氧化还原
电化学
化学
X射线光电子能谱
铜
电解质
超级电容器
无机化学
羧酸盐
电极
物理化学
化学工程
立体化学
有机化学
工程类
作者
Zhaoxia Song,Wei Liu,Xiaofei Wei,Quan Zhou,Hongda Liu,Zheng Zhang,Guichang Liu,Zhongfu Zhao
标识
DOI:10.1016/j.cclet.2019.07.022
摘要
The widely accepted theory concerning the electrochemical energy storage mechanism of copper hexacyanoferrate (CuHCF) for supercapacitors is that CuHCF stores charge by the reversible redox processes of Fe3+/Fe2+ couple and Cu cations are electrochemically inactive. In this work, CuHCF nanocubes (CuHCF-NC) were synthesized in the presence of potassium citrate and its electrochemical properties were tentatively studied in 1 mol/L Na2SO4 aqueous electrolyte. Good supercapacitive performance was exhibited. The combined analyses of cyclic voltammogram (CV) and X-ray photoelectron spectroscopy (XPS) disclosed that the CuHCF nanocubes underwent the redox reactions of Fe3+/Fe2+ and Cu2+/Cu+ couples to store charges. The Cu2+/Cu+ redox couple was activated due to the strong coordination interaction between the carboxylate groups of citrate ions and surface Cu cations.
科研通智能强力驱动
Strongly Powered by AbleSci AI