Cold start capability and durability of electrospun catalyst layer for proton exchange membrane fuel cell

被引:15
|
作者
Liu, Han [1 ]
Si, Dechun [2 ]
Ding, Han [3 ,4 ]
Wang, Shangshang [2 ]
Zhang, Jianbo [2 ,5 ]
Liu, Yong [6 ]
机构
[1] Beijing Univ Chem Technol, Coll Mech & Elect Engn, Beijing 100029, Peoples R China
[2] Tsinghua Univ, Dept Automot Engn, State Key Lab Automot Safety & Energy, Beijing 100084, Peoples R China
[3] State Key Lab Fluorinated Funct Membrane Mat, Huantai 256401, Peoples R China
[4] Shandong Dongyue Polymer Mat Co Ltd, Zibo 256401, Peoples R China
[5] Beijing Inst Technol, Beijing Coinnovat Ctr Elect Vehicles, Beijing 100081, Peoples R China
[6] Beijing Univ Chem Technol, Coll Mat Sci & Engn, Beijing Key Lab Adv Funct Polymer Composites, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrospun catalyst layer; Cold start; Pore size distribution; Electrospinning; Performance and structure;
D O I
10.1016/j.ijhydene.2020.06.032
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
The electrospun catalyst layer (E-spun CL) was found capable of improving both catalyst performance and durability under normal temperature operations. In this work, we first explored the reasons for this improvement, and then systematically compared the cold start capability and durability of E-spun CL with that of the commercial electro-sprayed catalyst layer (E-sprayed CL). Improved performance under normal temperature operations for E-spun CL was attributed to the optimized pore structure, which resulted in less mass transport losses. E-spun CL exhibited a better cold start capability in terms of more condensed product water due to longer survival time, possibly caused by the lower freezing probability of super-cooled water in micro-pores. After enduring several cold start tests, less performance and structural deterioration were observed for E-spun CL, mainly resulting from the high mechanical flexibility of porous nanofiber structure. (c) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:11140 / 11149
页数:10
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