Catalytic Activity of an Iron-Based Water Oxidation Catalyst: Substrate Effects of Graphitic Electrodes

The synthesis, characterization, and electrochemical studies of the dinuclear complex [(MeOH)­Fe­(Hbbpya)-μ-O-(Hbbpya)­Fe­(MeOH)]­(OTf)₄ (<b>1</b>) (with Hbbpya = <i>N,N</i>-bis­(2,2′-bipyrid-6-yl)­amine) are described. With the help of online electrochemical mass spectrometry, the complex is demonstrated to be active as a water oxidation catalyst. Comparing the results obtained for different electrode materials shows a clear substrate influence of the electrode, as the complex shows a significantly lower catalytic overpotential on graphitic working electrodes in comparison to other electrode materials. Cyclic voltammetry experiments provide evidence that the structure of complex <b>1</b> undergoes reversible changes under high-potential conditions, regenerating the original structure of complex <b>1</b> upon returning to lower potentials. Results from electrochemical quartz crystal microbalance experiments rule out that catalysis proceeds via deposition of catalytically active material on the electrode surface

Catalytic Activity of an Iron-Based Water Oxidation Catalyst: Substrate Effects of Graphitic Electrodes

The synthesis, characterization, and electrochemical studies of the dinuclear complex [(MeOH)­Fe­(Hbbpya)-μ-O-(Hbbpya)­Fe­(MeOH)]­(OTf)₄ (<b>1</b>) (with Hbbpya = <i>N,N</i>-bis­(2,2′-bipyrid-6-yl)­amine) are described. With the help of online electrochemical mass spectrometry, the complex is demonstrated to be active as a water oxidation catalyst. Comparing the results obtained for different electrode materials shows a clear substrate influence of the electrode, as the complex shows a significantly lower catalytic overpotential on graphitic working electrodes in comparison to other electrode materials. Cyclic voltammetry experiments provide evidence that the structure of complex <b>1</b> undergoes reversible changes under high-potential conditions, regenerating the original structure of complex <b>1</b> upon returning to lower potentials. Results from electrochemical quartz crystal microbalance experiments rule out that catalysis proceeds via deposition of catalytically active material on the electrode surface

Electrocatalytic Water Oxidation with α‑[Fe(mcp)(OTf)2] and Analogues

The complex α-[Fe(mcp)(OTf)2] (mcp = N,N′-dimethyl-N,N′-bis(pyridin-2-ylmethyl)-cyclohexane-1,2-diamine and OTf = trifluoromethanesulfonate anion) was reported in 2011 by some of us as an active water oxidation (WO) catalyst in the presence of sacrificial oxidants. However, because chemical oxidants are likely to take part in the reaction mechanism, mechanistic electrochemical studies are critical in establishing to what extent previous studies with sacrificial reagents have actually been meaningful. In this study, the complex α-[Fe(mcp)(OTf)2] and its analogues were investigated electrochemically under both acidic and neutral conditions. All the systems under investigation proved to be electrochemically active toward the WO reaction, with no major differences in activity despite the structural changes. Our findings show that WO-catalyzed by mcp–iron complexes proceeds via homogeneous species, whereas the analogous manganese complex forms a heterogeneous deposit on the electrode surface. Mechanistic studies show that the reaction proceeds with a different rate-determining step (rds) than what was previously proposed in the presence of chemical oxidants. Moreover, the different kinetic isotope effect (KIE) values obtained electrochemically at pH 7 (KIE ∼ 10) and at pH 1 (KIE = 1) show that the reaction conditions have a remarkable effect on the rds and on the mechanism. We suggest a proton-coupled electron transfer (PCET) as the rds under neutral conditions, whereas at pH 1 the rds is most likely an electron transfer (ET)

Detangling catalyst modification reactions from the oxygen evolution reaction by online mass spectrometry

\u3cp\u3eHere we showcase the synthesis and catalytic response of the anionic iridium(III) complex [IrCl\u3csub\u3e3\u3c/sub\u3e(pic)(MeOH)]\u3csup\u3e-\u3c/sup\u3e ([1]\u3csup\u3e-\u3c/sup\u3e, pic = picolinate) toward the evolution of oxygen. Online electrochemical mass spectrometry experiments illustrate that an initial burst of CO\u3csub\u3e2\u3c/sub\u3e due to catalyst degradation is expelled before the oxygen evolution reaction commences. Electrochemical features and XPS analysis illustrate the presence of iridium oxide, which is the true active species. (Chemical Equation Presented).\u3c/p\u3

Detangling catalyst modification reactions from the oxygen evolution reaction by online mass spectrometry

Here we showcase the synthesis and catalytic response of the anionic iridium(III) complex [IrCl(pic)(MeOH)] ([1], pic = picolinate) toward the evolution of oxygen. Online electrochemical mass spectrometry experiments illustrate that an initial burst of CO due to catalyst degradation is expelled before the oxygen evolution reaction commences. Electrochemical features and XPS analysis illustrate the presence of iridium oxide, which is the true active species.Generous financial support from the MINECO/FEDER (CTQ2014-53033-P; C.T.) and Gobierno de Aragon/FSE (GA/FSE, Inorganic Molecular Architecture Group, E70; C.T.) is gratefully acknowledged. P.A. and M.P.d.R. thank the MINECO/FEDER for a fellowship and a JdC contract, respectively.Peer Reviewe