Affiliation:
1. College of Materials Science and Engineering Sichuan University Chengdu Sichuan 610065 P. R. China
Abstract
AbstractMXenes 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 Ti3C2Tx MXene in a mild AlCl3 aqueous electrolyte can operate at a wide potential range from 0 to −1.3 V versus Hg/Hg2SO4 and retain high pseudocapacitive activity. Thus, a high capacity of up to 85 mAh g−1 is achieved, surpassing its performance in H2SO4 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.
Funder
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities
Subject
General Materials Science,General Chemistry
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献