Overall Design of a Gradient‐Ordered Membrane Electrode Assembly for Direct Liquid Fuel Cells

Author:

Pan Zhefei123,Xie Fengjia4,Zhang Zhewei3,Zhao Zhen3,Wu Lizhen3,Li Wenzhi3,Zhu Yao3,Huo Xiaoyu3,Liu Yun3,Zhang Xuming4,Chen Rong12,An Liang35ORCID

Affiliation:

1. Key Laboratory of Low‐Grade Energy Utilization Technologies and Systems (Chongqing University) Ministry of Education Chongqing 400030 China

2. Institute of Engineering Thermophysics Chongqing University Chongqing 400030 China

3. Department of Mechanical Engineering The Hong Kong Polytechnic University Hung Hom Kowloon Hong Kong SAR 999077 China

4. Department of Applied Physics The Hong Kong Polytechnic University Hung Hom Kowloon Hong Kong SAR 999077 China

5. Research Institute for Sports Science and Technology The Hong Kong Polytechnic University Hung Hom Kowloon Hong Kong SAR 999077 China

Abstract

AbstractThe direct liquid fuel cell (DLFC) constitutes a promising energy conversion system that directly conveys the chemical energy of liquid fuels into electrical energy. In certain DLFCs, gas is produced as a product of electrochemical reactions during operation. However, the accumulation of gas inside the porous electrode can significantly hinder the transport of reactants, leading to the failure of active sites and severe concentration loss. To address this issue, a gradient‐ordered membrane electrode assembly (MEA) is designed and fabricated, consisting of a dual‐gradient diffusion layer that comprises a pore‐size gradient and a wettability gradient as well as a catalyst layer constructed by nanoneedle catalyst. This MEA promptly removes the produced gas and delivers the fresh solution, thereby enhancing the cell power output and stability. The fuel cell with the gradient‐ordered MEA achieves a remarkable peak power density of 177 mW cm−2 and a discharging time of 19 h, which are more than four times and 30 times, respectively, higher than those of the conventional MEA.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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