Ultra-high activity methanol oxidation electrocatalyzed by a flexible integrated Pt-Zn array electrode

被引:1
作者
Liu, Yulan [1 ,2 ]
Zhang, Yu [1 ]
Tian, Xiaoyu [1 ,2 ]
Wang, He [1 ,2 ]
Huo, Lili [1 ,2 ]
机构
[1] Inner Mongolia Univ Technol, Chem Engn Coll, 49 Aimin St, Hohhot 010051, Peoples R China
[2] Key Lab CO2 Resource Utilizat Univ Inner Mongolia, 49 Aimin St, Hohhot 010051, Peoples R China
基金
中国国家自然科学基金;
关键词
65;
D O I
10.1039/d4tc04584j
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Maximizing the utilization of Pt-based materials is a fundamental objective for practical direct methanol fuel cell technology at the commercial scale. In this study, a flexible integrated electrode composed of a class of Pt-Zn alloys grown in situ on carbon cloth (CC) are fabricated via a simple one-step electro-deposition approach. The 3D self-supporting configuration can efficiently accelerate rapid electron diffusion and expose more utilizable active sites, thus achieving highly active electrodes with strong anti-CO poisoning properties for catalyzing the methanol oxidation reaction (MOR). By regulate the input Pt/Zn molar ratio, the Pt7Zn1/CC electrode exhibits a superior mass activity of 2.48/5.89 A mgPt-1 and specific activity of 310.36/905.99 mA cm-2, which are 10.78/10.15 and 24.53/29.25 fold enhancements in comparison with those of commercial Pt/C in acid and alkaline media, respectively. Additionally, the anti-CO poisoning ability of Pt-Zn/CC was greatly enhanced by introducing the Zn. The mass activity loss of the Pt7Zn1/CC electrode in acid and alkaline media is only 91.65% and 84.33%, much lower than those of Pt/CC (97.30% and 92.89%) and commercial Pt/C (98.61% and 98.07%) after successive 10 h tests in acid and alkaline media, respectively. This work indicates a strategic design for significant improvements of efficient Pt-based alloy electrocatalysts in fuel cell applications.
引用
收藏
页码:3054 / 3061
页数:8
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