1.Institute for Chemical Technology of Inorganic Materials,Johannes Kepler University Linz,Linz,Austria;2.Christian Doppler Laboratory for Combinatorial Oxide Chemistry at the Institute for Chemical Technology of Inorganic Materials,Johannes Kepler University Linz,Linz,Austria
Abstract:
In operando quantification of field-assisted ion release during high-voltage anodisation (up to 100 V SHE) of Nb in 0.1 M sulphuric acid was performed. Electrochemical high-field oxide formation under both potential and current control was studied separately. The quantification of in situ ion release via ICP-MS revealed an increase of the oxide dissolution factor (from 337 to 422 fm V?1) when decreasing the potential scan rate from 200 to 100 mV s?1. Dissolution rates measured during galvanostatic oxide formation allowed measuring oxide dissolution factors of 719 and 837 fm V?1 for current densities of 1.0 and 0.5 mA cm?2, respectively. As compared to the potentiodynamic case, higher dissolution rates and oxide dissolution factors were measured for galvanostatic anodisation. The overall fraction of the charge used for generation of soluble Nb species was below 0.4% for all oxide growth regimes. Cross-sectional SEM imaging proofs an oxide formation factor of 2.1 nm V?1. The surface of anodised films was extremely smooth and featureless without any cracks or voids. Based on X-ray diffraction, the films were found to be amorphous, indicating that no field crystallisation is occurring under the applied oxide growth conditions even at higher voltages.
