Detailed H2 and CO Electrochemistry for a MEA Model Fueled by Syngas

W. Y. Lee, K. M. Ong, A. F. Ghoniem

Research output: Chapter in Book/Report/Conference proceedingConference contribution

5 Scopus citations

Abstract

© The Electrochemical Society. SOFCs can directly oxidize CO in addition to H2, which allows them to be coupled to a gasifier. Many membrane-electrode-assembly (MEA) models neglect CO electrochemistry due to sluggish kinetics and the water-gas-shift reaction, but CO oxidation may be important for high CO-content syngas. The 1D-MEA model presented here incorporates detailed mechanisms for both H2 and CO oxidation, individually fitted to experimental data. These mechanisms are then combined into a single model, which provides a good fit to experimental data for H2/CO mixtures. Furthermore, the model fits H2/CO data best when a single chargetransfer step in the H2 mechanism is assumed to be rate-limiting for all current densities. This differs from the result for H2/H2O mixtures, where H2 adsorption becomes rate-limiting at high current densities. These results indicate that CO oxidation cannot be neglected in MEA models running on CO-rich syngas, and that CO oxidation can alter the H2 oxidation mechanism.
Original languageEnglish (US)
Title of host publicationECS Transactions
PublisherThe Electrochemical Society
Pages3059-3074
Number of pages16
ISBN (Print)9781607685395
DOIs
StatePublished - Jul 17 2015
Externally publishedYes

Bibliographical note

KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: This work has been supported by the Samsung Scholarship Foundation and an awardfrom King Abdullah University of Science and Technology.
This publication acknowledges KAUST support, but has no KAUST affiliated authors.

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