Effect of O<inf>2</inf> on the adsorption of SO<inf>2</inf> on carbon-supported pt electrocatalysts

• Main Authors: Punyawudho K., Ma S., Van Zee J., Monnier J.
• Format: Journal
• Published: 2017
• Online Access: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79959194285&origin=inward; http://cmuir.cmu.ac.th/jspui/handle/6653943832/43048
• Institution: Chiang Mai University

Adsorption of SO 2 in the presence of O 2 on Pt/C catalysts often used as electrocatalysts has been investigated by temperature programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS). The amounts of SO 2 adsorption on Pt/C in the presence of O 2 were much higher than those in the absence of O 2 (SO 2 -N 2 ) and from the carbon support (Vulcan XC-72) alone. Adsorption is dependent on oxygen concentration over the range 0-20% but reaches saturation at 20% O 2 . The spillover of SO 2 from Pt to the carbon support has been proposed for 10, 20, and 40% Pt loadings, characterized by desorption temperatures of approximately 150 and 260 °C for SO 2 adsorbed on Pt and carbon, respectively. Adsorbed Pt-S, C-S, C-SO x , and Pt-SO 4 species were identified by XPS as S-containing species on both Pt and carbon. Both TPD and XPS indicate that the carbon support plays a major role in SO 2 adsorption, primarily as SO x (x = 3, 4). The bonding of S and SO x on the carbon support was strong enough that back diffusion to the Pt surface did not occur. © 2011 American Chemical Society.