Paper Status Tracking
Contact us
[email protected]
Click here to send a message to me 3275638434
Paper Publishing WeChat

Article
Affiliation(s)

1. Division of Mechanical Engineering, Graduate School of Engineering, Mie University, Tsu-city, Mie 514-8507, Japan
2. School of Mechanical Engineering, the University of Adelaide, Adelaide, SA 5005, Australia

ABSTRACT

Polymer Electrolyte Fuel Cell (PEFC) is desired to be operated at temperature around 90 °C for stationary applications during the period from 2020 to 2025 in Japan. It can be expected thinner polymer electrolyte membrane (PEM) and gas diffusion layer (GDL) would promote the power generation performance of PEFC at this temperature. The aim of this study is to understand the impact of thickness of PEM and GDL on the temperature profile of interface between PEM and catalyst layer at the cathode (i.e., the reaction surface) in a single PEFC with an initial operation temperature (Tini). An 1D multi-plate heat transfer model based on temperature data of separator measured using thermograph in power generation process was developed to evaluate temperature of the reaction surface (Treact). This study investigated the effect of Tini, flow rate and relative humidity of supply gas on Treact distribution. The study finds that when using thin GDL, the even distribution of TreactTini is obtained irrespective of thickness of PEM, Tini and relative humidity conditions. TreactTini using Nafion 115 is higher than the other thin PEMs irrespective of Tini and relative humidity conditions. It can be concluded that the even temperature distribution could be achieved by using thin PEM and GDL.

KEYWORDS

PEFC, heat transfer model, temperature distribution, operation temperature around 90 °C, thickness of PEM and GDL, relative humidity condition.

Cite this paper

References

About | Terms & Conditions | Issue | Privacy | Contact us
Copyright © 2001 - David Publishing Company All rights reserved, www.davidpublisher.com
3 Germay Dr., Unit 4 #4651, Wilmington DE 19804; Tel: 001-302-3943358 Email: [email protected]