Adsorption and redox chemistry of cis-RuLL'(SCN)(2) with L=4,4'-dicarboxylic acid-2,2'-bipyridine and L'=4,4'-dinonyl-2,2'-bipyridine (Z907) at FTO and TiO2 electrode surfaces
Reference:
Fattori, A., Peter, L. M., McCall, K. L., Robertson, N. and Marken, F., 2010. Adsorption and redox chemistry of cis-RuLL'(SCN)(2) with L=4,4'-dicarboxylic acid-2,2'-bipyridine and L'=4,4'-dinonyl-2,2'-bipyridine (Z907) at FTO and TiO2 electrode surfaces. Journal of Solid State Electrochemistry, 14 (10), pp. 1929-1936.
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http://dx.doi.org/10.1007/s10008-010-1034-8
Abstract
The electrochemical and spectroelectrochemical properties of the sensitizer dye Z907 (cis-RuLL'(SCN)(2) with L=4,4'-dicarboxylic acid-2,2'-bipyridine and L'=4,4'-dinonyl-2,2'-bipyridine) adsorbed on fluorine-doped tin oxide (FTO) and TiO2 surfaces have been investigated. Langmuirian binding constants for FTO and TiO2 are estimated to be 3 x 10(6) M-1 and 4 x 10(4) M-1, respectively. The Ru(III/II) redox process is monitored by voltammetry and by spectroelectrochemistry. For Z907 adsorbed onto FTO, a slow EC-type electrochemical reaction is observed with a chemical rate constant of ca. k = 10(-2) s(-1) leading to Z907 dye degradation of a fraction of the FTO-adsorbed dye. The Z907 adsorption conditions affect the degradation process. No significant degradation was observed for TiO2-adsorbed dye. Degradation of the Z907 dye affects the electron hopping conduction at the FTO-TiO2 interface.
Details
| Item Type | Articles |
| Creators | Fattori, A., Peter, L. M., McCall, K. L., Robertson, N. and Marken, F. |
| DOI | 10.1007/s10008-010-1034-8 |
| Uncontrolled Keywords | semiconductor, tio2, dye, voltammetry, solar cell, fto, mechanism, sensitizer, conduction |
| Departments | Faculty of Science > Chemistry |
| Refereed | Yes |
| Status | Published |
| ID Code | 20237 |
| Additional Information | Symposium on Nanostructured Materials for Electrochemical Energy Systems - Lithium Batteries, Supercapacitors and Fuel Cells held at ICMAT 2009. 28 June - 3 July 2009. Singapore. |
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