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ISSN 1000-6818CN 11-1892/O6CODEN WHXUEU
Acta Phys Chim Sin >> 2012,Vol.28>> Issue(05)>> 1163-1168     doi: 10.3866/PKU.WHXB201202241         中文摘要
ELECTROCHEMISTRY AND NEW ENERGY
Direct Electrochemistry of Cytochrome c Adlayer on the ITO Electrode
ZHANG Zhe, QI Zhi-Mei, ZHANG Rong-Jun
State Key Laboratory of Transducer Technology, Institute of Electronics, Chinese Academy of Sciences, Beijing 100190, P. R. China
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The electrochemical redox reaction of a cytochrome c (Cyt c) adlayer on an indium tin oxide (ITO) electrode was directly monitored and the surface concentrations of Cyt c versus solution concentrations were obtained from cyclic voltammograms. The results indicate that the surface concentration increases from 0.35 × 10-12 to 1.53 × 10-12 mol·cm-2 when the solution concentration is increased from 2 to 10 μmol ·L-1. A quasi-linear relationship between the reciprocals of surface concentration and solution concentration was observed, indicating that Cyt c adsorption on the ITO electrode closely obeys the Langmuir isothermal adsorption model. The cyclic voltammograms of the Cyt c solutions with the ITO electrode reveal that both adsorbed and dissociated Cyt c molecules are involved in the electrode reaction and that the contribution of dissociated molecules is much larger than that of adsorbed ones. The electrode reaction is basically diffusion controlled and quasi-reversible. Based on the Nicholson method, the average standard heterogeneous rate constant was determined to be 1.65×10-3 cm· s-1. The electrochemical activity of the Cyt c adlayer was partially lost when it was kept at 25 °C for 1 h, and was completely lost at 80 °C. The denatured Cyt c adlayer on a gold electrode can effectively inhibit the electrode reaction of K3Fe(CN)6 solution.

Keywords: Cytochrome c adlayer   Direct electrochemistry   Langmuir isothermal adsorption   Surface concentration  
Received: 2011-12-02 Accepted: 2012-02-16 Publication Date (Web): 2012-02-24
Corresponding Authors: QI Zhi-Mei Email: zhimei-qi@mail.ie.ac.cn

Fund: The project was supported by the National Key Basic Research Program of China (973) (2009CB320300), National Natural Science Foundation of China (60978042, 61078039), and BaiRenJiHua Program of Chinese Academy of Sciences.

Cite this article: ZHANG Zhe, QI Zhi-Mei, ZHANG Rong-Jun. Direct Electrochemistry of Cytochrome c Adlayer on the ITO Electrode[J]. Acta Phys. -Chim. Sin., 2012,28 (05): 1163-1168.    doi: 10.3866/PKU.WHXB201202241
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