangjie [1 ,2 ]
机构
[1] Yanshan Univ, State key Lab Metastable Mat Sci & Technol, Qinhuangdao 066004, Peoples R China
[2] Yanshan Univ, Coll Environm & Chem Engn, Hebei Key Lab Appl Chem, Qinhuangdao 066004, Peoples R China
[3] Hebei Normal Univ Sci & Technol, Sch Phys & Chem, Qinhuangdao 066004, Peoples R China
关键词
Manganese oxides/carbon composites; Porous network; Electronic conductivity; Electrochemical performance; FACILE SYNTHESIS; ELECTROCHEMICAL PROPERTIES; MNO2; NANORODS; ENERGY; OXIDE; FOAM; CAPABILITY; NANOFIBERS; DIOXIDE; SPHERES;
D O I
10.1016/j.electacta.2015.02.097
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Manganese oxide/carbon (MnOx/C) composites have been successfully prepared via a high temperature heat treatment method followed by the electrochemical oxidation. The presence of carbon not only enhances the electronic conductivity of manganese oxides (MnOx), but also provides more active sites for the transformation of manganese monoxide (MnO) during the galvanostatic charge-discharge process. Simultaneity, the interconnected porous structures of MnOx/C samples are believed to provide a continuous channel for the diffusion of electrolyte ion and shorten the diffusion length of ions involved in the charge/discharge cycling processes. Consequently, these advantages endow the MnOx/C electrode a better capacitance performance, a superior long-term cyclic stability and outstanding rate capability compared with pristine MnOx. More importantly, the composites show a fascinating capacitance of 807 F g(-1) at 1 A g(-1), which is much higher than the reported hydrous RuO2 electrodes. It can be easily speculated that MnOx/C composites will act as a promising electrode materials for designing high-performance supercapacitors. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:32 / 39
页数:8
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