Controlling Proton and Electron Transfer Rates to Enhance the Activity of an Oxygen Reduction Electrocatalyst

An electrochemical approach is developed that allows for the control of both proton and electron transfer rates in the O2 reduction reaction (ORR). A dinuclear Cu ORR catalyst was prepared that can be covalently attached to thiol‐based self‐assembled monolayers (SAMs) on Au electrodes using azide–al...

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Veröffentlicht in:Angewandte Chemie International Edition 2018-10, Vol.57 (41), p.13480-13483
Hauptverfasser: Gautam, Rajendra P., Lee, Yi Teng, Herman, Gabriel L., Moreno, Cynthia M., Tse, Edmund C. M., Barile, Christopher J.
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Sprache:eng
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Zusammenfassung:An electrochemical approach is developed that allows for the control of both proton and electron transfer rates in the O2 reduction reaction (ORR). A dinuclear Cu ORR catalyst was prepared that can be covalently attached to thiol‐based self‐assembled monolayers (SAMs) on Au electrodes using azide–alkyne click chemistry. Using this architecture, the electron transfer rate to the catalyst is modulated by changing the length of the SAM, and the proton transfer rate to the catalyst is controlled with an appended lipid membrane modified with proton carriers. By tuning the relative rates of proton and electron transfer, the current density of the lipid‐covered catalyst is enhanced without altering its core molecular structure. This electrochemical platform will help identify optimal thermodynamic and kinetic parameters for ORR catalysts and catalysts of other reactions that involve the transfer of both protons and electrons. An electrochemical approach is developed to control both proton and electron transfer rates in the O2 reduction reaction. The electron transfer rate is modulated by changing the length of the self‐assembled monolayer, and the proton transfer rate by a modified lipid membrane. By tuning the relative proton and electron transfer rates, the current density is enhanced without altering its core molecular structure.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201806795