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TEMPO‐Modified Polymethacrylates as Mediators in Electrosynthesis – Redox Behavior and Electrocatalytic Activity toward Alcohol Substrates
Homogeneous catalysts (“mediators”) are useful for tuning selectivity in organic electrosynthesis. However, they can have a negative impact on the overall mass and energy balance if used only once or recycled inefficiently. In a previous work, we introduced the polymediator concept, in which soluble redox-active polymers catalyze the electrochemical reaction, allowing for recovery by dialysis or pressure-driven membrane filtration. Using anodic alcohol oxidation as a test case, it was shown that TEMPO-modified polymethacrylates (TPMA) can serve as efficient and reusable mediators. In the present study, the properties of a TPMA sample with well-defined molecular weight distribution were studied using cyclic voltammetry and compared to low-molecular TEMPO species. The non-catalytic profiles of TPMA are shaped by diffusive and adsorptive processes, whereby the latter only become pronounced at low mediator concentrations and high scan rates. Electrocatalytic studies suggest that under the applied conditions, TPMA-catalyzed alcohol oxidation is a predominantly homogeneous process. The homogeneous kinetics are determined rather by the mediator potential than by steric influences of the polymer backbone. © 2021 The Authors. ChemElectroChem published by Wiley-VCH GmbH
TEMPO-Modified Polymethacrylates as Mediators in Electrosynthesis: Influence of the Molecular Weight on Redox Properties and Electrocatalytic Activity
Homogeneous catalysts (“mediators”) are frequently employed in organic electrosynthesis to control selectivity. Despite their advantages, they can have a negative influence on the overall energy and mass balance if used only once or recycled inefficiently. Polymediators are soluble redox-active polymers applicable as electrocatalysts, enabling recovery by dialysis or membrane filtration. Using anodic alcohol oxidation as an example, we have demonstrated that TEMPO-modified polymethacrylates (TPMA) can act as efficient and recyclable catalysts. In the present work, the influence of the molecular size on the redox properties and the catalytic activity was carefully elaborated using a series of TPMAs with well-defined molecular weight distributions. Cyclic voltammetry studies show that the polymer chain length has a pronounced impact on the key-properties. Together with preparative-scale electrolysis experiments, an optimum size range was identified for polymediator-guided sustainable reaction control.
Electrochemical growth mechanism of nanoporous platinum layers
Porous platinum is a frequently used catalyst material in electrosynthesis and a robust broadband absorber in thermoelectrics. Pore size distribution and localization determine its properties by a large extent. However, the pore formation mechanism during the growth of the material remains unclear. In this work we elucidate the mechanism underlying electrochemical growth of nanoporous platinum layers and its control by ionic concentration and current density during electrolysis. The electrode kinetics and reduction steps of PtCl4 on platinum electrodes are investigated by cyclic voltammetry and impedance measurements. Cyclic voltammograms show three reduction steps: two steps relate to the platinum cation reduction, and one step relates to the hydrogen reduction. Hydrogen is not involved in the reduction of PtCl4, however it enables the formation of nanopores in the layers. These findings contribute to the understanding of electrochemical growth of nanoporous platinum layers in isopropanol with thickness of 100 nm to 500 nm.