Gold-promoted structurally ordered intermetallic palladium cobalt nanoparticles for the oxygen reduction reaction

被引:145
|
作者
Kuttiyiel, Kurian A. [1 ]
Sasaki, Kotaro [1 ]
Su, Dong [2 ]
Wu, Lijun [3 ]
Zhu, Yimei [3 ]
Adzic, Radoslav R. [1 ]
机构
[1] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
[2] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
[3] Brookhaven Natl Lab, Dept Condensed Matter Phys & Mat Sci, Upton, NY 11973 USA
来源
NATURE COMMUNICATIONS | 2014年 / 5卷
关键词
MEMBRANE FUEL-CELLS; SUPPORTED PD-CO; ALLOY ELECTROCATALYSTS; SHELL ELECTROCATALYSTS; HEAT-TREATMENT; PARTICLE-SIZE; MONOLAYER; CATALYSTS; PLATINUM; ALKALINE;
D O I
10.1038/ncomms6185
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Considerable efforts to make palladium and palladium alloys active catalysts and a possible replacement for platinum have had a marginal success. Here we report on a structurally ordered Au10Pd40Co50 catalyst that exhibits comparable activity to conventional platinum catalysts in both acid and alkaline media. Electron microscopic techniques demonstrate that, at elevated temperatures, palladium cobalt nanoparticles undergo an atomic structural transition from core-shell to a rare intermetallic ordered structure with twin boundaries forming stable {111}, {110} and {100} facets via addition of gold atoms. The superior stability of this catalyst compared with platinum after 10,000 potential cycles in alkaline media is attributed to the atomic structural order of PdCo nanoparticles along with protective effect of clusters of gold atoms on the surface. This strategy of making ordered palladium intermetallic alloy nanoparticles can be used in diverse heterogeneous catalysis where particle size and structural stability matter.
引用
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页数:8
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