Enhancing CO Tolerance in PEMFC Anodes via Thermal Oxidation Induced RuO2 Blocking Shell on a PtRu/C Catalyst

被引:3
|
作者
Chen, Lina [1 ,2 ]
Zhang, Pengyang [1 ,2 ]
Jin, Yan-Qi [1 ,2 ]
Yang, Huijuan [5 ]
Sheng, Tian [3 ]
Yan, Yifan [4 ]
Wang, Tao [1 ,2 ]
Chen, Zhixin [1 ,2 ]
Tian, Na [1 ,2 ]
Li, Xifei [5 ]
Zhou, Zhi-You [1 ,2 ]
Sun, Shi-Gang [1 ,2 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Tan Kah Kee Innovat Lab, Xiamen 361005, Peoples R China
[3] Anhui Normal Univ, Coll Chem & Mat Sci, Wuhu 241000, Peoples R China
[4] Univ Oxford, Dept Chem, Chem Res Lab, Oxford OX1 3TA, England
[5] Xian Univ Technol, Inst Adv Electrochem Energy, Shaanxi Int Joint Res Ctr Surface Technol Energy S, Sch Mat Sci & Engn, Xian 710048, Peoples R China
基金
中国国家自然科学基金;
关键词
CO tolerance; hydrogen oxidation reaction; thermal segregation; RuO2 blocking shell; proton exchange membrane fuel cells; PT-RU; ELECTROCATALYSIS; ADSORPTION; PLATINUM; ALLOY;
D O I
10.1021/acs.nanolett.4c02999
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CO poisoning in Pt-based anode catalysts significantly hampers the proton exchange membrane fuel cell (PEMFC) performance. Despite great advances in CO-tolerant catalysts, their effectiveness is often limited to fundamental three-electrode systems, which is inadequate for practical PEMFC applications. Herein, we present a straightforward thermal oxidation strategy for constructing a Ru oxide blocking layer on commercial PtRu/C through a one-step Ru-segregation-and-oxidation process. The resulting 0.7 nm thick Ru oxide layer effectively inhibits CO adsorption while maintaining hydrogen oxidation activity. PtRu@RuO2/C demonstrates exceptional CO tolerance, enduring 1% CO in rotating disk electrode tests, an similar to 10-fold improvement compared to that of PtRu/C. Crucially, it retains high HOR activity and CO tolerance in PEMFC, with negligible polarization curve loss in the presence of 100 ppm CO. Notably, 85% HOR activity is retained after a 4 h stability test. This enhancement contributes to the Ru oxide layer decelerating CO adsorption kinetics, rather than promoting CO oxidation via the classic bifunctional mechanism.
引用
收藏
页码:10642 / 10649
页数:8
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