Article ID Journal Published Year Pages File Type
69056 Journal of Molecular Catalysis A: Chemical 2006 9 Pages PDF
Abstract

Porphyrins and different metalloporphyrins have been synthesised and heterogenised on robust inorganic solids such as silica gel, purely siliceous MCM-41, and delaminated zeolites ITQ-2 and ITQ-6. Two different strategies for preparation of these catalysts have been explored, mainly based on immobilisation of a functionalisated porphyrin (route A) or heterogenisation of an aromatic aldehyde and consecutive porphyrin formation (route B). Route A yields stable materials and allows introduction of a larger quantity of metalloporphyrin onto the support (contents ranged from 0.3 to 0.4 mmol g−1) whereas route B was unsuccessful and no evidence was found to support the porphyrin formation. A multitechnique approach is employed for characterisation of samples and their catalytic behaviour has been tested in the electroreduction of oxygen. A cyclic voltammetry investigation, at varying scan rate, was carried out in an attempt to elucidate the net reaction for the oxygen reduction. The synthesised metalloporphyrins are active for electrocatalytic reduction of oxygen by a two-electron mechanism, producing hydrogen peroxide. The comparison between homogeneous and heterogenised catalysts confirms that heterogenisation avoids the catalyst desorption (lost of activity) from the electrode. Catalytic activity is directly related with the content of metalloporphyrin in heterogenised materials that are addressable electronically.

Graphical abstractA new general method to heterogenise porphyrins and different metalloporphyrins (Co, Fe) on inorganic supports, such as silica, mesoporous MCM-41 and delaminated zeolites ITQ-2 and ITQ-6, yields stable materials, which act as active catalysts for the electrochemical oxygen reduction, without catalyst desorption from the electrode or deactivation. Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
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