电解质
MXenes公司
材料科学
电化学窗口
电化学
超级电容器
插层(化学)
石英晶体微天平
水溶液
化学工程
电容
电极
无机化学
纳米技术
离子电导率
化学
吸附
工程类
物理化学
作者
Yongqiu Xian,Bin Wang,Zifeng Lin
出处
期刊:Small methods
[Wiley]
日期:2023-04-13
卷期号:7 (8): e2201526-e2201526
被引量:9
标识
DOI:10.1002/smtd.202201526
摘要
MXenes have been extensively explored as supercapacitor electrodes, especially in acidic aqueous electrolytes, where ultrahigh specific capacitance can be achieved; however, their narrow working potential window (≤ 1.0 V) limits the acquisition of high energy. Neutral and alkaline electrolytes can be used to extend the working potential window but MXenes in these electrolytes are less pseudocapacitive active, which leads to reduced charge storage. In this study, it is shown that Ti3 C2 Tx MXene in a mild AlCl3 aqueous electrolyte can operate at a wide potential range from 0 to -1.3 V versus Hg/Hg2 SO4 and retain high pseudocapacitive activity. Thus, a high capacity of up to 85 mAh g-1 is achieved, surpassing its performance in H2 SO4 electrolyte of 78 mAh g-1 . More interestingly, most of the capacity is released at a more negative potential range than that in acidic electrolytes, making it more suitable as a negative electrode material. In situ electrochemical quartz crystal microbalance results suggest that the high capacity originates from the pseudocapacitive intercalation/deintercalation of H+ instead of Al3+ , providing the possibility of coupling MXene anodes with proton redox active cathodes to achieve high-energy and high-power devices.
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