TY - JOUR
T1 - Electrolyte and temperature effects on the electron transfer kinetics of Fe(CN)6-3/-4 at boron-doped diamond thin film electrodes
AU - Kim, Doo Young
AU - Wang, Jian
AU - Yang, Juchan
AU - Kim, Hyoun Woo
AU - Swain, Greg M.
N1 - Copyright:
Copyright 2011 Elsevier B.V., All rights reserved.
PY - 2011/5/26
Y1 - 2011/5/26
N2 - 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 adventitious nondiamond carbon impurity by a twostep chemical-oxidation, and subsequently hydrogenated in hydrogen microwave plasma. The apparent heterogeneous electron-transfer rate constant, k° app, depended on the electrolyte concentration and the electrolyte cation type, increasing in order of Li+ < Na+ < K+ < Cs+. However, the dependence of k°app on the electrolyte cation was less than the dependence observed for other electrodes, like glassy carbon and gold. For example, k°app at the 1.0Mconcentration was only a factor of 1.6 greater in KCl than in LiCl for diamond. This is less than the factor of 5-10 seen for other electrodes, like glassy carbon and gold. The transfer coefficient for the oxidation was largely independent of the temperature and the electrolyte 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 respectively for KCl, NaCl, and LiCl. The results suggest that the electric double layer structure at sp3 diamond may be different from that found at sp 2 glassy carbon.
AB - 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 adventitious nondiamond carbon impurity by a twostep chemical-oxidation, and subsequently hydrogenated in hydrogen microwave plasma. The apparent heterogeneous electron-transfer rate constant, k° app, depended on the electrolyte concentration and the electrolyte cation type, increasing in order of Li+ < Na+ < K+ < Cs+. However, the dependence of k°app on the electrolyte cation was less than the dependence observed for other electrodes, like glassy carbon and gold. For example, k°app at the 1.0Mconcentration was only a factor of 1.6 greater in KCl than in LiCl for diamond. This is less than the factor of 5-10 seen for other electrodes, like glassy carbon and gold. The transfer coefficient for the oxidation was largely independent of the temperature and the electrolyte 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 respectively for KCl, NaCl, and LiCl. The results suggest that the electric double layer structure at sp3 diamond may be different from that found at sp 2 glassy carbon.
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U2 - 10.1021/jp1117954
DO - 10.1021/jp1117954
M3 - Article
AN - SCOPUS:79959955492
SN - 1932-7447
VL - 115
SP - 10026
EP - 10032
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 20
ER -