Electrochemical Oxidation of Isopropanol on Platinum-Ruthenium Nanoparticles Studied with Real-Time Product and Dissolution Analytics

Khanipour P, Speck F, Mangoufis Giasin I, Mayrhofer K, Cherevko S, Katsounaros I (2020)


Publication Type: Journal article

Publication year: 2020

Journal

Book Volume: 12

Pages Range: 33670-33678

Journal Issue: 30

DOI: 10.1021/acsami.0c07190

Abstract

The selective electrooxidation of 2-propanol to acetone can be used in fuel cells which, when combined with the transfer hydrogenation of acetone from liquid organic hydrogen carriers, will enable the realization of hydrogen economy without using molecular hydrogen gas for storage and transportation. We study the reaction on platinum and platinum-ruthenium nanocatalysts using unique tools for the real-time characterization of reaction and dissolution products. Acetone is the primary product on all investigated catalysts, and only traces of CO2 form at high potentials. We propose that the reaction occurs on Pt-Ru ensemble sites at low potentials and on Pt-Pt sites at high potentials. Dissolution of surface ruthenium atoms leads to suppression of the process at low overpotential. The main shortcomings to be addressed for an efficient catalyst performance are (a) the narrow potential range in which the bimetallic catalyst is active, (b) the surface poisoning from adsorbed acetone, and (c) the dissolution of ruthenium.

Authors with CRIS profile

Involved external institutions

How to cite

APA:

Khanipour, P., Speck, F., Mangoufis Giasin, I., Mayrhofer, K., Cherevko, S., & Katsounaros, I. (2020). Electrochemical Oxidation of Isopropanol on Platinum-Ruthenium Nanoparticles Studied with Real-Time Product and Dissolution Analytics. ACS Applied Materials and Interfaces, 12(30), 33670-33678. https://dx.doi.org/10.1021/acsami.0c07190

MLA:

Khanipour, Peyman, et al. "Electrochemical Oxidation of Isopropanol on Platinum-Ruthenium Nanoparticles Studied with Real-Time Product and Dissolution Analytics." ACS Applied Materials and Interfaces 12.30 (2020): 33670-33678.

BibTeX: Download