化学
循环伏安法
离子
铵
无机化学
超级电容器
水溶液
可控性
电化学
物理化学
电极
有机化学
应用数学
数学
作者
Ting Xiao,Can Tang,Hongxiang Lin,Xiuru Li,Yuting Mei,Can Xu,Lin Gao,Lihua Jiang,Peng Xiang,Shibing Ni,Yequan Xiao,Xinyu Tan
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-09-05
卷期号:63 (38): 17714-17726
被引量:5
标识
DOI:10.1021/acs.inorgchem.4c02554
摘要
Ion preintercalation is an effective method for fine-tuning the electrochemical characteristics of electrode materials, thereby enhancing the performance of aqueous ammonium-ion hybrid supercapacitors (A-HSCs). However, much of the current research on ion preintercalation lacks controllability, and the underlying mechanisms remain unclear. In this study, we employ a two-step electrochemical activation approach, involving galvanostatic charge-discharge and cyclic voltammetry, to modulate the preintercalation of NH4+ in MnO2. An in-depth analysis of the electrochemical activation mechanism is presented. This two-step electrochemical activation approach endows the final MnO2/AC electrode with a high capacitance of 917.4 F g-1, approximately 2.4 times higher than that of original MnO2. Furthermore, the MnO2/AC electrode retains approximately 93.4% of its capacitance after 10 000 cycles at a current density of 25 mA cm-2. Additionally, aqueous A-HSC, comprising MnO2/AC and P-MoO3, achieves a maximum energy density of 87.6 Wh kg-1. This study offers novel insights into the controllable ion preintercalation approach via electrochemical activation.
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