TY - JOUR
T1 - Self-supported PdxBi catalysts for the electrooxidation of glycerol in alkaline media
AU - Zalineeva, Anna
AU - Serov, Alexey
AU - Padilla, Monica
AU - Martinez, Ulises
AU - Artyushkova, Kateryna
AU - Baranton, Stève
AU - Coutanceau, Christophe
AU - Atanassov, Plamen B.
PY - 2014/3/12
Y1 - 2014/3/12
N2 - Highly active self-supported PdxBi catalysts are synthesized by the sacrificial support method. Self-supported PdxBi catalysts have a porous nanostructured morphology with high surface areas (in the range from 75 to 100 m2 g-1), making PdxBi a state-of-the-art catalyst. Pd4Bi displays the highest activity toward glycerol oxidation. In situ Fourier transform infrared spectroscopy highlights the unique catalytic behavior of self-supported PdxBi materials due to their particular structure and morphology. The confinement of reactants and intermediates in pores acting as nanoreactors is responsible for the high selectivity as a function of the electrode potential: aldehyde and ketone at low potentials, hydroxypyruvate at moderate potentials, and CO2 at high potentials. Moreover, the selectivity depends on the electrode history: it is different for the positive potential scan direction than for the reverse direction, where the catalyst becomes selective toward the production of carboxylates.
AB - Highly active self-supported PdxBi catalysts are synthesized by the sacrificial support method. Self-supported PdxBi catalysts have a porous nanostructured morphology with high surface areas (in the range from 75 to 100 m2 g-1), making PdxBi a state-of-the-art catalyst. Pd4Bi displays the highest activity toward glycerol oxidation. In situ Fourier transform infrared spectroscopy highlights the unique catalytic behavior of self-supported PdxBi materials due to their particular structure and morphology. The confinement of reactants and intermediates in pores acting as nanoreactors is responsible for the high selectivity as a function of the electrode potential: aldehyde and ketone at low potentials, hydroxypyruvate at moderate potentials, and CO2 at high potentials. Moreover, the selectivity depends on the electrode history: it is different for the positive potential scan direction than for the reverse direction, where the catalyst becomes selective toward the production of carboxylates.
UR - http://www.scopus.com/inward/record.url?scp=84896285074&partnerID=8YFLogxK
U2 - 10.1021/ja412429f
DO - 10.1021/ja412429f
M3 - Article
AN - SCOPUS:84896285074
SN - 0002-7863
VL - 136
SP - 3937
EP - 3945
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 10
ER -