Tuning the redox properties of Co-N4 macrocyclic complexes for the catalytic electrooxidation of glucose

• Published in: Electrochimica acta Vol. 53; no. 14; pp. 4883 - 4888
• Main Authors: Villagra, Evelyn, Bedioui, Fethi, Nyokong, Tebello, Canales, J. Carlos, Sancy, Mamie, Páez, Maritza A., Costamagna, Juan, Zagal, José H.
• Format: Journal Article
• Language: English
• Published: Oxford Elsevier Ltd 30.05.2008; Elsevier
• Subjects: Chemistry; Cobalt phthalocyanines; Cobalt pyridinoporphyrazine; Electrocatalysis; Electrochemistry; Exact sciences and technology; General and physical chemistry; Glucose oxidation; Kinetics and mechanism of reactions; Modified electrodes; Volcano plots; Electrocatalysis; Modified electrodes; Cobalt phthalocyanines; Cobalt pyridinoporphyrazine; Volcano plots; Glucose oxidation; Cobalt Complexes; Nitro compound; Organic hydroxysulfide; Aldose; Basic solution; Transition metal Complexes; Glucose; Pyrrole derivatives; Macrocycle; Electrodes; Electrochemical properties; Metallophthalocyanine; Graphite; Oxidation; Metalloporphyrin; Electrochemical reaction; Modified material
• ISSN: 0013-4686; 1873-3859
• DOI: 10.1016/j.electacta.2008.02.006

Graphite electrodes modified with four different cobalt N4 macrocyclics, namely Co tetrapentapyridinophthalocyanine, (CoTPenPyrPc), Co tetrapyridinoporphyrazine (CoTPyPz), Co octa(hydroxyethylthio)phthalocyanine (CoOEHTPc) and Co tetranitrophthalocyanine (CoTNPc) exhibit catalytic activity for the oxidation of glucose in alkaline media. The purpose of this work is to establish correlations between the catalytic activity of these complexes and their redox potential. The activity of the different modified electrodes was tested by linear voltammetry under hydrodynamic conditions using the rotating disk technique. Tafel plots constructed from mass-transport corrected currents give slopes ranging from 0.080 to 0.160 V/decade for the different catalysts which suggests that a first one-electron step is rate controlling with the symmetry of the energy barrier depending on the nature of the ligand of the Co complex. A plot of log I versus the Co(II)/(I) formal potential gives a volcano curve that also includes catalysts studied previously. This illustrates the concept that the formal potential of the catalyst needs to be tuned to a certain value for achieving maximum activity. A theoretical interpretation of these results is given in terms of Langmuir isotherms for the adsorption of glucose on the Co sites of the surface-confined metal complexes.