Effect of surface dynamic wettability in proton exchange membrane fuel cells

被引:29
作者
Jiao, Kui [1 ]
Li, Xianguo [1 ]
机构
[1] Univ Waterloo, Dept Mech & Mechatron Engn, Waterloo, ON N2L 3G1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Static contact angle; Dynamic wettability; Sliding angle; Proton exchange membrane fuel cell; Water transport; LIQUID WATER TRANSPORT; GAS-DIFFUSION LAYER; LEVERETT APPROACH; SLIDING BEHAVIOR; DROPLET; CHANNELS; REMOVAL; CASSIE; WENZEL; HYDROPHOBICITY;
D O I
10.1016/j.ijhydene.2010.05.027
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
It is known that the static contact angle reflecting the "contact area" between liquid and solid is insufficient to represent the dynamic wettability of a solid surface, and another parameter called the sliding angle is needed to describe the relative easiness of liquid moving on a solid surface. However, sliding angle has been largely neglected in the previous studies for proton exchange membrane fuel cell (PEMFC). In this study, three-dimensional multiphase simulations are carried out for a PEMFC with single straight flow channels considering both the static contact angles and sliding angles of gas diffusion layer (GDL) and catalyst layer (CL). The results show that the liquid water volume fraction in cathode CL (CCL) and GDL (CGDL) can be increased by several times when the sliding angle is increased while the static contact angle is kept constant. This could have significant implication on the water management strategy due to the considerable changes in the water transport and removal processes. Since GDL is much thicker than CL, changing the surface dynamic wettability of GDL has more significant effect on liquid water transport than changing the surface dynamic wettability of CL. (C) 2010 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:9095 / 9103
页数:9
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