Journal of Liaoning Petrochemical University
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Electrochemical Behaviors of Ferrocene Using Cyclic Voltammetry
Qiao Qingdong, Li Qi
Abstract2096)      PDF (1784KB)(1085)      
The ferrocene shows definite aromatic and redox properties, which can used as a switch model substance. In alcohol solution of lithium perchlorate, the redox reaction process of ferrocene is quasi-reversible, in which the electron transfer number determined is 1, and the diffusion coefficients of ferrocene ion (Fc+) and Fc are 2.24×10-3 cm2/s and 4.34×10-3 cm2/s, i.e. the diffusion velocity of Fc+ is faster than Fc. The standard rate constant tested is 2.79 cm/s.
2014, 34 (3): 5-7. DOI: 10.3696/j.issn.1672-6952.2014.03.002
Electrochemical Behaviors of Acetylferrocene at Disk  Electrode and Measurement of Diffusion Coefficient
ZHU Chongxiu, QIAO Qingdong, LI Qi, SONG Zhilin
Abstract614)      PDF (1831KB)(285)      
The electrochemical behaviors of acetylferrocene at a disk electrode in 0.2mol/L LiClO4 solution had been determined by using cyclic voltammetry. Two methods were used to determine the diffusion coefficient of acetylferrocene, in which the rotating disk electrode was motionless and rotational respectively. Electrochemistry experimental results show that the electrochemical process of acetylferrocene at the rotating disk electrode belongs to reversible redox reaction which was controlled by the diffusion. The peak-peak potential ΔEp and the number of transfer electron n were 56.5 mV and 1 respectively. The diffusion coefficient of AFc and AFc+ were 4.74×10-5 cm2/s and 4.47×10-5 cm2/s determined by the currentvoltage curve in static disk electrode. And the diffusion coefficient of AFc and AFc+ were 5.20×10-5 cm2/s and 5.07×10-5 cm2/s according to the relationship of the peak current and the scan rate in rotating disk electrode, which was little faster than that of in static disk electrode. Rate constants of reduction process and oxidation process were 7.17×10-3 cm2/s and 8.31×10-3 cm2/s, respectively.
2014, 34 (1): 12-15. DOI: 10.3696/j.issn.1672-6952.2014.01.004