TY - JOUR
T1 - Mass transport accompanied with electron transfer between the gold electrode modified with 11-ferrocenylundecanethiol monolayer and redox species in solution - an electrochemical quartz crystal microbalance study
AU - Sato, Yukari
AU - Mizutani, Fumio
AU - Shimazu, Katsuaki
AU - Ye, Shen
AU - Uosaki, Kohei
N1 - Funding Information:
This work was partially supported by a Grant-in-Aid for International Research Program (Joint Research 07044046) from the Ministry of Education, Science, Sports and Culture, Japan.
PY - 1999
Y1 - 1999
N2 - An electrochemical quartz crystal microbalance (EQCM) was employed to investigate mass transport during the redox reaction of the ferrocenylundecanethiolate (FcC11S(H)) monolayer modified gold electrode in solution containing other redox species. The FcC11S-monolayer on gold acts as a barrier for the electron transfer between a gold electrode and Fe(CN)64-/3- in solution and as a mediator for the reduction of Fe3+ in solution. In both cases, electrochemical current responses were complicated because the observed currents were due to the redox of both the ferrocenyl group immobilized on gold and others in electrolyte solutions. The frequency change, i.e. interfacial mass change on the gold electrode surface, was observed only during the redox of ferrocenyl groups. The complex current response was deconvoluted into the current components of the redox reaction of ferrocene and that of other redox species in solution by comparing cyclic voltammograms with the current calculated from frequency changes.
AB - An electrochemical quartz crystal microbalance (EQCM) was employed to investigate mass transport during the redox reaction of the ferrocenylundecanethiolate (FcC11S(H)) monolayer modified gold electrode in solution containing other redox species. The FcC11S-monolayer on gold acts as a barrier for the electron transfer between a gold electrode and Fe(CN)64-/3- in solution and as a mediator for the reduction of Fe3+ in solution. In both cases, electrochemical current responses were complicated because the observed currents were due to the redox of both the ferrocenyl group immobilized on gold and others in electrolyte solutions. The frequency change, i.e. interfacial mass change on the gold electrode surface, was observed only during the redox of ferrocenyl groups. The complex current response was deconvoluted into the current components of the redox reaction of ferrocene and that of other redox species in solution by comparing cyclic voltammograms with the current calculated from frequency changes.
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U2 - 10.1016/S0022-0728(99)00305-8
DO - 10.1016/S0022-0728(99)00305-8
M3 - Comment/debate
AN - SCOPUS:0033318664
SN - 1572-6657
VL - 474
SP - 94
EP - 99
JO - Journal of Electroanalytical Chemistry
JF - Journal of Electroanalytical Chemistry
IS - 1
ER -