材料科学
阳极
电池(电)
氧化钴
化学工程
氧化物
金属有机骨架
电极
热解
纳米线
金属
扫描电子显微镜
多孔性
纳米技术
复合材料
有机化学
冶金
化学
吸附
功率(物理)
物理
物理化学
量子力学
工程类
作者
Guangyu Zhao,Xin Sun,Li Zhang,Xuan Chen,Yachun Mao,Kening Sun
标识
DOI:10.1016/j.jpowsour.2018.04.001
摘要
Derivates of metal-organic frameworks are promising materials of self-supported Li ion battery anodes due to the good dispersion of active materials, conductive scaffold, and mass transport channels in them. However, the discontinuous growth and poor adherence of metal-organic framework films on substrates hamper their development in self-supported electrodes. In the present study, cobalt-based metal-organic frameworks are anchored on Ti nanowire arrays through an electrochemically assistant method, and then the metal-organic framework films are pyrolyzed to carbon-containing, porous, self-supported anodes of Li ion battery anodes. Scanning electron microscope images indicate that, a layer cobaltosic oxide polyhedrons inserted by the nanowires are obtained with the controllable in-situ synthesis. Thanks to the good dispersion and adherence of cobaltosic oxide polyhedrons on Ti substrates, the self-supported anodes exhibit remarkable rate capability and durability. They possess a capacity of 300 mAh g−1 at a rate current of 20 A g−1, and maintain 2000 charge/discharge cycles without obvious decay.
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