Prof. Alceo Macchioni Profile

Prof. Alceo Macchioni

at Univ of Perugia

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Proceedings Article | 7 October 2014 Paper

Homogeneous and heterogenized iridium water oxidation catalysts

Alceo Macchioni

Proceedings Volume 9176, 917608 (2014) https://doi.org/10.1117/12.2060957

KEYWORDS: Iridium, Oxygen, Electrons, Chlorine, Solar energy, Metals, Catalysis, X-ray diffraction, Oxidation, Titanium dioxide

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The development of an efficient catalyst for the oxidative splitting of water into molecular oxygen, protons and electrons is of key importance for producing solar fuels through artificial photosynthesis. We are facing the problem by means of a rational approach aimed at understanding how catalytic performance may be optimized by the knowledge of the reaction mechanism of water oxidation and the fate of the catalytic site under the inevitably harsh oxidative conditions. For the purposes of our study we selected iridium water oxidation catalysts, exhibiting remarkable performance (TOF > 5 s^-1 and TON > 20000). In particular, we recently focused our attention on [Cp*Ir(N,O)X] (N,O = 2-pyridincarboxylate; X = Cl or NO₃) and [IrCl(Hedta)]Na water oxidation catalysts. The former exhibited a remarkable TOF whereas the latter showed a very high TON. Furthermore, [IrCl(Hedta)]Na was heterogenized onto TiO₂ taking advantage of the presence of a dandling –COOH functionality. The heterogenized catalyst maintained approximately the same catalytic activity of the homogeneous analogous with the advantage that could be reused many times. Mechanistic studies were performed in order to shed some light on the rate-determining step and the transformation of catalysts when exposed to “oxidative stress”. It was found that the last oxidative step, preceding oxygen liberation, is the rate-determining step when a small excess of sacrificial oxidant is used. In addition, several intermediates of the oxidative transformation of the catalyst were intercepted and characterized by NMR, X-Ray diffractometry and ESI-MS.

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