假电容
材料科学
锰
腐蚀
电压
离子
化学工程
超级电容器
纳米技术
电极
电解质
电化学
冶金
电气工程
化学
工程类
物理化学
有机化学
作者
Lijin Yan,Chong Zhu,Jiangyu Hao,Xinyue Liang,Youcun Bai,Qin Hu,Bochuan Tan,Baibai Liu,Xuefeng Zou,Bin Xiang
标识
DOI:10.1002/adfm.202102693
摘要
Abstract Electrochemical activation can be appropriate for constructing tunable/controllable defects within the interior of electrode materials. However, the activation mechanisms under different applied electric fields urgently need to be systematically explored. Herein, the electrochemically activated manganese dioxide (MnO 2 ) samples are prepared via applying a positive/negative electric field, and two different activation mechanisms are revealed through a series of characterization methods. During the activation process, it is fascinating to discover that MnO 2 mainly generates the O vacancies under positive voltage, whereas the electrolyte cations are embedded in the interlayer under negative voltage. The generated O vacancies and intercalated ions not only act as active sites or participate in the charge‐transport process, but also enhance the transmission capability of carriers. In contrast, the specific capacitances of optimized MnO 2 samples are 2.9 and 2.8 times than that of pure‐MnO 2 after electrochemical activation under positive and negative voltage, respectively. In addition, the activated samples exhibit excellent cycle stability and resistance to electrochemical corrosion, which can well‐maintain the 3D network structure composed of nanosheets after 5000 cycles. This strategy opens up a promising approach for exploring efficient and corrosion‐resistant electrode materials.
科研通智能强力驱动
Strongly Powered by AbleSci AI