Identification and quantification of performance losses for PEM fuel cells as determined by selective chemisorption and ESA measurements

Membrane electrode assemblies (MEAs) were fabricated using a high frequency spraying technique. Electrocatalyst powders were directly sprayed onto an electrolyte membrane by ultrasonic spraying. The weight ratios of Nafion to Pt/C were studied, and the ratio about 50-62% yields the maximum current d...

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Main Authors: K. Punyawudho, N. Vorayos, Y. Zhang, S. Shimpalee, J. R. Monnier
Format: Journal
Published: 2018
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84903266186&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/45013
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spelling th-cmuir.6653943832-450132018-01-24T06:04:08Z Identification and quantification of performance losses for PEM fuel cells as determined by selective chemisorption and ESA measurements K. Punyawudho N. Vorayos Y. Zhang S. Shimpalee J. R. Monnier Membrane electrode assemblies (MEAs) were fabricated using a high frequency spraying technique. Electrocatalyst powders were directly sprayed onto an electrolyte membrane by ultrasonic spraying. The weight ratios of Nafion to Pt/C were studied, and the ratio about 50-62% yields the maximum current density at the ohmic and gas diffusion region of the polarization curve. Cross sections of the MEA were analyzed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM); images from SEM indicate that the supported catalysts are arranged in a layered manner and that pores in the catalyst coated layer (CCL) are formed. TEM images show the ionomer layer exists between the reaction zone and the electrolyte membrane. The concentration of Pt surface sites in the MEA was measured by selective H 2 chemisorption methods at dry conditions and by cyclic voltammetry (CV) for the electrochemical reaction. The chemisorption measurements indicate that ∼52% of the active Pt surface are lost due to ionomer coverage and CV shows an additional 28% of the Pt surface are lost due to blockage by condensed water and the isolation of Pt sites from ionomer and electrical conduction. In total 80% of the Pt surface sites present on the 20 wt% Pt/C starting material are lost during preparation and at operating conditions. Thu s, both mechanisms of activity loss are separately identified and quantified. © 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved. 2018-01-24T06:04:08Z 2018-01-24T06:04:08Z 2014-07-15 Journal 03603199 2-s2.0-84903266186 10.1016/j.ijhydene.2014.04.187 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84903266186&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/45013
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
description Membrane electrode assemblies (MEAs) were fabricated using a high frequency spraying technique. Electrocatalyst powders were directly sprayed onto an electrolyte membrane by ultrasonic spraying. The weight ratios of Nafion to Pt/C were studied, and the ratio about 50-62% yields the maximum current density at the ohmic and gas diffusion region of the polarization curve. Cross sections of the MEA were analyzed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM); images from SEM indicate that the supported catalysts are arranged in a layered manner and that pores in the catalyst coated layer (CCL) are formed. TEM images show the ionomer layer exists between the reaction zone and the electrolyte membrane. The concentration of Pt surface sites in the MEA was measured by selective H 2 chemisorption methods at dry conditions and by cyclic voltammetry (CV) for the electrochemical reaction. The chemisorption measurements indicate that ∼52% of the active Pt surface are lost due to ionomer coverage and CV shows an additional 28% of the Pt surface are lost due to blockage by condensed water and the isolation of Pt sites from ionomer and electrical conduction. In total 80% of the Pt surface sites present on the 20 wt% Pt/C starting material are lost during preparation and at operating conditions. Thu s, both mechanisms of activity loss are separately identified and quantified. © 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
format Journal
author K. Punyawudho
N. Vorayos
Y. Zhang
S. Shimpalee
J. R. Monnier
spellingShingle K. Punyawudho
N. Vorayos
Y. Zhang
S. Shimpalee
J. R. Monnier
Identification and quantification of performance losses for PEM fuel cells as determined by selective chemisorption and ESA measurements
author_facet K. Punyawudho
N. Vorayos
Y. Zhang
S. Shimpalee
J. R. Monnier
author_sort K. Punyawudho
title Identification and quantification of performance losses for PEM fuel cells as determined by selective chemisorption and ESA measurements
title_short Identification and quantification of performance losses for PEM fuel cells as determined by selective chemisorption and ESA measurements
title_full Identification and quantification of performance losses for PEM fuel cells as determined by selective chemisorption and ESA measurements
title_fullStr Identification and quantification of performance losses for PEM fuel cells as determined by selective chemisorption and ESA measurements
title_full_unstemmed Identification and quantification of performance losses for PEM fuel cells as determined by selective chemisorption and ESA measurements
title_sort identification and quantification of performance losses for pem fuel cells as determined by selective chemisorption and esa measurements
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84903266186&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/45013
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