材料科学
阳极
碳纤维
锂(药物)
煅烧
化学工程
纳米颗粒
石墨烯
沸石咪唑盐骨架
法拉第效率
复合数
电池(电)
储能
纳米技术
电极
金属有机骨架
复合材料
吸附
有机化学
催化作用
化学
物理化学
功率(物理)
内分泌学
工程类
物理
医学
量子力学
作者
Yulong Zhu,Yixian Wang,Cai Gao,Weinan Zhao,Xiaobo Wang,Mingbo Wu
标识
DOI:10.1016/s1872-5805(20)60494-2
摘要
Ultrafine transition metal oxides have great potential for efficient lithium storage but some key problems, such as a strong tendency to aggregate and poor electrical conductivity, need to be solved for their possible application. Here, hybrid nanoparticles of CoMoO4 and N-doped carbon were formed in a petroleum asphalt-based porous carbon prepared by a template method. A Co-based zeolitic imidazolate framework (ZIF-67) was then synthesized in-situ in its pores from Co(NO3)2·6H2O and 2-methylimidazole. The porous carbon was impregnated with Na2MoO4·2H2O and polyvinyl pyrrolidone, followed by solvothermal treatment at 180 oC for 24 h and finally calcination to convert the loaded components into hybrid nanoparticles of CoMoO4 and N-doped carbon. Results indicate that the N-doped carbon boosts the electron transport ability of CoMoO4 and efficiently prevents its aggregation. At an optimal CoMoO4 loading the composite was used as an anode material in a lithium ion battery and delivered a reversible specific capacity of 818 mAh g-1 at 1 A g-1, an initial coulombic efficiency of around 70%, and outstanding cycle and structural stability during cycling. The strategy reported here may open up a new avenue for the rational design and construction of well-designed electrode materials for energy storage.
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