Aqueous Phase Approach to Au-Modified Pt-Co/C toward Efficient and Durable Cathode Catalyst of PEMFCs

被引:8
作者
Ding, Chen [1 ]
Mao, Zijie [1 ]
Liang, Jia-Shun [2 ]
Qin, Xianxian [1 ]
Zhang, Qing [3 ]
Yang, Fan [3 ]
Li, Qing [2 ]
Cai, Wen-Bin [1 ]
机构
[1] Fudan Univ, Collaborat Innovat Ctr Chem Energy Mat, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200438, Peoples R China
[2] Huazhong Univ Sci & Technol, State Key Lab Mat Proc & Die & Mould Technol, Sch Mat Sci & Engn, Wuhan 430074, Hubei, Peoples R China
[3] Shanghai Tech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
关键词
OXYGEN REDUCTION ACTIVITY; ELECTROCATALYSTS; CARBON; NANOPARTICLES; TRANSITION; STABILITY;
D O I
10.1021/acs.jpcc.1c07696
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 commercialization of proton exchange membrane fuel cells (PEMFCs) calls for the development of active and durable Pt-based catalysts for oxygen reduction reaction (ORR) by means of a cost-effective and environmentally benign protocol. We report herein an all aqueous phase preparation of carbon supported Au-modified Pt-Co alloy catalyst (Au/PtCo/C), which involves the dimethylamine borane co-reduction of aqueous Pt(II) and Co(II) precursors to form a Pt-Co/C catalyst and the ethanol reduction of an aqueous Au(III) precursor to form Au/Pt-Co/C. This Au/PtCo/C catalyst not only shows a greatly enhanced ORR activity like the homemade Pt-Co/C and state-of-art Pt-Co/C(com) catalysts as compared to the Pt/C catalyst but also exhibits a much higher durability over the Pt/ C(com), homemade Pt-Co/C, and state-of-art Pt-Co/C(com) catalysts in accelerated degradation tests (ADTs) with both half-cell and single-cell configurations. Specifically, the maximum power density of a PEMFC involving the Au/Pt-Co/C cathode suffers only a 6% loss after 30 000 cycles of a standard ADT while that involving the state-of-art Pt-Co/C(com) suffers a 37% loss. This research provides an alternative route to prepare efficient and durable Pt-based ORR catalysts toward a widespread application of PEMFCs.
引用
收藏
页码:23821 / 23829
页数:9
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