The Electrocatalytic Activity of Au Electrodes Changes Significantly in Various Na⁺/K⁺ Supporting Electrolyte...

The potential of maximum entropy (PME) is an indicator of extreme disorder at the electrode/electrolyte interface and can predict changes in catalytic activity within electrolytes of varying compositions. The laser-induced current transient technique is employed to evaluate the PME for Au polycrystalline (Au_pc) electrodes immersed in Ar-saturated cation electrolyte mixtures containing potassium and sodium ions at pH = 8. Five cation ratios (0.5 M K₂SO₄:0.5 M Na₂SO₄ = 0:1, 0.25:0.75, 0.5:0.5, 0.75:0.25, and 1:0) are explored, considering earlier studies that unveil cation-dependent shifts at near-neutral pH. Moreover, for all electrolyte compositions, electrochemical impedance spectroscopy is utilized to determine the double-layer capacitance (C _DL), the minimum of which should be close to the potential of zero charge (PZC). By correlating cation molar ratios with the PMEs and PZCs, the impact on the model oxygen reduction reaction (ORR) activity, assessed via the rotating disk electrode method, is analyzed. The results demonstrate a linear relationship between electrolyte cation mixtures and PME, while ORR activity exhibits an exponential trend. This observation validates the PME-activity link hypothesis, underscoring electrolyte components' pivotal role in tailoring interfacial properties for electrocatalytic systems. These findings introduce a new degree of freedom for designing optimal electrocatalytic systems by adjusting various electrolyte components.