Hard-Magnet L10-CoPt Nanoparticles Advance Fuel Cell Catalysis

被引:432
作者
Li, Junrui [1 ]
Sharma, Shubham [2 ]
Liu, Xiaoming [3 ]
Pan, Yung-Tin [4 ]
Spendelow, Jacob S. [4 ]
Chi, Miaofang [3 ]
Jia, Yukai [5 ]
Zhang, Peng [5 ]
Cullen, David A. [6 ]
Xi, Zheng [1 ]
Lin, Honghong [1 ]
Yin, Zhouyang [1 ]
Shen, Bo [1 ]
Muzzio, Michelle [1 ]
Yu, Chao [1 ]
Kim, Yu Seung [4 ]
Peterson, Andrew A. [2 ]
More, Karren L. [3 ]
Zhu, Huiyuan [7 ]
Sun, Shouheng [1 ]
机构
[1] Brown Univ, Dept Chem, Providence, RI 02912 USA
[2] Brown Univ, Sch Engn, Providence, RI 02912 USA
[3] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci Div, Oak Ridge, TN 37831 USA
[4] Los Alamos Natl Lab, Mat Phys & Applicat Div, Los Alamos, NM 87545 USA
[5] Dalhousie Univ, Dept Chem, Halifax, NS B3H 4R2, Canada
[6] Oak Ridge Natl Lab, Mat Sci & Technol Div, Oak Ridge, TN 37831 USA
[7] Oak Ridge Natl Lab, Chem Sci Div, Oak Ridge, TN 37831 USA
基金
美国国家科学基金会;
关键词
OXYGEN REDUCTION; ALLOY NANOPARTICLES; FEPT NANOPARTICLES; NANOWIRES; STRAIN; COPT;
D O I
10.1016/j.joule.2018.09.016
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
Stabilizing transition metals (M) in MPt alloy under acidic conditions is challenging, yet crucial to boost Pt catalysis toward oxygen reduction reaction (ORR). We synthesized similar to 9 nm hard-magnet core/shell L1(0)-CoPt/Pt nanoparticles with 2-3 atomic layers of strained Pt shell for ORR. At 60 degrees C in acid, the hard-magnet L1(0)-CoPt better stabilizes Co (5% loss after 24 hr) than soft-magnet A1-CoPt (34% loss in 7 hr). L1(0)-CoPt/Pt achievesmass activities (MA) of 0.56 A/mg(Pt) initially and 0.45 A/mg(Pt) after 30,000 voltage cycles in the membrane electrode assembly at 80 degrees C, exceeding the DOE 2020 targets on Pt activity and durability (0.44 A/mg(Pt) in MA and < 40% loss in MA after 30,000 cycles). Density functional theory calculations suggest that the ligand effect of Co and the biaxial strain (-4.50%/-4.25%) of the Pt shell weaken the binding of oxygenated species, leading to enhanced ORR performance in fuel cells.
引用
收藏
页码:124 / 135
页数:12
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