Electrocatalytic reduction of CO2 using the dinuclear rhenium(I) complex [ReCl(CO)3(μ-tptzH)Re(CO)3]. (24th November 2015)

• Record Type: Journal Article
• Authors: Rezaei, Behzad; Mokhtarianpour, Maryam; Ensafi, Ali Asghar; Hadadzadeh, Hassan; Shakeri, Jamaladin
• Is Part Of: Polyhedron. Volume 101(2015)
• Page Start: 160
• Page End: 164
• Publication Date: 2015-11-24
• Subjects: Carbon dioxide -- Electrocatalyst -- Electrochemical reduction -- Rhenium complex -- Carboxylated multiwall carbon nanotubes modified; Chemistry, Inorganic -- Periodicals; Chimie inorganique -- Périodiques; Organometaalverbindingen; Anorganische chemie; 546.05
• DOI: 10.1016/j.poly.2015.08.014
• Languages: English
• ISSNs: 0277-5387

Abstract

Graphical abstract: A dinuclear rhenium(I) complex was studied by voltammetric experiments for CO2 reduction. It was revealed that the complex displayed catalytic properties for CO2 reduction under both homogeneous and heterogeneous conditions. Abstract: The dinuclear rhenium(I) complex [ReCl(CO)3 ( μ -tptzH)Re(CO)3 ] (where tptz-H is 2, 4, 6-tri(pyridine-2-yl)-2H-1, 3, 5-triazine-1-ide) was used as an electrocatalyst for the homogeneous and heterogeneous reduction of CO2 . The electrochemical behavior of the complex in solution and at the surface of an electrode after its adsorption was studied for the reduction of CO2 on a carboxylated multiwall carbon nanotubes modified (CMWCNTs) pencil graphite electrode (PGE) using cyclic voltammetric methods. The reduction potential of CO2 in homogenous studies was −853 mV versus NHE in acetonitrile. The results show that methanol (MeOH) as a weak Brönsted acid enhances the rate of the catalytic process for the reduction of CO2 in acetonitrile. Under heterogonous conditions, the dinuclear complex was only casted on the CMWCNTs–PGE and investigated in an acidic solution of MeOH. In comparison with the homogeneous catalyst, the heterogeneous catalyst shows a higher cathodic current and a lower over potential (about 650 mV).