Electrolytic ion diffusion properties and their effects on charge storage potentials of pseudocapacitive Co3O4 electrode film

被引:1
|
作者
Akintayo, Olamide A. [1 ,2 ]
Al-Senani, Ghadah M. [3 ]
Ajayeoba, Yetunde A. [1 ]
Al-Qahtani, Salhah D. [3 ]
Adewinbi, Saheed A. [1 ]
机构
[1] Osun State Univ, Dept Phys, Osogbo 210001, Osun State, Nigeria
[2] Yaba Coll Technol, Dept Phys Sci, Yaba 101212, Lagos State, Nigeria
[3] Princess Nourah Bint Abdulrahman Univ, Coll Sci, Dept Chem, POB 84428, Riyadh 11671, Saudi Arabia
关键词
Co(3)O(4)Electrode; Electrolyte ions; Specific capacitance; Electrochemical impedance spectroscopy; Diffusion coefficient; SUPERCAPACITOR ELECTRODE; COBALT; PERFORMANCE; NANOSTRUCTURES; HYBRID; NICKEL;
D O I
10.1007/s11581-024-05877-8
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this report, we have employed an electrodeposition approach under three-electrode configuration to fabricate Co3O4 electrode film and investigated the effect of electrolytic Na+ and K+ from KOH, NaOH, and Na2SO4 aqueous electrolytes, on its charge storage characteristics. The microstructural studies validated the formation of stable phases and cubic crystal structure. The film grew with slightly dense sphere-shaped nanostructure and large surface area and is composed of corresponding elements, as revealed from microstructural studies. The charge storage measurements on fabricated Co3O4 film electrode were carried out extensively under three-electrode mode. The electrode's performance was found to be dependent on ion diffusion nature of the electrolytes and hence displayed optimum specific capacitance/capacity of 240 Fg(-1)/46.6mAh g(-1) in Na2SO4 compared to in NaOH due to multiple redox peaks, with better ion diffusion in KOH due to smaller Na+ ions, constituting relatively low solution resistance with faster ion kinetic and transport. The study unveiled that the performance of Co3O4 electrode in aqueous electrolyte is dependent on the electrolyte's ionic strengths, mobility and diffusion, and pH.
引用
收藏
页码:587 / 600
页数:14
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