Electrochemical characterisation and oxygen evolution at a heavily boron doped diamond electrode

Abstract

Characterisation of a commercial heavily doped BDD electrode demonstrated it contains a small sp 2 content, which on anodic potential scanning, is oxidised to CO/CO 2. This surface modification alters the electrode activity, increasing the overpotential for the hydrogen and oxygen evolution reactions (HER and OER). Ex situ and in situ investigations indicate film morphology is mainly composed of “chain of hills”, presenting relatively high differential capacitance values and morphology factor, which is attributed to the effect of surface states and high surface roughness of the BDD film. The voltammetric behaviour depends on the applied potential; the heavily doped BDD electrode behaving as a metallic electrode at more anodic potentials. Polarisation curves (potentiostatic (1 mV s −1) or galvanostatic (point-by-point)), recorded at different temperatures and H 2SO 4 concentrations, lead to the same conclusions. The high Tafel coefficients and low apparent electronic transfer coefficient ( α A) are independent of overpotential and temperature but show a dependence on H 2SO 4 concentration. The linear relationship observed between the apparent electrochemical enthalpy of activation (Δ H # η) and overpotential supports α A is constant. An OER mechanism was proposed taking into account the absence of adsorption sites at the BDD surface. The OER is inhibited, explaining the high overpotentials and elevated Δ H # η values.