Abstract

Herein, water-oxidation reaction by cobalt(II) phthalocyanine, N,N′-bis (salicylidene) ethylenediamino cobalt(II), nickel(II) Schiff base (N,N′-bis (salicylidene)ethylenediamino nickel(II), nickel(II)) phthalocyanine-tetrasulfonate tetrasodium, manganese(II) phthalocyanine, 5,10,15,20-Tetraphenyl-21H,23H-porphine manganese(III) chloride, manganese(III) 5,10,15,20-tetra(4-pyridyl)-21H,23H-porphine chloride tetrakis(methochloride) was investigated using electrochemistry, UV-vis spectroscopy and spectroelectrochemistry. According to our results, a new decomposition pathway for these metal complexes under water-oxidation conditions was proposed. The produced metal oxide obtained by decomposition of metal complex under water -oxidation conditions not only catalyzes water-oxidation reaction but this metal oxide also accelerates decomposition of the corresponding complex to form higher amounts of the metal oxide. We hypothesize that such a mechanism could be investigated for many metal complexes under different oxidation or reduction reactions.

Highlights

  • Hydrogen is a promising molecule to store sustainable, intermittent and fluctuating energies[1]

  • Metal complexes were investigated in the presence of the corresponding metal oxides covered on fluorine-doped tin oxide electrode (FTO) in the absence of potential

  • The aim of this step was to track the adsorption of the metal complexes on the surface of the metal oxide covered on FTO in the absence of water-oxidation reaction

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Summary

Introduction

Hydrogen is a promising molecule to store sustainable, intermittent and fluctuating energies[1]. An approach to producing hydrogen is water-splitting reaction. In the presence of these metal complexes and under water-oxidation reaction, finding a true catalyst remains a challenging issue[11–15]. It is proposed that in some cases a metal complex is not stable and may decompose to metal oxides; subsequently, obtained metal oxides from decomposition of metal complex could serve as suitable catalysts for water-oxidation reaction. The details of the decomposition of metal complexes under water-oxidation reaction remain unknown. As metal oxides were reported to be a decomposition agent for organic compounds, it is needed to explore if formed metal oxides could affect the metal complexes under water-oxidation reactions. We reported a decomposition mechanism for Mn, Co and Ni-based complexes (Fig. S1) under water-oxidation reaction

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