标题:Biological cell template synthesis of nitrogen-doped porous hollow carbon spheres/MnO2 composites for high-performance asymmetric supercapacitors
作者:Du, Wei; Wang, Xiaoning; Zhan, Jie; Sun, Xueqin; Kang, Litao; Jiang, Fuyi; Zhang, Xiaoyu; Shao, Qian; Dong, Mengyao; Liu, Hu; Muru 更多
作者机构:[Du, Wei; Wang, Xiaoning; Sun, Xueqin; Kang, Litao; Jiang, Fuyi; Zhang, Xiaoyu] Yantai Univ, Sch Environm & Mat Engn, Yantai 264005, Shandong, Peoples 更多
通讯作者:Du, W
通讯作者地址:[Du, W]Yantai Univ, Sch Environm & Mat Engn, Yantai 264005, Shandong, Peoples R China.
来源:ELECTROCHIMICA ACTA
出版年:2019
卷:296
页码:907-915
DOI:10.1016/j.electacta.2018.11.074
关键词:Asymmetric supercapacitor; Biological cell template; Carbon material;; Manganese dioxide; Composite
摘要:Nitrogen-doped porous hollow carbon spheres were fabricated via hydrothermal pre-carbonization and pyrolysis carbonization using yeast cell templates. After that, the MnO2 nanowires were deposited by the in-situ hydrothermal reaction. By controlling the reaction concentration, various MnO2 nanostructures with different morphologies and electrochemical properties were obtained. The as-prepared sample exhibited an ultrahigh specific capacitance of 255 F g(-1) at a current density 1 A g(-1) in 1 M Na2SO4 electrolyte. The MnO2/HCS-30 material was used as the positive electrode, and the HCS was used as the negative electrode to assemble the asymmetric supercapacitor. The maximum energy density operating at the 2.0 V voltage window is 41.4 Wh kg(-1) at a power density of 500 W kg(-1) and still maintains 23.0 Wh kg(-1) at a power density of 7901 W kg(-1). Moreover, it displayed excellent cycle stability, retained approximately 93.9% of the capacitance after 5000 cycles. This work innovatively combines biomass and energy, provides an environmentally benign strategy and new insights for the preparation of electrode materials. (C) 2018 Elsevier Ltd. All rights reserved.
收录类别:SCOPUS;SCIE
WOS核心被引频次:14
Scopus被引频次:36
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85058998562&doi=10.1016%2fj.electacta.2018.11.074&partnerID=40&md5=2eb01c02b682ca7fa7f56869d93095db
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