首页> 外文期刊>Applied Surface Science >Birnessite manganese oxide nanosheets assembled on Ni foam as high- performance pseudocapacitor electrodes: Electrochemical oxidation driven porous honeycomb architecture formation
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Birnessite manganese oxide nanosheets assembled on Ni foam as high- performance pseudocapacitor electrodes: Electrochemical oxidation driven porous honeycomb architecture formation

机译:作为高性能伪电容器电极,在泡沫镍上组装的水钠锰矿锰氧化物纳米片:电化学氧化驱动的多孔蜂窝结构的形成

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摘要

It has not been considered in the reported literatures that the current or the cyclic number of galvanostatic charge-discharge process controls the morphology growth of manganese oxide materials. Here, standing birnessite nanosheets assembled porous honeycomb architecture is in situ formed on Ni foam by electrochemical oxidation of hydro thermally synthesized Mn3O4 nanospheres electrodes via a electrochemical cycling technique. The birnessite morphology much depends on the conditions of the electrochemical cycling. By tuning the current and cycle number, Mn3O4 nanospheres are converted to birnessite with optimal morphology, while a high pseudocapacitive performance is achieved. The optimized birnessite electrodes exhibit a high level of specific capacitance (377 Fg(-1) at 1 Ag-1), a superior rate capability (227 F g(-1) at 30 Ag-1) and a good cycling stability (75% retention after 4000 cycles). This work provides useful strategies for developing high-performance manganese oxide electrodes.
机译:在已报道的文献中尚未考虑到恒电流充放电过程的当前或循环数控制氧化锰材料的形态生长。在此,通过水热合成的Mn3O4纳米球电极的电化学氧化,通过电化学循环技术,在Ni泡沫上原位形成了组装的水钠锰矿纳米片组装的多孔蜂窝结构。水钠锰矿的形态很大程度上取决于电化学循环的条件。通过调节电流和循环次数,Mn3O4纳米球被转化为具有最佳形态的水钠锰矿,同时获得了较高的假电容性能。优化的水钠锰矿电极显示出高水平的比电容(在1 Ag-1时为377 Fg(-1)),出色的倍率能力(在30 Ag-1时为227 F g(-1))和良好的循环稳定性(75 4000次循环后保留率%)。这项工作为开发高性能氧化锰电极提供了有用的策略。

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