The Library
Microelectrochemical measurements of electron transfer rates at the interface between two immiscible electrolyte solutions: Potential dependence of the ferro/ferricyanide-7,7,8,8-tetracyanoquinodimethane (TCNQ)/TCNQ(center dot-) system
Tools
Tools
Tools
UNSPECIFIED (2002) Microelectrochemical measurements of electron transfer rates at the interface between two immiscible electrolyte solutions: Potential dependence of the ferro/ferricyanide-7,7,8,8-tetracyanoquinodimethane (TCNQ)/TCNQ(center dot-) system. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 4 (15). pp. 3820-3827. doi:10.1039/b108882c ISSN 1463-9076.
Research output not available from this repository.
Request-a-Copy directly from author or use local Library Get it For Me service.
Official URL: http://dx.doi.org/10.1039/b108882c
Abstract
The reduction of 7,7,8,8-tetracyanoquinodimethane (TCNQ) in both 1,2-dichloroethane (DCE) and nitrobenzene (NB), by aqueous ferrocyanide, and the back reaction have been studied by scanning electrochemical microscopy (SECM) and microelectrochemical measurements at expanding droplets (MEMED). The main focus has been to elucidate the effect of galvanic potential at the interface between two immiscible electrolyte solutions (ITIES) on electron transfer (ET) rates, with different electrolyte concentrations in the organic phase. SECM studies show that the ET rate constants for both the forward and back reaction depend strongly on the interfacial potential drop, with an apparent ET coefficient close to 0.5. MEMED demonstrates that TCNQ is confined to DCE, but transfers from NB to water under certain experimental conditions, which could complicate kinetic analysis. The ET kinetics for the water/DCE system have been analysed further using Marcus theory. Close to zero driving force, the rate constants for the forward and back reaction are found to be similar and in good agreement with predictions from Marcus theory with a sharp liquid/liquid interface. The results suggest that Butler-Volmer kinetics describe ET at the ITIES when the driving force is low and the ionic strength in both the aqueous and organic phases is relatively high.
| Item Type: | Journal Article | ||||
|---|---|---|---|---|---|
| Subjects: | Q Science > QD Chemistry Q Science > QC Physics |
||||
| Journal or Publication Title: | PHYSICAL CHEMISTRY CHEMICAL PHYSICS | ||||
| Publisher: | ROYAL SOC CHEMISTRY | ||||
| ISSN: | 1463-9076 | ||||
| Official Date: | 2002 | ||||
| Dates: |
|
||||
| Volume: | 4 | ||||
| Number: | 15 | ||||
| Number of Pages: | 8 | ||||
| Page Range: | pp. 3820-3827 | ||||
| DOI: | 10.1039/b108882c | ||||
| Publication Status: | Published |
Data sourced from Thomson Reuters' Web of Knowledge
Request changes or add full text files to a record
Repository staff actions (login required)
 |
View Item |
