Hydride phase formation in carbon supported palladium nanoparticle electrodes investigated using in situ EXAFS and XRD
Hydride phase formation in carbon supported palladium nanoparticle electrodes investigated using in situ EXAFS and XRD
In situ EXAFS (extended X-ray absorption. ne structure), in situ XRD (X-ray diffraction) and electrochemical studies have been used to investigate the palladium hydride phases of carbon supported palladium nanoparticles as a function of applied potential. Electrochemical investigations showed an increase in the hydrogen to palladium ratio with an increasingly negative potential. The H/Pd ratio could be divided into four distinct regions, which described the palladium hydride phase present; the alpha-phase, a mixture of the alpha- and beta-phases, the beta-phase, and a hyperstoichiometric region. The beta-hydride phase stoichiometry obtained from the electrochemical data corresponded to PdH. However, the composition obtained from the lattice expansions observed from the in situ EXAFS and XRD, 3.3% and 3.8%, correspond to compositions of PdH0.59 to PdH0.68. The excess hydrogen and hyperstoichiometric amounts found at more negative potentials are attributed to either spillover on to the carbon support or trapping and subsequent reoxidation of H-2 in the porous electrode structure.
x-ray-absorption, fuel-cell electrocatalysts, hydrogen absorption, acidic solutions, fine-structure, pd, adsorption, particles, deuterium, spectroscopy
3220-3225
Rose, Abigail
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Maniguet, Stephanie
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Mathew, Rebeca J.
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Slater, Claire
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Yao, Jun
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Russell, Andrea E.
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2003
Rose, Abigail
7e1f0e36-2ad5-4e29-b9b9-756484f1f8c6
Maniguet, Stephanie
cd69841b-03b4-4c98-9ef7-141d56e67228
Mathew, Rebeca J.
cda2fbaa-bdd3-499d-a4b2-02c9c72c8c4a
Slater, Claire
eafe3bbc-5c4b-44f0-a53d-903f3cb3651f
Yao, Jun
cd8e4e0e-ed2d-4590-be1f-fc6340f6a441
Russell, Andrea E.
b6b7c748-efc1-4d5d-8a7a-8e4b69396169
Rose, Abigail, Maniguet, Stephanie, Mathew, Rebeca J., Slater, Claire, Yao, Jun and Russell, Andrea E.
(2003)
Hydride phase formation in carbon supported palladium nanoparticle electrodes investigated using in situ EXAFS and XRD.
Physical Chemistry Chemical Physics, 5 (15), .
(doi:10.1039/b302956e).
Abstract
In situ EXAFS (extended X-ray absorption. ne structure), in situ XRD (X-ray diffraction) and electrochemical studies have been used to investigate the palladium hydride phases of carbon supported palladium nanoparticles as a function of applied potential. Electrochemical investigations showed an increase in the hydrogen to palladium ratio with an increasingly negative potential. The H/Pd ratio could be divided into four distinct regions, which described the palladium hydride phase present; the alpha-phase, a mixture of the alpha- and beta-phases, the beta-phase, and a hyperstoichiometric region. The beta-hydride phase stoichiometry obtained from the electrochemical data corresponded to PdH. However, the composition obtained from the lattice expansions observed from the in situ EXAFS and XRD, 3.3% and 3.8%, correspond to compositions of PdH0.59 to PdH0.68. The excess hydrogen and hyperstoichiometric amounts found at more negative potentials are attributed to either spillover on to the carbon support or trapping and subsequent reoxidation of H-2 in the porous electrode structure.
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Published date: 2003
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PCCP
Keywords:
x-ray-absorption, fuel-cell electrocatalysts, hydrogen absorption, acidic solutions, fine-structure, pd, adsorption, particles, deuterium, spectroscopy
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Local EPrints ID: 20073
URI: http://eprints.soton.ac.uk/id/eprint/20073
ISSN: 1463-9076
PURE UUID: cab8a565-d6aa-41af-90c9-9e1dabb42c87
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Date deposited: 24 Feb 2006
Last modified: 16 Mar 2024 02:59
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Contributors
Author:
Abigail Rose
Author:
Stephanie Maniguet
Author:
Rebeca J. Mathew
Author:
Claire Slater
Author:
Jun Yao
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