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Electrolyte and Temperature Effects on the Electron Transfer Kinetics of Fe(CN)(6)(-3/-4) at Boron-Doped Diamond Thin Film Electrodes

Authors
Kim, Doo YoungWang, JianYang, JuchanKim, Hyoun WooSwain, Greg M.
Issue Date
May-2011
Publisher
AMER CHEMICAL SOC
Citation
JOURNAL OF PHYSICAL CHEMISTRY C, v.115, no.20, pp.10026 - 10032
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF PHYSICAL CHEMISTRY C
Volume
115
Number
20
Start Page
10026
End Page
10032
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/168443
DOI
10.1021/jp1117954
ISSN
1932-7447
Abstract
Cyclic and linear sweep voltammetry were used to investigate the effects of the electrolyte composition and temperature on the electrontransfer kinetics of Fe(CN)6 3/4 at well-characterized, boron-doped diamond thin-film electrodes. Highly conductive films were employed, which were first cleaned of any dventitious nondiamond carbon impurity by a twostep chemical-oxidation, and subsequently hydrogenated in hydrogen microwave plasma. The apparent heterogeneous electron-transfer rate constant, kapp, depended on the electrolyte concentration and the electrolyte cation type, increasing in order of Liþ ˂ aþ ˂ Kþ ˂ Csþ. However, the dependence of koapp on the electrolyte cation was less than the dependence observed for other electrodes, like glassy carbon and gold. For example, koapp at the 1.0 M concentration was only a factor of 1.6 greater in KCl than in LiCl for diamond. This is less than the factor of 510 seen for other electrodes, like glassy carbon and gold. The transfer coefficient for the oxidation was largely independent of the temperature and the lectrolyte composition with a value ranging from 0.52 to 0.55. The activation energy for electron transfer was found to be 14.3, 15.6, and 16.5 kJ/mol espectively for KCl, NaCl, and LiCl. The results suggest that the electric double layer structure at sp3 diamond may be different from that found at sp2 glassy carbon.
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