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Electrochemical, top-down nanostructured pseudocapacitive electrodes for enhanced specific capacitance and cycling efficiency

机译:电化学,自上而下的纳米为增强特定pseudocapacitive电极电容和循环效率

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Stabilization of the electroactive redox centers on ideally polarisable conductive electrodes is a critical challenge for realizing stable, high performing pseudocapacitive energy storage devices. Here, we report a top-down, electrochemical nanostructuring route based on voltammetric cycling to stabilize beta-MnO2 on a single walled carbon nanotube (CNT) scaffold from a MnMoO4 precursor. Such in situ nanostructuring results in controlled disintegration of an similar to 8 mu m almond like structure to form similar to 29 nm beta-MnO2 resulting in a 59 increase in the specific surface area and a 31 increase in the porosity of the pseudocapacitive electrode. Consequently, the specific capacitance and areal capacitance increase by similar to 75 and similar to 40, respectively. Such controlled, top-down nanostructuring is confirmed through binding energy changes to Mo 3d, C 1s, O 1s and Mn 2p respectively in XPS. Furthermore, Raman spectral mapping confirms the sequential nanostructuring initiating from the interface of CNTs with MnMoO4 and proceeding outwards. Thus, the process yields the final CNT/beta-MnO2 electrode that is electrically conductive, facilitates rapid charge transfer, and has increased capacitance and longer stability. Furthermore, the charge-transfer resistance and equivalent resistance are significantly lower compared to conventional activated carbon based electrodes.
机译:稳定的电活性氧化还原中心在理想情况下可极化的导电电极关键的挑战实现稳定、高执行pseudocapacitive能量储存设备。基于电化学纳米结构路线伏安循环稳定beta-MnO2上单壁碳纳米管(CNT)脚手架MnMoO4前体。导致解体的控制类似于8μm杏仁等结构形式类似于29海里beta-MnO2导致59%增加比表面积和31%pseudocapacitive的孔隙度增加电极。和面积电容增加类似于75%分别和类似于40%。控制,自上而下的纳米结构是证实通过结合能变化莫3 d、C 1 s, O1 s, XPS Mn 2 p分别。拉曼光谱证实了连续映射纳米结构界面的启动碳纳米管MnMoO4和向外进行。收益率最后问/ beta-MnO2过程导电电极,促进快速的电荷转移,并且增加电容和不再稳定。此外,电荷转移电阻等效电阻大大降低相比传统的活性炭电极。

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