The influence of the carbon support and platinum particle size on degradation of cathode for low platinum-loading catalyst layer

Haoran Yu, Andrea Baricci, Andrea Casalegno, Laure Guetaz, Radenka Maric

Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

2 Scopus citations

Abstract

We demonstrated the ability to control the platinum particle size in the synthesis of carbon supported Pt (Pt/C) electrocatalyst with reactive spray deposition technology (RSDT). The degradation of Pt cathode with loading of 0.1 mg/cm2 in membrane electrode assembly (MEA) under simulated drive cycles (30000 triangular wave cycles between 0.6 and 1.0 Vrhe) showed similar electrochemical surface area (ECSA) at the end of life (EOL), regardless of the initial Pt particle size or carbon support type. However, it is possible to reduce the loss of ECSA using a gradient catalyst layer consisting of a 6 um layer with Pt particles of 5 nm toward the membrane and another 6 μm layer with Pt particles of 2 nm toward the GDL. Microscopy studies suggested that the gradient catalyst layer have less Pt loss% into the electrolyte, thereby maintained higher ECSA at EOL.

Original languageEnglish
Title of host publicationHeterogeneous Functional Materials for Energy Conversion and Storage
EditorsW. K. S. Chiu, F. Chen, A. Herring, D. Chu, S. Gopalan, T. Markus, P. J. Masset
PublisherElectrochemical Society Inc.
Pages41-55
Number of pages15
Edition25
ISBN (Electronic)9781607687528
ISBN (Print)9781623323943
DOIs
StatePublished - 2016
Externally publishedYes
EventSymposium on Heterogeneous Functional Materials for Energy Conversion and Storage - 229th ECS Meeting - San Diego, United States
Duration: May 29 2016Jun 2 2016

Publication series

NameECS Transactions
Number25
Volume72
ISSN (Print)1938-6737
ISSN (Electronic)1938-5862

Conference

ConferenceSymposium on Heterogeneous Functional Materials for Energy Conversion and Storage - 229th ECS Meeting
Country/TerritoryUnited States
CitySan Diego
Period05/29/1606/2/16

Funding

The authors gratefully acknowledge the National Science Foundation (award number CMMI-1265893) for financial support.

FundersFunder number
National Science FoundationCMMI-1265893

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