“…This corrosive/dissolution agent in the electrolyte attacks niobium species or niobium oxide leaching niobium precursor ionic species to the solution. Regarding the present experimental conditions (where pH ≈ 1 and 0.7M HF), the tendency of Nb(V) to be complexed by fluorides, resulting NbF6complex could be expected, which afterwards can be reduced to a metallic niobium [29,30,32]. Besides, in a HF-based electrolyte, in the near location of the working electrode oxygen (O 2-) species are generated which are needed for different kinds of niobium oxides NbO, NbO2, Nb2O5 and NbO4formation [32].…”