Journal
JOULE
Volume 3, Issue 1, Pages 124-135Publisher
CELL PRESS
DOI: 10.1016/j.joule.2018.09.016
Keywords
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Funding
- US Department of Energy (DOE), Energy Efficiency and Renewable Energy, Fuel Cell Technologies Office
- Los Alamos National Security, LLC [DE-AC52-06NA25396]
- US DOE [DE-AC02-06CH11357]
- Canadian Light Source
- National Science Foundation Graduate Research Fellowship [1644760]
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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.
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