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Effect of deposited Pt particles on the surface charge of TiO/sub 2/ aqueous suspensions by potentiometry, electrophoresis, and labeled ion adsorption

Journal Article · · J. Phys. Chem.; (United States)
DOI:https://doi.org/10.1021/j100403a035· OSTI ID:5697758
Potentiometry, electrophoresis, and radiotracer technique have been used to study the charge density in different parts of the double layer at the TiO/sub 2/-electrolyte interface for powder samples supporting 0.5-10 wt % platinum as particles of homogeneous size (ca. 2 nm diameter). Less positive charge densities were measured by potentiometry for increasing Pt content; the value of point of zero charge decreases accordingly. More negative electrophoretic mobilities were found for the metal-loaded samples from pH 3 to pH approx.8; as a result the value of the point of zero zeta potential decreases with increasing Pt content. From a comparison between the surface charge density, the charge density of the diffuse part of the double layer, and the charge density of the counterions (determined from adsorption isotherms of labeled Na/sup +/ and Cl/sup -/ ions for TiO/sub 2/ and 10 wt % Pt/TiO/sub 2/), it is deduced that a part of the Cl/sup -/ ions form neutral adsorbed species at the Pt surface. Therefore, the changes observed in potentiometric titrations and electrophoretic mobilities are attributed to an increase in TiO/sub 2/ acidity induced by the Pt particles, which reflects the decreased TiO/sub 2/ electron density.
Research Organization:
Ecole Centrale de Lyon, Ecully, France
OSTI ID:
5697758
Journal Information:
J. Phys. Chem.; (United States), Journal Name: J. Phys. Chem.; (United States) Vol. 90:12; ISSN JPCHA
Country of Publication:
United States
Language:
English