期刊文献+

电化学氧化工艺对NiO/Ni(OH)2电极材料电容性能的影响 被引量:1

Effect of electrochemical oxidation process on capacitance properties of NiO/Ni(OH)2 electrode materials
下载PDF
导出
摘要 通过化学镀再电化学氧化的方法在铜片表面制备出带有微坑的均一NiO/Ni(OH)2电极材料,采用扫描电镜、X射线衍射、X射线光电子能谱和电化学技术对所制备的NiO/Ni(OH)2电极材料进行表征和电化学性能测试。结果表明,所制备的电极材料由Ni、NiO和Ni(OH)2组成,电化学氧化电解液中添加2种助氧化剂过硫酸钾和亚硝酸钠均能提高NiO/Ni(OH)2电极材料的比电容值50%~69%;在1 A/g的充放电电流密度下,2种助氧化剂存在下阳极氧化所制得的NiO/Ni(OH)2电极材料经历10000次充放电循环后分别给出了1410 F/g和1380 F/g的比电容,显示出良好的可逆性及电化学稳定性。化学镀表面的非晶组织和添加助氧化剂进行电化学原位氧化使得表面氧化物含量增大及致密性提高是其显示优异赝电容性能的主要原因。 Homogeneous NiO/Ni(OH)2 electrode materials with micropits were prepared on the surface of copper sheet by electroless-electrochemical anodic oxidation.SEM,XRD and XPS test results show that the prepared electrode materials are composed of Ni,NiO and Ni(OH)2,and the addition of two assistant oxidants(K2S2O8 and NaNO2)in the electrochemical anodic oxidation electrolyte can improve the surface NiO/Ni(OH)2 content of the electrode materials.Cyclic voltammetry measurements show that the specific capacitance of NiO/Ni(OH)2 electrode materials are increased by 50%~69%with the addition of two kinds of assistant oxidants.At the charge/discharge current density of 1 A/g,the specific capacitance of 1410 F/g and 1380 F/g are obtained by anodic oxidation of the NiO/Ni(OH)2 electrode material in the presence of two kinds of assistant oxidants after 10000 charge/discharge cycles,showing good reversibility and electrochemical stability.The Ragone curves reveals that the prepared NiO/Ni(OH)2 samples have higher power density and lower energy density.The electroless Ni plating is amorphous structure,and the content of surface oxide is increased by in-situ electrochemical anodic oxidation with the addition of two kinds of assistant oxidants.These factors are responsible for the superior pseudocapacitive performance of NiO/Ni(OH)2 electrode materials.
作者 张轲 高晨 周岩 曹中秋 ZHANG Ke;GAO Chen;ZHOU Yan;CAO Zhongqiu(College of Chemistry and Chemical Engineering,Shenyang Normal University,Shenyang 110034,China)
出处 《沈阳师范大学学报(自然科学版)》 CAS 2020年第5期400-406,共7页 Journal of Shenyang Normal University:Natural Science Edition
基金 辽宁省科技厅重点研发计划项目(2018304025) 辽宁省教育厅科学研究经费项目(LJC201911)。
关键词 电化学电容器 NiO/Ni(OH)2电极材料 比电容 阳极氧化 助氧化剂 electrochemical capacitor NiO/Ni(OH)2 electrode materials specific capacitance electrochemical anodic oxidation assistant oxidant
  • 相关文献

参考文献3

二级参考文献62

  • 1Sherif S A, Barbir F, Veziroglu T N. Wind energy and the hydrogen economy-review of the technology[J]. Solar Ener- gy, 2005,78 : 647.
  • 2Satyapal S, Petrovic J, Read C, et al. The U. S. depart- ment of energy's national hydrogen storage project: Pro- gress towards meeting hydrogen-powered vehicle require- ments[J]. Catal Today,2007,120(3-4) :246.
  • 3Sakintuna B, Lamari-Darkrim F, Hirscher M. Metal hy- dride materials for solid hydrogen storage: A review[J]. Int J Hydrogen Energy, 2007,32(9) : 1121.
  • 4Ross D K. Hydrogen storage: The major technological bar- rier to the development of hydrogen fuel cell cars[J]. Va- cuum, 2006,10(80) : 1084.
  • 5Sakata K, Mizutani E, Fukuda K. A review of topics in hy- drogen-related innovative materials in Japan [J]. J Power Sources, 2006,159 : 100.
  • 6第十届全国氢能学术会议暨第二届两岸三地氢能研讨会论文摘要集前言.天津:南开大学,2009.
  • 7Sigfusson T I. Hydrogen energy -abundant, efficient, clean a debate over the energy-system-of-change[J]. Int J Hydro- gen Energy, 2009, 34 (10): 4452.
  • 8O'Brien C M, McKellar J E, et al. High-temperature elec- trolysis for large-scale hydrogen and syngas production from nuclear energy-summary of system simulation and economic analyses[J]. Int J Hydrogen Energy, 2010,35 (10) :4808.
  • 9Kelly D B, Gibson N A, Ouwerkerk T L. A solar-powered, high-efficiency hydrogen fueling system using high-pressure electrolysis of water. Design and initial results [J]. Int J Hydrogen Energy, 2008,33 (11) : 2747.
  • 10Balat E, Kirtay H. Hydrogen from biomass Present sce- na-rio and future prospects[J]. Int J Hydrogen Energy, 2010,35(14) :7416.

共引文献45

同被引文献2

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部