Investigation of the electrochemical oxidation reaction of the borohydride anion in palladium layers on Pt(111)

Abstract The electrooxidation reaction of 0.001 mol L −1 NaBH 4 in 0.1 mol L −1 sodium hydroxide solution is studied on a set of Pd xML /Pt(111) surfaces with x  = 0 (Pt(111) substrate), 1, 2, 5, 10 and 16 monolayers (ML) as equivalent thickness. The Pd xML /Pt(111) surfaces are all more active than Pt(111), and present smaller reaction onset potential and larger faradaic current in the kinetics region. The most active surface, at 400 rpm is Pd 1ML /Pt(111). As hydrogen insertion is not possible in this case, the superior activity of Pd xML /Pt(111) surfaces cannot be linked to the formation of Pd-hydrides. Instead, the activity improvement of the Pd xML /Pt(111) surfaces versus Pt(111) may originate from (i) the larger oxophilicity of Pd than Pt facilitates the removal of strongly-adsorbed BH ad intermediates in a Langmuir-Hinshelwood pathway, (ii) the redirection of the heterogeneous hydrolysis of BH 4 − towards the partial dissociation into BH 3 species, that are oxidized faster than BH ad species and (iii) the slower hydrogen evolution reaction (HER) at Pd than at Pt surface, which shifts negatively the BOR onset potential and oxidation current generation. Pd xML /Pt(111) surfaces are sensitive to surface poisoning and deactivation by either the final products of the BOR (BO x ) and/or their intermediates (BH x,ad species), but this deactivation is much less than observed for Pt(111). Finally, the Pd xML /Pt(111) and Pt(111) surfaces lose their long-range order after being used for the BOR, most likely because of the “irreversible” adsorption of strong adsorbates ( e.g . BO x species), even if their restructuration cannot be completely ruled out.