The influence of the Pt crystalline surface orientation on the glycerol electro-oxidation in acidic media

Abstract We investigated the electrochemical oxidation of glycerol on low-index Pt single crystals in acidic media (H 2 SO 4 and HClO 4 ) by cyclic voltammetry and Fourier Transform Infrared (FTIR) spectroscopy and we verified that this is a surface sensitive reaction. Pt(1 0 0) and Pt(1 1 0) surface structures favor the breaking of the C C C bond at low potentials (say 0.05 V), as seen by the formation of CO, one of the adsorbed residues of the glycerol dissociation, which poisons these surfaces even at high potentials. Pt(1 1 1) surface structure does not favor the C C C bond breaking at potentials as low as 0.05 V. However, Pt(1 1 1) is less poisoned by residues of glycerol dissociation and, for this reason, it is more active for glycerol oxidation than Pt(1 0 0) and Pt(1 1 0) at low potentials. Carbonyl containing compounds and CO 2 were detected as reaction products of the glycerol oxidation on all investigated single-crystal Pt surfaces. The ratio between CO 2 and carbonyl containing compounds is clearly much higher for Pt(1 0 0) and Pt(1 1 0) than for Pt(1 1 1).