TY - JOUR
T1 - Ceria Entrapped Palladium Novel Composites for Hydrogen Oxidation Reaction in Alkaline Medium
AU - Ralbag, Noam
AU - Davydova, Elena S.
AU - Mann-Lahav, Meirav
AU - Cong, Peixi
AU - He, Jin
AU - Beale, Andrew M.
AU - Grader, Gideon S.
AU - Avnir, David
AU - Dekel, Dario R.
N1 - Publisher Copyright:
© 2020 The Author(s). Published on behalf of The Electrochemical Society by IOP Publishing Limited.
PY - 2020/1/4
Y1 - 2020/1/4
N2 - A new heterogeneous catalyst for hydrogen oxidation reaction (HOR), metallic palladium within which nanoparticles of ceria are entrapped, CeO2@Pd, is described. Its preparation is based on a new materials methodology of molecular doping of metals. The metallic matrix, which encages the nanoparticles, is prepared in foam architecture, to ensure easy molecular diffusion. Characterization of the structural properties of the CeO2@Pd composite using SEM, STEM, TEM, XRD, EXAFS and nitrogen adsorption reveals its morphological architecture, which leads to improved catalytic activity. In-situ electrochemical and H2 temperature-programmed reduction (H2-TPR) spectra provide direct experimental evidence of the weakening of PdH bond in the CeO2@Pd composites, relative to pure (undoped) Pd catalysts. Gas diffusion electrodes based on the entrapped CeO2@Pd catalysts demonstrated one order of magnitude higher activity than pure Pd analog in the HOR reaction in an alkaline medium.
AB - A new heterogeneous catalyst for hydrogen oxidation reaction (HOR), metallic palladium within which nanoparticles of ceria are entrapped, CeO2@Pd, is described. Its preparation is based on a new materials methodology of molecular doping of metals. The metallic matrix, which encages the nanoparticles, is prepared in foam architecture, to ensure easy molecular diffusion. Characterization of the structural properties of the CeO2@Pd composite using SEM, STEM, TEM, XRD, EXAFS and nitrogen adsorption reveals its morphological architecture, which leads to improved catalytic activity. In-situ electrochemical and H2 temperature-programmed reduction (H2-TPR) spectra provide direct experimental evidence of the weakening of PdH bond in the CeO2@Pd composites, relative to pure (undoped) Pd catalysts. Gas diffusion electrodes based on the entrapped CeO2@Pd catalysts demonstrated one order of magnitude higher activity than pure Pd analog in the HOR reaction in an alkaline medium.
UR - http://www.scopus.com/inward/record.url?scp=85082395396&partnerID=8YFLogxK
U2 - 10.1149/1945-7111/ab74be
DO - 10.1149/1945-7111/ab74be
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AN - SCOPUS:85082395396
SN - 0013-4651
VL - 167
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 5
M1 - 054514
ER -