Optimizing catalyst layer structure design for improved water management of anion exchange membrane fuel cells

被引:0
|
作者
Xiao, Cailin [1 ,2 ]
Huang, Haodong [1 ,2 ]
Zhang, Zijie [1 ,2 ]
Jiang, Yuting [1 ,2 ]
Wang, Guanxiong [3 ]
Liu, Hongxiao [4 ]
Liu, Yu [4 ]
Xing, Lei [5 ]
Zeng, Lin [1 ,2 ]
机构
[1] Southern Univ Sci & Technol, Dept Mech & Energy Engn, Shenzhen Key Lab Adv Energy Storage, Shenzhen 518055, Peoples R China
[2] Southern Univ Sci & Technol, SUSTech Energy Inst Carbon Neutral, Shenzhen 518055, Peoples R China
[3] Shenzhen Acad Aerosp Technol, Shenzhen 518057, Peoples R China
[4] Shenyang Univ Chem Technol, Coll Sci, Shenyang 110142, Peoples R China
[5] Univ Surrey, Sch Chem & Chem Engn, Guildford GU2 7XH, England
基金
中国国家自然科学基金;
关键词
Anion exchange membrane fuel cells; Pore structure; Gradient pores; Water transport; Reverse diffusion; MICRO-POROUS LAYER; PERFORMANCE; STRATEGIES; IMPEDANCE; IONOMERS; STACK;
D O I
10.1016/j.jpowsour.2024.234509
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
Recent research into anion exchange membrane fuel cells (AEMFCs) highlights challenges in achieving high performance, primarily due to poor water management. This study delves into how the structure and thickness of the catalyst layer, specifically the pore design, affect AEMFC efficiency. Our study reveals that H-2/O-2 AEMFC performance is significantly influenced by the distribution and structure of anode porous sizes, which affects water generation and transport kinetics. It has become evident that, instead of oxygen availability at the cathode, the primary factors constraining AEMFC performance are water supply through back-diffusion and water flooding at the anode. Notably, by controlling the carbon content of the anode catalyst layer to create gradient pores, we successfully alleviate mass transport limitations of gases in AEMFCs, while simultaneously improving water transport. Furthermore, insights from surface water transport and detailed phase field model analysis further confirmed that these gradient pores enhance water transportation rates. These results indicate that the fabrication of a porosity-gradient anode catalyst layer using carbon powder significantly increased the limit current density by 24 % (from 4.10 W cm(-2) to 5.20 W cm(-2)) and the power density by 34.6 % (from 1.56 W cm(-2) to 2.10 W cm(-2)), compared to the catalyst layer without carbon powder.
引用
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页数:9
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